Next Generation Sequencing Competence Network

Next Generation Sequencing Competence Network

e.g. CCGA
(min 2 characters)

Per Hoffmann

Dr.
University of Bonn
Genomics, Institute for Human Genetics
Venusberg-Campus 1, 53127 Bonn, Germany
Bonn 53127
+49 228 68854
Download vCard

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Schumann G, Andreassen OA, Banaschewski T, Calhoun VD, Clinton N, Desrivieres S, Brandlistuen RE, Feng J, Hese S, Hitchen E, Hoffmann P, Jia T, Jirsa V, Marquand AF, Nees F, N?then MM, Novarino G, Polemiti E, Ralser M, Rapp M, Schepanski K, Schikowski T, Slater M, Sommer P, Stahl BC, Thompson PM, Twardziok S, van der Meer D, Walter H, Westlye L, environMENTAL Consortium. Addressing Global Environmental Challenges to Mental Health Using Population Neuroscience: A Review. JAMA Psychiatry. 2023 Oct 01; 80(10):1066-1074. PMID: 37610741.
      Citations: 1     Fields:    Translation:HumansPHPublic Health
    2. Hess T, Maj C, Gehlen J, Borisov O, Haas SL, Gockel I, Vieth M, Piessen G, Alakus H, Vashist Y, Pereira C, Knapp M, Sch?ller V, Quaas A, Grabsch HI, Trautmann J, Malecka-Wojciesko E, Mokrowiecka A, Speller J, Mayr A, Schr?der J, Hillmer AM, Heider D, Lordick F, P?rez-A?sa ?, Campo R, Espinel J, Geijo F, Thomson C, Bujanda L, Sope?a F, Lanas ?, Pellis? M, Pauligk C, Goetze TO, Zelck C, Reingruber J, Hassanin E, Elbe P, Alsabeah S, Lindblad M, Nilsson M, Kreuser N, Thieme R, Tavano F, Pastorino R, Arzani D, Persiani R, Jung JO, Nienh?ser H, Ott K, Schumann RR, Kumpf O, Burock S, Arndt V, Jakubowska A, Lawniczak M, Moreno V, Mart?n V, Kogevinas M, Poll?n M, Dabrowska J, Salas A, Cussenot O, Boland-Auge A, Daian D, Deleuze JF, Salvi E, Teder-Laving M, Tomasello G, Ratti M, Senti C, De Re V, Steffan A, H?lscher AH, Messerle K, Bruns CJ, Sivin? A, Bogdanova I, Skieceviciene J, Arstikyte J, Moehler M, Lang H, Grimminger PP, Kruschewski M, Vassos N, Schildberg C, Lingohr P, Ridwelski K, Lippert H, Fricker N, Krawitz P, Hoffmann P, N?then MM, Veits L, Izbicki JR, Mostowska A, Martin?n-Torres F, Cusi D, Adolfsson R, Cancel-Tassin G, H?blinger A, Rodermann E, Ludwig M, Keller G, Metspalu A, Brenner H, Heller J, Neef M, Schepke M, Dumoulin FL, Hamann L, Cannizzaro R, Ghidini M, Pla?mann D, Geppert M, Malfertheiner P, Glehen O, Skoczylas T, Majewski M, Lubinski J, Palmieri O, Boccia S, Latiano A, Aragones N, Schmidt T, Dinis-Ribeiro M, Medeiros R, Al-Batran SE, Leja M, Kupcinskas J, Garc?a-Gonz?lez MA, Venerito M, Schumacher J. Corrigendum to "Dissecting the genetic heterogeneity of gastric cancer". EBioMedicine. 2023 Aug; 94:104709. PMID: 37480624; PMCID: PMC10393529.
      Citations:    Fields:    
    3. Lechner L, Opitz R, Silver MJ, Krabusch PM, Prentice AM, Field MS, Stachelscheid H, Leit?o E, Schr?der C, Fernandez Vallone V, Horsthemke B, J?ckel KH, Schmidt B, N?then MM, Hoffmann P, Herms S, Kleyn PW, Megges M, Blume-Peytavi U, Weiss K, Mai K, Blankenstein O, Obermayer B, Wiegand S, K?hnen P. Early-set POMC methylation variability is accompanied by increased risk for obesity and is addressable by MC4R agonist treatment. Sci Transl Med. 2023 07 19; 15(705):eadg1659. PMID: 37467315.
      Citations: 1     Fields:    Translation:HumansCells
    4. Amare AT, Thalamuthu A, Schubert KO, Fullerton JM, Ahmed M, Hartmann S, Papiol S, Heilbronner U, Degenhardt F, Tekola-Ayele F, Hou L, Hsu YH, Shekhtman T, Adli M, Akula N, Akiyama K, Ardau R, Arias B, Aubry JM, Hasler R, Richard-Lepouriel H, Perroud N, Backlund L, Bhattacharjee AK, Bellivier F, Benabarre A, Bengesser S, Biernacka JM, Birner A, Marie-Claire C, Cervantes P, Chen HC, Chillotti C, Cichon S, Cruceanu C, Czerski PM, Dalkner N, Del Zompo M, DePaulo JR, ?tain B, Jamain S, Falkai P, Forstner AJ, Frisen L, Frye MA, Gard S, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Fallgatter AJ, Stegmaier S, Ethofer T, Biere S, Petrova K, Schuster C, Adorjan K, Budde M, Heilbronner M, Kalman JL, Kohshour MO, Reich-Erkelenz D, Schaupp SK, Schulte EC, Senner F, Vogl T, Anghelescu IG, Arolt V, Dannlowski U, Dietrich D, Figge C, J?ger M, Lang FU, Juckel G, Konrad C, Reimer J, Schmau? M, Schmitt A, Spitzer C, von Hagen M, Wiltfang J, Zimmermann J, Andlauer TFM, Fischer A, Bermpohl F, Ritter P, Matura S, Gryaznova A, Falkenberg I, Yildiz C, Kircher T, Schmidt J, Koch M, Gade K, Trost S, Haussleiter IS, Lambert M, Rohenkohl AC, Kraft V, Grof P, Hashimoto R, Hauser J, Herms S, Hoffmann P, Jim?nez E, Kahn JP, Kassem L, Kuo PH, Kato T, Kelsoe J, Kittel-Schneider S, Ferensztajn-Rochowiak E, K?nig B, Kusumi I, Laje G, Land?n M, Lavebratt C, Leboyer M, Leckband SG, Tortorella A, Manchia M, Martinsson L, McCarthy MJ, McElroy S, Colom F, Millischer V, Mitjans M, Mondimore FM, Monteleone P, Nievergelt CM, N?then MM, Nov?k T, O'Donovan C, Ozaki N, Pfennig A, Pisanu C, Potash JB, Reif A, Reininghaus E, Rouleau GA, Rybakowski JK, Schalling M, Schofield PR, Schweizer BW, Severino G, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Squassina A, Stamm T, Stopkova P, Maj M, Turecki G, Vieta E, Veeh J, Witt SH, Wright A, Zandi PP, Mitchell PB, Bauer M, Alda M, Rietschel M, McMahon FJ, Schulze TG, Clark SR, Baune BT. Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder. Mol Psychiatry. 2023 Jul 11. PMID: 37433967.
      Citations: 8     Fields:    
    5. Herrera-Rivero M, Guti?rrez-Fragoso K, Thalamuthu A, Amare AT, Adli M, Akiyama K, Akula N, Ardau R, Arias B, Aubry JM, Backlund L, Bellivier F, Benabarre A, Bengesser S, Abesh B, Biernacka J, Birner A, Cearns M, Cervantes P, Chen HC, Chillotti C, Cichon S, Clark S, Colom F, Cruceanu C, Czerski P, Dalkner N, Degenhardt F, Zompo MD, DePaulo JR, Etain B, Falkai P, Ferensztajn-Rochowiak E, Forstner AJ, Frank J, Frisen L, Frye M, Fullerton J, Gallo C, Gard S, Garnham J, Goes F, Grigoroiu-Serbanescu M, Grof P, Hashimoto R, Hasler R, Hauser J, Heilbronner U, Herms S, Hoffmann P, Hou L, Hsu Y, Jamain S, Jim?nez E, Kahn JP, Kassem L, Kato T, Kelsoe J, Kittel-Schneider S, Kuo PH, Kurtz J, Kusumi I, K?nig B, Laje G, Land?n M, Lavebratt C, Leboyer M, Leckband S, Maj M, Manchia M, Marie-Claire C, Martinsson L, McCarthy M, McElroy SL, Millischer V, Mitjans M, Mondimore F, Monteleone P, Nievergelt C, Novak T, N?then M, Odonovan C, Ozaki N, Papiol S, Pfennig A, Pisanu C, Potash J, Reif A, Reininghaus E, Richard-Lepouriel H, Roberts G, Rouleau G, Rybakowski JK, Schalling M, Schofield P, Schubert KO, Schulte E, Schweizer B, Severino G, Shekhtman T, Shilling P, Shimoda K, Simhandl C, Slaney C, Squassina A, Stamm T, Stopkova P, Streit F, Ayele F, Tortorella A, Turecki G, Veeh J, Vieta E, Viswanath B, Witt S, Zandi P, Alda M, Bauer M, McMahon F, Mitchell P, Rietschel M, Schulze T, Baune B. Immunogenetics of lithium response and psychiatric phenotypes in patients with bipolar disorder. Res Sq. 2023 Jun 26. PMID: 37461719; PMCID: PMC10350128.
      Citations:    
    6. Gl?ssner A, Wurpts G, R?seler S, Yazdi AS, Kr?mer C, Fatangare A, Sickmann A, Hoffmann P, N?then M, Sachs B. IFN-? secretion of PBMC from non-drug-allergic control persons: Considerations for the validity of a positive lymphocyte transformation test. J Immunol Methods. 2023 Aug; 519:113515. PMID: 37331693.
      Citations:    Fields:    Translation:HumansCells
    7. Hess T, Maj C, Gehlen J, Borisov O, Haas SL, Gockel I, Vieth M, Piessen G, Alakus H, Vashist Y, Pereira C, Knapp M, Sch?ller V, Quaas A, Grabsch HI, Trautmann J, Malecka-Wojciesko E, Mokrowiecka A, Speller J, Mayr A, Schr?der J, Hillmer AM, Heider D, Lordick F, P?rez-A?sa ?, Campo R, Espinel J, Geijo F, Thomson C, Bujanda L, Sope?a F, Lanas ?, Pellis? M, Pauligk C, Goetze TO, Zelck C, Reingruber J, Hassanin E, Elbe P, Alsabeah S, Lindblad M, Nilsson M, Kreuser N, Thieme R, Tavano F, Pastorino R, Arzani D, Persiani R, Jung JO, Nienh?ser H, Ott K, Schumann RR, Kumpf O, Burock S, Arndt V, Jakubowska A, Lawniczak M, Moreno V, Mart?n V, Kogevinas M, Poll?n M, Dabrowska J, Salas A, Cussenot O, Boland-Auge A, Daian D, Deleuze JF, Salvi E, Teder-Laving M, Tomasello G, Ratti M, Senti C, De Re V, Steffan A, H?lscher AH, Messerle K, Bruns CJ, Sivin? A, Bogdanova I, Skieceviciene J, Arstikyte J, Moehler M, Lang H, Grimminger PP, Kruschewski M, Vassos N, Schildberg C, Lingohr P, Ridwelski K, Lippert H, Fricker N, Krawitz P, Hoffmann P, N?then MM, Veits L, Izbicki JR, Mostowska A, Martin?n-Torres F, Cusi D, Adolfsson R, Cancel-Tassin G, H?blinger A, Rodermann E, Ludwig M, Keller G, Metspalu A, Brenner H, Heller J, Neef M, Schepke M, Dumoulin FL, Hamann L, Cannizzaro R, Ghidini M, Pla?mann D, Geppert M, Malfertheiner P, Gehlen O, Skoczylas T, Majewski M, Lubinski J, Palmieri O, Boccia S, Latiano A, Aragones N, Schmidt T, Dinis-Ribeiro M, Medeiros R, Al-Batran SE, Leja M, Kupcinskas J, Garc?a-Gonz?lez MA, Venerito M, Schumacher J. Dissecting the genetic heterogeneity of gastric cancer. EBioMedicine. 2023 Jun; 92:104616. PMID: 37209533; PMCID: PMC10212786.
      Citations: 1     Fields:    Translation:Humans
    8. Gehlen J, Stundl A, Debiec R, Fontana F, Sharipova D, Nelson CP, Al-Kassou B, Zelck CF, Koebbe LL, Braund PS, Webb TR, Hetherington S, Shrestha M, Krueger H, Siepe M, Kari FA, Kelm M, Veulemans V, Adam M, Baldus S, Karck M, Mehlhorn U, Conzelmann LO, Breitenbach I, Lebherz C, Kandels J, Ellinghaus D, Hoffmann P, Wirth F, Doppler S, Lahm H, von Scheidt M, Knoll K, Kessler T, Schunkert H, Nickenig G, Bolger AP, Abdelilah-Seyfried S, Samani NJ, Trenkwalder T, Schumacher J, Ensminger S, Fujita B, Mohamed SA, Nordbeck P, Buravezky L, Haas Y, Nowak-Goettl U, Dre?en M, N?then MM, Erdmann J, Krane M, Giel AS, Sinning JM, Bruenger CMH, Laugwitz KL, Urbanski P, Kim WK, Hengstenberg C. Elucidation of the genetic causes of bicuspid aortic valve disease. Cardiovasc Res. 2023 05 02; 119(3):857-866. PMID: 35727948; PMCID: PMC10153415.
      Citations: 4     Fields:    Translation:HumansAnimalsCells
    9. Zhao L, M?hleisen TW, Pelzer DI, Burger B, Beins EC, Forstner AJ, Herms S, Hoffmann P, Amunts K, Palomero-Gallagher N, Cichon S. Relationships between neurotransmitter receptor densities and expression levels of their corresponding genes in the human hippocampus. Neuroimage. 2023 06; 273:120095. PMID: 37030412; PMCID: PMC10167541.
      Citations: 1     Fields:    Translation:Humans
    10. Yde Ohki CM, Walter NM, Rickli M, Van Puyenbroeck P, D?ring C, Hoffmann P, Herms S, Maria Werling A, Walitza S, Gr?nblatt E. Generation of induced pluripotent stem cells from two ADHD patients and two healthy controls. Stem Cell Res. 2023 06; 69:103084. PMID: 37004448.
      Citations: 1     Fields:    Translation:HumansCells
    11. Garnham J, Goes F, Amare A, Thalamuthu A, Schubert KO, Fullerton J, Ahmed M, Hartmann S, Papiol S, Heilbronner U, Degenhardt F, Tekola-Ayele F, Hou L, Hsu YH, Shekhtman T, Adli M, Akula N, Akiyama K, Ardau R, Arias B, Aubry JM, Backlund L, Bhattacharjee AK, Bellivier F, Benabarre A, Bengesser S, Biernacka J, Birner A, Marie-Claire C, Cervantes P, Chen HC, Chillotti C, Cichon S, Cruceanu C, Czerski P, Dalkner N, Del Zompo M, DePaulo JR, Etain B, Jamain S, Falkai P, Forstner AJ, Fris?n L, Frye M, Gard S, Grigoroiu-Serbanescu M, Fallgatter A, Stegmaier S, Ethofer T, Biere S, Petrova K, Schuster C, Adorjan K, Budde M, Heilbronner M, Kalman J, Oraki Kohshour M, Reich-Erkelenz D, Schaupp S, Schulte E, Senner F, Vogl T, Anghelescu IG, Arolt V, Dannlowski U, Dietrich DE, Figge C, J?ger M, Lang F, Juckel G, Spitzer C, Reimer J, Schmau? M, Schmitt A, Konrad C, von Hagen M, Wiltfang J, Zimmermann J, Andlauer T, Fischer A, Bermpohl F, Kraft V, Matura S, Gryaznova A, Falkenberg I, Yildiz C, Kircher T, Schmidt J, Koch M, Gade K, Trost S, Hau?leiter I, Lambert M, Rohenkohl AC, Kraft V, Grof P, Hashimoto R, Hauser J, Herms S, Hoffmann P, Jim?nez E, Kahn JP, Kassem L, Kuo PH, Kato T, Kelsoe J, Kittel-Schneider S, Ferensztajn-Rochowiak E, K?nig B, Kusumi I, Laje G, Land?n M, Lavebratt C, Leboyer M, Leckband SG, Tortorella A, Manchia M, Martinsson L, McCarthy M, McElroy SL, Colom F, Mitjans M, Mondimore F, Monteleone P, Nievergelt C, N?then M, Novak T, O'Donovan C, Ozaki N, Pfennig A, Pisanu C, Potash J, Reif A, Reininghaus E, Rouleau G, Rybakowski JK, Schalling M, Schofield P, Schweizer BW, Severino G, Shilling PD, Shimoda K, Simhandl C, Slaney C, Squassina A, Stamm T, Stopkova P, Maj M, Turecki G, Vieta E, Veeh J, Witt S, Wright A, Zandi P, Mitchell P, Bauer M, Alda M, Rietschel M, McMahon F, Schulze TG, Millischer V, Clark S, Baune B. Association of Polygenic Score and the involvement of Cholinergic and Glutamatergic Pathways with Lithium Treatment Response in Patients with Bipolar Disorder. Res Sq. 2023 Feb 14. PMID: 36824922; PMCID: PMC9949170.
      Citations:    
    12. de Rojas I, Moreno-Grau S, Tesi N, Grenier-Boley B, Andrade V, Jansen IE, Pedersen NL, Stringa N, Zettergren A, Hern?ndez I, Montrreal L, Ant?nez C, Antonell A, Tankard RM, Bis JC, Sims R, Bellenguez C, Quintela I, Gonz?lez-Perez A, Calero M, Franco-Mac?as E, Mac?as J, Blesa R, Cervera-Carles L, Men?ndez-Gonz?lez M, Frank-Garc?a A, Royo JL, Moreno F, Huerto Vilas R, Baquero M, Diez-Fairen M, Lage C, Garc?a-Madrona S, Garc?a-Gonz?lez P, Alarc?n-Mart?n E, Valero S, Sotolongo-Grau O, Ullgren A, Naj AC, Lemstra AW, Benaque A, P?rez-Cord?n A, Benussi A, R?bano A, Padovani A, Squassina A, de Mendon?a A, Arias Pastor A, Kok AAL, Meggy A, Pastor AB, Espinosa A, Corma-G?mez A, Mart?n Montes A, Sanabria ?, DeStefano AL, Schneider A, Haapasalo A, Kinhult St?hlbom A, Tybj?rg-Hansen A, Hartmann AM, Spottke A, Corbat?n-Anchuelo A, Rongve A, Borroni B, Arosio B, Nacmias B, Nordestgaard BG, Kunkle BW, Charbonnier C, Abdelnour C, Masullo C, Mart?nez Rodr?guez C, Mu?oz-Fernandez C, Dufouil C, Graff C, Ferreira CB, Chillotti C, Reynolds CA, Fenoglio C, Van Broeckhoven C, Clark C, Pisanu C, Satizabal CL, Holmes C, Buiza-Rueda D, Aarsland D, Rujescu D, Alcolea D, Galimberti D, Wallon D, Seripa D, Gr?nblatt E, Dardiotis E, D?zel E, Scarpini E, Conti E, Rubino E, Gelpi E, Rodriguez-Rodriguez E, Duron E, Boerwinkle E, Ferri E, Tagliavini F, K???kali F, Pasquier F, Sanchez-Garcia F, Mangialasche F, Jessen F, Nicolas G, Selb?k G, Ortega G, Ch?ne G, Hadjigeorgiou G, Rossi G, Spalletta G, Giaccone G, Grande G, Binetti G, Papenberg G, Hampel H, Bailly H, Zetterberg H, Soininen H, Karlsson IK, Alvarez I, Appollonio I, Giegling I, Skoog I, Saltvedt I, Rainero I, Rosas Allende I, Hort J, Diehl-Schmid J, Van Dongen J, Vidal JS, Lehtisalo J, Wiltfang J, Thomassen JQ, Kornhuber J, Haines JL, Vogelgsang J, Pineda JA, Fortea J, Popp J, Deckert J, Buerger K, Morgan K, Flie?bach K, Sleegers K, Molina-Porcel L, Kilander L, Weinhold L, Farrer LA, Wang LS, Kleineidam L, Farotti L, Parnetti L, Tremolizzo L, Hausner L, Benussi L, Froelich L, Ikram MA, Deniz-Naranjo MC, Tsolaki M, Rosende-Roca M, L?wenmark M, Hulsman M, Spallazzi M, Pericak-Vance MA, Esiri M, Bernal S?nchez-Arjona M, Dalmasso MC, Mart?nez-Larrad MT, Arcaro M, N?then MM, Fern?ndez-Fuertes M, Dichgans M, Ingelsson M, Herrmann MJ, Scherer M, Vyhnalek M, Kosmidis MH, Yannakoulia M, Schmid M, Ewers M, Heneka MT, Wagner M, Scamosci M, Kivipelto M, Hiltunen M, Zulaica M, Alegret M, Fornage M, Roberto N, van Schoor NM, Seidu NM, Banaj N, Armstrong NJ, Scarmeas N, Scherbaum N, Goldhardt O, Hanon O, Peters O, Skrobot OA, Quenez O, Lerch O, Boss? P, Caffarra P, Dionigi Rossi P, Sakka P, Mecocci P, Hoffmann P, Holmans PA, Fischer P, Riederer P, Yang Q, Marshall R, Kalaria RN, Mayeux R, Vandenberghe R, Cecchetti R, Ghidoni R, Frikke-Schmidt R, Sorbi S, H?gg S, Engelborghs S, Helisalmi S, Botne Sando S, Kern S, Archetti S, Boschi S, Fostinelli S, Gil S, Mendoza S, Mead S, Ciccone S, Djurovic S, Heilmann-Heimbach S, Riedel-Heller S, Kuulasmaa T, Del Ser T, Lebouvier T, Polak T, Ngandu T, Grimmer T, Bessi V, Escott-Price V, Giedraitis V, Deramecourt V, Maier W, Jian X, Pijnenburg YAL, EADB contributors, GR@ACE study group, DEGESCO consortium, IGAP (ADGC, CHARGE, EADI, GERAD), PGC-ALZ consortia, Kehoe PG, Garcia-Ribas G, S?nchez-Juan P, Pastor P, P?rez-Tur J, Pi?ol-Ripoll G, Lopez de Munain A, Garc?a-Alberca JM, Bullido MJ, ?lvarez V, Lle? A, Real LM, Mir P, Medina M, Scheltens P, Holstege H, Marqui? M, S?ez ME, Carracedo ?, Amouyel P, Schellenberg GD, Williams J, Seshadri S, van Duijn CM, Mather KA, S?nchez-Valle R, Serrano-R?os M, Orellana A, T?rraga L, Blennow K, Huisman M, Andreassen OA, Posthuma D, Clarim?n J, Boada M, van der Flier WM, Ramirez A, Lambert JC, van der Lee SJ, Ruiz A. Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores. Nat Commun. 2023 Feb 09; 14(1):716. PMID: 36759603; PMCID: PMC9911386.
      Citations:    Fields:    
    13. David FS, Stein F, Andlauer TFM, Streit F, Witt SH, Herms S, Hoffmann P, Heilmann-Heimbach S, Opel N, Repple J, Jansen A, Nenadic I, Papiol S, Heilbronner U, Kalman JL, Schaupp SK, Senner F, Schulte EC, Falkai PG, Schulze TG, Dannlowski U, Kircher T, Rietschel M, N?then MM, Krug A, Forstner AJ. Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders. Schizophr Res. 2023 02; 252:161-171. PMID: 36652833.
      Citations: 3     Fields:    Translation:Humans
    14. Degenhardt F, Ellinghaus D, Juzenas S, Wendorff M, Uellendahl-Werth F, ElAbd H, Arora J, Wacker EM, Wienbrandt L, Palom A, Garcia-Fernandez AE, Blanco-Grau A, Zanella A, Holten AR, Bandera A, Cherubini A, Gerussi A, Ramirez A, Nebel A, Barreira A, Ganna A, Gori A, Lind A, Tanck A, Hinney A, Fracanzani AL, Peschuck A, Cavallero A, Dyrhol-Riise AM, Ruello A, Muscatello A, Pesenti A, Rando-Segura A, Schmidt A, Bellinghausen C, Scollo C, Gassner C, Paccapelo C, Lehmann C, Angelini C, COVICAT study group, Aachen Study (COVAS), Bianco C, Cea C, Sancho C, Hoff DAL, Galimberti D, Prati D, Haschka D, Toapanta D, Sandoval E, Binatti E, Scarpini E, Urrechaga E, Pontali E, Reverter E, Arana-Arri E, Ceriotti F, Malvestiti F, Medrano FJ, Hanses F, Hemmrich-Stanisak G, Bellani G, Grasselli G, Pezzoli G, Costantino G, Albano G, Bellelli G, Citerio G, Foti G, Lamorte G, Baselli G, Kurihara H, Neb H, Kurth I, Pink I, Holter JC, Rybniker J, Dopazo J, Bergan J, Barretina J, Goikoetxea J, Fazaal J, Risnes K, Banasik K, Tonby K, Sumoy L, Terranova L, Knopp L, Gustad LT, Garbarino L, Santoro L, Ostadreza M, Intxausti M, Berger MM, Schaefer M, Niemi MEK, Carrabba M, Figuera Basso ME, Valsecchi MG, Vehreschild MJGT, Manunta M, Acosta-Herrera M, Baldini M, Grimsrud MM, Cornberg M, Castoldi M, Cordioli M, D'Amato M, Augustin M, Tomasi M, Seilmaier MJ, Joannidis M, Wittig M, Mazzocco M, Ciccarelli M, Bocciolone M, Miozzo M, Chueca N, Montano N, Braun N, Marx N, Norwegian SARS-CoV-2 Study group, Witzke O, Palmieri O, Pa Study Group, Faverio P, Preatoni P, Bonfanti P, Omodei P, Castro P, Hoffmann P, Rosenstiel P, Schommers P, Ferrer R, Gualtierotti R, Carpani R, Ciesek S, May S, Marsal S, Pigazzini S, Klein S, Pelusi S, Wilfling S, Bosari S, Volland S, Raychaudhuri S, Schreiber S, Heilmann-Heimbach S, Dudman S, Wesse T, Zheng T, STORM Study group, The Humanitas Task Force, The Humanitas Gavazzeni Task Force, Eggermann T, Illig T, Brenner T, Pumarola T, Feldt T, Folseraas T, Monzani V, Keitel V, Kopfnagel V, Andrade V, Albrecht W, Peter W, Yi X, Khodamoradi Y, Latiano A, Bacher P, Tran F, Ludwig KU, Invernizzi P, Hov JR, Valenti L, Karlsen TH, Franke A, Lenning OB, Myhre R, Vadla MS, Garrido Chercoles A, Mantovani A, Protti A, Aghemo A, Lleo A, Biondi A, Caballero-Garralda A, Carreras Nolla A, Voza A, Cortes B, Nafria-Jimenez B, Schaefer B, Maj C, Herr C, Spinner CD, Hu C, Cappadona C, Azzolini E, Paraboschi EM, Contro E, Martinelli-Boneschi F, Peyvandi F, Blasi F, Cardamone G, My I, de Rojas I, Afset JE, Schneider J, Gaede KI, Heggelund L, Bettini LR, Nkambule L, Cazzaniga M, Cecconi M, Dreher M, Imaz Ayo N, Blay N, Ludwig N, Cornely OA, Tentorio P, Bals R, Badalamenti S, Bombace S, Aliberti S, Gonzalez Cejudo T, Rimoldi V, Farre X, Goerg S, Koehler P, Zoller H, Duga S, Asselta R, de Cid R, Lerga-Jaso J, Maya-Miles D, R?hlemann MC, ?zer O, Blandino Ortiz A, de Salazar A, Ruiz A, Mayer A, Braun A, Teles A, Kildal AB, Gl?ck A, Juli? A, Solier A, Mateos B, Jensen B, Ferrando C, de la Horra C, Quereda C, Skurk C, Thibeault C, Lange C, Azuure C, Jim?nez D, Pesta?a D, Mu?iz-Diaz E, Helbig ET, Casalone E, Calder?n EJ, Navas E, Sollig?rd E, Aziz F, Garcia F, Garc?a S?nchez F, Kurth F, Mesonero F, Rodriguez-Frias F, M?ller F, Matullo G, Hern?ndez I, Galv?n-Femenia I, Heyckendorf J, K?ssens J, Dam?s JK, Altm?ller J, Ampuero J, Mart?n J, Erdmann J, Banales JM, Badia JR, Walter J, Hern?ndez Quero J, Delgado J, Guerrero JM, Kraft J, Schr?der J, M?ller KE, Garcia-Etxebarria K, Izquierdo-Sanchez L, Sander LE, Lippert LJ, T?llez L, Roade L, Kogevinas M, Riveiro-Barciela M, Guti?rrez-Stampa MA, Hernandez-Tejero M, D'Angi? M, N?then MM, Marqui? M, Boada M, Rodr?guez-Gand?a M, Mart?nez N, et al. Detailed stratified GWAS analysis for severe COVID-19 in four European populations. Hum Mol Genet. 2022 11 28; 31(23):3945-3966. PMID: 35848942; PMCID: PMC9703941.
      Citations: 28     Fields:    Translation:HumansCells
    15. Tielke A, Martins H, Pelzl MA, Maaser-Hecker A, David FS, Reinbold CS, Streit F, Sirignano L, Schwarz M, Vedder H, Kammerer-Ciernioch J, Albus M, Borrmann-Hassenbach M, Hautzinger M, H?nten K, Degenhardt F, Fischer SB, Beins EC, Herms S, Hoffmann P, Schulze TG, Witt SH, Rietschel M, Cichon S, N?then MM, Schratt G, Forstner AJ. Genetic and functional analyses implicate microRNA 499A in bipolar disorder development. Transl Psychiatry. 2022 10 07; 12(1):437. PMID: 36207305; PMCID: PMC9547016.
      Citations: 2     Fields:    Translation:Humans
    16. Fritz N, Berens S, Dong Y, Mart?nez C, Schmitteckert S, Houghton LA, Goebel-Stengel M, Wahl V, Kabisch M, G?tze D, D'Amato M, Zheng T, R?th R, M?nnikes H, Tesarz J, Engel F, Gauss A, Raithel M, Andresen V, Keller J, Frieling T, Pehl C, Stein-Th?ringer C, Clarke G, Kennedy PJ, Cryan JF, Dinan TG, Quigley EMM, Spiller R, Beltr?n C, Madrid AM, Torres V, Mayer EA, Sayuk G, Gazouli M, Karamanolis G, Bustamante M, Estivil X, Rabionet R, Hoffmann P, N?then MM, Heilmann-Heimbach S, Schmidt B, Franke A, Lieb W, Herzog W, Boeckxstaens G, Wouters MM, Simr?n M, Rappold GA, Vicario M, Santos J, Schaefert R, Lorenzo-Bermejo J, Niesler B. The serotonin receptor 3E variant is a risk factor for female IBS-D. J Mol Med (Berl). 2022 Nov; 100(11):1617-1627. PMID: 36121467; PMCID: PMC9592668.
      Citations: 1     Fields:    Translation:Humans
    17. Kumar V, Pouw RB, Autio MI, Sagmeister MG, Phua ZY, Borghini L, Wright VJ, Hoggart C, Pan B, Tan AKY, Binder A, Brouwer MC, Pinnock E, De Groot R, Hazelzet J, Emonts M, Van Der Flier M, Reiter K, N?then MM, Hoffmann P, EUCLIDS consortium, Schlapbach LJ, Bellos E, Anderson S, Secka F, Martin?n-Torres F, Salas A, Fink C, Carrol ED, Pollard AJ, Coin LJ, Zenz W, Wouters D, Ang LT, Hibberd ML, Levin M, Kuijpers TW, Davila S. Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrations. Am J Hum Genet. 2022 Sep 01; 109(9):1680-1691. PMID: 36007525; PMCID: PMC9502058.
      Citations: 2     Fields:    Translation:Humans
    18. Ludwig KU, Schmithausen RM, Li D, Jacobs ML, Hollstein R, Blumenstock K, Liebing J, Slabicki M, Ben-Shmuel A, Israeli O, Weiss S, Ebert TS, Paran N, Wilbring G, Feldman D, Ishorst N, Hochfeld LM, Beins EC, Kaltheuner IH, Schmitz M, Sib E, Jentzsch M, Moench EC, Borrajo JD, Strecker J, Reinhardt J, Cleary B, Geyer M, Macrae R, Hoffmann P, Exner M, Regev A, Zhang F, Schmid-Burgk JL, R?diger W, Lippke B, W?hler A, D?hla M, H?lzel M, N?then MM. Author Correction: LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding. Nat Biotechnol. 2022 Aug; 40(8):1295. PMID: 35851378; PMCID: PMC9294830.
      Citations:    Fields:    
    19. Cearns M, Amare AT, Schubert KO, Thalamuthu A, Frank J, Streit F, Adli M, Akula N, Akiyama K, Ardau R, Aubry J, Backlund L, Bhattacharjee AK, Bellivier F, Benabarre A, Bengesser S, Biernacka JM, Birner A, Brichant-Petitjean C, Cervantes P, Chen H, Chillotti C, Cichon S, Cruceanu C, Czerski PM, Dalkner N, Dayer A, Degenhardt F, Zompo MD, DePaulo JR, Falkai P, Forstner AJ, Frisen L, Frye MA, Fullerton JM, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Grof P, Hashimoto R, Hauser J, Heilbronner U, Herms S, Hoffmann P, Hofmann A, Hou L, Hsu YH, Jamain S, Kahn JP, Kassem L, Kuo PH, Kato T, Kelsoe J, Kittel-Schneider S, Kliwicki S, Kusumi I, Laje G, Lavebratt C, Leboyer M, Leckband SG, Maj M, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Manchia M, Martinsson L, McCarthy MJ, McElroy S, Colom F, Mitjans M, Mondimore FM, Monteleone P, Nievergelt CM, O'Donovan C, Ozaki N, Millischer V, Papiol S, Pfennig A, Pisanu C, Potash JB, Reif A, Reininghaus E, Rouleau GA, Rybakowski JK, Schalling M, Schofield PR, Schweizer BW, Severino G, Shekhtman T, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Squassina A, Stamm T, Stopkova P, TekolaAyele F, Tortorella A, Turecki G, Veeh J, Vieta E, Witt SH, Roberts G, Zandi PP, Alda M, Bauer M, McMahon FJ, Mitchell PB, Schulze TG, Rietschel M, Clark SR, Baune BT, Arias B, ?tain B, Gard S, Jim?nez E, K?nig B, Land?n M, N?then MM, Nov?k T. Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach - CORRIGENDUM. Br J Psychiatry. 2022 08; 221(2):494. PMID: 35505515.
      Citations: 1     Fields:    Translation:Humans
    20. Mathey CM, Maj C, Scheer AB, Fazaal J, Wedi B, Wieczorek D, Amann PM, L?ffler H, Koch L, Sch?ffl C, Dickel H, Ganjuur N, Hornung T, Forkel S, Greve J, Wurpts G, Hallberg P, Bygum A, Von Buchwald C, Karawajczyk M, Steffens M, Stingl J, Hoffmann P, Heilmann-Heimbach S, Mangold E, Ludwig KU, Rasmussen ER, Wadelius M, Sachs B, N?then MM, Forstner AJ. Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes. Front Genet. 2022; 13:914376. PMID: 35923707; PMCID: PMC9339951.
      Citations: 2     
    21. Schubert KO, Thalamuthu A, Amare AT, Frank J, Streit F, Akula N, Akiyama K, Ardau R, Aubry JM, Backlund L, Bhattacharjee AK, Benabarre A, Bengesser S, Biernacka JM, Birner A, Cearns M, Cervantes P, Chen HC, Chillotti C, Cichon S, Clark SR, Cruceanu C, Czerski PM, Dalkner N, Dayer A, Degenhardt F, Del Zompo M, DePaulo JR, Falkai P, Forstner AJ, Frisen L, Frye MA, Fullerton JM, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Grof P, Hashimoto R, Hauser J, Heilbronner U, Herms S, Hoffmann P, Hou L, Hsu YH, Kassem L, Kuo PH, Kato T, Kelsoe J, Kittel-Schneider S, Ferensztajn-Rochowiak E, Kusumi I, Laje G, Lavebratt C, Leckband SG, Maj M, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Manchia M, Martinsson L, McCarthy MJ, McElroy S, Colom F, Mondimore FM, Monteleone P, Nievergelt CM, O'Donovan C, Ozaki N, Papiol S, Pisanu C, Potash JB, Reif A, Reininghaus E, Rouleau GA, Rybakowski JK, Schalling M, Schofield PR, Schweizer BW, Severino G, Shekhtman T, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Squassina A, Stopkova P, Tekola-Ayele F, Tortorella A, Turecki G, Veeh J, Vieta E, Witt SH, Roberts G, Zandi PP, Alda M, McMahon FJ, Mitchell PB, Schulze TG, Rietschel M, Adl M, Arias B, Bellivier F, Marie-Claire C, ?tain B, Gard S, Jamain S, Jim?nez E, Kahn JP, K?nig B, Land?n M, Leboyer M, Mitjans M, N?then MM, Nov?k T, ?sby U, Pfennig A, Stamm T, Bauer M, Baune BT. Correction: Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients. Transl Psychiatry. 2022 Jul 11; 12(1):278. PMID: 35817769; PMCID: PMC9273602.
      Citations:    Fields:    
    22. Tremmel R, Nies AT, van Eijck BAC, Handin N, Haag M, Winter S, Klein F, Mazzola P, Hofmann U, Klein K, Hoffmann P, Gaugaz FZ, Artursson P, Schwab M, Schaeffeler E, B?ttner FA, K?lz C, N?then MM. Hepatic Expression of the Na+-Taurocholate Cotransporting Polypeptide Is Independent from Genetic Variation. Int J Mol Sci. 2022 Jul 05; 23(13). PMID: 35806468; PMCID: PMC9267852.
      Citations: 2     Fields:    Translation:HumansCells
    23. Zillich L, Poisel E, Frank J, Foo JC, Friske MM, Streit F, Sirignano L, Heilmann-Heimbach S, Hoffmann P, Degenhardt F, Hansson AC, Bakalkin G, Rietschel M, Spanagel R, Witt SH, Heimbach A, N?then MM. Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum. Transl Psychiatry. 2022 05 06; 12(1):190. PMID: 35523767; PMCID: PMC9076849.
      Citations: 7     Fields:    Translation:Humans
    24. Clay-Gilmour A, Chattopadhyay S, Hildebrandt MAT, Thomsen H, Weinhold N, Vodicka P, Vodickova L, Hoffmann P, Langer C, Hajek R, Pettersson-Kymmer U, Ohlsson C, Houlston R, Goldschmidt H, Manasanch EE, Norman A, Kumar S, Rajkumar SV, Slager S, Vachon CM, Hemminki K, N?then MM, J?ckel KH, Schmidt B, Hallmans G, Sp?th F, F?rsti A. Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6. Blood Cancer J. 2022 04 13; 12(4):60. PMID: 35418122; PMCID: PMC9007981.
      Citations:    Fields:    Translation:Humans
    25. Qi T, Bigdeli TB, Bryois J, Chen CY, Dennison CA, Hall LS, Lam M, Watanabe K, Frei O, Ge T, Harwood JC, Koopmans F, Magnusson S, Richards AL, Sidorenko J, Wu Y, Zeng J, Grove J, Kim M, Li Z, Voloudakis G, Zhang W, Adams M, Agartz I, Atkinson EG, Agerbo E, Al Eissa M, Albus M, Alexander M, Alizadeh BZ, Als TD, Amin F, Athanasiu L, Azevedo MH, Bacanu SA, Bass NJ, Belliveau RA, Benyamin B, Bergen SE, Blasi G, Bonassi S, Bromet EJ, Bruggeman R, Buckley PF, Buckner RL, Bybjerg-Grauholm J, Cahn W, Cairns MJ, Calkins ME, Carr VJ, Castle D, Catts SV, Chambert KD, Chan RCK, Cheng W, Cheung EFC, Chong SA, Curtis C, Davidson M, Davis KL, de Haan L, Degenhardt F, DeLisi LE, Demontis D, Dickerson F, Dikeos D, Dinan T, Djurovic S, Duan J, Ducci G, Dudbridge F, Eriksson JG, Faraone SV, Fiorentino A, Forstner A, Frank J, Freimer NB, Fromer M, Frustaci A, Genovese G, Gershon ES, Giegling I, Goldstein JI, Gopal S, Gratten J, Green MF, Greenwood TA, Guillin O, Gur RE, Gur RC, Hakonarson H, Haroutunian V, Hartmann AM, Harvey C, Hayward C, Henskens FA, Herms S, Hoffmann P, Howrigan DP, Ikeda M, Iyegbe C, Joa I, Kam-Thong T, Kamatani Y, Karachanak-Yankova S, Keller MC, Kelly BJ, Khrunin A, Kim SW, Klovins J, Kondratiev N, Konte B, Kubo M, Kucinskas V, Kucinskiene ZA, Kusumawardhani A, Kuzelova-Ptackova H, Landi S, Lazzeroni LC, Lee PH, Legge SE, Lehrer DS, Lerer B, Li M, Lieberman J, Light GA, Limborska S, Liu CM, Loughland CM, Lubinski J, Luykx JJ, Lynham A, Macek M, Mackinnon A, Magnusson PKE, Maher BS, Maier W, Malaspina D, Marder SR, Marsal S, Martin AR, Martorell L, Mattheisen M, McCarley RW, McDonald C, McGrath JJ, Medeiros H, Meier S, Melle I, Mesholam-Gately RI, Metspalu A, Michie PT, Milani L, Milanova V, Molden E, Molina E, Mondelli V, Morley CP, Murphy KC, Myin-Germeys I, Nestadt G, Nikitina-Zake L, Nuechterlein KH, O'Brien NL, O'Neill FA, Oh SY, Olincy A, Pantelis C, Papadimitriou GN, Paunio T, Pellegrino R, Periyasamy S, Perkins DO, Pimm J, Porteous D, Powell J, Quattrone D, Quested D, Radant AD, Rampino A, Rapaport MH, Rautanen A, Reichenberg A, Roe C, Roffman JL, Rutten BPF, Salomaa V, Savitz A, Schall U, Scott RJ, Seidman LJ, Sharp SI, Shi J, Siever LJ, Sigurdsson E, Sim K, Slominsky P, So HC, Sobell JL, Stain HJ, Steen NE, Stone WS, Straub RE, Streit F, Strengman E, Stroup TS, Subramaniam M, Sugar CA, Suvisaari J, Svrakic DM, Swerdlow NR, Szatkiewicz JP, Takahashi A, Terao C, Toncheva D, Tooney PA, Torretta S, Tosato S, Tura GB, Turetsky BI, Vaaler A, van Amelsvoort T, van Winkel R, Veijola J, Waddington J, Waterreus A, Webb BT, Weiser M, Williams NM, Witt SH, Wormley BK, Wu JQ, Xu Z, Yolken R, Zai CC, Zhou W, Zhu F, Zimprich F, Atbasoglu EC, Ayub M, Benner C, Bertolino A, Black DW, Bray NJ, Breen G, Buccola NG, Byerley WF, Chen WJ, Cloninger CR, Crespo-Facorro B, Donohoe G, Freedman R, Galletly C, Gandal MJ, Gennarelli M, Hougaard DM, Hwu HG, Jablensky AV, McCarroll SA, Moran JL, Mors O, Mortensen PB, Neil AL, Nordentoft M, Pato MT, Petryshen TL, Pirinen M, Pulver AE, Schulze TG, Silverman JM, Smoller JW, Stahl EA, Tsuang DW, Vilella E, Wang SH, Xu S, Indonesia Schizophrenia Consortium, PsychENCODE, Psychosis Endophenotypes International Consortium, SynGO Consortium, Braff D, Bramon E, Buxbaum JD, Campion D, Cervilla JA, Cichon S, Collier DA, Corvin A, Curtis D, Forti MD, Domenici E, Escott-Price V, Fanous AH, Gareeva A, Gejman PV, Gill M, Glatt SJ, Golimbet V, Hong KS, Hultman CM, Hyman SE, Iwata N, Kennedy JL, Khusnutdinova E, Kirov G, Knowles JA, Lee J, Lencz T, Levinson DF, Li QS, Liu J, Malhotra AK, Malhotra D, McIntosh A, McQuillin A, Morgan VA, Morris DW, Mowry BJ, Murray RM, Nimgaonkar V, Ophoff RA, Paciga SA, Palotie A, Pato CN, Qin S, Rietschel M, Riley BP, Rivera M, Rujescu D, Saka MC, Sanders AR, Schwab SG, Serretti A, Sham PC, Shi Y, St Clair D, Stefansson K, Tsuang MT, van Os J, Vawter MP, Weinberger DR, Werge T, Wildenauer DB, et al. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. 2022 04; 604(7906):502-508. PMID: 35396580; PMCID: PMC9392466.
      Citations: 460     Fields:    Translation:Humans
    26. Jansen IE, Kleineidam L, Amin N, Naj AC, Campos-Martin R, Andrade V, Holmans PA, van der Lee SJ, Kuulasmaa T, Yang Q, Bis JC, Yaqub A, Prokic I, Ahmad S, Giedraitis V, Aarsland D, Alcolea D, Armstrong NJ, Tsolaki A, Appollonio I, Arcaro M, Archetti S, Pastor AA, Arosio B, Athanasiu L, Banaj N, Barral S, Beiser A, Below JE, Benchek P, Benussi L, Bessi V, Binetti G, Bizarro A, Blesa R, Boerwinkle E, Borroni B, Boschi S, Bressler J, Bresner C, Brodaty H, Brookes KJ, Buiza-Rueda D, Burholt V, Bush WS, Cantwell LB, Chung J, Cuccaro ML, Cecchetti R, Cervera-Carles L, Charbonnier C, Chen HH, Chillotti C, Claassen JAHR, Conti E, Costantini E, Custodero C, Dalmasso MC, Daniele A, Dardiotis E, de Deyn PP, de Paiva Lopes K, de Witte LD, Del Ser T, Denning N, DeStefano A, Diehl-Schmid J, Djurovic S, Eiriksdottir G, Engelborghs S, Escott-Price V, Faber KM, Fabrizio T, Nielsen SF, Fardo DW, Farotti L, Fenoglio C, Ferrari R, Ferreira CB, Fischer P, Fladby T, Fongang B, Fornage M, Fortea J, Foroud TM, Fostinelli S, Fox NC, Froelich L, Fulton-Howard B, Galimberti D, Garcia-Madrona S, Garcia-Ribas G, Ghidoni R, Giegling I, Giorgio G, Goate AM, Goldhardt O, Gomez-Fonseca D, Graff C, Grande G, Green E, Grimmer T, Grunin M, Gudnason V, Guetta-Baranes T, Haapasalo A, Hadjigeorgiou G, Haines JL, Hamilton-Nelson KL, Hardy J, Hartmann AM, Hausner L, Harwood J, Heilmann-Heimbach S, Helisalmi S, Heneka MT, Herrmann MJ, Hoffmann P, Holmes C, Holstege H, Vilas RH, Hulsman M, Humphrey J, Biessels GJ, Jian X, Johansson C, Jun GR, Kastumata Y, Kauwe J, Kehoe PG, Kilander L, Kivipelto M, Koivisto A, Kosmidis MH, Kukull WA, Kuksa PP, Kunkle BW, Kuzma AB, Lage C, Laukka EJ, Launer L, Lauria A, Lee CY, Lehtisalo J, Lerch O, Longstreth W, Lopez O, de Munain AL, Love S, Luckcuck L, Lunetta KL, Ma Y, MacLeod CA, Maier W, Mangialasche F, Spallazzi M, Marshall R, Martin ER, Masullo C, Mayeux R, Mead S, Mecocci P, Medina M, Meggy A, Mehrabian S, Mir P, Moebus S, Mol M, Morelli L, Moreno F, Morgan K, Mosley T, Mukherjee S, Nacmias B, Ngandu T, Nicolas G, Orsini M, Padovani A, Paolo C, Papenberg G, Parnetti L, Pasquier F, Peloso G, Pijnenburg YAL, Pisanu C, Polak T, Popp J, Posthuma D, Priller J, Quenez O, Thomassen JQ, Rainero I, Rajabli F, Ramakers I, Reinders MJT, Reitz C, Reyes-Dumeyer D, Ridge P, Riedel-Heller S, Rodriguez-Rodriguez E, Rongve A, Rujescu D, Sakka P, Saltvedt I, Sando SB, Satizabal CL, Scamosci M, Scarmeas N, Scarpini E, Scheltens P, Scherbaum N, Scherer M, Schmid M, Schneider A, Schott JM, Seripa D, Sha J, Shadrin AA, Skrobot O, Slifer S, Snijders GJL, Soininen H, Solfrizzi V, Solomon A, Song Y, Sorbi S, Spalletta G, Spottke A, Squassina A, Stordal E, Thalamuthu A, Thomas T, Tosto G, Traykov L, Tremolizzo L, Uitterlinden A, Ullgren A, Ulstein I, Valladares O, Broeckhoven CV, Vance J, Vardarajan BN, van der Lugt A, Dongen JV, van Rooij J, van Swieten J, Vandenberghe R, Verhey F, Vogelgsang J, Vyhnalek M, Wagner M, Wallon D, Wang LS, Wang R, Weinhold L, Wiltfang J, Windle G, Woods B, Yannakoulia M, Zare H, Zhao Y, Zhang X, Zhu C, Zulaica M, EADB, GR@ACE, DEGESCO, EADI, GERAD, Demgene, FinnGen, ADGC, CHARGE, Farrer LA, Psaty BM, Ghanbari M, Raj T, Sachdev P, Mather K, Jessen F, Ikram MA, Hort J, Tsolaki M, Pericak-Vance MA, Williams J, Frikke-Schmidt R, Clarimon J, Rossi G, Seshadri S, Andreassen OA, Ingelsson M, Hiltunen M, Sleegers K, Schellenberg GD, van Duijn CM, Sims R, van der Flier WM, Ramirez A, Bellenguez C, K???kali F, Moreno-Grau S, Grenier-Boley B, Boland A, Damotte V, Costa MR, de Rojas I, Chapuis J, Garcia-Gonzalez P, Abdelnour C, Alarc?n-Mart?n E, Alegret M, Alvarez I, ?lvarez V, Ant?nez C, Bailly H, Baquero M, Pastor AB, Berr C, Besse C, Boada M, Boss? P, Br?then G, Brusco LI, B?rger K, Calero M, Chene G, Carracedo ?, Ciccone S, Clark C, Corma-G?mez A, Daian D, Dartigues JF, Debette S, Deckert J, Dichgans M, Diez-Fairen M, Rossi PD, Duron E, D?zel E, Dufouil C, Espinosa A, Ewers M, Fern?ndez-Fuertes M, Ferri E, Fin B, et al. New insights into the genetic etiology of Alzheimer's disease and related dementias. Nat Genet. 2022 04; 54(4):412-436. PMID: 35379992; PMCID: PMC9005347.
      Citations: 395     Fields:    Translation:Humans
    27. Rickenbacher M, Herms S, Hoffmann P, Cichon S, Wueest AS, Monsch AU, Steiner LA, Goettel N, Reinbold CS. Genome-wide Association Study of Postoperative Cognitive Dysfunction in Older Surgical Patients. J Neurosurg Anesthesiol. 2022 Apr 01; 34(2):248-250. PMID: 33264229.
      Citations: 3     Fields:    Translation:Humans
    28. Kaut O, Schmitt I, Hoffmann P, Gonzalez FJ, Stahl F, Fr?hlich H, W?llner U. Epigenome-Wide Analysis of DNA Methylation in Parkinson's Disease Cortex. Life (Basel). 2022 Mar 29; 12(4). PMID: 35454993; PMCID: PMC9025601.
      Citations: 10     
    29. Baak L, Frank M, Hoffmann P, Erbel R, D?rig J, D?hrsen U, N?then MM, Dragano N, J?ckel KH, Schmidt B. A genetic risk score of alleles related to MGUS interacts with socioeconomic position in a population-based cohort. Sci Rep. 2022 03 15; 12(1):4409. PMID: 35292679; PMCID: PMC8924237.
      Citations:    Fields:    Translation:Humans
    30. Kopp JF, Schwerdtle T, Cabral M, Hoffmann P, Ng E, Whitfield JB, Morris AP, Lind L, Schulze MB, J?ger S. Blood copper and risk of cardiometabolic diseases: a Mendelian randomization study. Hum Mol Genet. 2022 03 03; 31(5):783-791. PMID: 34523676; PMCID: PMC8895748.
      Citations: 6     Fields:    Translation:Humans
    31. Cearns M, Amare AT, Schubert KO, Thalamuthu A, Frank J, Streit F, Akula N, Akiyama K, Ardau R, Aubry JM, Backlund L, Bhattacharjee AK, Benabarre A, Bengesser S, Biernacka JM, Birner A, Cervantes P, Chen HC, Chillotti C, Cichon S, Cruceanu C, Czerski PM, Dalkner N, Dayer A, Degenhardt F, Zompo MD, DePaulo JR, Falkai P, Forstner AJ, Frisen L, Frye MA, Fullerton JM, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Grof P, Hashimoto R, Hauser J, Herms S, Hoffmann P, Hofmann A, Hou L, Hsu YH, Kassem L, Kuo PH, Kato T, Kelsoe J, Kittel-Schneider S, Kliwicki S, Kusumi I, Laje G, Lavebratt C, Leckband SG, Maj M, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Manchia M, Martinsson L, McCarthy MJ, McElroy S, Mondimore FM, Monteleone P, Nievergelt CM, O'Donovan C, Ozaki N, Millischer V, Papiol S, Pisanu C, Potash JB, Reif A, Reininghaus E, Rouleau GA, Rybakowski JK, Schalling M, Schofield PR, Schweizer BW, Severino G, Shekhtman T, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Squassina A, Stopkova P, Tekola-Ayele F, Tortorella A, Turecki G, Veeh J, Vieta E, Witt SH, Roberts G, Zandi PP, Alda M, McMahon FJ, Mitchell PB, Rietschel M, Clark SR, Adli M, Arias B, Bellivier F, Brichant-Petitjean C, ?tain B, Gard S, Heilbronner U, Jamain S, Jim?nez E, Kahn JP, K?nig B, Land?n M, Leboyer M, Colom F, Mitjans M, N?then MM, Nov?k T, Pfennig A, Stamm T, Bauer M, Schulze TG, Baune BT. Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach. Br J Psychiatry. 2022 Feb 28; 1-10. PMID: 35225756.
      Citations: 3     Fields:    
    32. Uellendahl-Werth F, Maj C, Borisov O, Juzenas S, Wacker EM, Steiert TA, Bej S, Krawitz P, Hoffmann P, Schramm C, Wolkenhauer O, Banasik K, Schreiber S, Karlsen TH, Degenhardt F, Franke A, Folseraas T, Ellinghaus D, J?rgensen IF, Brunak S, N?then M. Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease. Commun Biol. 2022 01 20; 5(1):80. PMID: 35058554; PMCID: PMC8776955.
      Citations: 8     Translation:HumansCells
    33. Schubert KO, Thalamuthu A, Amare AT, Frank J, Streit F, Akula N, Akiyama K, Ardau R, Aubry JM, Backlund L, Bhattacharjee AK, Benabarre A, Bengesser S, Biernacka JM, Birner A, Cearns M, Cervantes P, Chen HC, Chillotti C, Cichon S, Clark SR, Cruceanu C, Czerski PM, Dalkner N, Dayer A, Degenhardt F, Del Zompo M, DePaulo JR, Falkai P, Forstner AJ, Frisen L, Frye MA, Fullerton JM, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Grof P, Hashimoto R, Hauser J, Heilbronner U, Herms S, Hoffmann P, Hou L, Hsu YH, Kassem L, Kuo PH, Kato T, Kelsoe J, Kittel-Schneider S, Ferensztajn-Rochowiak E, Kusumi I, Laje G, Lavebratt C, Leckband SG, Maj M, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Manchia M, Martinsson L, McCarthy MJ, McElroy S, Colom F, Mondimore FM, Monteleone P, Nievergelt CM, O'Donovan C, Ozaki N, Papiol S, Pisanu C, Potash JB, Reif A, Reininghaus E, Rouleau GA, Rybakowski JK, Schalling M, Schofield PR, Schweizer BW, Severino G, Shekhtman T, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Squassina A, Stopkova P, Tekola-Ayele F, Tortorella A, Turecki G, Veeh J, Vieta E, Witt SH, Roberts G, Zandi PP, Alda M, McMahon FJ, Mitchell PB, Schulze TG, Rietschel M, Adl M, Arias B, Bellivier F, Marie-Claire C, ?tain B, Gard S, Jamain S, Jim?nez E, Kahn JP, K?nig B, Land?n M, Leboyer M, Mitjans M, N?then MM, Nov?k T, ?sby U, Pfennig A, Stamm T, Bauer M, Baune BT. Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients. Transl Psychiatry. 2021 11 29; 11(1):606. PMID: 34845190; PMCID: PMC8630000.
      Citations: 12     Fields:    Translation:Humans
    34. Smigielski L, Papiol S, Theodoridou A, Heekeren K, Gerstenberg M, Wotruba D, Buechler R, Hoffmann P, Herms S, Adorjan K, Budde M, Comes AL, Heilbronner M, Heilbronner U, Kalman JL, Reich-Erkelenz D, Schaupp SK, Schulte EC, Senner F, Anghelescu IG, Dietrich DE, Figge C, Juckel G, Konrad C, Reimer J, Reininghaus E, Spitzer C, Gryaznova A, Flatau-Nagel L, Meyers M, Emons B, Witt SH, Degenhardt F, Forstner AJ, Rietschel M, Andlauer TFM, Walitza S, Falkai P, Schulze TG, Anderson-Schmidt H, Gade K, Kl?hn-Saghatolislam F, Arolt V, Baune BT, Dannlowski U, Fallgatter AJ, J?ger M, Nieratschker V, Schmau? M, von Hagen M, Wiltfang J, Zimmermann J, Reitt M, Hau?leiter IS, Lang FU, Becker T, Wigand ME, N?then MM, R?ssler W, Gr?nblatt E. Polygenic risk scores across the extended psychosis spectrum. Transl Psychiatry. 2021 11 26; 11(1):600. PMID: 34836939; PMCID: PMC8626446.
      Citations: 3     Fields:    Translation:Humans
    35. Coombes BJ, Millischer V, Batzler A, Larrabee B, Hou L, Papiol S, Heilbronner U, Adli M, Akiyama K, Akula N, Amare AT, Ardau R, Arias B, Aubry JM, Backlund L, Bauer M, Baune BT, Bellivier F, Benabarre A, Bengesser S, Bhattacharjee AK, Cervantes P, Chen HC, Chillotti C, Cichon S, Clark SR, Colom F, Cruceanu C, Czerski PM, Dalkner N, Degenhardt F, Del Zompo M, DePaulo JR, ?tain B, Falkai P, Ferensztajn-Rochowiak E, Forstner AJ, Frisen L, Gard S, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Grof P, Hashimoto R, Hauser J, Herms S, Hoffmann P, Jamain S, Jim?nez E, Kahn JP, Kassem L, Kato T, Kelsoe JR, Kittel-Schneider S, K?nig B, Kuo PH, Kusumi I, Laje G, Land?n M, Lavebratt C, Leboyer M, Leckband SG, Maj M, Manchia M, Martinsson L, McCarthy MJ, McElroy SL, Mitchell PB, Mitjans M, Mondimore FM, Monteleone P, Nievergelt CM, N?then MM, Nov?k T, O'Donovan C, Osby U, Ozaki N, Pfennig A, Pisanu C, Potash JB, Reif A, Reininghaus E, Rietschel M, Rouleau GA, Rybakowski JK, Schalling M, Schofield PR, Schubert KO, Schweizer BW, Severino G, Shekhtman T, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Squassina A, Stamm T, Stopkova P, Tortorella A, Turecki G, Vieta E, Witt SH, Zandi PP, Fullerton JM, Alda M, Frye MA, Schulze TG, McMahon FJ, Biernacka JM. Association of Attention-Deficit/Hyperactivity Disorder and Depression Polygenic Scores with Lithium Response: A Consortium for Lithium Genetics Study. Complex Psychiatry. 2021 Dec; 7(3-4):80-89. PMID: 36408127; PMCID: PMC8740189.
      Citations: 4     
    36. Thalamuthu A, Mills NT, Forstner AJ, Hoffmann P, Witt S, Rietschel M, Adams M, McIntosh AM, Porteous DJ, Deary IJ, Hayward C, Campbell A, Teumer A, Homuth G, van der Auwera-Palitschka S, Baune BT, Berger K, Minnerup H, Grotegerd D, Dannlowski U, Meinert S, Opel N, Repple J, Gruber M, Nenadic I, Stein F, Brosch K, Meller T, Pfarr JK, N?then MM, Kircher T, Grabe HJ, Schubert KO. Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Mol Psychiatry. 2022 02; 27(2):1111-1119. PMID: 34782712; PMCID: PMC7612684.
      Citations: 14     Fields:    Translation:Humans
    37. Zillich L, Frank J, Streit F, Friske MM, Foo JC, Sirignano L, Heilmann-Heimbach S, Dukal H, Degenhardt F, Hoffmann P, Hansson AC, Rietschel M, Spanagel R, Witt SH, N?then MM. Epigenome-wide association study of alcohol use disorder in five brain regions. Neuropsychopharmacology. 2022 03; 47(4):832-839. PMID: 34775485; PMCID: PMC8882178.
      Citations: 11     Fields:    Translation:HumansCells
    38. Schreier PH, Heilmann-Heimbach S, Hoffmann P, Slooter AJC, Heinrich M, Sieg M, Kruppa J, N?rnberg P, N?then MM, Janke J, Pischon T, Winterer G, Spies CD. Association between genetic variants of the cholinergic system and postoperative delirium and cognitive dysfunction in elderly patients. BMC Med Genomics. 2021 10 21; 14(1):248. PMID: 34674705; PMCID: PMC8529799.
      Citations: 4     Fields:    Translation:Humans
    39. Mullins N, Kang J, Campos AI, Coleman JRI, Edwards AC, Galfalvy H, Levey DF, Lori A, Shabalin A, Starnawska A, Su MH, Watson HJ, Adams M, Gandal M, Hafferty JD, Hishimoto A, Kim M, Okazaki S, Otsuka I, Ware EB, Bergen AW, Berrettini WH, Bohus M, Brandt H, Chang X, Chen WJ, Chen HC, Crawford S, Crow S, DiBlasi E, Gallinger S, Glatt SJ, Guo Y, Hakonarson H, Halmi KA, Hwu HG, Jain S, Johnson C, Kaplan AS, Kaye WH, Keel PK, Kennedy JL, Klump KL, Li D, Liao SC, Lieb K, Lilenfeld L, Liu CM, Magistretti PJ, Marshall CR, Mitchell JE, Monson ET, Myers RM, Pinto D, Powers A, Rozanov V, Scherer SW, Schmahl C, Sokolowski M, Strober M, Thornton LM, Treasure J, Tsuang MT, Witt SH, Woodside DB, Yilmaz Z, Zillich L, Agartz I, Air TM, Alda M, Alfredsson L, Andreassen OA, Anjorin A, Appadurai V, Van der Auwera S, Azevedo MH, Bass N, Biernacka JM, Bigdeli TB, Binder EB, Boehnke M, Boks MP, Braff DL, Bryant R, Budde M, Byrne EM, Cahn W, Castelao E, Cervilla JA, Corvin A, Craddock N, Craig D, Degenhardt F, Djurovic S, Edenberg HJ, Fanous AH, Foo JC, Frye M, Fullerton JM, Gatt JM, Gejman PV, Giegling I, Grabe HJ, Green MJ, Grigoroiu-Serbanescu M, Gutierrez B, Hamilton SP, Hamshere ML, Hartmann A, Hauser J, Heilmann-Heimbach S, Hoffmann P, Ising M, Jones I, Jones LA, Jonsson L, Kelsoe JR, Kendler KS, Kloiber S, Koenen KC, Kogevinas M, Konte B, Lawrence J, Lee PH, Levinson DF, Lissowska J, Lucae S, McElroy SL, McGrath P, McGuffin P, McQuillin A, Medland SE, Mehta D, Melle I, Milaneschi Y, Mitchell PB, Molina E, Morken G, Mortensen PB, Nievergelt C, Nimgaonkar V, O'Donovan MC, Ophoff RA, Owen MJ, Pato C, Pato MT, Penninx BWJH, Pimm J, Pistis G, Potash JB, Power RA, Preisig M, Quested D, Reif A, Rietschel M, Rivera M, Roberts A, Roberts G, Rujescu D, Sanders AR, Schofield PR, Scott LJ, Serretti A, Shi J, Shyn SI, Sirignano L, Sklar P, Smeland OB, Smoller JW, Sonuga-Barke EJS, Spalletta G, Strauss JS, Trzaskowski M, Vincent JB, Walters JTR, Shannon Weickert C, Weickert TW, Weissman MM, Williams LM, Wray NR, Zai CC, Ashley-Koch AE, Beckham JC, Hauser ER, Hauser MA, Kimbrel NA, Lindquist JH, McMahon B, Oslin DW, Qin X, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Eating Disorders Working Group of the Psychiatric Genomics Consortium, German Borderline Genomics Consortium, MVP Suicide Exemplar Workgroup, VA Million Veteran Program, Agerbo E, Breen G, Erlangsen A, Gelernter J, Hougaard DM, Kessler RC, Kranzler HR, Li QS, Martin NG, McIntosh AM, Mors O, Nordentoft M, Olsen CM, Porteous D, Ursano RJ, Wasserman D, Werge T, Whiteman DC, Bulik CM, Coon H, Demontis D, Docherty AR, Kuo PH, Lewis CM, Mann JJ, Smith DJ, Stahl EA, Stein MB, Streit F, Willour V, Ruderfer DM, Awasthi S, Ripke S, Duriez P, Fern?ndez-Aranda F, Fichter MM, Gorwood P, Jamain S, Jim?nez-Murcia S, Ramoz N, Roepke S, Adolfsson R, Soler Artigas M, Bau CHD, Baune BT, Bellivier F, Berger K, Bosch R, Casas M, Chaumette B, Cichon S, Forstner AJ, Grevet EH, Guzman-Parra J, Kahn RS, Krebs MO, Land?n M, Leboyer M, Liao C, Mayoral F, M?ller-Myhsok B, N?then MM, Ramos-Quiroga JA, Ribas?s M, Richarte V, Rouleau GA, Rovaris DL, S?nchez-Mora C, Schulze TG, Swiatkowska B, Turecki G, Vilar-Rib? L, V?lzke H, B?rglum AD, Esko T, Renter?a ME. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biol Psychiatry. 2022 02 01; 91(3):313-327. PMID: 34861974; PMCID: PMC8851871.
      Citations: 60     Fields:    Translation:Humans
    40. Amare AT, Schubert KO, Hou L, Clark SR, Cearns M, Degenhardt F, Tekola-Ayele F, Hsu YH, Shekhtman T, Akula N, Akiyama K, Ardau R, Aubry JM, Backlund L, Bhattacharjee AK, Benabarre A, Bengesser S, Biernacka JM, Birner A, Cervantes P, Chen HC, Chillotti C, Cichon S, Cruceanu C, Czerski PM, Dalkner N, Dayer A, Del Zompo M, DePaulo JR, Falkai P, Forstner AJ, Frisen L, Frye MA, Fullerton JM, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Grof P, Hashimoto R, Hauser J, Herms S, Hoffmann P, Kassem L, Kuo PH, Kato T, Kelsoe JR, Kittel-Schneider S, Ferensztajn-Rochowiak E, Kusumi I, Laje G, Lavebratt C, Leckband SG, Tortorella A, Manchia M, Martinsson L, McCarthy MJ, McElroy SL, Colom F, Millischer V, Mondimore FM, Monteleone P, Nievergelt CM, O'Donovan C, Ozaki N, Potash JB, Reif A, Reininghaus E, Rouleau GA, Rybakowski JK, Schalling M, Schofield PR, Schweizer BW, Severino G, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Pisanu C, Squassina A, Stopkova P, Maj M, Turecki G, Vieta E, Veeh J, Witt SH, Wright A, Zandi PP, Mitchell PB, Alda M, Rietschel M, McMahon FJ, Schulze TG, Le Clerc S, Lombardi L, Baune BT, Papiol S, Heilbronner U, Adli M, Arias B, Bellivier F, Brichant-Petitjean C, ?tain B, Jamain S, Gard S, Jim?nez E, Kahn JP, K?nig B, Land?n M, Mitjans M, N?then MM, Nov?k T, ?sby U, Pfennig A, Stamm T, Bauer M, Spadoni JL, Boukouaci W, Richard JR, Le Corvoisier P, Barrau C, Zagury JF, Leboyer M, Tamouza R. HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders. Sci Rep. 2021 09 08; 11(1):17823. PMID: 34497278; PMCID: PMC8426488.
      Citations: 6     Fields:    Translation:Humans
    41. Polushina T, Banerjee N, Giddaluru S, Bettella F, Espeseth T, Lundervold AJ, Djurovic S, Cichon S, Hoffmann P, Steen VM, Andreassen OA, N?then MM, Le Hellard S. Identification of pleiotropy at the gene level between psychiatric disorders and related traits. Transl Psychiatry. 2021 07 29; 11(1):410. PMID: 34326310; PMCID: PMC8322263.
      Citations: 4     Fields:    Translation:Humans
    42. Saunders CN, Chattopadhyay S, Huhn S, Weinhold N, Hoffmann P, Landi S, Goldschmidt H, Milani P, Merlini G, Rowcieno D, Hawkins P, Hegenbart U, Palladini G, Wechalekar A, Houlston R, Hemminki K, N?then MM, J?ckel KH, Schmidt B, Sch?nland SO, F?rsti A. Search for AL amyloidosis risk factors using Mendelian randomization. Blood Adv. 2021 07 13; 5(13):2725-2731. PMID: 34228109; PMCID: PMC8288669.
      Citations: 3     Fields:    Translation:Humans
    43. Kim H, Momen-Heravi F, Chen S, Hoffmann P, Kebschull M, Papapanou PN. Differential DNA methylation and mRNA transcription in gingival tissues in periodontal health and disease. J Clin Periodontol. 2021 09; 48(9):1152-1164. PMID: 34101221; PMCID: PMC8376779.
      Citations: 12     Fields:    Translation:HumansCells
    44. Ludwig KU, Schmithausen RM, Li D, Jacobs ML, Hollstein R, Blumenstock K, Liebing J, Slabicki M, Ben-Shmuel A, Israeli O, Weiss S, Ebert TS, Paran N, Wilbring G, Feldman D, Ishorst N, Hochfeld LM, Beins EC, Kaltheuner IH, Schmitz M, Sib E, Jentzsch M, Borrajo JD, Strecker J, Reinhardt J, Cleary B, Geyer M, Macrae R, Hoffmann P, Exner M, Regev A, Zhang F, Schmid-Burgk JL, Moench EC, R?diger W, Lippke B, W?hler A, D?hla M, H?lzel M, N?then MM. LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding. Nat Biotechnol. 2021 12; 39(12):1556-1562. PMID: 34188222; PMCID: PMC8678193.
      Citations: 26     Fields:    Translation:Humans
    45. Niazi Y, Thomsen H, Smolkova B, Vodickova L, Vodenkova S, Kroupa M, Vymetalkova V, Kazimirova A, Barancokova M, Volkovova K, Staruchova M, Hoffmann P, Dusinska M, Musak L, Vodicka P, Hemminki K, N?then MM, F?rsti A. DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations. Front Genet. 2021; 12:691947. PMID: 34220964; PMCID: PMC8242355.
      Citations: 2     
    46. Tesi N, Grenier-Boley B, Andrade V, Jansen IE, Pedersen NL, Stringa N, Zettergren A, Tankard RM, Bis JC, Sims R, Calero M, Blesa R, Cervera-Carles L, Moreno F, Huerto Vilas R, Lage C, Ullgren A, Naj AC, Lemstra AW, Benussi A, Padovani A, Squassina A, Arias Pastor A, Kok AAL, Meggy A, DeStefano AL, Schneider A, Haapasalo A, Hartmann AM, Spottke A, Rongve A, Borroni B, Arosio B, Nacmias B, Kunkle BW, Masullo C, Dufouil C, Graff C, Chillotti C, Reynolds CA, Fenoglio C, Van Broeckhoven C, Pisanu C, Satizabal CL, Holmes C, Buiza-Rueda D, Aarsland D, Rujescu D, Alcolea D, Galimberti D, Seripa D, Dardiotis E, Scarpini E, Conti E, Rodriguez-Rodriguez E, Boerwinkle E, Tagliavini F, Pasquier F, Mangialasche F, Jessen F, Hadjigeorgiou G, Rossi G, Spalletta G, Giaccone G, Grande G, Binetti G, Papenberg G, Soininen H, Karlsson IK, Appollonio I, Giegling I, Skoog I, Saltvedt I, Rainero I, Hort J, Diehl-Schmid J, Van Dongen J, Lehtisalo J, Wiltfang J, Thomassen JQ, Haines JL, Vogelgsang J, Fortea J, Morgan K, Sleegers K, Kilander L, Weinhold L, Farrer LA, Wang LS, Kleineidam L, Farotti L, Parnetti L, Tremolizzo L, Hausner L, Benussi L, Froelich L, Ikram MA, Tsolaki M, Hulsman M, Spallazzi M, Pericak-Vance MA, Esiri M, Dalmasso MC, Arcaro M, Ingelsson M, Herrmann MJ, Scherer M, Vyhnalek M, Kosmidis MH, Yannakoulia M, Schmid M, Heneka MT, Wagner M, Scamosci M, Kivipelto M, Hiltunen M, Zulaica M, Fornage M, van Schoor NM, Seidu NM, Banaj N, Armstrong NJ, Scarmeas N, Scherbaum N, Goldhardt O, Skrobot OA, Lerch O, Caffarra P, Sakka P, Hoffmann P, Holmans PA, Fischer P, Yang Q, Marshall R, Kalaria RN, Mayeux R, Vandenberghe R, Cecchetti R, Ghidoni R, Frikke-Schmidt R, Sorbi S, Engelborghs S, Helisalmi S, Botne Sando S, Kern S, Archetti S, Boschi S, Fostinelli S, Mead S, Djurovic S, Heilmann-Heimbach S, Riedel-Heller S, Kuulasmaa T, Del Ser T, Lebouvier T, Polak T, Ngandu T, Grimmer T, Bessi V, Escott-Price V, Giedraitis V, Deramecourt V, Maier W, Jian X, Pijnenburg YAL, EADB contributors, GR@ACE study group, DEGESCO consortium, IGAP (ADGC, CHARGE, EADI, GERAD), PGC-ALZ consortia, Garcia-Ribas G, Lopez de Munain A, Mir P, Medina M, Scheltens P, Holstege H, Amouyel P, Schellenberg GD, Williams J, Seshadri S, van Duijn CM, Mather KA, Huisman M, Andreassen OA, Posthuma D, van der Flier WM, Ramirez A, Lambert JC, van der Lee SJ, de Rojas I, Moreno-Grau S, Hern?ndez I, Montrreal L, Ant?nez C, Antonell A, Bellenguez C, Quintela I, Gonz?lez-Perez A, Franco-Mac?as E, Mac?as J, Men?ndez-Gonz?lez M, Frank-Garc?a A, Royo JL, Baquero M, Diez-Fairen M, Garc?a-Madrona S, Garc?a-Gonz?lez P, Alarc?n-Mart?n E, Valero S, Sotolongo-Grau O, Benaque A, P?rez-Cord?n A, R?bano A, de Mendon?a A, Pastor AB, Espinosa A, Corma-G?mez A, Mart?n Montes A, Sanabria ?, Kinhult St?hlbom A, Tybj?rg-Hansen A, Corbat?n-Anchuelo A, Nordestgaard BG, Charbonnier C, Abdelnour C, Mart?nez Rodr?guez C, Mu?oz-Fernandez C, Ferreira CB, Clark C, Wallon D, Gr?nblatt E, D?zel E, Rubino E, Gelpi E, Duron E, Ferri E, K???kali F, Sanchez-Garcia F, Nicolas G, Selb?k G, Ortega G, Ch?ne G, Hampel H, Bailly H, Zetterberg H, Alvarez I, Rosas Allende I, Vidal JS, Kornhuber J, Pineda JA, Popp J, Deckert J, Buerger K, Flie?bach K, Molina-Porcel L, Deniz-Naranjo MC, Rosende-Roca M, L?wenmark M, Bernal S?nchez-Arjona M, Mart?nez-Larrad MT, N?then MM, Fern?ndez-Fuertes M, Dichgans M, Ewers M, Alegret M, Roberto N, Hanon O, Peters O, Quenez O, Boss? P, Dionigi Rossi P, Riederer P, H?gg S, Gil S, Mendoza S, Ciccone S, S?nchez-Juan P, Pastor P, P?rez-Tur J, Pi?ol-Ripoll G, Garc?a-Alberca JM, Bullido MJ, ?lvarez V, Lle? A, Real LM, Marqui? M, S?ez ME, Carracedo ?, S?nchez-Valle R, Serrano-R?os M, Orellana A, T?rraga L, Blennow K, Clarim?n J, Boada M, Ruiz A, Mecocci P, Kehoe PG. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores. Nat Commun. 2021 06 07; 12(1):3417. PMID: 34099642; PMCID: PMC8184987.
      Citations: 80     Fields:    Translation:Humans
    47. Pechlivanis S, Jung D, Moebus S, Lehmann N, Mahabadi AA, Hoffmann P, Erbel R, Bachmann HS, N?then MM. Pharmacogenetic association of diabetes-associated genetic risk score with rapid progression of coronary artery calcification following treatment with HMG-CoA-reductase inhibitors -results of the Heinz Nixdorf Recall Study. Naunyn Schmiedebergs Arch Pharmacol. 2021 08; 394(8):1713-1725. PMID: 34021798; PMCID: PMC8298241.
      Citations: 3     Fields:    Translation:Humans
    48. Mullins N, Forstner AJ, O'Connell KS, Coombes B, Coleman JRI, Qiao Z, Als TD, Bigdeli TB, Bryois J, Charney AW, Drange OK, Gandal MJ, Hagenaars SP, Ikeda M, Kamitaki N, Kim M, Krebs K, Schilder BM, Sloofman LG, Steinberg S, Winsvold BS, Won HH, Abramova L, Adorjan K, Agerbo E, Al Eissa M, Albani D, Alliey-Rodriguez N, Anjorin A, Antilla V, Antoniou A, Baek JH, Bass N, Beins EC, Bergen SE, Birner A, Boks MP, Bosch R, Brum M, Brumpton BM, Brunkhorst-Kanaan N, Budde M, Bybjerg-Grauholm J, Byerley W, Cairns M, Casas M, Cervantes P, Clarke TK, Cruceanu C, Cuellar-Barboza A, Cunningham J, Curtis D, Czerski PM, Dale AM, Dalkner N, David FS, Degenhardt F, Djurovic S, Dobbyn AL, Douzenis A, Escott-Price V, Ferrier IN, Fiorentino A, Foroud TM, Forty L, Frank J, Frei O, Freimer NB, Gade K, Garnham J, Gelernter J, Gizer IR, Gordon SD, Gordon-Smith K, Greenwood TA, Grove J, Ha K, Haraldsson M, Heilbronner U, Hellgren D, Herms S, Hoffmann P, Holmans PA, Huckins L, Johnson JS, Kalman JL, Kamatani Y, Kennedy JL, Kittel-Schneider S, Knowles JA, Kogevinas M, Koromina M, Kranz TM, Kranzler HR, Kubo M, Kupka R, Kushner SA, Lavebratt C, Lawrence J, Leber M, Lee HJ, Lee PH, Levy SE, Lewis C, Lucae S, Lundberg M, MacIntyre DJ, Magnusson SH, Maier W, Maihofer A, Malaspina D, Maratou E, Martinsson L, Mattheisen M, McCarroll SA, McGregor NW, McGuffin P, McKay JD, Medeiros H, Medland SE, Millischer V, Montgomery GW, Moran JL, Morris DW, O'Brien N, O'Donovan C, Olde Loohuis LM, Oruc L, Papiol S, Perry A, Porichi E, Potash JB, Quested D, Raj T, Rapaport MH, DePaulo JR, Regeer EJ, Rice JP, Rivera M, Roussos P, Ruderfer DM, Schulte EC, Senner F, Sharp S, Shilling PD, Sigurdsson E, Sirignano L, Slaney C, Smeland OB, Smith DJ, Sobell JL, Soler Artigas M, Spijker AT, Stein DJ, Strauss JS, Swiatkowska B, Terao C, Thorgeirsson TE, Toma C, Tooney P, Tsermpini EE, Vawter MP, Vedder H, Walters JTR, Witt SH, Xi S, Xu W, Yang JMK, Young AH, Young H, Zandi PP, Zhou H, Zillich L, HUNT All-In Psychiatry, Agartz I, Alda M, Alfredsson L, Babadjanova G, Backlund L, Bengesser S, Berrettini WH, Blackwood DHR, Boehnke M, Breen G, Carr VJ, Catts S, Corvin A, Craddock N, Dikeos D, Ferentinos P, Frye M, Fullerton JM, Gershon ES, Goes FS, Green MJ, Grigoroiu-Serbanescu M, Hauser J, Henskens F, Hillert J, Hong KS, Hougaard DM, Hultman CM, Hveem K, Iwata N, Jablensky AV, Jones I, Jones LA, Kelsoe JR, Kirov G, Lewis CM, Li QS, Lissowska J, Lochner C, Loughland C, Martin NG, Mathews CA, McElroy SL, McIntosh AM, McMahon FJ, Melle I, Michie P, Milani L, Mitchell PB, Morken G, Mors O, Mortensen PB, Mowry B, Myers RM, Neale BM, Nievergelt CM, Nordentoft M, O'Donovan MC, Oedegaard KJ, Olsson T, Owen MJ, Paciga SA, Pantelis C, Pato C, Pato MT, Patrinos GP, Perlis RH, Posthuma D, Ramos-Quiroga JA, Reif A, Reininghaus EZ, Rietschel M, Ripke S, Saito T, Schall U, Schalling M, Schofield PR, Schulze TG, Scott LJ, Scott RJ, Serretti A, Shannon Weickert C, Smoller JW, Stefansson H, Stefansson K, Stordal E, Streit F, Sullivan PF, Turecki G, Vaaler AE, Vieta E, Vincent JB, Waldman ID, Weickert TW, Werge T, Wray NR, Zwart JA, Biernacka JM, Nurnberger JI, Cichon S, Edenberg HJ, Stahl EA, McQuillin A, Di Florio A, Ophoff RA, Andreassen OA, B?rte S, Panagiotaropoulou G, Trubetskoy V, Awasthi S, B?kvad-Hansen M, Bauer M, B?cker Pedersen C, B?en E, Elvs?shagen T, Fris?n L, Gi?rtz Pedersen M, Guzman-Parra J, Hautzinger M, Jamain S, Liao C, M?hleisen TW, Pardi?as AF, Pfennig A, Rivas F, Roth J, S?nchez-Mora C, S?holm Hansen C, Adolfsson R, Baune BT, Bellivier F, B?rglum AD, Dannlowski U, Esko T, Etain B, Gawlik M, Kahn RS, Land?n M, Leboyer M, Mayoral F, M?ller-Myhsok B, N?then MM, Ribas?s M, Rouleau GA. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nat Genet. 2021 06; 53(6):817-829. PMID: 34002096; PMCID: PMC8192451.
      Citations: 305     Fields:    Translation:HumansCells
    49. Torres GG, Nygaard M, Caliebe A, Lieb W, Christiansen L, Christensen K, Hoffmann P, Flachsbart F, Schreiber S, Ellinghaus D, Franke A, Dose J, Nebel A, Blanch? H, Chantalat S, Galan P, Deleuze JF, Strauch K, M?ller-Nurasyid M, Peters A, N?then MM. Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes. J Gerontol A Biol Sci Med Sci. 2021 04 30; 76(5):786-795. PMID: 33491046; PMCID: PMC8087267.
      Citations: 11     Fields:    Translation:Humans
    50. Khanam T, Sandmann S, Seggewiss J, Ruether C, Zimmermann M, Norvil AB, Bartenhagen C, Randau G, Mueller S, Herbrueggen H, Hoffmann P, Herms S, Wei L, Woeste M, Wuensch C, Gowher H, Oschlies I, Klapper W, Woessmann W, Dugas M, Burkhardt B. Integrative genomic analysis of pediatric T-cell lymphoblastic lymphoma reveals candidates of clinical significance. Blood. 2021 04 29; 137(17):2347-2359. PMID: 33152759; PMCID: PMC8759350.
      Citations: 16     Fields:    Translation:Humans
    51. Andlauer TFM, Teumer A, Wittfeld K, Herms S, Moebus S, Etkin A, Grabe HJ, M?hleisen TW, Hoffstaedter F, Teuber A, Reinbold CS, Grotegerd D, B?low R, Caspers S, Dannlowski U, Hoffmann P, Kircher T, Minnerup H, Nenadic I, Teismann H, V?lker U, Berger K, N?then MM, Amunts K, Eickhoff SB, S?mann PG, M?ller-Myhsok B, Cichon S. Genetic factors influencing a neurobiological substrate for psychiatric disorders. Transl Psychiatry. 2021 03 29; 11(1):192. PMID: 33782385; PMCID: PMC8007575.
      Citations: 2     Fields:    Translation:Humans
    52. van der Meer D, Moreau C, Kaufmann T, Ellegaard M, Abdellaoui A, Ames D, Armstrong NJ, Bernard M, Blackburn NB, Blangero J, Boomsma DI, Brodaty H, Brouwer RM, Cahn W, Calhoun VD, Ching CRK, Ciufolini S, Curran JE, Dale AM, Dalvie S, Dazzan P, de Geus EJC, de Zubicaray GI, de Zwarte SMC, Desrivieres S, Doherty JL, Donohoe G, Draganski B, Ehrlich S, Eising E, Espeseth T, Fejgin K, Fisher SE, Fladby T, Frei O, Fukunaga M, Ge T, Glahn DC, Grabe HJ, Groenewold NA, Haavik J, Haberg AK, Hall J, Hashimoto R, Hibar DP, Hillegers MHJ, Hoffmann P, Holleran L, Holmes AJ, Homuth G, Hottenga JJ, Hulshoff Pol HE, Ikeda M, Jahanshad N, Johansson S, Kikuchi M, Knowles EEM, Kumar K, Le Hellard S, Leu C, Linden DEJ, Liu J, Lundervold A, Lundervold AJ, Martin NG, Martin-Brevet S, Mather KA, Mathias SR, McMahon KL, McRae AF, Medland SE, Meyer-Lindenberg A, Moberget T, Modenato C, Morris DW, Murray RM, Nielsen J, Nordvik JE, Loohuis LMO, Ophoff RA, Owen MJ, Paus T, Pausova Z, Peralta JM, Pike GB, Prieto C, Quinlan EB, Marques TR, Rucker JJH, Sachdev PS, Sando SB, Schofield PR, Schork AJ, Schumann G, Shin J, Shumskaya E, Silva AI, Sisodiya SM, Steen VM, Stein DJ, Strike LT, Suzuki IK, Tamnes CK, Teumer A, Thalamuthu A, Uhlmann A, van 't Ent D, van den Bree MBM, Vanderhaeghen P, Vassos E, Wen W, Wittfeld K, Wright MJ, Agartz I, Djurovic S, Westlye LT, Thompson PM, Andreassen OA, ENIGMA-CNV working group, S?nderby IE, Walters GB, Amunts K, Andersson M, B?low R, B?en R, Caspers S, Cichon S, Crespo-Facorro B, Frouin V, Gareau T, G?stafsson ?, Hehir-Kwa JY, Jockwitz C, J?nsson EG, J?rgensen NR, Maillard AM, S?nchez JM, M?hleisen TW, Nyberg L, Reinbold CS, Tordesillas-Guti?rrez D, Ulfarsson MO, Stefansson H, Stefansson K, Jacquemont S. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans. Transl Psychiatry. 2021 03 22; 11(1):182. PMID: 33753722; PMCID: PMC7985307.
      Citations: 17     Fields:    Translation:Humans
    53. Niazi Y, Thomsen H, Smolkova B, Vodickova L, Vodenkova S, Kroupa M, Vymetalkova V, Kazimirova A, Barancokova M, Volkovova K, Staruchova M, Hoffmann P, Dusinska M, Vodicka P, Hemminki K, N?then MM, Musak L, F?rsti A. DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population. DNA Repair (Amst). 2021 05; 101:103079. PMID: 33676360.
      Citations: 3     Fields:    Translation:HumansCells
    54. Grossmann L, Yde Ohki CM, Hoffmann P, Herms S, Werling AM, Walitza S, D?ring C, Gr?nblatt E. Generation of integration-free induced pluripotent stem cell lines from four pediatric ADHD patients. Stem Cell Res. 2021 05; 53:102268. PMID: 33662736.
      Citations: 5     Fields:    Translation:HumansCells
    55. Yde Ohki CM, Grossmann L, Hoffmann P, Herms S, Werling AM, Walitza S, D?ring C, Gr?nblatt E. Generation of integration-free induced pluripotent stem cells from healthy individuals. Stem Cell Res. 2021 05; 53:102269. PMID: 33667761.
      Citations: 3     Fields:    Translation:HumansCells
    56. Hoffmann P, Herrera-Rivero M, Stoll M, Hegenbarth JC, R?hle F, Limperger V, Junker R, Franke A, Shneyder M, Stach M, Nowak-G?ttl U. Single- and Multimarker Genome-Wide Scans Evidence Novel Genetic Risk Modifiers for Venous Thromboembolism. Thromb Haemost. 2021 Sep; 121(9):1169-1180. PMID: 33592630.
      Citations: 8     Fields:    Translation:Humans
    57. Streit F, Forstner AJ, Strohmaier J, Gil Flores S, Cabaleiro Fabeiro FJ, Auburger G, Degenhardt F, Heilmann-Heimbach S, Herms S, Hoffmann P, Frank J, Foo JC, Sirignano L, Witt SH, Cichon S, Andlauer TFM, Rietschel M, Guzman-Parra J, Gonz?lez MJ, Del R?o Noriega F, Perez Perez F, Haro Gonz?lez J, Orozco Diaz G, de Diego-Otero Y, Moreno-Kustner B, Rivas F, Mayoral F, N?then MM. Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families. Transl Psychiatry. 2021 01 11; 11(1):31. PMID: 33431802; PMCID: PMC7801527.
      Citations: 13     Fields:    Translation:Humans
    58. Frank M, Hensel J, Baak L, Schramm S, Weimar C, Hoffmann P, Erbel R, Jokisch M, Dragano N, N?then MM, J?ckel KH, Schmidt B. Interaction of Alzheimer's Disease-Associated Genetic Risk with Indicators of Socioeconomic Position on Mild Cognitive Impairment in the Heinz Nixdorf Recall Study. J Alzheimers Dis. 2021; 82(4):1715-1725. PMID: 34219719; PMCID: PMC8461721.
      Citations: 5     Fields:    Translation:Humans
    59. Cuadrat R, Wittenbecher C, Floegel A, Hoffmann P, Adamski J, Pischon T, Schulze MB, J?ger S, Prehn C. Mendelian Randomization Study on Amino Acid Metabolism Suggests Tyrosine as Causal Trait for Type 2 Diabetes. Nutrients. 2020 Dec 19; 12(12). PMID: 33352682; PMCID: PMC7766372.
      Citations: 2     Fields:    Translation:Humans
    60. Palladino VS, Chiocchetti AG, Frank L, Haslinger D, Till A, Haupt S, Edenhofer F, Hoffmann P, Reif A, Kittel-Schneider S, McNeill R, Radtke F, Br?stle O, G?nther K. Energy Metabolism Disturbances in Cell Models of PARK2 CNV Carriers with ADHD. J Clin Med. 2020 Dec 18; 9(12). PMID: 33353000; PMCID: PMC7766864.
      Citations: 2     
    61. Streeck H, Schulte B, Richter E, Fuhrmann C, Bartok E, Dolscheid-Pommerich R, Berger M, Wessendorf L, Eschbach-Bludau M, Kellings A, Schwaiger A, Coenen M, Hoffmann P, Stoffel-Wagner B, Exner M, Schmithausen RM, Schmid M, Hartmann G, K?mmerer BM, H?ller T, N?then MM, Eis-H?binger AM. Infection fatality rate of SARS-CoV2 in a super-spreading event in Germany. Nat Commun. 2020 11 17; 11(1):5829. PMID: 33203887; PMCID: PMC7672059.
      Citations: 196     Fields:    Translation:HumansCells
    62. Shadrin AA, Ellinghaus D, Makarious MB, Blauwendraat C, Heras-Garvin A, Ding J, Hammer M, Pavy-Le Traon A, Frei O, O'Connell KS, Bahrami S, Schreiber S, Lieb W, Schminke U, Homuth G, Schmidt CO, Hoffmann P, Wenning G, European Multiple System Atrophy Study Group, Gibbs JR, Franke A, Hardy J, Stefanova N, Singleton A, Houlden H, Scholz SW, Andreassen OA, Mucha S, Sreelatha AAK, Foubert-Samier A, Meissner WG, Rascol O, M?ller-Nurasyid M, N?then MM, Gieger C, Gasser T, Sharma M. Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease. Mov Disord. 2021 02; 36(2):449-459. PMID: 33107653; PMCID: PMC8985479.
      Citations: 7     Fields:    Translation:HumansAnimals
    63. Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, Pourcain BS, Iannuzzi S, Demonet JF, Morris AP, Hulslander J, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Peyrard-Janvid M, Brandeis D, Bonte M, Stein JF, Talcott JB, Wilcke A, Kirsten H, Francks C, Monaco AP, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Honbolyg? F, T?th D, Cs?pe V, Huguet G, Chaix Y, Lyytinen H, Lepp?nen PHT, Fauchereau F, M?ller B, Bourgeron T, Ramus F, N?then MM, M?ller-Myhsok B, Schulte-K?rne G. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Mol Psychiatry. 2021 07; 26(7):3004-3017. PMID: 33057169; PMCID: PMC8505236.
      Citations: 28     Fields:    Translation:Humans
    64. Niazi Y, Thomsen H, Smolkova B, Vodickova L, Vodenkova S, Kroupa M, Vymetalkova V, Kazimirova A, Barancokova M, Volkovova K, Staruchova M, Hoffmann P, Dusinska M, Vodicka P, Hemminki K, N?then MM, Musak L, F?rsti A. Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans. Mutat Res Genet Toxicol Environ Mutagen. 2020 Oct - Dec; 858-860:503253. PMID: 33198934.
      Citations: 1     Fields:    Translation:HumansCells
    65. Imahorn E, Aushev M, Herms S, Hoffmann P, Cichon S, Reichelt J, Itin PH, Burger B. Gene expression is stable in a complete CIB1 knockout keratinocyte model. Sci Rep. 2020 09 11; 10(1):14952. PMID: 32917957; PMCID: PMC7486891.
      Citations: 1     Fields:    Translation:HumansCells
    66. Pechlivanis S, Lehmann N, Hoffmann P, Erbel R, Moebus S, N?then MM, J?ckel KH. Risk prediction for coronary heart disease by a genetic risk score - results from the Heinz Nixdorf Recall study. BMC Med Genet. 2020 09 10; 21(1):178. PMID: 32912153; PMCID: PMC7487988.
      Citations: 8     Fields:    Translation:Humans
    67. Cuadrat R, Hoffmann P, Wittenbecher C, Schulze MB, J?ger S. Desaturase Activity and the Risk of Type 2 Diabetes and Coronary Artery Disease: A Mendelian Randomization Study. Nutrients. 2020 Jul 28; 12(8). PMID: 32731631; PMCID: PMC7469057.
      Citations: 9     Fields:    Translation:Humans
    68. Krug A, Seffer D, Rippberger H, Dietsche B, Stein F, Sivalingam S, Forstner AJ, Witt SH, Dukal H, Streit F, Maaser A, Heilmann-Heimbach S, Andlauer TFM, Herms S, Hoffmann P, Rietschel M, Koch M, Schwarting RKW, Kircher T, W?hr M, Sungur A?, N?then MM, Lackinger M, Schratt G. Advanced paternal age as a risk factor for neurodevelopmental disorders: a translational study. Mol Autism. 2020 06 23; 11(1):54. PMID: 32576230; PMCID: PMC7310295.
      Citations: 11     Fields:    Translation:HumansAnimalsCells
    69. Jansen A, Krug A, Nenadic I, Rietschel M, Witt SH, Heilmann-Heimbach S, Hoffmann P, Forstner AJ, Kircher T, Goltermann J, Opel N, Redlich R, Repple J, Kaehler C, Grotegerd D, Dohm K, Leehr EJ, B?hnlein J, F?rster K, Meinert S, Enneking V, Emden D, Leenings R, Winter NR, Hahn T, Mikhail S, N?then MM, Baune BT, Dannlowski U. Replication of a hippocampus specific effect of the tescalcin regulating variant rs7294919 on gray matter structure. Eur Neuropsychopharmacol. 2020 07; 36:10-17. PMID: 32451266.
      Citations:    Fields:    Translation:Humans
    70. Pechlivanis S, Moebus S, Lehmann N, Erbel R, Mahabadi AA, Hoffmann P, Bachmann HS, Heinz Nixdorf Recall Study Investigative Group, J?ckel KH, N?then MM. Genetic risk scores for coronary artery disease and its traditional risk factors: Their role in the progression of coronary artery calcification-Results of the Heinz Nixdorf Recall study. PLoS One. 2020; 15(5):e0232735. PMID: 32379805; PMCID: PMC7205301.
      Citations: 5     Fields:    Translation:Humans
    71. Thomsen H, Chattopadhyay S, Hoffmann P, Kalirai H, Coupland SE, Jonas JB, Hemminki K, N?then MM, F?rsti A. Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1. Melanoma Res. 2020 04; 30(2):166-172. PMID: 31626034.
      Citations: 5     Fields:    Translation:HumansCells
    72. Writing Committee for the ENIGMA-CNV Working Group, van der Meer D, Kaufmann T, Abdellaoui A, Ames D, Amunts K, Armstrong NJ, Bernard M, Blackburn NB, Blangero J, Boomsma DI, Brodaty H, Brouwer RM, Cahn W, Calhoun VD, Caspers S, Cavalleri GL, Ching CRK, Cichon S, Ciufolini S, Corvin A, Curran JE, Dalvie S, Dazzan P, de Geus EJC, de Zubicaray GI, de Zwarte SMC, Delanty N, den Braber A, Desrivieres S, Di Forti M, Doherty JL, Donohoe G, Ehrlich S, Eising E, Espeseth T, Fisher SE, Fladby T, Frei O, Fukunaga M, Glahn DC, Grabe HJ, Groenewold NA, Haavik J, Haberg AK, Hashimoto R, Hibar DP, Hillegers MHJ, Hoffmann P, Holleran L, Hottenga JJ, Hulshoff Pol HE, Ikeda M, Jahanshad N, Jockwitz C, Johansson S, Kikuchi M, Knowles EEM, Kwok JB, Le Hellard S, Linden DEJ, Liu J, Lundervold A, Lundervold AJ, Martin NG, Mather KA, Mathias SR, McMahon KL, McRae AF, Medland SE, Moberget T, Moreau C, Morris DW, Murray RM, Nordvik JE, Olde Loohuis LM, Ophoff RA, Owen MJ, Paus T, Pausova Z, Peralta JM, Pike B, Prieto C, Quinlan EB, Reis Marques T, Rucker JJH, Sachdev PS, Sando SB, Schofield PR, Schork AJ, Schumann G, Shin J, Shumskaya E, Silva AI, Sisodiya SM, Steen VM, Stein DJ, Strike LT, Tamnes CK, Teumer A, Thalamuthu A, Uhlmann A, van 't Ent D, van den Bree MBM, Vassos E, Wen W, Wittfeld K, Wright MJ, Zayats T, Dale AM, Djurovic S, Agartz I, Westlye LT, Thompson PM, Andreassen OA, S?nderby IE, Walters GB, Andersson M, B?low R, Crespo-Facorro B, Frouin V, Gareau T, G?stafsson ?, Hehir-Kwa JY, Jacquemont S, J?nsson EG, M?hleisen TW, Nyberg L, Reinbold CS, Tordesillas-Guti?rrez D, ?lfarsson M?, Stef?nsson H, Stef?nsson K. Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. JAMA Psychiatry. 2020 04 01; 77(4):420-430. PMID: 31665216; PMCID: PMC6822096.
      Citations: 39     Fields:    Translation:HumansCells
    73. Pechlivanis S, Mahabadi AA, Hoffmann P, Broecker-Preuss M, Erbel R, Moebus S, Stang A, N?then MM, J?ckel KH. Association between lipoprotein(a) (Lp(a)) levels and Lp(a) genetic variants with coronary artery calcification. BMC Med Genet. 2020 03 27; 21(1):62. PMID: 32220223; PMCID: PMC7099786.
      Citations: 7     Fields:    Translation:Humans
    74. Teumer A, Herms S, Moebus S, Caspers S, R?ckner ME, Jockwitz C, Bittner N, Hoffmann P, N?then MM, Amunts K, Cichon S, M?hleisen TW. Pathway-Specific Genetic Risk for Alzheimer's Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults. Cereb Cortex. 2020 03 21; 30(2):801-811. PMID: 31402375.
      Citations: 9     Fields:    Translation:Humans
    75. Nashef A, Weiss E, Loos BG, van der Velde N, Hoffmann P, Laudes M, Lieb W, Franke A, Dommisch H, Houri-Haddad Y, Iraqi FA, Matthias M, Jepsen S, Uitterlinden AG, Wellmann J, Berger K, Sch?fer A. Translation of mouse model to human gives insights into periodontitis etiology. Sci Rep. 2020 03 17; 10(1):4892. PMID: 32184465; PMCID: PMC7078197.
      Citations: 6     Fields:    Translation:HumansAnimals
    76. Amare AT, Schubert KO, Hou L, Clark SR, Papiol S, Cearns M, Heilbronner U, Degenhardt F, Tekola-Ayele F, Hsu YH, Shekhtman T, Akula N, Akiyama K, Ardau R, Aubry JM, Backlund L, Bhattacharjee AK, Benabarre A, Bengesser S, Biernacka JM, Birner A, Cervantes P, Chen HC, Chillotti C, Cichon S, Cruceanu C, Czerski PM, Dalkner N, Dayer A, Del Zompo M, DePaulo JR, Falkai P, Forstner AJ, Frisen L, Frye MA, Fullerton JM, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Grof P, Hashimoto R, Hauser J, Herms S, Hoffmann P, Hofmann A, Kassem L, Kuo PH, Kato T, Kelsoe JR, Kittel-Schneider S, Kliwicki S, Kusumi I, Laje G, Lavebratt C, Leckband SG, Tortorella A, Manchia M, Martinsson L, McCarthy MJ, McElroy SL, Colom F, Mondimore FM, Monteleone P, Nievergelt CM, O'Donovan C, Ozaki N, Potash JB, Reif A, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Reininghaus E, Rouleau GA, Rybakowski JK, Schalling M, Schofield PR, Schweizer BW, Severino G, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Squassina A, Stopkova P, Maj M, Turecki G, Vieta E, Veeh J, Witt SH, Wright A, Zandi PP, Mitchell PB, Alda M, Rietschel M, McMahon FJ, Schulze TG, Adli M, Arias B, Bellivier F, Brichant-Petitjean C, ?tain B, Jamain S, Gard S, Jim?nez E, Kahn JP, K?nig B, Land?n M, Leboyer M, Mitjans M, N?then MM, Nov?k T, ?sby U, Pfennig A, Stamm T, Bauer M, Baune BT. Association of polygenic score for major depression with response to lithium in patients with bipolar disorder. Mol Psychiatry. 2021 06; 26(6):2457-2470. PMID: 32203155.
      Citations: 24     Fields:    Translation:Humans
    77. Doan NT, Hibar DP, Martin-Brevet S, Abdellaoui A, Ames D, Amunts K, Armstrong NJ, Bernard M, Blackburn N, Blangero J, Boomsma DI, Bralten J, Brattbak HR, Brodaty H, Brouwer RM, Calhoun V, Caspers S, Cavalleri G, Chen CH, Ciufolini S, Corvin A, Curran JE, Dale AM, Dalvie S, Dazzan P, de Geus EJC, de Zubicaray GI, de Zwarte SMC, Delanty N, den Braber A, Donohoe G, Ehrlich S, Espeseth T, Fisher SE, Franke B, Fukunaga M, Glahn DC, Grabe H, Groenewold NA, Haavik J, Hashimoto R, Heinz A, Hillegers MHJ, Hoffmann P, Holleran L, Hottenga JJ, Hulshoff HE, Ikeda M, Jahanshad N, Jernigan T, Jockwitz C, Johansson S, Jonsdottir GA, Kahn R, Kaufmann T, Kelly S, Kikuchi M, Knowles EEM, Kwok JB, Hellard SL, Leu C, Liu J, Lundervold AJ, Lundervold A, Martin NG, Mather K, Mathias SR, McCormack M, McMahon KL, McRae A, Milaneschi Y, Morris D, Mothersill D, Murray R, Nordvik JE, Olde Loohuis LM, Ophoff R, Paus T, Pausova Z, Penninx B, Peralta JM, Pike B, Prieto C, Quinlan E, Quintana DS, Marques TR, Reymond A, Richard G, Rodriguez-Herreros B, Rokicki J, Rucker J, Sachdev P, Sanders AM, Sando SB, Schmaal L, Schofield PR, Schork AJ, Schumann G, Shin J, Shumskaya E, Sisodiya S, Steen VM, Stein DJ, Steinberg S, Strike L, Teumer A, Thalamuthu A, Turner J, Ueland T, Uhlmann A, Ulfarsson MO, van 't Ent D, van der Meer D, van Haren NEM, Vaskinn A, Vassos E, Walters GB, Wang Y, Wen W, Whelan CD, Wittfeld K, Wright M, Yamamori H, Zayats T, Agartz I, Westlye LT, Djurovic S, Thompson P, Andreassen OA, 16p11.2 European Consortium, for the ENIGMA-CNV working group, S?nderby IE, G?stafsson ?, Andersson M, B?low R, Cichon S, Crespo-Facorro B, Desrivi?res S, Draganski B, Frouin V, Gareau T, H?berg A, Hehir-Kwa JY, J?nsson EG, Kolsk?r KK, Moreau C, M?hleisen TW, Nyberg L, Pudas S, Reinbold CS, Roiz-Santia?ez R, Tordesillas-Gutierrez D, Jacquemont S, Stef?nsson H, Stef?nsson K. Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia. Mol Psychiatry. 2020 Mar; 25(3):692-695. PMID: 30705424; PMCID: PMC7608381.
      Citations:    Fields:    
    78. Munn-Chernoff MA, Johnson EC, Chou YL, Coleman JRI, Thornton LM, Walters RK, Yilmaz Z, Baker JH, Gordon S, Medland SE, Watson HJ, Bryois J, Hinney A, Mattheisen M, Ripke S, Yao S, Hanscombe KB, Adan RAH, Alfredsson L, Ando T, Andreassen OA, Berrettini WH, Boni C, Boraska Perica V, Buehren K, Burghardt R, Cassina M, Cichon S, Clementi M, Cone RD, Courtet P, Crow S, Crowley JJ, Danner UN, Davis OSP, de Zwaan M, Dedoussis G, Degortes D, DeSocio JE, Dick DM, Dikeos D, Dina C, Dmitrzak-Weglarz M, Docampo E, Duncan LE, Estivill X, Farmer A, Favaro A, Fichter MM, Fischer K, Foretova L, Forstner AJ, Forzan M, Franklin CS, Gallinger S, Giegling I, Giuranna J, Gonidakis F, Gorwood P, Gratacos Mayora M, Guo Y, Hakonarson H, Hatzikotoulas K, Hauser J, Hebebrand J, Helder SG, Herms S, Herpertz-Dahlmann B, Herzog W, Huckins LM, Hudson JI, Imgart H, Inoko H, Janout V, Kalsi G, Karhunen L, Karwautz A, Kas MJH, Kennedy JL, Keski-Rahkonen A, Kiezebrink K, Kim YR, Klump KL, Knudsen GPS, La Via MC, Le Hellard S, Levitan RD, Li D, Lilenfeld L, Lin BD, Lissowska J, Luykx J, Magistretti PJ, Maj M, Mannik K, Marsal S, Marshall CR, Mattingsdal M, McDevitt S, McGuffin P, Metspalu A, Meulenbelt I, Micali N, Mitchell K, Monteleone AM, Monteleone P, Nacmias B, Navratilova M, Ntalla I, O'Toole JK, Ophoff RA, Padyukov L, Palotie A, Pantel J, Papezova H, Pinto D, Raevuori A, Ramoz N, Reichborn-Kjennerud T, Ricca V, Ripatti S, Roberts M, Rotondo A, Rujescu D, Rybakowski F, Santonastaso P, Scherer SW, Schmidt U, Schork NJ, Schosser A, Seitz J, Slachtova L, Slagboom PE, Slof-Op't Landt MCT, Slopien A, Sorbi S, Swiatkowska B, Szatkiewicz JP, Tachmazidou I, Tenconi E, Tortorella A, Tozzi F, Treasure J, Tsitsika A, Tyszkiewicz-Nwafor M, Tziouvas K, van Elburg AA, van Furth EF, Wagner G, Widen E, Zeggini E, Zerwas S, Zipfel S, Bergen AW, Boden JM, Brandt H, Crawford S, Halmi KA, Horwood LJ, Johnson C, Kaplan AS, Kaye WH, Mitchell J, Olsen CM, Pearson JF, Pedersen NL, Strober M, Werge T, Whiteman DC, Woodside DB, Grove J, Henders AK, Larsen JT, Parker R, Petersen LV, Jordan J, Kennedy MA, Lichtenstein P, Norring C, Mortensen PB, Polimanti R, McClintick JN, Adkins AE, Aliev F, Bacanu SA, Batzler A, Bertelsen S, Biernacka JM, Bigdeli TB, Chen LS, Clarke TK, Degenhardt F, Docherty AR, Edwards AC, Foo JC, Fox L, Frank J, Hack LM, Hartmann AM, Hartz SM, Heilmann-Heimbach S, Hodgkinson C, Hoffmann P, Hottenga JJ, Konte B, Lahti J, Lahti-Pulkkinen M, Lai D, Ligthart L, Loukola A, Maher BS, Mbarek H, McIntosh AM, McQueen MB, Meyers JL, Milaneschi Y, Palviainen T, Peterson RE, Ryu E, Saccone NL, Salvatore JE, Sanchez-Roige S, Schwandt M, Sherva R, Streit F, Strohmaier J, Thomas N, Wang JC, Webb BT, Wedow R, Wetherill L, Wills AG, Zhou H, Boardman JD, Chen D, Choi DS, Copeland WE, Culverhouse RC, Dahmen N, Degenhardt L, Domingue BW, Frye MA, Hayward C, Ising M, Keyes M, Kiefer F, Koller G, Kramer J, Kuperman S, Lucae S, Lynskey MT, Maier W, Mann K, Murray AD, Nurnberger JI, Preuss U, Reynolds MD, Ridinger M, Scherbaum N, Schuckit MA, Soyka M, Treutlein J, Witt SH, Wodarz N, Zill P, Adkins DE, Boomsma DI, Bierut LJ, Brown SA, Bucholz KK, Costello EJ, de Wit H, Diazgranados N, Eriksson JG, Farrer LA, Foroud TM, Gillespie NA, Goate AM, Goldman D, Grucza RA, Hancock DB, Harris KM, Hesselbrock V, Hewitt JK, Hopfer CJ, Iacono WG, Johnson EO, Karpyak VM, Kendler KS, Kranzler HR, Krauter K, Lind PA, McGue M, MacKillop J, Madden PAF, Maes HH, Magnusson PKE, Nelson EC, Palmer AA, Penninx BWJH, Porjesz B, Rice JP, Rietschel M, Riley BP, Rose RJ, Shen PH, Silberg J, Stallings MC, Tarter RE, Vanyukov MM, Vrieze S, Wall TL, Whitfield JB, Zhao H, Neale BM, Wade TD, Heath AC, Montgomery GW, Martin NG, Sullivan PF, Kaprio J, Breen G, Gelernter J, Edenberg HJ, Bulik CM, Agrawal A, H?bel C, Gaspar HA, Lepp? VM, Giusti-Rodr?guez P, Boehm I, Egberts K, Ehrlich S, Escaram?s G, Esko T, Fern?ndez-Aranda F, et al. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addict Biol. 2021 01; 26(1):e12880. PMID: 32064741; PMCID: PMC7429266.
      Citations: 21     Fields:    Translation:Humans
    79. Forstner AJ, Fischer SB, Schenk LM, Strohmaier J, Maaser-Hecker A, Sivalingam S, Hecker J, Streit F, Degenhardt F, Witt SH, Schumacher J, Thiele H, Auburger G, Gil Flores S, Rivas F, Mayoral F, Reif A, Herms S, Hoffmann P, Pirooznia M, Goes FS, Rietschel M, Cichon S, Reinbold CS, N?rnberg P, Guzman-Parra J, Orozco Diaz G, Albus M, Borrmann-Hassenbach M, Gonz?lez MJ, Cabaleiro Fabeiro FJ, Del R?o Noriega F, Perez Perez F, Haro Gonz?lez J, Bauer M, Pfennig A, N?then MM. Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families. Transl Psychiatry. 2020 02 04; 10(1):57. PMID: 32066727; PMCID: PMC7026119.
      Citations: 14     Fields:    Translation:Humans
    80. Adorjan K, Mekonnen Z, Tessema F, Ayana M, Degenhardt F, Hoffmann P, Fricker N, Widmann M, Riedke H, Toennes SW, Soboka M, Suleman S, Andlauer TFM, Tesfaye M, Rietschel M, Susser E, Odenwald M, Schulze TG, Mattheisen M. Genotype-phenotype feasibility studies on khat abuse, traumatic experiences and psychosis in Ethiopia. Psychiatr Genet. 2020 02; 30(1):34-38. PMID: 31568069.
      Citations:    Fields:    Translation:HumansAnimals
    81. Niazi Y, Thomsen H, Smolkova B, Vodickova L, Vodenkova S, Kroupa M, Vymetalkova V, Kazimirova A, Barancokova M, Volkovova K, Staruchova M, Hoffmann P, Dusinska M, Musak L, Vodicka P, Hemminki K, N?then MM, F?rsti A. Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Mutagenesis. 2019 12 19; 34(4):323-330. PMID: 31586183.
      Citations: 1     Fields:    Translation:Humans
    82. Haertle L, Lardenoije R, Maierhofer A, Dittrich M, Riemens RJM, Leber M, Riedel-Heller S, Wagner M, Scherer M, van de Hove DLA, Hoffmann P, Ramirez A, Haaf T, El Hajj N, M?ller T, Stora S, Roche M, Ravel A, Mircher C, Cieuta-Walti C, Durand S, M?garban? A. Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer's disease-related dysregulation. Clin Epigenetics. 2019 12 16; 11(1):195. PMID: 31843015; PMCID: PMC6916110.
      Citations: 10     Fields:    Translation:HumansCells
    83. Lardenoije R, Roubroeks JAY, Pishva E, Leber M, Wagner H, Iatrou A, Smith AR, Smith RG, Eijssen LMT, Kleineidam L, Kawalia A, Hoffmann P, Luck T, Riedel-Heller S, Jessen F, Maier W, Wagner M, Kenis G, Ali M, Del Sol A, Mastroeni D, Delvaux E, Coleman PD, Mill J, Rutten BPF, Lunnon K, Ramirez A, Hurlemann R, van den Hove DLA. Alzheimer's disease-associated (hydroxy)methylomic changes in the brain and blood. Clin Epigenetics. 2019 11 27; 11(1):164. PMID: 31775875; PMCID: PMC6880587.
      Citations: 49     Fields:    Translation:HumansCells
    84. Forstner AJ, Maron E, Erhardt A, Czamara D, Eriksson E, Lavebratt C, Allgulander C, Friedrich N, Becker J, Hecker J, Rambau S, Conrad R, Geiser F, McMahon FJ, Moebus S, Hess T, Buerfent BC, Hoffmann P, Herms S, Heilmann-Heimbach S, Kockum I, Olsson T, Alfredsson L, Alpers GW, Fehm L, Fydrich T, Gerlach AL, Hamm A, Kircher T, Lang T, Meier S, Metspalu A, Domschke K, Reif A, Hovatta I, Lindefors N, Andersson E, Schalling M, Mbarek H, Milaneschi Y, de Geus EJC, Boomsma DI, Penninx BWJH, Thorgeirsson TE, Steinberg S, Stefansson K, Stefansson H, Hansen TF, Werge T, Mortensen PB, Nordentoft M, Hougaard DM, Hultman CM, Sullivan PF, Woldbye DPD, Mors O, Binder EB, Schumacher J, Awasthi S, Wolf C, Weber H, Arolt V, Pan?-Farr? CA, Pauli P, Rief W, Str?hle A, Plag J, Wittchen HU, Mattheisen M, M?ller-Myhsok B, B?rglum AD, N?then MM, R?ck C, Ripke S, Deckert J. Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression. Mol Psychiatry. 2021 08; 26(8):4179-4190. PMID: 31712720.
      Citations: 24     Fields:    Translation:Humans
    85. Andlauer TFM, Streit F, Strohmaier J, Auburger G, Degenhardt F, Heilmann-Heimbach S, Herms S, Hoffmann P, Frank J, Foo JC, Treutlein J, Witt SH, Cichon S, Kogevinas M, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Forstner AJ, Rietschel M, Guzman-Parra J, Gonz?lez MJ, Gil Flores S, Cabaleiro Fabeiro FJ, Del R?o Noriega F, Perez FP, Haro Gonz?lez J, Orozco Diaz G, de Diego-Otero Y, Moreno-K?stner B, Rivas F, Mayoral F, M?ller-Myhsok B, N?then MM. Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. Mol Psychiatry. 2021 04; 26(4):1286-1298. PMID: 31712721; PMCID: PMC7985020.
      Citations: 14     Fields:    Translation:Humans
    86. Novak N, Bej S, Mayr G, Emmert H, Gerdes S, Jung ES, Degenhardt F, Ellinghaus E, Wienbrandt L, Lieb W, Hotze M, Dand N, Arnold A, Homuth G, Schmidt CO, Wehkamp U, Hoffmann P, Paternoster L, Early Genetics and Lifecourse Epidemiology (EAGLE) Eczema Consortium, Ahluwalia TS, Bisgaard H, Werfel T, Lee YA, Wolfien M, Rosenstiel P, Wolkenhauer O, Schreiber S, Franke A, Weidinger S, Ellinghaus D, Mucha S, Baurecht H, Rodr?guez E, St?lzl D, H?benthal M, K?ssens JC, M?ller-Nurasyid M, Grosche S, Marenholz I, N?then MM, Standl M, B?nnelykke K, Peters A, Gieger C, Waldenberger M, Schulz H, Strauch K. Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression. J Allergy Clin Immunol. 2020 04; 145(4):1208-1218. PMID: 31707051.
      Citations: 15     Fields:    Translation:HumansCells
    87. Chattopadhyay S, Thomsen H, Weinhold N, Meziane I, Huhn S, da Silva Filho MI, Vodicka P, Vodickova L, Hoffmann P, Landi S, Hajek R, Pettersson-Kymmer U, Ohlsson C, Milani P, Merlini G, Rowcieno D, Hawkins P, Hegenbart U, Palladini G, Wechalekar A, Houlston R, Goldschmidt H, Hemminki K, N?then MM, J?ckel KH, Schmidt B, Hallmans G, Sch?nland SO, F?rsti A. Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance. Leukemia. 2020 04; 34(4):1187-1191. PMID: 31695157.
      Citations: 8     Fields:    Translation:Humans
    88. Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Frizatti A, Chouraki V, Martin ER, Sleegers K, Badarinarayan N, Jakobsdottir J, Hamilton-Nelson KL, Raybould R, Chen Y, Kuzma AB, Hiltunen M, Morgan T, Ahmad S, Vardarajan BN, Hoffmann P, Beecham GW, Harold D, Fitzpatrick AL, Valladares O, Gerrish A, Smith AV, Qu L, Denning N, Jian X, Zhao Y, Del Zompo M, Fox NC, Hughes JT, Adams HH, Malamon J, Patel Y, Brody JA, Dombroski BA, Daniilidou M, Eiriksdottir G, Mukherjee S, Wallon D, Uphill J, Aspelund T, Cantwell LB, Galimberti D, Hofer E, Butkiewicz M, Scarpini E, Sarnowski C, Bush WS, Kornhuber J, White CC, Song Y, Barber RC, Engelborghs S, Sordon S, Voijnovic D, Adams PM, Vandenberghe R, Mayhaus M, Cupples LA, Albert MS, De Deyn PP, Gu W, Himali JJ, Beekly D, Squassina A, Hartmann AM, Blacker D, Lovestone S, Garcia ME, Doody RS, Sussams R, Lin H, Fairchild TJ, Holmes C, Karamujic-Comic H, Frosch MP, Thonberg H, Maier W, Roshchupkin G, Ghetti B, Giedraitis V, Kawalia A, Li S, Huebinger RM, Kilander L, Moebus S, Kamboh MI, Brundin R, Turton J, Yang Q, Katz MJ, Concari L, Lord J, Beiser AS, Keene CD, Helisalmi S, Kloszewska I, Kukull WA, Koivisto AM, Lynch A, Larson EB, Haapasalo A, Lawlor B, Mosley TH, Lipton RB, Solfrizzi V, Gill M, Longstreth WT, Montine TJ, Frisardi V, Rivadeneira F, Petersen RC, Salani F, Ciaramella A, Boerwinkle E, Reiman EM, Fievet N, Rotter JI, Reisch JS, Cupidi C, Uitterlinden AGA, Royall DR, Dufouil C, Maletta RG, Sano M, Cecchetti R, George-Hyslop PS, Tsolaki M, Tsuang DW, Craig D, Wu CK, Soininen H, Avramidou D, Albin RL, Fratiglioni L, Germanou A, Apostolova LG, Keller L, Koutroumani M, Arnold SE, Panza F, Gkatzima O, Asthana S, Hannequin D, Whitehead P, Atwood CS, Caffarra P, Hampel H, Lannfelt L, Rubinsztein DC, Barnes LL, Barral S, McGuinness B, Beach TG, Johnston JA, Becker JT, Passmore P, Bigio EH, Schott JM, Bird TD, Warren JD, Boeve BF, Lupton MK, Bowen JD, Proitsi P, Boxer A, Powell JF, Burke JR, Kauwe JSK, Burns JM, Mancuso M, Buxbaum JD, Bonuccelli U, Cairns NJ, McQuillin A, Cao C, Livingston G, Carlson CS, Bass NJ, Carlsson CM, Hardy J, Carney RM, Bras J, Carrasquillo MM, Guerreiro R, Allen M, Chui HC, Fisher E, Masullo C, Crocco EA, DeCarli C, Bisceglio G, Dick M, Ma L, Duara R, Graff-Radford NR, Evans DA, Hodges A, Faber KM, Scherer M, Fallon KB, Riemenschneider M, Fardo DW, Heun R, Farlow MR, Ferris S, Leber M, Foroud TM, Galasko DR, Giegling I, Gearing M, Geschwind DH, Gilbert JR, Morris J, Green RC, Mayo K, Growdon JH, Feulner T, Hamilton RL, Harrell LE, Drichel D, Honig LS, Cushion TD, Huentelman MJ, Hollingworth P, Hulette CM, Hyman BT, Marshall R, Jarvik GP, Meggy A, Abner E, Menzies GE, Leonenko G, Jun GR, Baldwin CT, Grozeva D, Karydas A, Russo G, Kaye JA, Kim R, Jessen F, Kowall NW, Vellas B, Kramer JH, Vardy E, LaFerla FM, Lah JJ, Leverenz JB, Mann D, Levey AI, Pickering-Brown S, Lieberman AP, Lunetta KL, Wichmann HE, Lyketsos CG, Morgan K, Marson DC, Brown K, Martiniuk F, Medway C, Mash DC, Masliah E, Hooper NM, McCormick WC, Daniele A, McCurry SM, Bayer A, McDavid AN, Gallacher J, McKee AC, van den Bussche H, Mesulam M, Brayne C, Miller BL, Riedel-Heller S, Miller CA, Miller JW, Morris JC, Myers AJ, Wiltfang J, O'Bryant S, Olichney JM, Alvarez V, Parisi JE, Singleton AB, Paulson HL, Collinge J, Perry WR, Mead S, Peskind E, Cribbs DH, Rossor M, Pierce A, Ryan NS, Poon WW, Nacmias B, Potter H, Sorbi S, Quinn JF, Sacchinelli E, Raj A, Spalletta G, Raskind M, Caltagirone C, Orfei MD, Reisberg B, Clarke R, Reitz C, Smith AD, Ringman JM, Warden D, Roberson ED, Wilcock G, Rogaeva E, Bruni AC, Rosen HJ, Gallo M, Rosenberg RN, Ben-Shlomo Y, Sager MA, Mecocci P, Saykin AJ, Cuccaro ML, Vance JM, Schneider JA, Schneider LS, Slifer S, Seeley WW, Smith AG, Sonnen JA, Spina S, Stern RA, Swerdlow RH, Tang M, Tanzi RE, Trojanowski JQ, Troncoso JC, Van Deerlin VM, Van Eldik LJ, Vinters HV, Vonsattel JP, Weintraub S, et al. Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates A?, tau, immunity and lipid processing. Nat Genet. 2019 Sep; 51(9):1423-1424. PMID: 31417202; PMCID: PMC7265117.
      Citations: 28     Fields:    
    89. Went M, Kinnersley B, Sud A, Johnson DC, Weinhold N, van Duin M, Orlando G, Mitchell JS, Kuiper R, Walker BA, Gregory WM, Hoffmann P, Jackson GH, da Silva Filho MI, Thomsen H, Broyl A, Davies FE, Thorsteinsdottir U, Kaiser M, Sonneveld P, Goldschmidt H, Stefansson K, Hemminki K, Morgan GJ, Houlston RS, F?rsti A, N?then MM, Hansson M, Nilsson B. Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes. Hum Genomics. 2019 08 20; 13(1):37. PMID: 31429796; PMCID: PMC6700979.
      Citations: 8     Fields:    Translation:HumansCells
    90. Mullins N, Bigdeli TB, B?rglum AD, Coleman JRI, Demontis D, Mehta D, Power RA, Ripke S, Stahl EA, Starnawska A, Anjorin A, M.R.C.Psych, Corvin A, Sanders AR, Forstner AJ, Reif A, Koller AC, Swiatkowska B, Baune BT, M?ller-Myhsok B, Penninx BWJH, Pato C, Zai C, Rujescu D, Hougaard DM, Quested D, Levinson DF, Binder EB, Byrne EM, Agerbo E, Dr.Med.Sc, Streit F, Mayoral F, Bellivier F, Degenhardt F, Breen G, Morken G, Turecki G, Rouleau GA, Grabe HJ, V?lzke H, Jones I, Giegling I, Agartz I, Melle I, Lawrence J, Walters JTR, Strohmaier J, Shi J, Hauser J, Biernacka JM, Vincent JB, Kelsoe J, Strauss JS, Lissowska J, Pimm J, Smoller JW, Guzman-Parra J, Berger K, Scott LJ, Jones LA, Azevedo MH, Trzaskowski M, Kogevinas M, Rietschel M, Boks M, Ising M, Grigoroiu-Serbanescu M, Hamshere ML, Leboyer M, Frye M, N?then MM, Alda M, Preisig M, Nordentoft M, Boehnke M, O'Donovan MC, Owen MJ, Pato MT, Renteria ME, Budde M, Dipl.-Psych, Weissman MM, Wray NR, Bass N, Craddock N, Smeland OB, Andreassen OA, Mors O, Gejman PV, Sklar P, McGrath P, Hoffmann P, McGuffin P, Lee PH, Mortensen PB, Kahn RS, Ophoff RA, Adolfsson R, Van der Auwera S, Djurovic S, Kloiber S, Heilmann-Heimbach S, Jamain S, Hamilton SP, McElroy SL, Lucae S, Cichon S, Schulze TG, Hansen T, Werge T, Air TM, Nimgaonkar V, Appadurai V, Cahn W, Milaneschi Y, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Fanous AH, Kendler KS, McQuillin A, Lewis CM. GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. Am J Psychiatry. 2019 08 01; 176(8):651-660. PMID: 31164008; PMCID: PMC6675659.
      Citations: 101     Fields:    Translation:Humans
    91. Takahashi H, Cornish AJ, Sud A, Law PJ, Kinnersley B, Ostrom QT, Labreche K, Eckel-Passow JE, Armstrong GN, Claus EB, Il'yasova D, Schildkraut J, Barnholtz-Sloan JS, Olson SH, Bernstein JL, Lai RK, Schoemaker MJ, Simon M, Hoffmann P, Chanock S, Rajaraman P, Johansen C, Jenkins RB, Wrensch MR, Bondy ML, Turnbull C, Houlston RS, N?then MM, J?ckel KH, Melin BS, Sanson M. Publisher Correction: Mendelian randomisation study of the relationship between vitamin D and risk of glioma. Sci Rep. 2019 May 23; 9(1):7924. PMID: 31118477; PMCID: PMC6531429.
      Citations:    Fields:    
    92. Law PJ, Timofeeva M, Broderick P, Studd J, Fernandez-Tajes J, Farrington S, Svinti V, Palles C, Orlando G, Sud A, Holroyd A, Penegar S, Theodoratou E, Vaughan-Shaw P, Campbell H, Zgaga L, Hayward C, Campbell A, Harris S, Deary IJ, Starr J, Gatcombe L, Pinna M, Briggs S, Martin L, Jaeger E, Sharma-Oates A, East J, Leedham S, Arnold R, Johnstone E, Wang H, Kerr D, Kerr R, Maughan T, Kaplan R, Al-Tassan N, Palin K, Cajuso T, Tanskanen T, Kondelin J, Kaasinen E, Sarin AP, Rissanen H, Knekt P, Pukkala E, Jousilahti P, Salomaa V, Ripatti S, Palotie A, Renkonen-Sinisalo L, Buchanan DD, Win AK, Hopper J, Jenkins ME, Lindor NM, Newcomb PA, Gallinger S, Duggan D, Casey G, Hoffmann P, Easton DF, Pharoah PDP, Peto J, Canzian F, Swerdlow A, Eeles RA, Kote-Jarai Z, Muir K, Pashayan N, PRACTICAL consortium, Harkin A, Allan K, McQueen J, Paul J, Iveson T, Saunders M, Butterbach K, Chang-Claude J, Hoffmeister M, Brenner H, Kirac I, Hofer P, Brezina S, Gsur A, Cheadle JP, Aaltonen LA, Tomlinson I, Houlston RS, Dunlop MG, Fernandez-Rozadilla C, H?nninen UA, Eriksson JG, Lepist? A, B?hm J, Mecklin JP, N?then MM, J?ckel KH, Mato?evic P. Association analyses identify 31 new risk loci for colorectal cancer susceptibility. Nat Commun. 2019 05 14; 10(1):2154. PMID: 31089142; PMCID: PMC6517433.
      Citations: 103     Fields:    Translation:Humans
    93. Stahl EA, Breen G, Forstner AJ, McQuillin A, Ripke S, Mattheisen M, Wang Y, Coleman JRI, de Leeuw CA, Steinberg S, Pavlides JMW, Trzaskowski M, Byrne EM, Pers TH, Holmans PA, Richards AL, Abbott L, Agerbo E, Akil H, Albani D, Alliey-Rodriguez N, Als TD, Anjorin A, Antilla V, Badner JA, Barchas JD, Bass N, Belliveau R, Bergen SE, Boks MP, Boocock J, Budde M, Bunney W, Burmeister M, Bybjerg-Grauholm J, Byerley W, Casas M, Cerrato F, Cervantes P, Chambert K, Charney AW, Chen D, Churchhouse C, Clarke TK, Coryell W, Craig DW, Cruceanu C, Curtis D, Czerski PM, Dale AM, de Jong S, Degenhardt F, Del-Favero J, DePaulo JR, Dobbyn AL, Dumont A, Escott-Price V, Fan CC, Fischer SB, Flickinger M, Foroud TM, Forty L, Frank J, Fraser C, Freimer NB, Gade K, Gage D, Garnham J, Giambartolomei C, Goldstein J, Gordon SD, Gordon-Smith K, Green EK, Green MJ, Greenwood TA, Grove J, Guan W, Hamshere ML, Heilbronner U, Herms S, Hipolito M, Hoffmann P, Holland D, Huckins L, Johnson JS, Kandaswamy R, Karlsson R, Kennedy JL, Kittel-Schneider S, Knowles JA, Kogevinas M, Koller AC, Kupka R, Lavebratt C, Lawrence J, Lawson WB, Leber M, Lee PH, Levy SE, Li JZ, Liu C, Lucae S, Maaser A, MacIntyre DJ, Mahon PB, Maier W, Martinsson L, McCarroll S, McGuffin P, McInnis MG, McKay JD, Medeiros H, Medland SE, Meng F, Milani L, Montgomery GW, Morris DW, Mullins N, Nguyen H, Nievergelt CM, Nwulia EA, O'Donovan C, Loohuis LMO, Ori APS, Oruc L, Perlis RH, Perry A, Potash JB, Purcell SM, Regeer EJ, Reif A, Rice JP, Rivera M, Roussos P, Ruderfer DM, Ryu E, Schatzberg AF, Scheftner WA, Schork NJ, Shannon Weickert C, Shehktman T, Shilling PD, Sigurdsson E, Slaney C, Smeland OB, Sobell JL, Spijker AT, St Clair D, Steffens M, Strauss JS, Streit F, Strohmaier J, Szelinger S, Thompson RC, Thorgeirsson TE, Treutlein J, Vedder H, Wang W, Watson SJ, Weickert TW, Witt SH, Xi S, Xu W, Young AH, Zandi P, Zhang P, eQTLGen Consortium, BIOS Consortium, Agartz I, Alda M, Backlund L, Baune BT, Bellivier F, Berrettini WH, Biernacka JM, Blackwood DHR, Boehnke M, Corvin A, Craddock N, Daly MJ, Dannlowski U, Etain B, Frye M, Fullerton JM, Gershon ES, Gill M, Goes F, Grigoroiu-Serbanescu M, Hauser J, Hougaard DM, Hultman CM, Jones I, Jones LA, Kirov G, Lewis CM, Li QS, Lissowska J, Martin NG, McElroy SL, McIntosh AM, McMahon FJ, Melle I, Metspalu A, Mitchell PB, Morken G, Mors O, Mortensen PB, Myers RM, Neale BM, Nimgaonkar V, Nordentoft M, O'Donovan MC, Oedegaard KJ, Owen MJ, Paciga SA, Pato C, Pato MT, Posthuma D, Ramos-Quiroga JA, Rietschel M, Rouleau GA, Schalling M, Schofield PR, Schulze TG, Serretti A, Smoller JW, Stefansson H, Stefansson K, Stordal E, Sullivan PF, Turecki G, Vaaler AE, Vieta E, Vincent JB, Werge T, Nurnberger JI, Wray NR, Di Florio A, Edenberg HJ, Cichon S, Ophoff RA, Scott LJ, Andreassen OA, Kelsoe J, Sklar P, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Trubetskoy V, Gaspar HA, Awasthi S, B?kvad-Hansen M, Bauer M, Pedersen CB, B?en E, Djurovic S, Elvs?shagen T, Fris?n L, Pedersen MG, Guzman-Parra J, Hautzinger M, Jamain S, Jur?us A, M?hleisen TW, Adolfsson AN, ?sby U, Pfennig A, Reinbold CS, Rivas F, S?nchez-Mora C, S?holm Hansen C, Z?llner S, Adolfsson R, B?rglum AD, Esko T, Kahn RS, Land?n M, Leboyer M, Mayoral F, M?ller-Myhsok B, N?then MM, Ribas?s M. Genome-wide association study identifies 30 loci associated with bipolar disorder. Nat Genet. 2019 05; 51(5):793-803. PMID: 31043756; PMCID: PMC6956732.
      Citations: 600     Fields:    Translation:Humans
    94. Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Frizatti A, Chouraki V, Martin ER, Sleegers K, Badarinarayan N, Jakobsdottir J, Hamilton-Nelson KL, Raybould R, Chen Y, Kuzma AB, Hiltunen M, Morgan T, Ahmad S, Vardarajan BN, Hoffmann P, Beecham GW, Harold D, Fitzpatrick AL, Valladares O, Gerrish A, Smith AV, Qu L, Denning N, Jian X, Zhao Y, Del Zompo M, Fox NC, Hughes JT, Adams HH, Malamon J, Patel Y, Brody JA, Dombroski BA, Daniilidou M, Eiriksdottir G, Mukherjee S, Wallon D, Uphill J, Aspelund T, Cantwell LB, Galimberti D, Hofer E, Butkiewicz M, Scarpini E, Sarnowski C, Bush WS, Kornhuber J, White CC, Song Y, Barber RC, Engelborghs S, Sordon S, Voijnovic D, Adams PM, Vandenberghe R, Mayhaus M, Cupples LA, Albert MS, De Deyn PP, Gu W, Himali JJ, Beekly D, Squassina A, Hartmann AM, Blacker D, Lovestone S, Garcia ME, Doody RS, Sussams R, Lin H, Fairchild TJ, Holmes C, Karamujic-Comic H, Frosch MP, Thonberg H, Maier W, Roshchupkin G, Ghetti B, Giedraitis V, Kawalia A, Li S, Huebinger RM, Kilander L, Moebus S, Kamboh MI, Brundin R, Turton J, Yang Q, Katz MJ, Concari L, Lord J, Beiser AS, Keene CD, Helisalmi S, Kloszewska I, Kukull WA, Koivisto AM, Lynch A, Larson EB, Haapasalo A, Lawlor B, Mosley TH, Lipton RB, Solfrizzi V, Gill M, Longstreth WT, Montine TJ, Frisardi V, Rivadeneira F, Petersen RC, Salani F, Ciaramella A, Boerwinkle E, Reiman EM, Fievet N, Rotter JI, Reisch JS, Cupidi C, Andre Uitterlinden AG, Royall DR, Dufouil C, Maletta RG, Sano M, Cecchetti R, George-Hyslop PS, Tsolaki M, Tsuang DW, Craig D, Wu CK, Soininen H, Avramidou D, Albin RL, Fratiglioni L, Germanou A, Apostolova LG, Keller L, Koutroumani M, Arnold SE, Panza F, Gkatzima O, Asthana S, Hannequin D, Whitehead P, Atwood CS, Caffarra P, Hampel H, Lannfelt L, Rubinsztein DC, Barnes LL, Barral S, McGuinness B, Beach TG, Johnston JA, Becker JT, Passmore P, Bigio EH, Schott JM, Bird TD, Warren JD, Boeve BF, Lupton MK, Bowen JD, Proitsi P, Boxer A, Powell JF, Burke JR, Kauwe JSK, Burns JM, Mancuso M, Buxbaum JD, Bonuccelli U, Cairns NJ, McQuillin A, Cao C, Livingston G, Carlson CS, Bass NJ, Carlsson CM, Hardy J, Carney RM, Bras J, Carrasquillo MM, Guerreiro R, Allen M, Chui HC, Fisher E, Masullo C, Crocco EA, DeCarli C, Bisceglio G, Dick M, Ma L, Duara R, Graff-Radford NR, Evans DA, Hodges A, Faber KM, Scherer M, Fallon KB, Riemenschneider M, Fardo DW, Heun R, Farlow MR, Ferris S, Leber M, Foroud TM, Galasko DR, Giegling I, Gearing M, Geschwind DH, Gilbert JR, Morris J, Green RC, Mayo K, Growdon JH, Feulner T, Hamilton RL, Harrell LE, Drichel D, Honig LS, Cushion TD, Huentelman MJ, Hollingworth P, Hulette CM, Hyman BT, Marshall R, Jarvik GP, Meggy A, Abner E, Menzies GE, Leonenko G, Jun GR, Baldwin CT, Grozeva D, Karydas A, Russo G, Kaye JA, Kim R, Jessen F, Kowall NW, Vellas B, Kramer JH, Vardy E, LaFerla FM, Lah JJ, Leverenz JB, Mann D, Levey AI, Pickering-Brown S, Lieberman AP, Lunetta KL, Wichmann HE, Lyketsos CG, Morgan K, Marson DC, Brown K, Martiniuk F, Medway C, Mash DC, Masliah E, Hooper NM, McCormick WC, Daniele A, McCurry SM, Bayer A, McDavid AN, Gallacher J, McKee AC, van den Bussche H, Mesulam M, Brayne C, Miller BL, Riedel-Heller S, Miller CA, Miller JW, Morris JC, Myers AJ, Wiltfang J, O'Bryant S, Olichney JM, Alvarez V, Parisi JE, Singleton AB, Paulson HL, Collinge J, Perry WR, Mead S, Peskind E, Cribbs DH, Rossor M, Pierce A, Ryan NS, Poon WW, Nacmias B, Potter H, Sorbi S, Quinn JF, Sacchinelli E, Raj A, Spalletta G, Raskind M, Caltagirone C, Orfei MD, Reisberg B, Clarke R, Reitz C, Smith AD, Ringman JM, Warden D, Roberson ED, Wilcock G, Rogaeva E, Bruni AC, Rosen HJ, Gallo M, Rosenberg RN, Ben-Shlomo Y, Sager MA, Mecocci P, Saykin AJ, Cuccaro ML, Vance JM, Schneider JA, Schneider LS, Slifer S, Seeley WW, Smith AG, Sonnen JA, Spina S, Stern RA, Swerdlow RH, Tang M, Tanzi RE, Trojanowski JQ, Troncoso JC, Van Deerlin VM, Van Eldik LJ, Vinters HV, Vonsattel JP, Weintraub S, et al. Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates A?, tau, immunity and lipid processing. Nat Genet. 2019 03; 51(3):414-430. PMID: 30820047; PMCID: PMC6463297.
      Citations: 1105     Fields:    Translation:Humans
    95. Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Brandler W, Huguet G, Morris AP, Hulslander J, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Peyrard-Janvid M, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Wilcke A, Francks C, Bourgeron T, Monaco AP, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Honbolyg? F, T?th D, Cs?pe V, Lyytinen H, Lepp?nen PHT, Ramus F, N?then MM, M?ller-Myhsok B, Schulte-K?rne G. Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Transl Psychiatry. 2019 02 11; 9(1):77. PMID: 30741946; PMCID: PMC6370792.
      Citations: 36     Fields:    Translation:Humans
    96. Thomsen H, Chattopadhyay S, Weinhold N, Vodicka P, Vodickova L, Hoffmann P, Langer C, Hajek R, Pettersson-Kymmer U, Ohlsson C, Houlston R, Goldschmidt H, Hemminki K, N?then MM, J?ckel KH, Hallmans G, Sp?th F, F?rsti A. Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma. Leukemia. 2019 07; 33(7):1817-1821. PMID: 30737484.
      Citations: 9     Fields:    Translation:Humans
    97. Schulz H, Ruppert AK, Zara F, Madia F, Iacomino M, S Vari M, Balagura G, Minetti C, Striano P, Bianchi A, Marini C, Guerrini R, Kunz WS, Oliver KL, Bellows ST, Mullen SA, Berkovic SF, Scheffer IE, Ozbek U, Hoffmann P, Schramm S, Tsortouktzidis D, Becker AJ, Sander T, Weber YG, Becker F, Lerche H, Kapser C, Schankin CJ, M?ller RS, Caglayan H. No evidence for a BRD2 promoter hypermethylation in?blood leukocytes of Europeans with juvenile myoclonic?epilepsy. Epilepsia. 2019 05; 60(5):e31-e36. PMID: 30719712.
      Citations: 2     Fields:    Translation:HumansCells
    98. Atkins I, Kinnersley B, Ostrom QT, Labreche K, Il'yasova D, Armstrong GN, Eckel-Passow JE, Schoemaker MJ, Barnholtz-Sloan JS, Swerdlow AJ, Simon M, Rajaraman P, Chanock SJ, Shildkraut J, Bernstein JL, Hoffmann P, Lai RK, Claus EB, Olson SH, Johansen C, Wrensch MR, Jenkins RB, Bondy ML, Houlston RS, N?then MM, J?ckel KH, Melin B, Sanson M. Transcriptome-Wide Association Study Identifies New Candidate Susceptibility Genes for Glioma. Cancer Res. 2019 04 15; 79(8):2065-2071. PMID: 30709929; PMCID: PMC6522343.
      Citations: 16     Fields:    Translation:HumansCells
    99. Hanses C, Milz E, Becker J, Heilmann-Heimbach S, Hoffmann P, Avalos MSS, Bosco P, Spalletta G, Galimberti D, Mancuso M, Nacmias B, Sorbi S, Mecocci P, Pilotto A, Caffarra P, Panza F, Coto E, Graff C, Ingelsson M, Scaro H, Maier W, Jessen F, Lambert JC, Ramirez A, Dalmasso MC, Brusco LI, Olivar N, Muchnik C, Prestia FA, Galeano P, Martinez LE, Carulla ME, Azurmendi PJ, Liberczuk C, Fezza C, Sampa?o M, Fierens M, Jemar G, Solis P, Medel N, Lisso J, Sevillano Z, Boss? P, Bullido M, Clarimon J, S?nchez-Juan P, Sanchez-Garcia F, Bellenguez C, Casta?o EM, Kairiyama C, Politis DG, Kochen S, Mangone CA, Morelli L. Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease. Transl Psychiatry. 2019 01 31; 9(1):55. PMID: 30705288; PMCID: PMC6355764.
      Citations: 19     Fields:    Translation:Humans
    100. Takahashi H, Cornish AJ, Sud A, Law PJ, Disney-Hogg L, Calvocoressi L, Lu L, Hansen HM, Smirnov I, Walsh KM, Schramm J, Hoffmann P, Schildkraut JM, Simon M, Bondy M, Wrensch M, Wiemels JL, Claus EB, Turnbull C, Houlston RS, N?then MM, J?ckel KH. Mendelian randomization provides support for obesity as a risk factor for meningioma. Sci Rep. 2019 01 22; 9(1):309. PMID: 30670737; PMCID: PMC6343031.
      Citations: 12     Fields:    Translation:Humans
    101. Vijayakrishnan J, Studd J, Broderick P, Kinnersley B, Holroyd A, Law PJ, Kumar R, Allan JM, Harrison CJ, Moorman AV, Vora A, Roman E, Rachakonda S, Kinsey SE, Sheridan E, Thompson PD, Irving JA, Koehler R, Hoffmann P, Heilmann-Heimbach S, Easton DF, Pharaoh PDP, Dunning AM, Peto J, Canzian F, Swerdlow A, Eeles RA, Kote-Jarai Z, Muir K, Pashayan N, PRACTICAL consortium, Greaves M, Zimmerman M, Bartram CR, Schrappe M, Stanulla M, Hemminki K, Houlston RS, N?then MM, J?ckel KH. Author Correction: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. Nat Commun. 2019 01 21; 10(1):419. PMID: 30664635; PMCID: PMC6341085.
      Citations:    Fields:    
    102. Went M, Sud A, Halvarsson BM, Weinhold N, Kimber S, van Duin M, Thorleifsson G, Holroyd A, Johnson DC, Li N, Orlando G, Law PJ, Ali M, Chen B, Mitchell JS, Gudbjartsson DF, Kuiper R, Stephens OW, Bertsch U, Broderick P, Campo C, Bandapalli OR, Gregory WA, Gullberg U, Hillengass J, Hoffmann P, Jackson GH, Johnsson E, Mellqvist UH, Nahi H, Easton D, Pharoah P, Dunning A, Peto J, Canzian F, Swerdlow A, Eeles RA, Kote-Jarai Z, Muir K, Pashayan N, PRACTICAL consortium, Nickel J, Rafnar T, Ross FM, da Silva Filho MI, Thomsen H, Vangsted A, Andersen NF, Waage A, Walker BA, Wihlborg AK, Broyl A, Davies FE, Thorsteinsdottir U, Langer C, Hansson M, Goldschmidt H, Kaiser M, Sonneveld P, Stefansson K, Morgan GJ, Hemminki K, Houlston RS, F?rsti A, Einsele H, J?ckel KH, Kristinsson SY, N?then MM, Turesson I, Nilsson B. Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. Nat Commun. 2019 01 10; 10(1):213. PMID: 30631080; PMCID: PMC6328616.
      Citations:    Fields:    
    103. Sud A, Thomsen H, Law PJ, da Silva Filho MI, Holroyd A, Broderick P, Orlando G, Lenive O, Wright L, Cooke R, Easton D, Pharoah P, Dunning A, Peto J, Canzian F, Eeles R, Kote-Jarai Z, Muir K, Pashayan N, PRACTICAL consortium, Hoffmann P, von Strandmann EP, Lightfoot T, Kane E, Roman E, Lake A, Montgomery D, Jarrett RF, Swerdlow AJ, Engert A, Orr N, Hemminki K, Houlston RS, F?rsti A, N?then MM, J?ckel KH. Author Correction: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility. Nat Commun. 2019 01 08; 10(1):157. PMID: 30622283; PMCID: PMC6325156.
      Citations:    Fields:    
    104. Lackner P, Hoffmann P, Stanzial F, Parmeggiani L, Benedicenti F, Pellegrin S, Casara G, Domingues FS, K?nig E, Schwienbacher C, Volpato CB, Picard A, Cantaloni C, Mascalzoni D, Heimbach A, Hicks AA, Pramstaller PP. Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly. Seizure. 2019 Mar; 66:81-85. PMID: 30818181.
      Citations: 9     Fields:    Translation:Humans
    105. Went M, Sud A, Speedy H, Sunter NJ, Law PJ, Johnson DC, Mirabella F, Holroyd A, Li N, Orlando G, Weinhold N, van Duin M, Chen B, Mitchell JS, Mansouri L, Juliusson G, Smedby KE, Jayne S, Majid A, Dearden C, Allsup DJ, Bailey JR, Pratt G, Pepper C, Fegan C, Rosenquist R, Kuiper R, Stephens OW, Bertsch U, Broderick P, Gregory WM, Hillengass J, Hoffmann P, Jackson GH, Nickel J, da Silva Filho MI, Thomsen H, Walker BA, Broyl A, Davies FE, Hansson M, Goldschmidt H, Dyer MJS, Kaiser M, Sonneveld P, Morgan GJ, Hemminki K, Catovsky D, Allan JM, Houlston RS, F?rsti A, Einsele H, J?ckel KH, N?then MM, Nilsson B. Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology. Blood Cancer J. 2018 12 21; 9(1):1. PMID: 30602759; PMCID: PMC6315026.
      Citations: 8     Fields:    Translation:Humans
    106. Walters RK, Polimanti R, Johnson EC, McClintick JN, Adams MJ, Adkins AE, Aliev F, Bacanu SA, Batzler A, Bertelsen S, Biernacka JM, Bigdeli TB, Chen LS, Clarke TK, Chou YL, Degenhardt F, Docherty AR, Edwards AC, Fontanillas P, Foo JC, Fox L, Frank J, Giegling I, Gordon S, Hack LM, Hartmann AM, Hartz SM, Heilmann-Heimbach S, Herms S, Hodgkinson C, Hoffmann P, Jan Hottenga J, Kennedy MA, Alanne-Kinnunen M, Konte B, Lahti J, Lahti-Pulkkinen M, Lai D, Ligthart L, Loukola A, Maher BS, Mbarek H, McIntosh AM, McQueen MB, Meyers JL, Milaneschi Y, Palviainen T, Pearson JF, Peterson RE, Ripatti S, Ryu E, Saccone NL, Salvatore JE, Sanchez-Roige S, Schwandt M, Sherva R, Streit F, Strohmaier J, Thomas N, Wang JC, Webb BT, Wedow R, Wetherill L, Wills AG, 23andMe Research Team, Boardman JD, Chen D, Choi DS, Copeland WE, Culverhouse RC, Dahmen N, Degenhardt L, Domingue BW, Elson SL, Frye MA, Hayward C, Ising M, Keyes M, Kiefer F, Kramer J, Kuperman S, Lucae S, Lynskey MT, Maier W, Mann K, Murray AD, Nurnberger JI, Palotie A, Preuss U, Reynolds MD, Ridinger M, Scherbaum N, Schuckit MA, Soyka M, Treutlein J, Witt S, Wodarz N, Zill P, Adkins DE, Boden JM, Boomsma DI, Bierut LJ, Brown SA, Bucholz KK, Cichon S, Costello EJ, de Wit H, Diazgranados N, Dick DM, Eriksson JG, Farrer LA, Foroud TM, Gillespie NA, Goate AM, Goldman D, Grucza RA, Hancock DB, Harris KM, Heath AC, Hesselbrock V, Hewitt JK, Hopfer CJ, Horwood J, Iacono W, Johnson EO, Kaprio JA, Karpyak VM, Kendler KS, Kranzler HR, Krauter K, Lichtenstein P, Lind PA, McGue M, MacKillop J, Madden PAF, Maes HH, Magnusson P, Martin NG, Medland SE, Montgomery GW, Nelson EC, Palmer AA, Pedersen NL, Penninx BWJH, Porjesz B, Rice JP, Rietschel M, Riley BP, Rose R, Rujescu D, Shen PH, Silberg J, Stallings MC, Tarter RE, Vanyukov MM, Vrieze S, Wall TL, Whitfield JB, Zhao H, Neale BM, Gelernter J, Edenberg HJ, Agrawal A, G?bel W, M?nnist? S, M?ller-Myhsok B, R?ikk?nen K, N?then MM. Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nat Neurosci. 2018 12; 21(12):1656-1669. PMID: 30482948; PMCID: PMC6430207.
      Citations: 244     Fields:    Translation:Humans
    107. Spinell T, Hoffmann P, Enkling N, Renvert S, Schwarz F, Demmer RT, Papapanou PN, Kebschull M, Kr?ger A, H?lsmann C, Fickl S, H?ttig F, Kaufmann F, Heimbach A, Jepsen S. The severity of human peri-implantitis lesions correlates with the level of submucosal microbial dysbiosis. J Clin Periodontol. 2018 12; 45(12):1498-1509. PMID: 30341964.
      Citations: 15     Fields:    Translation:HumansPHPublic Health
    108. Bihl M, Bratic Hench I, Hoffmann P, Tolnay M, Mariani L, Frank S, Hench J, B?sch Al Jadooa N, Capper D. Satisfying your neuro-oncologist: a fast approach to routine molecular glioma diagnostics. Neuro Oncol. 2018 11 12; 20(12):1682-1683. PMID: 30169880; PMCID: PMC6231198.
      Citations: 6     Fields:    Translation:HumansCells
    109. Maaser A, Forstner AJ, Strohmaier J, Hecker J, Ludwig KU, Sivalingam S, Streit F, Degenhardt F, Witt SH, Koller AC, Raff R, Heilmann-Heimbach S, Fischer SB, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Herms S, Hoffmann P, Thiele H, Carmenate-Naranjo D, Proenza-Barzaga N, Auburger GWJ, Andlauer TFM, Cichon S, Marcheco-Teruel B, Mors O, Rietschel M, Reinbold CS, N?rnberg P, L?hlein Fier H, Orozco-D?az G, N?then MM. Exome sequencing in large, multiplex bipolar disorder families from Cuba. PLoS One. 2018; 13(10):e0205895. PMID: 30379966; PMCID: PMC6209204.
      Citations: 9     Fields:    Translation:Humans
    110. Claus EB, Cornish AJ, Broderick P, Schildkraut JM, Dobbins SE, Holroyd A, Calvocoressi L, Lu L, Hansen HM, Smirnov I, Walsh KM, Schramm J, Hoffmann P, Swerdlow A, Larsen SB, Johansen C, Simon M, Bondy M, Wrensch M, Houlston RS, Wiemels JL, N?then MM, J?ckel KH. Genome-wide association analysis identifies a meningioma risk locus at 11p15.5. Neuro Oncol. 2018 10 09; 20(11):1485-1493. PMID: 29762745; PMCID: PMC6176799.
      Citations: 13     Fields:    Translation:HumansCells
    111. Hughes T, Polushina T, Hansson L, Athanasiu L, Hassani S, Hoeffding LK, Herms S, Bergen SE, Karlsson R, Song J, Rietschel M, Forstner AJ, Hoffmann P, Hultman CM, Cichon S, Werge T, Andreassen OA, Le Hellard S, Djurovic S, S?nderby IE, Holmgren A, Melb?-J?rgensen C, N?then MM, Land?n M. Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder. Transl Psychiatry. 2018 10 08; 8(1):210. PMID: 30297702; PMCID: PMC6175894.
      Citations: 16     Fields:    Translation:Humans
    112. Niazi Y, Thomsen H, Smolkova B, Vodickova L, Vodenkova S, Kroupa M, Vymetalkova V, Kazimirova A, Barancokova M, Volkovova K, Staruchova M, Hoffmann P, Musak L, Vodicka P, Hemminki K, N?then MM, Du?insk? M, F?rsti A. Genetic variation associated with chromosomal aberration frequency: A genome-wide association study. Environ Mol Mutagen. 2019 01; 60(1):17-28. PMID: 30368896.
      Citations: 1     Fields:    Translation:HumansCells
    113. Doan NT, Hibar DP, Martin-Brevet S, Abdellaoui A, Ames D, Amunts K, Armstrong NJ, Bernard M, Blackburn N, Blangero J, Boomsma DI, Bralten J, Brattbak HR, Brodaty H, Brouwer RM, Calhoun V, Caspers S, Cavalleri G, Chen CH, Ciufolini S, Corvin A, Curran JE, Dale AM, Dalvie S, Dazzan P, de Geus EJC, de Zubicaray GI, de Zwarte SMC, Delanty N, den Braber A, Donohoe G, Ehrlich S, Espeseth T, Fisher SE, Franke B, Fukunaga M, Glahn DC, Grabe H, Groenewold NA, Haavik J, Hashimoto R, Heinz A, Hillegers MHJ, Hoffmann P, Holleran L, Hottenga JJ, Hulshoff HE, Ikeda M, Jahanshad N, Jernigan T, Jockwitz C, Johansson S, Jonsdottir GA, Kahn R, Kaufmann T, Kelly S, Kikuchi M, Knowles EEM, Kwok JB, Hellard SL, Leu C, Liu J, Lundervold AJ, Lundervold A, Martin NG, Mather K, Mathias SR, McCormack M, McMahon KL, McRae A, Milaneschi Y, Morris D, Mothersill D, Murray R, Nordvik JE, Olde Loohuis LM, Ophoff R, Paus T, Pausova Z, Penninx B, Peralta JM, Pike B, Prieto C, Quinlan E, Quintana DS, Marques TR, Reymond A, Richard G, Rodriguez-Herreros B, Rokicki J, Rucker J, Sachdev P, Sanders AM, Sando SB, Schmaal L, Schofield PR, Schork AJ, Schumann G, Shin J, Shumskaya E, Sisodiya S, Steen VM, Stein DJ, Steinberg S, Strike L, Teumer A, Thalamuthu A, Turner J, Ueland T, Uhlmann A, Ulfarsson MO, van 't Ent D, van der Meer D, van Haren NEM, Vaskinn A, Vassos E, Walters GB, Wang Y, Wen W, Whelan CD, Wittfeld K, Wright M, Yamamori H, Zayats T, Agartz I, Westlye LT, Djurovic S, Thompson P, Andreassen OA, 16p11.2 European Consortium, for the ENIGMA-CNV working group, S?nderby IE, G?stafsson ?, Andersson M, B?low R, Cichon S, Crespo-Facorro B, Desrivi?res S, Draganski B, Frouin V, Gareau T, H?berg A, Hehir-Kwa JY, J?nsson EG, Kolsk?r KK, Moreau C, M?hleisen TW, Nyberg L, Pudas S, Reinbold CS, Roiz-Santia?ez R, Tordesillas-Gutierrez D, Jacquemont S, Stef?nsson H, Stef?nsson K. Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia. Mol Psychiatry. 2020 03; 25(3):584-602. PMID: 30283035; PMCID: PMC7042770.
      Citations: 28     Fields:    Translation:HumansCells
    114. Kayser K, Degenhardt F, Holzapfel S, Horpaopan S, Peters S, Spier I, Vangala D, von Knebel-Doeberitz M, Engel C, Wijnen J, Doerks T, Bork P, Moebus S, Herms S, Fischer S, Hoffmann P, Aretz S, Steinke-Lange V, Morak M, Rahner N, Schackert HK, B?ttner R. Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes. Int J Cancer. 2018 12 01; 143(11):2800-2813. PMID: 29987844.
      Citations: 7     Fields:    Translation:HumansCells
    115. Palladino VS, Subrata NOC, Geburtig-Chiocchetti A, McNeill R, Hoffmann P, Reif A, Kittel-Schneider S. Generation of human induced pluripotent stem cell lines (hiPSC) from one bipolar disorder patient carrier of a DGKH risk haplotype and one non-risk-variant-carrier bipolar disorder patient. Stem Cell Res. 2018 10; 32:104-109. PMID: 30266033.
      Citations: 2     Fields:    Translation:HumansCells
    116. Loos BG, Divaris K, Offenbacher S, Teumer A, Holtfreter B, Kocher T, Bruckmann C, Graetz C, Staufenbiel I, van der Velde N, de Groot LCPGM, Krone B, Hoffmann P, Laudes M, Lieb W, Franke A, Munz M, Richter GM, Jepsen S, Jockel-Schneider Y, Ahmad I, Uitterlinden AG, Wellmann J, Berger K, Erdmann J, Dommisch H, Schaefer AS. Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci. Eur J Hum Genet. 2019 01; 27(1):102-113. PMID: 30218097; PMCID: PMC6303247.
      Citations: 35     Fields:    Translation:HumansCells
    117. Went M, Sud A, Halvarsson BM, Weinhold N, Kimber S, van Duin M, Thorleifsson G, Holroyd A, Johnson DC, Li N, Orlando G, Law PJ, Ali M, Chen B, Mitchell JS, Gudbjartsson DF, Kuiper R, Stephens OW, Bertsch U, Broderick P, Campo C, Bandapalli OR, Gregory WA, Gullberg U, Hillengass J, Hoffmann P, Jackson GH, Johnsson E, Mellqvist UH, Nahi H, Easton D, Pharoah P, Dunning A, Peto J, Canzian F, Swerdlow A, Eeles RA, Kote-Jarai Z, Muir K, Pashayan N, Nickel J, Rafnar T, Ross FM, da Silva Filho MI, Thomsen H, Vangsted A, Andersen NF, Waage A, Walker BA, Wihlborg AK, Broyl A, Davies FE, Thorsteinsdottir U, Langer C, Hansson M, Goldschmidt H, Kaiser M, Sonneveld P, Stefansson K, Morgan GJ, Hemminki K, Houlston RS, PRACTICAL consortium, F?rsti A, Einsele H, J?ckel KH, Kristinsson SY, N?then MM, Turesson I, Nilsson B. Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. Nat Commun. 2018 09 13; 9(1):3707. PMID: 30213928; PMCID: PMC6137048.
      Citations: 55     Fields:    Translation:HumansCells
    118. Loos BG, Divaris K, Offenbacher S, Teumer A, Holtfreter B, Kocher T, Bruckmann C, Graetz C, Staufenbiel I, van der Velde N, de Groot LCPGM, Krone B, Hoffmann P, Laudes M, Lieb W, Franke A, Munz M, Richter GM, Jepsen S, Jockel-Schneider Y, Munoz L, Bhandari A, Tennstedt S, Uitterlinden AG, Wellmann J, Berger K, Dommisch H, Erdmann J, Schaefer AS. Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus. Sci Rep. 2018 09 12; 8(1):13678. PMID: 30209331; PMCID: PMC6135769.
      Citations: 18     Fields:    Translation:Humans
    119. Sud A, Thomsen H, Orlando G, Law PJ, Broderick P, Cooke R, Hariri F, Pastinen T, Easton DF, Pharoah PDP, Dunning AM, Peto J, Canzian F, Eeles R, Kote-Jarai Z, Muir K, Pashayan N, Campa D, PRACTICAL Consortium, Hoffmann P, von Strandmann EP, Swerdlow AJ, Engert A, Orr N, Hemminki K, Houlston RS, F?rsti A, N?then MM, J?ckel KH. Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma. Blood. 2018 11 08; 132(19):2040-2052. PMID: 30194254; PMCID: PMC6236462.
      Citations: 14     Fields:    Translation:HumansCells
    120. Corominas J, Klein M, Zayats T, Pauper M, Neveling K, Poelmans G, Reif A, Arias Vasquez A, Galesloot TE, Kiemeney LALM, Buitelaar JK, Ramos-Quiroga JA, Cormand B, Hveem K, Gabrielsen ME, Hoffmann P, Cichon S, Haavik J, Johansson S, Franke B, Rivero O, Ziegler GC, Jansch C, Svirin E, Geissler J, Weber H, Ribas?s M, Jacob CP, Romanos M, Lesch KP. Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing. Mol Psychiatry. 2020 09; 25(9):2047-2057. PMID: 30116028; PMCID: PMC7473839.
      Citations: 12     Fields:    Translation:Humans
    121. Foo JC, Streit F, Treutlein J, Ripke S, Witt SH, Strohmaier J, Degenhardt F, Forstner AJ, Hoffmann P, Soyka M, Dahmen N, Scherbaum N, Wodarz N, Heilmann-Heimbach S, Herms S, Cichon S, Preuss U, Ridinger M, Hoffmann S, Schulze TG, Maier W, Zill P, Ising M, Lucae S, Mann K, Kiefer F, Rietschel M, Frank J, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Gaebel W, M?ller-Myhsok B, N?then MM. Shared genetic etiology between alcohol dependence and major depressive disorder. Psychiatr Genet. 2018 08; 28(4):66-70. PMID: 29901528; PMCID: PMC6039372.
      Citations: 11     Fields:    Translation:Humans
    122. Kalman JL, Papiol S, Forstner AJ, Heilbronner U, Degenhardt F, Strohmaier J, Adorjan K, Akula N, Alda M, Anderson-Schmidt H, Andlauer TF, Anghelescu IG, Ardau R, Aubry JM, Backlund L, Bartholdi K, Baune BT, Benabarre A, Bengesser S, Bhattacharjee AK, Biernacka JM, Birner A, Budde M, Cervantes P, Chillotti C, Cichon S, Clark SR, Colom F, Comes AL, Cruceanu C, Czerski PM, Dayer A, Del Zompo M, DePaulo JR, Dietrich DE, Falkai P, Figge C, Flatau L, Folkerts H, Frisen L, Frye MA, Fullerton JM, Gade K, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Gryaznova A, Hake M, Hauser J, Herms S, Hoffmann P, Hou L, Jamain S, Juckel G, Kassem L, Kelsoe J, Kittel-Schneider S, Kliwicki S, Klohn-Sagatholislam F, Konrad C, Lackner N, Laje G, Lavebratt C, Leboyer M, Leckband SG, Maj M, Manchia M, Martinsson L, McCarthy MJ, McElroy SL, McMahon FJ, Mitchell PB, Mondimore FM, Monteleone P, Nievergelt CM, Potash JB, Reich-Erkelenz D, Reif A, Reimer J, Reininghaus E, Rouleau GA, Rybakowski JK, Schalling M, Schofield PR, Schubert KO, Schulte EC, Schulz S, Senner F, Severino G, Shekhtman T, Shilling PD, Simhandl C, Slaney CM, Spitzer C, Squassina A, Stopkova P, Thiel A, Tighe SK, Tortorella A, Turecki G, Vieta E, Veeh J, Witt S, Wright A, Zandi PP, Rietschel M, Schulze TG, Adli M, Arias B, Arolt V, Bauer M, Becker T, Bellivier F, Brichant-Petitjean C, Dannlowski U, ?tain B, Ethofer T, Fallgatter A, Gard S, J?ger M, Jim?nez E, Kahn JP, Koller M, K?nig B, Land?n M, Lang FU, Mitjans M, Nieratschker V, Nov?k T, ?sby U, Pfennig A, Reitt M, Ripke S, Scherk H, Schmau? M, Stamm T, Stegmaier S, Stierl S, von Hagen M, Wigand ME, Wiltfang J, Zimmermann J, N?then M. Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study. Bipolar Disord. 2019 02; 21(1):68-75. PMID: 29956436; PMCID: PMC6585855.
      Citations: 11     Fields:    Translation:Humans
    123. Brainstorm Consortium, Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, Lee PH, Turley P, Grenier-Boley B, Chouraki V, Kamatani Y, Berr C, Letenneur L, Hannequin D, Amouyel P, Vardarajan BN, Reitz C, Goate AM, Huentelman MJ, Kamboh MI, Larson EB, Rogaeva E, St George-Hyslop P, Hakonarson H, Kukull WA, Farrer LA, Barnes LL, Beach TG, Demirci FY, Head E, Hulette CM, Jicha GA, Kauwe JSK, Kaye JA, Leverenz JB, Levey AI, Lieberman AP, Pankratz VS, Poon WW, Quinn JF, Saykin AJ, Schneider LS, Smith AG, Sonnen JA, Stern RA, Van Deerlin VM, Van Eldik LJ, Harold D, Russo G, Rubinsztein DC, Bayer A, Tsolaki M, Proitsi P, Fox NC, Owen MJ, Mead S, Passmore P, Morgan K, Rossor M, Lupton MK, Hoffmann P, Lawlor B, McQuillin A, Al-Chalabi A, Bis JC, Seshadri S, Beiser A, Rice K, van der Lee SJ, De Jager PL, Geschwind DH, Riemenschneider M, Riedel-Heller S, Rotter JI, Ransmayr G, Hyman BT, Cruchaga C, Winsvold B, Palta P, Farh KH, Cuenca-Leon E, Furlotte N, Ligthart L, Terwindt GM, Freilinger T, Ran C, Gordon SD, Borck G, Adams HHH, Wedenoja J, Buring JE, Hrafnsdottir M, Hottenga JJ, Penninx B, Artto V, Kaunisto M, Martin NG, Montgomery GW, Kurki MI, Huang H, Huang J, Sandor C, Webber C, Muller-Myhsok B, Schreiber S, Salomaa V, Loehrer E, Macaya A, Pozo-Rosich P, Hansen T, Werge T, Kaprio J, Metspalu A, Kubisch C, Ferrari MD, Belin AC, van den Maagdenberg AMJM, Zwart JA, Boomsma D, Eriksson N, Olesen J, Chasman DI, Nyholt DR, Avbersek A, Baum L, Berkovic S, Bradfield J, Buono RJ, Catarino CB, De Jonghe P, Dlugos D, Ferraro TN, French J, Hjalgrim H, Jamnadas-Khoda J, Kunz WS, Lerche H, Leu C, Lindhout D, Lo W, Lowenstein D, McCormack M, Molloy A, Ng PW, Oliver K, Privitera M, Radtke R, Ruppert AK, Sander T, Schachter S, Schankin C, Scheffer I, Schoch S, Sisodiya SM, Smith P, Sperling M, Striano P, Surges R, Thomas GN, Visscher F, Whelan CD, Zara F, Heinzen EL, Marson A, Becker F, Stroink H, Zimprich F, Gibbs R, Martinez M, Morris HR, Sharma M, Ryten M, Mok KY, Pulit S, Bevan S, Holliday E, Attia J, Battey T, Boncoraglio G, Thijs V, Chen WM, Mitchell B, Rothwell P, Sharma P, Sudlow C, Markus H, Kourkoulis C, Raffeld M, Silliman S, Boraska Perica V, Thornton LM, Huckins LM, William Rayner N, Lewis CM, Gratacos M, Rybakowski F, Keski-Rahkonen A, Raevuori A, Hudson JI, Reichborn-Kjennerud T, Monteleone P, Karwautz A, Mannik K, Baker JH, O'Toole JK, Trace SE, Davis OSP, Helder SG, Herpertz-Dahlmann B, Danner UN, van Elburg AA, Clementi M, Forzan M, Lissowska J, Hauser J, Tortorella A, Maj M, Gonidakis F, Tziouvas K, Papezova H, Yilmaz Z, Wagner G, Cohen-Woods S, Herms S, Dick DM, Ripatti S, Andreassen OA, Espeseth T, Lundervold AJ, Steen VM, Pinto D, Scherer SW, Aschauer H, Schosser A, Alfredsson L, Padyukov L, Halmi KA, Mitchell J, Strober M, Bergen AW, Kaye W, Szatkiewicz JP, Ramos-Quiroga JA, Haavik J, Zayats T, Johansson S, Williams N, Dempfle A, Rothenberger A, Kuntsi J, Oades RD, Banaschewski T, Franke B, Buitelaar JK, Arias Vasquez A, Doyle AE, Reif A, Lesch KP, Freitag C, Rivero O, Palmason H, Romanos M, Langley K, Rietschel M, Witt SH, Dalsgaard S, Waldman I, Wilmot B, Molly N, Crosbie J, Schachar R, Loo SK, McGough JJ, Medland SE, Robinson E, Weiss LA, Bacchelli E, Bailey A, Bal V, Battaglia A, Bolton P, Cantor R, Dawson G, De Rubeis S, Green A, Klauck SM, Levitt P, Maestrini E, Mane S, De-Luca DM, Parr J, Regan R, Reichenberg A, Sandin S, Vorstman J, Wassink T, Wijsman E, Cook E, Santangelo S, Delorme R, Magalhaes T, Arking D, Schulze TG, Thompson RC, Strohmaier J, Matthews K, Melle I, Morris D, Blackwood D, McIntosh A, Bergen SE, Schalling M, Maaser A, Fischer SB, Fullerton JM, Mayoral F, Schofield PR, Cichon S, Degenhardt F, Schumacher J, Mitchell PB, Gershon ES, Rice J, et al. Analysis of shared heritability in common disorders of the brain. Science. 2018 06 22; 360(6395). PMID: 29930110; PMCID: PMC6097237.
      Citations: 685     Fields:    Translation:Humans
    124. Chattopadhyay S, Thomsen H, da Silva Filho MI, Weinhold N, Hoffmann P, Marina A, Pechlivanis S, Langer C, Goldschmidt H, Hemminki K, N?then MM, J?ckel KH, Schmidt B, F?rsti A. Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study. Mol Med. 2018 06 11; 24(1):30. PMID: 30134812; PMCID: PMC6016882.
      Citations: 5     Fields:    Translation:Humans
    125. Forstner AJ, Hecker J, Fullerton JM, Hoffmann P, Hou L, Heilbronner U, Degenhardt F, Akiyama K, Akula N, Ardau R, Backlund L, Benabarre A, Bengesser S, Bhattacharjee AK, Biernacka JM, Birner A, Cervantes P, Chen GB, Chen HC, Chillotti C, Clark SR, Colom F, Cousins DA, Cruceanu C, Czerski PM, Dayer A, Falkai P, Garnham JS, Goes FS, Grof P, Hashimoto R, Hauser J, Herms S, Kassem L, Kittel-Schneider S, Kliwicki S, Kusumi I, Lackner N, Laje G, Lavebratt C, Leckband SG, MacQueen G, Manchia M, Martinsson L, Mattheisen M, McCarthy MJ, McElroy SL, Mitjans M, Mondimore FM, Monteleone P, Nievergelt CM, Ozaki N, Perlis RH, Reich-Erkelenz D, Rouleau GA, Schofield PR, Schubert KO, Schweizer BW, Severino G, Shekhtman T, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Smoller JW, Squassina A, Stopkova P, Tighe SK, Tortorella A, Turecki G, Volkert J, Witt SH, Wright AJ, Young LT, Zandi PP, Potash JB, DePaulo JR, Reininghaus E, Aubry JM, Maj M, Baune BT, Mitchell PB, Vieta E, Rybakowski JK, Kuo PH, Kato T, Grigoroiu-Serbanescu M, Reif A, Del Zompo M, Schalling M, Wray NR, Kelsoe JR, Alda M, McMahon FJ, Schulze TG, Rietschel M, Cichon S, Reinbold CS, Adli M, Arias B, Marie-Claire C, ?tain B, Fris?n L, Gard S, Gruber O, Jamain S, Jim?nez E, Kahn JP, K?nig B, Land?n M, Leboyer M, L?pez Jaramillo CA, ?sby U, Pfennig A, Seem?ller F, Stamm TJ, Bauer M, Nov?k T, Frye MA, Bellivier F, N?then MM. Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder. Front Psychiatry. 2018; 9:207. PMID: 29904359; PMCID: PMC5991073.
      Citations: 13     
    126. Wray NR, Ripke S, Mattheisen M, Trzaskowski M, Byrne EM, Abdellaoui A, Adams MJ, Agerbo E, Air TM, Andlauer TMF, Bacanu SA, Beekman AFT, Bigdeli TB, Binder EB, Blackwood DRH, Bryois J, Bybjerg-Grauholm J, Cai N, Castelao E, Christensen JH, Clarke TK, Coleman JIR, Couvy-Duchesne B, Craddock N, Crawford GE, Crowley CA, Dashti HS, Davies G, Deary IJ, Degenhardt F, Derks EM, Direk N, Dolan CV, Dunn EC, Eley TC, Eriksson N, Escott-Price V, Kiadeh FHF, Finucane HK, Forstner AJ, Frank J, Gill M, Goes FS, Gordon SD, Grove J, Hall LS, Hannon E, Hansen TF, Herms S, Hickie IB, Hoffmann P, Homuth G, Horn C, Hottenga JJ, Hougaard DM, Hu M, Hyde CL, Ising M, Jansen R, Jin F, Jorgenson E, Knowles JA, Kohane IS, Kretzschmar WW, Krogh J, Lane JM, Li Y, Li Y, Lind PA, Liu X, Lu L, MacIntyre DJ, MacKinnon DF, Maier RM, Maier W, Marchini J, Mbarek H, McGrath P, McGuffin P, Medland SE, Mehta D, Middeldorp CM, Mihailov E, Milaneschi Y, Milani L, Mill J, Mondimore FM, Montgomery GW, Mostafavi S, Mullins N, Nauck M, Ng B, Nivard MG, Nyholt DR, O'Reilly PF, Oskarsson H, Owen MJ, Painter JN, Peterson RE, Pettersson E, Peyrot WJ, Pistis G, Posthuma D, Purcell SM, Quiroz JA, Qvist P, Rice JP, Riley BP, Rivera M, Saeed Mirza S, Saxena R, Schoevers R, Schulte EC, Shen L, Shi J, Shyn SI, Sigurdsson E, Sinnamon GBC, Smit JH, Smith DJ, Stefansson H, Steinberg S, Stockmeier CA, Streit F, Strohmaier J, Tansey KE, Teumer A, Thompson W, Thomson PA, Thorgeirsson TE, Tian C, Traylor M, Treutlein J, Umbricht D, Van der Auwera S, van Hemert AM, Viktorin A, Visscher PM, Wang Y, Webb BT, Weinsheimer SM, Willemsen G, Witt SH, Wu Y, Xi HS, Yang J, Zhang F, eQTLGen, 23andMe, Baune BT, Boomsma DI, Cichon S, de Geus ECJ, DePaulo JR, Domschke K, Grabe HJ, Hamilton SP, Hayward C, Heath AC, Hinds DA, Kendler KS, Kloiber S, Lewis G, Li QS, Lucae S, Madden PFA, Magnusson PK, Martin NG, McIntosh AM, Metspalu A, Mors O, Mortensen PB, Nordentoft M, O'Donovan MC, Paciga SA, Pedersen NL, Penninx BWJH, Perlis RH, Porteous DJ, Potash JB, Preisig M, Rietschel M, Schaefer C, Schulze TG, Smoller JW, Stefansson K, Tiemeier H, Uher R, Weissman MM, Werge T, Winslow AR, Lewis CM, Levinson DF, Breen G, Sullivan PF, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, B?kvad-Hansen M, Buttensch?n HN, Colodro-Conde L, Gaspar HA, Giusti-Rodr?guez P, Hansen CS, Kraft J, Kutalik Z, Pedersen CB, Pedersen MG, Teismann H, Trubetskoy V, Uitterlinden AG, Wellmann J, Arolt V, Berger K, Dannlowski U, Domenici E, Esko T, M?ller-Myhsok B, N?then MM, V?lzke H, B?rglum AD. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nat Genet. 2018 05; 50(5):668-681. PMID: 29700475; PMCID: PMC5934326.
      Citations: 1108     Fields:    Translation:Humans
    127. Vijayakrishnan J, Studd J, Broderick P, Kinnersley B, Holroyd A, Law PJ, Kumar R, Allan JM, Harrison CJ, Moorman AV, Vora A, Roman E, Rachakonda S, Kinsey SE, Sheridan E, Thompson PD, Irving JA, Koehler R, Hoffmann P, Heilmann-Heimbach S, Easton DF, Pharaoh PDP, Dunning AM, Peto J, Canzian F, Swerdlow A, Eeles RA, Kote-Jarai Z, Muir K, Pashayan N, PRACTICAL Consortium, Greaves M, Zimmerman M, Bartram CR, Schrappe M, Stanulla M, Hemminki K, Houlston RS, N?then MM, J?ckel KH. Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. Nat Commun. 2018 04 09; 9(1):1340. PMID: 29632299; PMCID: PMC5890276.
      Citations: 41     Fields:    Translation:Humans
    128. Disney-Hogg L, Cornish AJ, Sud A, Law PJ, Kinnersley B, Jacobs DI, Ostrom QT, Labreche K, Eckel-Passow JE, Armstrong GN, Claus EB, Il'yasova D, Schildkraut J, Barnholtz-Sloan JS, Olson SH, Bernstein JL, Lai RK, Schoemaker MJ, Simon M, Hoffmann P, Chanock S, Rajaraman P, Johansen C, Jenkins RB, Wrensch MR, Bondy ML, Houlston RS, N?then MM, J?ckel KH, Melin BS, Sanson M. Impact of atopy on risk of glioma: a Mendelian randomisation study. BMC Med. 2018 03 15; 16(1):42. PMID: 29540232; PMCID: PMC5853158.
      Citations: 27     Fields:    Translation:Humans
    129. Disney-Hogg L, Sud A, Law PJ, Cornish AJ, Kinnersley B, Ostrom QT, Labreche K, Eckel-Passow JE, Armstrong GN, Claus EB, Il'yasova D, Schildkraut J, Barnholtz-Sloan JS, Olson SH, Bernstein JL, Lai RK, Swerdlow AJ, Simon M, Hoffmann P, Chanock S, Rajaraman P, Johansen C, Jenkins RB, Wrensch MR, Bondy ML, Houlston RS, N?then MM, J?ckel KH, Melin BS, Sanson M. Influence of obesity-related risk factors in the aetiology of glioma. Br J Cancer. 2018 04; 118(7):1020-1027. PMID: 29531326; PMCID: PMC5931112.
      Citations: 23     Fields:    Translation:Humans
    130. Graetz C, Staufenbiel I, Krone B, Hoffmann P, van der Velde N, de Groot LCPGM, Sawalha AH, Direskeneli H, Guzeldemir-Akcakanat E, Keceli HG, Laudes M, Noack B, Teumer A, Holtfreter B, Kocher T, Eickholz P, Doerfer C, Bruckmann C, Lieb W, Franke A, Schreiber S, Nohutcu RM, Loos BG, Jepsen S, Munz M, Willenborg C, Richter GM, Jockel-Schneider Y, Wellmann J, Berger K, Uitterlinden AG, Saruhan-Direskeneli G, Meyle J, Erdmann J, Dommisch H, Schaefer AS. A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis. Hum Mol Genet. 2018 03 01; 27(5):941-942. PMID: 29346566.
      Citations: 7     Fields:    
    131. Takahashi H, Cornish AJ, Sud A, Law PJ, Kinnersley B, Ostrom QT, Labreche K, Eckel-Passow JE, Armstrong GN, Claus EB, Il'yasova D, Schildkraut J, Barnholtz-Sloan JS, Olson SH, Bernstein JL, Lai RK, Schoemaker MJ, Simon M, Hoffmann P, Chanock S, Rajaraman P, Johansen C, Jenkins RB, Wrensch MR, Bondy ML, Turnbull C, Houlston RS, N?then MM, J?ckel KH, Melin BS, Sanson M. Mendelian randomisation study of the relationship between vitamin D and risk of glioma. Sci Rep. 2018 02 05; 8(1):2339. PMID: 29402980; PMCID: PMC5799201.
      Citations: 14     Fields:    Translation:Humans
    132. International Consortium on Lithium Genetics (ConLi+Gen), Amare AT, Schubert KO, Hou L, Clark SR, Papiol S, Heilbronner U, Degenhardt F, Tekola-Ayele F, Hsu YH, Shekhtman T, Akula N, Akiyama K, Ardau R, Aubry JM, Backlund L, Bhattacharjee AK, Bengesser S, Biernacka JM, Birner A, Cervantes P, Chen HC, Chillotti C, Cichon S, Cruceanu C, Czerski PM, Dalkner N, Dayer A, Del Zompo M, DePaulo JR, Falkai P, Forstner AJ, Frisen L, Frye MA, Fullerton JM, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Grof P, Hashimoto R, Hauser J, Herms S, Hoffmann P, Hofmann A, Kassem L, Kuo PH, Kato T, Kelsoe J, Kittel-Schneider S, Kliwicki S, Kusumi I, Laje G, Lavebratt C, Leckband SG, Tortorella A, Manchia M, Martinsson L, McCarthy MJ, McElroy S, Mondimore FM, Monteleone P, Nievergelt CM, O'Donovan C, Ozaki N, Potash JB, Reif A, Reininghaus E, Rouleau GA, Rybakowski JK, Schalling M, Schofield PR, Schweizer BW, Severino G, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Squassina A, Stopkova P, Maj M, Turecki G, Volkert J, Witt S, Wright A, Zandi PP, Mitchell PB, Alda M, Rietschel M, McMahon FJ, Schulze TG, Baune BT, Adli M, Arias B, Bellivier F, Benabarre A, Brichant-Petitjean C, ?tain B, Gard S, Jamain S, Jim?nez E, Kahn JP, K?nig B, Land?n M, Leboyer M, Colom F, Mitjans M, N?then MM, Nov?k T, ?sby U, Pfennig A, Stamm T, Vieta E, Bauer M. Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study. JAMA Psychiatry. 2018 01 01; 75(1):65-74. PMID: 29121268; PMCID: PMC5833535.
      Citations: 68     Fields:    Translation:Humans
    133. Polushina T, Giddaluru S, Bettella F, Espeseth T, Lundervold AJ, Djurovic S, Cichon S, Hoffmann P, Steen VM, Andreassen OA, N?then MM, Le Hellard S. Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data. Transl Psychiatry. 2017 12 18; 7(12):1289. PMID: 29249828; PMCID: PMC5802566.
      Citations: 4     Fields:    Translation:Humans
    134. Sud A, Thomsen H, Law PJ, Filho MIDS, Holroyd A, Broderick P, Orlando G, Lenive O, Wright L, Cooke R, Easton D, Pharoah P, Dunning A, Peto J, Canzian F, Eeles R, Kote-Jarai Z, Muir K, Pashayan N, PRACTICAL consortium, Hoffmann P, Strandmann EPV, Lightfoot T, Kane E, Roman E, Lake A, Montgomery D, Jarrett RF, Swerdlow AJ, Engert A, Orr N, Hemminki K, Houlston RS, F?rsti A, N?then MM, J?ckel KH. Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility. Nat Commun. 2017 12 01; 8(1):1892. PMID: 29196614; PMCID: PMC5711884.
      Citations: 25     Fields:    Translation:Humans
    135. Horpaopan S, Kirfel J, Peters S, Kloth M, Drichel D, Odenthal M, Kristiansen G, Strassburg C, Nattermann J, Hoffmann P, Thiele H, Spier I, Aretz S, H?neburg R, Altm?ller J, N?rnberg P, B?ttner R, Kahl P. Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS). Hered Cancer Clin Pract. 2017; 15:22. PMID: 29213343; PMCID: PMC5707812.
      Citations: 5     
    136. Schulz H, Ruppert AK, Herms S, Wolf C, Mirza-Schreiber N, Stegle O, Czamara D, Forstner AJ, Sivalingam S, Schoch S, Moebus S, Hillmer A, Fricker N, Vatter H, Becker AJ, Hoffmann P, Sander T, Cichon S, P?tz B, M?ller-Myhsok B, N?then MM. Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. Nat Commun. 2017 11 15; 8(1):1511. PMID: 29142228; PMCID: PMC5688097.
      Citations: 38     Fields:    Translation:HumansCells
    137. Abramova LI, Alda M, Babadjanova G, Bauer M, Brennan P, Chuchalin A, Cruceanu C, Czerski PM, Fullerton JM, Grigoroiu-Serbanescu M, Hauser J, Kammerer-Ciernioch J, Pantelejeva G, Pfennig A, Rouleau GA, Schofield PR, Tiganov AS, M?hleisen TW, Reinbold CS, Forstner AJ, Degenhardt F, Fischer SB, Gordon SD, Grof P, Hautzinger M, Herms S, Hoffmann P, Khusnutdinova E, Kogevinas M, Krasnov V, Lacour A, Laprise C, Leber M, Lissowska J, Lucae S, Maaser A, Maier W, Martin NG, Mattheisen M, Mayoral F, McKay JD, Medland SE, Mitchell PB, Moebus S, Montgomery GW, M?ller-Myhsok B, Oruc L, Pojskic L, Polonikov A, Reif A, Rivas F, Schenk LM, Schwarz M, Streit F, Strohmaier J, Szeszenia-Dabrowska N, Treutlein J, Turecki G, Vedder H, Witt SH, Schulze TG, Rietschel M, N?then MM, Cichon S. Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. J Affect Disord. 2018 03 01; 228:20-25. PMID: 29197740.
      Citations: 2     Fields:    Translation:HumansCells
    138. Hoffmann P, Strathmann K, Fernandez-Rebollo E, Eipel M, Seefried L, Jakob F, Wagner W. Primary Osteoporosis Is Not Reflected by Disease-Specific DNA Methylation or Accelerated Epigenetic Age in Blood. J Bone Miner Res. 2018 02; 33(2):356-361. PMID: 28926142.
      Citations: 20     Fields:    Translation:HumansCells
    139. Wallner S, Schmitz G, Klein-Hitpass L, Sinha A, Heilmann-Heimbach S, Hoffmann P, Steffens M, Rahmann S, Schr?der C, Leit?o E, J?ckel KH, N?then MM, Ebert P, Horsthemke B. Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential function. Epigenetics Chromatin. 2017 07 26; 10(1):37. PMID: 28747224; PMCID: PMC5530492.
      Citations: 8     Fields:    Translation:HumansCells
    140. Wahl S, Sharma S, Hoffmann P, Floegel A, Pischon T, Adamski J, Peters A, Suhre K, Grallert H, Boeing H, Schulze MB, Meidtner K, J?ger S, Kr?ger J, Prehn C, M?ller-Nurasyid M, Waldenberger M, Strauch K, Gieger C. Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes. Sci Rep. 2017 07 20; 7(1):6037. PMID: 28729637; PMCID: PMC5519666.
      Citations: 7     Fields:    Translation:Humans
    141. Treutlein J, Frank J, Streit F, Juraeva D, Degenhardt F, Rietschel L, Witt SH, Forstner AJ, Ridinger M, Strohmaier J, Wodarz N, Dukal H, Foo JC, Hoffmann P, Herms S, Heilmann-Heimbach S, Soyka M, Maier W, Dahmen N, Scherbaum N, Lucae S, Ising M, Stickel F, Berg T, Roggenbuck U, Scholz H, Zimmermann US, Buch S, Sommer WH, Spanagel R, Brors B, Cichon S, Mann K, Kiefer F, Hampe J, Rosendahl J, Rietschel M, Reinbold CS, Gaebel W, M?ller-Myhsok B, J?ckel KH, N?then MM. Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. Genes (Basel). 2017 Jul 17; 8(7). PMID: 28714907; PMCID: PMC5541316.
      Citations: 4     Fields:    
    142. Sims R, van der Lee SJ, Naj AC, Badarinarayan N, Jakobsdottir J, Kunkle BW, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, Sleegers K, Vronskaya M, Graham RR, Hoffmann P, Grove ML, Vardarajan BN, Hiltunen M, White CC, Hamilton-Nelson KL, Maier W, Choi SH, Beecham GW, Herms S, Smith AV, Funk CC, Forstner AJ, Ahmad S, Li H, Harold D, Satizabal CL, Valladares O, Squassina A, Thomas R, Brody JA, Qu L, Morgan T, Wolters FJ, Zhao Y, Denning N, Fornage M, Malamon J, Majounie E, Mosley TH, Dombroski B, Wallon D, Lupton MK, Whitehead P, Fratiglioni L, Medway C, Jian X, Mukherjee S, Keller L, Brown K, Lin H, Cantwell LB, Panza F, McGuinness B, Burgess JD, Solfrizzi V, Proitsi P, Adams HH, Allen M, Seripa D, Pastor P, Cupples LA, Price ND, Hannequin D, Levy D, Chakrabarty P, Caffarra P, Giegling I, Beiser AS, Giedraitis V, Hampel H, Garcia ME, Wang X, Lannfelt L, Mecocci P, Eiriksdottir G, Crane PK, Pasquier F, Boccardi V, Barber RC, Scherer M, Adams PM, Leber M, Chen Y, Albert MS, Riedel-Heller S, Emilsson V, Beekly D, Braae A, Schmidt R, Blacker D, Masullo C, Schmidt H, Doody RS, Spalletta G, Longstreth WT, Fairchild TJ, Lopez OL, Frosch MP, Sacchinelli E, Ghetti B, Yang Q, Huebinger RM, Jessen F, Li S, Kamboh MI, Morris J, Katz MJ, Corcoran C, Dunstan M, Braddel A, Thomas C, Meggy A, Marshall R, Gerrish A, Chapman J, Taylor S, Hill M, Hodges A, Vellas B, Soininen H, Kloszewska I, Daniilidou M, Uphill J, Patel Y, Hughes JT, Lord J, Turton J, Hartmann AM, Cecchetti R, Fenoglio C, Serpente M, Arcaro M, Caltagirone C, Orfei MD, Ciaramella A, Pichler S, Mayhaus M, Gu W, Barber IS, Brookes K, Cupidi C, Maletta RG, Carrell D, Sorbi S, Moebus S, Urbano M, Pilotto A, Kornhuber J, Bosco P, Todd S, Craig D, Johnston J, Gill M, Lawlor B, Lynch A, Fox NC, Hardy J, ARUK Consortium, Albin RL, Apostolova LG, Arnold SE, Asthana S, Atwood CS, Baldwin CT, Barnes LL, Barral S, Beach TG, Becker JT, Bigio EH, Bird TD, Boeve BF, Bowen JD, Boxer A, Burke JR, Burns JM, Buxbaum JD, Cairns NJ, Cao C, Carlson CS, Carlsson CM, Carney RM, Carrasquillo MM, Carroll SL, Diaz CC, Chui HC, Clark DG, Cribbs DH, Crocco EA, DeCarli C, Dick M, Duara R, Evans DA, Faber KM, Fallon KB, Fardo DW, Farlow MR, Ferris S, Foroud TM, Galasko DR, Gearing M, Geschwind DH, Gilbert JR, Graff-Radford NR, Green RC, Growdon JH, Hamilton RL, Harrell LE, Honig LS, Huentelman MJ, Hulette CM, Hyman BT, Jarvik GP, Abner E, Jin LW, Jun G, Karydas A, Kaye JA, Kim R, Kowall NW, Kramer JH, LaFerla FM, Lah JJ, Leverenz JB, Levey AI, Li G, Lieberman AP, Lunetta KL, Lyketsos CG, Marson DC, Martiniuk F, Mash DC, Masliah E, McCormick WC, McCurry SM, McDavid AN, McKee AC, Mesulam M, Miller BL, Miller CA, Miller JW, Morris JC, Murrell JR, Myers AJ, O'Bryant S, Olichney JM, Pankratz VS, Parisi JE, Paulson HL, Perry W, Peskind E, Pierce A, Poon WW, Potter H, Quinn JF, Raj A, Raskind M, Reisberg B, Reitz C, Ringman JM, Roberson ED, Rogaeva E, Rosen HJ, Rosenberg RN, Sager MA, Saykin AJ, Schneider JA, Schneider LS, Seeley WW, Smith AG, Sonnen JA, Spina S, Stern RA, Swerdlow RH, Tanzi RE, Thornton-Wells TA, Trojanowski JQ, Troncoso JC, Van Deerlin VM, Van Eldik LJ, Vinters HV, Vonsattel JP, Weintraub S, Welsh-Bohmer KA, Wilhelmsen KC, Williamson J, Wingo TS, Woltjer RL, Wright CB, Yu CE, Yu L, Engelborghs S, Vandenberghe R, De Deyn PP, Thonberg H, Forsell C, Lilius L, Kilander L, Brundin R, Concari L, Helisalmi S, Koivisto AM, Haapasalo A, Fievet N, Dufouil C, Himali JJ, Keene CD, Tschanz J, Fitzpatrick AL, Kukull WA, Norton M, Aspelund T, Larson EB, Munger R, Rotter JI, Lipton RB, Hofman A, Montine TJ, Coto E, Boerwinkle E, Petersen RC, Alvarez V, Rivadeneira F, Reiman EM, Gallo M, O'Donnell CJ, Reisch JS, Bruni AC, Royall DR, Sano M, Galimberti D, St George-Hyslop P, Scarpini E, Tsuang DW, Mancuso M, Bonuccelli U, Winslow AR, Daniele A, Wu CK, GERAD/PERADES, CHARGE, ADGC, EADI, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nat Genet. 2017 09; 49(9):1373-1384. PMID: 28714976; PMCID: PMC5669039.
      Citations: 459     Fields:    Translation:HumansCells
    143. Fernandez-Rebollo E, Franzen J, Abagnale G, Sieben T, Ostrowska A, Hoffmann P, Lemaitre JM, Bischof O, Wagner W, Mentrup B, Ebert R, Roux PF, Rath B, Goodhardt M, Jakob F. Human Platelet Lysate versus Fetal Calf Serum: These Supplements Do Not Select for Different Mesenchymal Stromal Cells. Sci Rep. 2017 07 11; 7(1):5132. PMID: 28698620; PMCID: PMC5506010.
      Citations: 31     Fields:    Translation:HumansAnimalsCells
    144. Meziane I, Huhn S, Filho MIDS, Weinhold N, Campo C, Nickel J, Hoffmann P, Landi S, Mitchell JS, Johnson D, Jauch A, Morgan GJ, Houlston R, Goldschmidt H, Milani P, Merlini G, Rowcieno D, Hawkins P, Hegenbart U, Palladini G, Wechalekar A, Hemminki K, N?then MM, J?ckel KH, F?rsti A, Sch?nland SO. Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. Haematologica. 2017 10; 102(10):e411-e414. PMID: 28679651; PMCID: PMC5622874.
      Citations: 3     Fields:    Translation:Humans
    145. Graetz C, Staufenbiel I, Krone B, Hoffmann P, van der Velde N, de Groot LCPGM, Sawalha AH, Direskeneli H, Guzeldemir-Akcakanat E, Keceli HG, Laudes M, Noack B, Teumer A, Holtfreter B, Kocher T, Eickholz P, Doerfer C, Bruckmann C, Lieb W, Franke A, Schreiber S, Nohutcu RM, Loos BG, Jepsen S, Munz M, Willenborg C, Richter GM, Jockel-Schneider Y, Wellmann J, Berger K, Uitterlinden AG, Saruhan-Direskeneli G, Meyle J, Erdmann J, Dommisch H, Schaefer AS. A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis. Hum Mol Genet. 2017 07 01; 26(13):2577-2588. PMID: 28449029.
      Citations: 48     Fields:    Translation:Humans
    146. Tsoi LC, Stuart PE, Tian C, Gudjonsson JE, Das S, Zawistowski M, Ellinghaus E, Barker JN, Chandran V, Dand N, Duffin KC, Franke A, Gladman DD, Hoffmann P, Krueger GG, Lim HW, Metspalu A, Mrowietz U, Rahman P, Tejasvi T, Trembath R, Voorhees JJ, Weidinger S, Weichenthal M, Wen X, Eriksson N, Kang HM, Hinds DA, Nair RP, Elder JT, Enerb?ck C, Esko T, Kingo K, K?ks S, Mucha S, Reis A, Abecasis GR. Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants. Nat Commun. 2017 05 24; 8:15382. PMID: 28537254; PMCID: PMC5458077.
      Citations: 128     Fields:    Translation:HumansCells
    147. Thomsen H, Campo C, Weinhold N, da Silva Filho MI, Pour L, Vodicka P, Vodickova L, Hoffmann P, Langer C, Hajek R, Goldschmidt H, Hemminki K, Gregora E, N?then MM, J?ckel KH, F?rsti A. Genomewide association study on monoclonal gammopathy of unknown significance (MGUS). Eur J Haematol. 2017 Jul; 99(1):70-79. PMID: 28375557.
      Citations: 9     Fields:    Translation:Humans
    148. Webb TR, Stirrups KE, Stitziel NO, Masca NG, Kanoni S, Nelson CP, Eicher JD, Johnson AD, Hamby SE, Betsholtz C, Ruusalepp A, Schadt EE, Weeke PE, Auer PL, Schick UM, Lu Y, Zhang H, Goel A, Farrall M, Peloso GM, Won HH, Do R, van Iperen E, Kruppa J, Mahajan A, Scott RA, Braund PS, van Capelleveen JC, Doney AS, Donnelly LA, Asselta R, Merlini PA, Duga S, Marziliano N, Denny JC, Shaffer C, Franke A, Heilmann S, Hoffmann P, Holmen OL, Marouli E, Martinelli N, McCarthy MI, Van Zuydam NR, Mihailov E, Alver M, Moebus S, Morris AD, Virtamo J, Nikpay M, Olivieri O, Provost S, AlQarawi A, Robertson NR, Akinsansya KO, Reilly DF, Vogt TF, Yin W, Asselbergs FW, Kooperberg C, Jackson RD, Stahl E, Wellcome Trust Case Control Consortium, Chowdhury R, Salomaa V, Ford I, Jukema JW, Kontto J, MORGAM Investigators, Saleheen D, Sattar N, Young R, Howson JM, Butterworth AS, Danesh J, Ardissino D, Bottinger EP, Erbel R, Girelli D, Hall AS, Hovingh GK, Lieb W, Kraus WE, Shah SH, McPherson R, Orho-Melander M, Melander O, Metspalu A, Palmer CN, Rader DJ, Reilly MP, Loos RJ, Reiner AP, Roden DM, Thompson JR, Wareham NJ, Watkins H, Samani NJ, Deloukas P, Kathiresan S, Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators, Erdmann J, Jansen H, Ferrario PG, K?nig IR, Franz?n O, Bj?rkegren JL, Dube MP, Willenborg C, El-Mokhtari NE, Hengstenberg C, Hveem K, Jansson JH, J?ckel KH, Kessler T, Kriebel J, Laugwitz KL, Meisinger C, Esko T, Escher SA, M?ller-Nurasyid M, Strauch K, Varga TV, Waldenberger M, Zeng L, Amouyel P, Nordestgaard BG, Ferri?res J, Surendran P, Wagner A, Franks PW, Kastrati A, Meitinger T, Peters A, Tardif JC, Willer CJ, Schunkert H. Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With?Coronary Artery?Disease. J Am Coll Cardiol. 2017 Feb 21; 69(7):823-836. PMID: 28209224; PMCID: PMC5314135.
      Citations: 124     Fields:    Translation:Humans
    149. Forstner AJ, Hecker J, Hofmann A, Maaser A, Leber M, Strohmaier J, Degenhardt F, Treutlein J, Mattheisen M, Schumacher J, Streit F, Meier S, Herms S, Hoffmann P, Witt SH, Reif A, Lucae S, Maier W, Schwarz M, Vedder H, Kammerer-Ciernioch J, Pfennig A, Bauer M, Moebus S, Schenk LM, Fischer SB, Sivalingam S, Czerski PM, Hauser J, Lissowska J, Szeszenia-Dabrowska N, Brennan P, McKay JD, Wright A, Mitchell PB, Fullerton JM, Schofield PR, Montgomery GW, Medland SE, Gordon SD, Martin NG, Krasnov V, Chuchalin A, Babadjanova G, Pantelejeva G, Abramova LI, Tiganov AS, Polonikov A, Khusnutdinova E, Alda M, Cruceanu C, Rouleau GA, Turecki G, Rivas F, Mayoral F, Kogevinas M, Grigoroiu-Serbanescu M, Becker T, Schulze TG, Rietschel M, Cichon S, Fier H, Reinbold CS, M?hleisen TW, Lacour A, M?ller-Myhsok B, Hautzinger M, Laprise C, N?then MM. Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. PLoS One. 2017; 12(2):e0171595. PMID: 28166306; PMCID: PMC5293228.
      Citations: 36     Fields:    Translation:HumansCells
    150. Treutlein J, Strohmaier J, Frank J, Witt SH, Rietschel L, Forstner AJ, Lang M, Degenhardt F, Dukal H, Herms S, Streit F, Hoffmann P, Cichon S, Rietschel M, N?then MM. Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder. Psychiatr Genet. 2017 02; 27(1):34-37. PMID: 27584037.
      Citations: 7     Fields:    Translation:HumansCells
    151. Law PJ, Sud A, Mitchell JS, Henrion M, Orlando G, Lenive O, Broderick P, Speedy HE, Johnson DC, Kaiser M, Weinhold N, Cooke R, Sunter NJ, Jackson GH, Summerfield G, Harris RJ, Pettitt AR, Allsup DJ, Carmichael J, Bailey JR, Pratt G, Rahman T, Pepper C, Fegan C, von Strandmann EP, Engert A, Chen B, Filho MI, Thomsen H, Hoffmann P, Noethen MM, Eisele L, Allan JM, Swerdlow AJ, Goldschmidt H, Catovsky D, Morgan GJ, Hemminki K, Houlston RS, F?rsti A, J?ckel KH. Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci. Sci Rep. 2017 01 23; 7:41071. PMID: 28112199; PMCID: PMC5253627.
      Citations: 21     Fields:    Translation:Humans
    152. Kebschull M, Hoffmann P, Papapanou PN, H?lsmann C. Genome-Wide Analysis of Periodontal and Peri-Implant Cells and Tissues. Methods Mol Biol. 2017; 1537:307-326. PMID: 27924602; PMCID: PMC6554644.
      Citations: 3     Fields:    Translation:HumansCells
    153. Heinemann B, Strohmaier J, Pfohl MA, Giegling I, Hofmann A, Ludwig KU, Witt SH, Ludwig M, Forstner AJ, Albus M, Schwab SG, Borrmann-Hassenbach M, Lennertz L, Wagner M, Hoffmann P, Rujescu D, Maier W, Cichon S, Rietschel M, Degenhardt F, N?then MM. Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2. Psychiatr Genet. 2016 12; 26(6):293-296. PMID: 27668412; PMCID: PMC5087564.
      Citations: 3     Fields:    Translation:HumansCells
    154. Weinhold L, Pechlivanis S, Hoffmann P, Schmid M, Wahl S. A statistical model for the analysis of beta values in DNA methylation studies. BMC Bioinformatics. 2016 Nov 22; 17(1):480. PMID: 27875981; PMCID: PMC5120494.
      Citations: 23     Fields:    Translation:HumansCells
    155. Marshall CR, Howrigan DP, Merico D, Thiruvahindrapuram B, Wu W, Greer DS, Antaki D, Shetty A, Holmans PA, Pinto D, Gujral M, Brandler WM, Malhotra D, Wang Z, Fajarado KVF, Maile MS, Ripke S, Agartz I, Albus M, Alexander M, Amin F, Atkins J, Bacanu SA, Belliveau RA, Bergen SE, Bertalan M, Bevilacqua E, Bigdeli TB, Black DW, Bruggeman R, Buccola NG, Buckner RL, Bulik-Sullivan B, Byerley W, Cahn W, Cai G, Cairns MJ, Campion D, Cantor RM, Carr VJ, Carrera N, Catts SV, Chambert KD, Cheng W, Cloninger CR, Cohen D, Cormican P, Craddock N, Crowley JJ, Curtis D, Davidson M, Davis KL, Degenhardt F, Del Favero J, DeLisi LE, Dikeos D, Dinan T, Djurovic S, Donohoe G, Drapeau E, Duan J, Dudbridge F, Eichhammer P, Escott-Price V, Essioux L, Fanous AH, Farh KH, Farrell MS, Frank J, Franke L, Freedman R, Freimer NB, Friedman JI, Forstner AJ, Fromer M, Genovese G, Georgieva L, Gershon ES, Giegling I, Goldstein JI, Gratten J, de Haan L, Hamshere ML, Hansen M, Hansen T, Haroutunian V, Hartmann AM, Henskens FA, Herms S, Hirschhorn JN, Hoffmann P, Hofman A, Huang H, Ikeda M, Joa I, Kalaydjieva L, Karjalainen J, Kavanagh D, Keller MC, Kelly BJ, Kennedy JL, Kim Y, Knowles JA, Konte B, Laurent C, Lee P, Lee SH, Legge SE, Lerer B, Levy DL, Liang KY, Lieberman J, Loughland CM, Magnusson PKE, Maher BS, Maier W, Mattheisen M, Mattingsdal M, McCarley RW, McDonald C, McIntosh AM, Meier S, Meijer CJ, Melle I, Mesholam-Gately RI, Metspalu A, Michie PT, Milani L, Milanova V, Mokrab Y, Morris DW, Murphy KC, Murray RM, Myin-Germeys I, Nenadic I, Nertney DA, Nestadt G, Nicodemus KK, Nisenbaum L, O'Callaghan E, O'Dushlaine C, Oh SY, Olincy A, Olsen L, O'Neill FA, Van Os J, Pantelis C, Papadimitriou GN, Parkhomenko E, Pato MT, Paunio T, Psychosis Endophenotypes International Consortium, Perkins DO, Pers TH, Pimm J, Pocklington AJ, Powell J, Price A, Pulver AE, Purcell SM, Quested D, Rasmussen HB, Reichenberg A, Reimers MA, Richards AL, Roffman JL, Roussos P, Ruderfer DM, Salomaa V, Sanders AR, Savitz A, Schall U, Schulze TG, Schwab SG, Scolnick EM, Scott RJ, Seidman LJ, Shi J, Silverman JM, Smoller JW, Spencer CCA, Stahl EA, Strengman E, Strohmaier J, Stroup TS, Suvisaari J, Svrakic DM, Szatkiewicz JP, Thirumalai S, Tooney PA, Veijola J, Visscher PM, Waddington J, Walsh D, Webb BT, Weiser M, Wildenauer DB, Williams NM, Williams S, Witt SH, Wolen AR, Wormley BK, Wray NR, Wu JQ, Zai CC, Andreassen OA, Blackwood DHR, Bramon E, Buxbaum JD, Cichon S, Collier DA, Corvin A, Daly MJ, Darvasi A, Domenici E, Gejman PV, Gill M, Gurling H, Hultman CM, Iwata N, Jablensky AV, Kendler KS, Kirov G, Knight J, Levinson DF, Li QS, McCarroll SA, McQuillin A, Moran JL, Mowry BJ, Ophoff RA, Owen MJ, Palotie A, Pato CN, Petryshen TL, Posthuma D, Rietschel M, Riley BP, Rujescu D, Sklar P, St Clair D, Walters JTR, Werge T, Sullivan PF, O'Donovan MC, Scherer SW, Neale BM, Sebat J, CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium, Crespo-Facorro B, Eriksson J, Giusti-Rodr?guez P, Godard S, K?hler AK, Kahn RS, L?nnqvist J, Mallet J, M?ller-Myhsok B, Nordin A, Pietil?inen O, S?derman E, Adolfsson R, Esko T, J?nsson EG, N?then MM. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nat Genet. 2017 01; 49(1):27-35. PMID: 27869829; PMCID: PMC5737772.
      Citations: 449     Fields:    Translation:Humans
    156. Brosens E, Marsch F, de Jong EM, Zaveri HP, Hilger AC, Choinitzki VG, Hoffmann P, Herms S, Boemers TM, Ure BM, Lacher M, Ludwig M, Eussen BH, van der Helm RM, Douben H, Van Opstal D, Wijnen RM, Beverloo HB, van Bever Y, Brooks AS, IJsselstijn H, Scott DA, Schumacher J, Tibboel D, Reutter H, de Klein A, H?lscher A. Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula. Eur J Hum Genet. 2016 12; 24(12):1715-1723. PMID: 27436264; PMCID: PMC5117935.
      Citations: 18     Fields:    Translation:Humans
    157. Mitchell JS, Li N, Weinhold N, Ali M, van Duin M, Thorleifsson G, Johnson DC, Chen B, Halvarsson BM, Gudbjartsson DF, Kuiper R, Stephens OW, Bertsch U, Broderick P, Campo C, Gregory WA, Gullberg U, Henrion M, Hillengass J, Hoffmann P, Jackson GH, Johnsson E, Lenive O, Mellqvist UH, Migliorini G, Nahi H, Nelander S, Nickel J, Rafnar T, Ross FM, da Silva Filho MI, Swaminathan B, Thomsen H, Vangsted A, Vogel U, Waage A, Walker BA, Wihlborg AK, Broyl A, Davies FE, Thorsteinsdottir U, Langer C, Hansson M, Kaiser M, Sonneveld P, Stefansson K, Morgan GJ, Goldschmidt H, Hemminki K, Houlston RS, F?rsti A, Einsele H, J?ud M, Kristinsson SY, Lenhoff S, N?then MM, Turesson I, Nilsson B. Genome-wide association study identifies multiple susceptibility loci for multiple myeloma. Nat Commun. 2016 07 01; 7:12050. PMID: 27363682; PMCID: PMC4932178.
      Citations: 84     Fields:    Translation:Humans
    158. Hou L, Bergen SE, Akula N, Song J, Hultman CM, Alda M, Ardau R, Aubry JM, Backlund L, Badner JA, Barrett TB, Baune BT, Benabarre A, Bengesser S, Berrettini WH, Bhattacharjee AK, Biernacka JM, Birner A, Bloss CS, Bui ET, Byerley W, Cervantes P, Chillotti C, Cichon S, Colom F, Coryell W, Craig DW, Cruceanu C, Czerski PM, Davis T, Dayer A, Degenhardt F, Del Zompo M, DePaulo JR, Edenberg HJ, Falkai P, Foroud T, Forstner AJ, Frye MA, Fullerton JM, Garnham JS, Gershon ES, Goes FS, Greenwood TA, Grigoroiu-Serbanescu M, Hauser J, Heilbronner U, Heilmann-Heimbach S, Herms S, Hipolito M, Hitturlingappa S, Hoffmann P, Hofmann A, Kassem L, Kelsoe JR, Kittel-Schneider S, Kliwicki S, Koller DL, Lackner N, Laje G, Lang M, Lavebratt C, Lawson WB, Leckband SG, Liu C, Maaser A, Mahon PB, Maier W, Maj M, Manchia M, Martinsson L, McCarthy MJ, McElroy SL, McInnis MG, McKinney R, Mitchell PB, Mondimore FM, Monteleone P, Nievergelt CM, Nurnberger JI, Nwulia EA, Potash JB, Propping P, Reif A, Reininghaus E, Rice J, Rietschel M, Rouleau GA, Rybakowski JK, Schalling M, Scheftner WA, Schofield PR, Schork NJ, Schulze TG, Schumacher J, Schweizer BW, Severino G, Shekhtman T, Shilling PD, Simhandl C, Slaney CM, Smith EN, Squassina A, Stopkova P, Streit F, Strohmaier J, Szelinger S, Tighe SK, Tortorella A, Turecki G, Vieta E, Volkert J, Witt SH, Wright A, Zandi PP, Zhang P, Zollner S, McMahon FJ, Land?n M, Adli M, Arias B, Bauer M, Bellivier F, Brichant-Petitjean C, ?tain B, Fris?n L, Gard S, Jamain S, Jim?nez E, Kahn JP, K?nig B, Leboyer M, Mitjans M, M?hleisen TW, N?then MM, Nov?k T, ?sby U, Pfennig A, Stamm T. Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. Hum Mol Genet. 2016 08 01; 25(15):3383-3394. PMID: 27329760; PMCID: PMC5179929.
      Citations: 82     Fields:    Translation:HumansCells
    159. Thomsen H, Inacio da Silva Filho M, Fuchs M, Ponader S, Pogge von Strandmann E, Eisele L, Herms S, Hoffmann P, Engert A, Hemminki K, F?rsti A. Evidence of Inbreeding in Hodgkin Lymphoma. PLoS One. 2016; 11(4):e0154259. PMID: 27123581; PMCID: PMC4849743.
      Citations: 7     Fields:    Translation:Humans
    160. Spier I, Kerick M, Drichel D, Horpaopan S, Holzapfel S, Peters S, Adam R, Zhao B, Becker T, Lifton RP, Perner S, Thiele H, Hoffmann P, Timmermann B, Schweiger MR, Aretz S, Altm?ller J, Laner A, Holinski-Feder E, N?then MM. Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis. Fam Cancer. 2016 Apr; 15(2):281-8. PMID: 26780541.
      Citations: 26     Fields:    Translation:Humans
    161. Flachsbart F, Ellinghaus D, Gentschew L, Heinsen FA, Caliebe A, Christiansen L, Nygaard M, Christensen K, Brand S, Hoffmann P, Lieb W, Franke A, Schreiber S, Nebel A, Blanch? H, Deleuze JF, Derbois C, Galan P, B?ning C, Peters A, Strauch K, M?ller-Nurasyid M, N?then MM. Immunochip analysis identifies association of the RAD50/IL13 region with human longevity. Aging Cell. 2016 06; 15(3):585-8. PMID: 27004735; PMCID: PMC4854908.
      Citations: 13     Fields:    Translation:HumansCells
    162. Thomsen H, Chen B, Figlioli G, Elisei R, Romei C, Cipollini M, Cristaudo A, Bambi F, Hoffmann P, Herms S, Landi S, Hemminki K, Gemignani F, F?rsti A. Runs of homozygosity and inbreeding in thyroid cancer. BMC Cancer. 2016 Mar 16; 16:227. PMID: 26984635; PMCID: PMC4794977.
      Citations: 13     Fields:    Translation:Humans
    163. Hou L, Degenhardt F, Akiyama K, Akula N, Ardau R, Backlund L, Banzato CEM, Benabarre A, Bengesser S, Bhattacharjee AK, Biernacka JM, Birner A, Bui ET, Cervantes P, Chen GB, Chen HC, Chillotti C, Cichon S, Clark SR, Colom F, Cousins DA, Cruceanu C, Czerski PM, Dantas CR, Dayer A, Falkai P, Forstner AJ, Fullerton JM, Garnham JS, Goes FS, Grof P, Hashimoto R, Hauser J, Herms S, Hoffmann P, Hofmann A, Kassem L, Kittel-Schneider S, Kliwicki S, Kusumi I, Lackner N, Laje G, Lavebratt C, Leckband SG, MacQueen G, Manchia M, Martinsson L, Mattheisen M, McCarthy MJ, McElroy SL, Mondimore FM, Monteleone P, Nievergelt CM, Ozaki N, Perlis RH, Reich-Erkelenz D, Rouleau GA, Schofield PR, Schubert KO, Schweizer BW, Severino G, Shekhtman T, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Smoller JW, Squassina A, Stopkova P, Tighe SK, Tortorella A, Turecki G, Volkert J, Witt S, Wright A, Young LT, Zandi PP, Potash JB, DePaulo JR, Reininghaus EZ, Aubry JM, Maj M, Baune BT, Mitchell PB, Vieta E, Frye MA, Rybakowski JK, Kuo PH, Kato T, Grigoroiu-Serbanescu M, Reif A, Del Zompo M, Schalling M, Wray NR, Kelsoe JR, Alda M, Rietschel M, McMahon FJ, Heilbronner U, Adli M, Arias B, Brichant-Petitjean C, ?tain B, Fris?n L, Gard S, Gruber O, Jamain S, Jim?nez E, Kahn JP, K?nig B, Land?n M, Leboyer M, Jaramillo CAL, Mitjans M, N?then MM, ?sby U, Pfennig A, Seem?ller F, Stamm T, Bauer M, Nov?k T, Bellivier F, Schulze TG. Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. Lancet. 2016 Mar 12; 387(10023):1085-1093. PMID: 26806518; PMCID: PMC4814312.
      Citations: 124     Fields:    Translation:HumansCTClinical Trials
    164. Johnson DC, Weinhold N, Mitchell JS, Chen B, Kaiser M, Begum DB, Hillengass J, Bertsch U, Gregory WA, Cairns D, Jackson GH, Nickel J, Hoffmann P, Stephens OW, Barlogie B, Davis FE, Hemminki K, Goldschmidt H, Houlston RS, Morgan GJ, F?rsti A, N?ethen MM. Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma. Nat Commun. 2016 Jan 08; 7:10290. PMID: 26743840; PMCID: PMC4729868.
      Citations: 15     Fields:    Translation:HumansCells
    165. Stuart PE, Nair RP, Tsoi LC, Tejasvi T, Das S, Kang HM, Chandran V, Callis-Duffin K, Ike R, Li Y, Wen X, Gudjonsson JE, Mrowietz U, Reis A, Wichmann HE, Hoffmann P, Kunz M, Moreta EG, Mease PJ, Ritchlin CT, Bowcock AM, Krueger GG, Lim HW, Weidinger S, Weichenthal M, Voorhees JJ, Rahman P, Gregersen PK, Gladman DD, Elder JT, Ellinghaus E, Enerb?ck C, K?ks S, Kingo K, Esko T, Gieger C, N?then MM, Winkelmann J, Franke A, Abecasis GR. Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. Am J Hum Genet. 2015 Dec 03; 97(6):816-36. PMID: 26626624; PMCID: PMC4678416.
      Citations: 127     Fields:    Translation:Humans
    166. Spier I, Drichel D, Kerick M, Kirfel J, Horpaopan S, Laner A, Holzapfel S, Peters S, Adam R, Zhao B, Becker T, Lifton RP, Perner S, Hoffmann P, Kristiansen G, Timmermann B, Holinski-Feder E, Schweiger MR, Aretz S, N?then MM. Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases. J Med Genet. 2016 Mar; 53(3):172-9. PMID: 26613750.
      Citations: 25     Fields:    Translation:Humans
    167. Thomsen H, Filho MI, Woltmann A, Hamann U, Herms S, Hoffmann P, Chen B, Huhn S, Hemminki K, Johansson R, Eyfj?rd JE, Manjer J, Enquist-Olsson K, Henriksson R, Lenner P, F?rsti A. Inbreeding and homozygosity in breast cancer survival. Sci Rep. 2015 Nov 12; 5:16467. PMID: 26558712; PMCID: PMC4642301.
      Citations: 3     Fields:    Translation:Humans
    168. Vijayakrishnan J, Henrion M, Moorman AV, Fiege B, Kumar R, da Silva Filho MI, Holroyd A, Koehler R, Thomsen H, Irving JA, Allan JM, Lightfoot T, Roman E, Kinsey SE, Sheridan E, Thompson PD, Hoffmann P, Eisele L, Bartram CR, Schrappe M, Greaves M, Hemminki K, Harrison CJ, Stanulla M, Houlston RS, N?then MM, M?hleisen TW. The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A. Sci Rep. 2015 Oct 14; 5:15065. PMID: 26463672; PMCID: PMC4604478.
      Citations: 20     Fields:    Translation:HumansCells
    169. Schwantes-An TH, Zhang J, Chen LS, Hartz SM, Culverhouse RC, Chen X, Coon H, Frank J, Kamens HM, Kovanen L, Latvala A, Legrand LN, Maher BS, Melroy WE, Nelson EC, Reid MW, Robinson JD, Shen PH, Yang BZ, Andrews JA, Aveyard P, Beltcheva O, Brown SA, Cannon DS, Cichon S, Corley RP, Degenhardt L, Foroud T, Glatt SJ, Grucza RA, Hardin J, Heath AC, Herms S, Hodgkinson CA, Hoffmann P, Hops H, Huizinga D, Ising M, Johnson EO, Johnstone E, Kaneva RP, Kendler KS, Kiefer F, Kranzler HR, Krauter KS, Levran O, Lucae S, Lynskey MT, Maier W, Mann K, Martin NG, Mattheisen M, Montgomery GW, Murphy MF, Neale MC, Nikolov MA, Nishita D, Nurnberger J, Partonen T, Pergadia ML, Reynolds M, Ridinger M, Rose RJ, Scherbaum N, Soyka M, Stallings MC, Steffens M, Treutlein J, Tsuang M, Wall TL, Wodarz N, Yuferov V, Zill P, Bergen AW, Chen J, Cinciripini PM, Edenberg HJ, Ehringer MA, Ferrell RE, Gelernter J, Goldman D, Hewitt JK, Hopfer CJ, Iacono WG, Kaprio J, Kreek MJ, Kremensky IM, Madden PA, McGue M, Philibert RA, Rietschel M, Roy A, Saarikoski ST, Swan GE, Todorov AA, Vanyukov MM, Weiss RB, Bierut LJ, Saccone NL, Konte B, Dahmen N, Gaebel W, Giegling I, Hartmann AM, M?ller-Myhsok B, N?then MM, Rouvinen-Lagerstr?m N, Schm?l C, Munaf? MR, Rujescu D. Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behav Genet. 2016 Mar; 46(2):151-69. PMID: 26392368; PMCID: PMC4752855.
      Citations: 55     Fields:    Translation:Humans
    170. Nettersheim D, Jostes S, Sharma R, Schneider S, Hofmann A, Ferreira HJ, Hoffmann P, Kristiansen G, Schorle H, Esteller MB. BMP Inhibition in Seminomas Initiates Acquisition of Pluripotency via NODAL Signaling Resulting in Reprogramming to an Embryonal Carcinoma. PLoS Genet. 2015 Jul; 11(7):e1005415. PMID: 26226633; PMCID: PMC4520454.
      Citations: 34     Fields:    Translation:HumansAnimalsCells
    171. Sharma A, Jamil MA, Nuesgen N, Schreiner F, Priebe L, Hoffmann P, Herns S, Oldenburg J, Woelfle J, El-Maarri O, N?then MM, Fr?hlich H. DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations. Clin Epigenetics. 2015; 7:76. PMID: 26221191; PMCID: PMC4517491.
      Citations: 36     Fields:    
    172. Lal D, Pernhorst K, Klein KM, Reif P, Tozzi R, Toliat MR, Winterer G, Neubauer B, Rosenow F, Kunz WS, Kurki MI, Becker AJ, Perucca E, Zara F, Sander T, N?rnberg P, Becker F, Lerche H, Hoffmann P, Weber YG. Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy. Epilepsia. 2015 Sep; 56(9):e129-33. PMID: 26174448.
      Citations: 23     Fields:    Translation:Humans
    173. Basmanav FB, Forstner AJ, Fier H, Herms S, Meier S, Degenhardt F, Hoffmann P, Barth S, Fricker N, Strohmaier J, Witt SH, Ludwig M, Schmael C, Moebus S, Maier W, Rujescu D, Rietschel M, Lange C, Cichon S, M?ssner R, N?then MM. Investigation of the role of TCF4 rare sequence variants in schizophrenia. Am J Med Genet B Neuropsychiatr Genet. 2015 Jul; 168B(5):354-62. PMID: 26010163.
      Citations: 7     Fields:    Translation:Humans
    174. Hofmann A, Herms S, Hoffmann P, Weber S, Doerfler W. Destabilization of the human epigenome: consequences of foreign DNA insertions. Epigenomics. 2015 Aug; 7(5):745-55. PMID: 26088384.
      Citations: 6     Fields:    Translation:HumansCells
    175. Figlioli G, Chen B, Elisei R, Romei C, Campo C, Cipollini M, Cristaudo A, Bambi F, Paolicchi E, Hoffmann P, Herms S, Kalemba M, Kula D, Jarzab B, Landi S, Gemignani F, Pastor S, Marcos R, Vel?zquez A, Hemminki K, F?rsti A. Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk. Sci Rep. 2015 Mar 10; 5:8922. PMID: 25753578; PMCID: PMC4354074.
      Citations: 14     Fields:    Translation:Humans
    176. Wessel J, Chu AY, Willems SM, Wang S, Yaghootkar H, Brody JA, Dauriz M, Raghavan S, Lipovich L, Hidalgo B, Fox K, Huffman JE, An P, Lu Y, Rasmussen-Torvik LJ, Grarup N, Ehm MG, Li L, Baldridge AS, Abrol R, Bork-Jensen J, Fornage M, Freitag DF, Garcia ME, Guo X, Hara K, Isaacs A, Jakobsdottir J, Lange LA, Layton JC, Li M, Hua Zhao J, Morrison AC, Nalls MA, Peters MJ, Sabater-Lleal M, Schurmann C, Silveira A, Smith AV, Southam L, Stoiber MH, Strawbridge RJ, Taylor KD, Allin KH, Amin N, Aponte JL, Aung T, Barbieri C, Bihlmeyer NA, Boehnke M, Bombieri C, Bowden DW, Burns SM, Chen Y, Chen YD, Cheng CY, Correa A, Czajkowski J, Dehghan A, Ehret GB, Eiriksdottir G, Farmaki AE, Gambaro G, Giulianini F, Goddard WA, Goel A, Gottesman O, Grove ML, Gustafsson S, Hai Y, Heo J, Hoffmann P, Ikram MK, Jensen RA, Karaleftheri M, Khor CC, Kirkpatrick A, Kraja AT, Kuusisto J, Lange EM, Lee IT, Lee WJ, Leong A, Liao J, Liu C, Liu Y, Lindgren CM, Linneberg A, Malerba G, Mamakou V, Marouli E, Maruthur NM, Matchan A, McKean-Cowdin R, McLeod O, Metcalf GA, Mohlke KL, Muzny DM, Ntalla I, Palmer ND, Pasko D, Rayner NW, Rice K, Sala CF, Sennblad B, Serafetinidis I, Smith JA, Soranzo N, Speliotes EK, Stahl EA, Stirrups K, Tentolouris N, Thanopoulou A, Torres M, Traglia M, Tsafantakis E, Javad S, Yanek LR, Zengini E, Becker DM, Bis JC, Brown JB, Cupples LA, Hansen T, Ingelsson E, Karter AJ, Lorenzo C, Mathias RA, Norris JM, Peloso GM, Sheu WH, Toniolo D, Vaidya D, Varma R, Wagenknecht LE, Bottinger EP, Dedoussis G, Deloukas P, Ferrannini E, Franco OH, Gibbs RA, Gudnason V, Hamsten A, Harris TB, Hattersley AT, Hayward C, Hofman A, Langenberg C, Launer LJ, Levy D, Oostra BA, O'Donnell CJ, O'Rahilly S, Padmanabhan S, Pankow JS, Polasek O, Province MA, Rich SS, Ridker PM, Rudan I, Smith BH, Walker M, Watkins H, Wong TY, Zeggini E, EPIC-InterAct Consortium, Laakso M, Borecki IB, Chasman DI, Pedersen O, Psaty BM, Tai ES, van Duijn CM, Wareham NJ, Waterworth DM, Boerwinkle E, Kao WH, Florez JC, Loos RJ, Wilson JG, Frayling TM, Siscovick DS, Rotter JI, Meigs JB, Scott RA, Goodarzi MO, Hivert MF, Stanc?kov? A, Besse C, Boland A, Meidtner K, Varga TV, Escher SA, Fr?nberg M, Hallmans G, J?rgensen ME, J?rgensen T, Peter A, Renstr?m F, Boeing H, Franks PW, Jansson JH, Schulze MB, Uitterlinden AG, Dupuis J. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nat Commun. 2015 Jan 29; 6:5897. PMID: 25631608; PMCID: PMC4311266.
      Citations: 100     Fields:    Translation:Humans
    177. Johnson MR, Behmoaras J, Bottolo L, Krishnan ML, Pernhorst K, Santoscoy PLM, Rossetti T, Speed D, Srivastava PK, Chadeau-Hyam M, Hajji N, Dabrowska A, Rotival M, Razzaghi B, Kovac S, Wanisch K, Grillo FW, Slaviero A, Langley SR, Shkura K, Roncon P, De T, Mattheisen M, Niehusmann P, O'Brien TJ, Petrovski S, von Lehe M, Hoffmann P, Coffey AJ, Cichon S, Walker M, Simonato M, Mazzuferi M, Foerch P, Schoch S, De Paola V, Kaminski RM, Cunliffe VT, Becker AJ, Petretto E, Eriksson J, Danis B. Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus. Nat Commun. 2015 Jan 23; 6:6031. PMID: 25615886; PMCID: PMC4627576.
      Citations: 67     Fields:    Translation:HumansAnimalsCells
    178. Spier I, Holzapfel S, Zhao B, Horpaopan S, Vogt S, Chen S, Morak M, Raeder S, Kayser K, Stienen D, Adam R, Plotz G, Holinski-Feder E, Lifton RP, Thiele H, Hoffmann P, Steinke V, Aretz S, Altm?ller J, N?rnberg P. Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas. Int J Cancer. 2015 Jul 15; 137(2):320-31. PMID: 25529843.
      Citations: 73     Fields:    Translation:Humans
    179. van Setten J, Pechlivanis S, Tragante V, de Jong PA, Smolonska J, Platteel M, Hoffmann P, Oudkerk M, de Koning HJ, Moebus S, Erbel R, Viergever MA, Mali WP, de Bakker PI, I?gum I, N?then MM, J?ckel KH. Serum lipid levels, body mass index, and their role in coronary artery calcification: a polygenic analysis. Circ Cardiovasc Genet. 2015 Apr; 8(2):327-33. PMID: 25577604.
      Citations: 8     Fields:    Translation:HumansCTClinical Trials
    180. Kaut O, Schmitt I, Hofmann A, Hoffmann P, Schlaepfer TE, W?llner U, Hurlemann R. Aberrant NMDA receptor DNA methylation detected by epigenome-wide analysis of hippocampus and prefrontal cortex in major depression. Eur Arch Psychiatry Clin Neurosci. 2015 Jun; 265(4):331-41. PMID: 25571874.
      Citations: 27     Fields:    Translation:HumansCells
    181. Weinhold N, Meissner T, Johnson DC, Seckinger A, Chen B, Nickel J, Chubb D, Rawstron AC, Doughty C, Dahir NB, Begum DB, Young K, Walker BA, Hoffmann P, Davies FE, Goldschmidt H, Morgan GJ, Houlston RS, Hose D, Hemminki K, Moreaux J, F?rsti A, N?then MM, Klein B. The 7p15.3 (rs4487645) association for multiple myeloma shows strong allele-specific regulation of the MYC-interacting gene CDCA7L in malignant plasma cells. Haematologica. 2015 Mar; 100(3):e110-3. PMID: 25480495; PMCID: PMC4349291.
      Citations: 20     Fields:    Translation:HumansCells
    182. Forstner AJ, Basmanav FB, Mattheisen M, Hollegaard MV, Janson E, Strengman E, Priebe L, Degenhardt F, Hoffmann P, Herms S, Maier W, Rujescu D, Ophoff RA, Moebus S, Mortensen PB, Hougaard DM, Frank J, Witt SH, Rietschel M, Zimmer A, Cichon S, B?hmer AC, M?ssner R, B?rglum AD, N?then MM, Mir? X. Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia. J Psychiatry Neurosci. 2014 Nov; 39(6):386-96. PMID: 24936775; PMCID: PMC4214873.
      Citations: 17     Fields:    Translation:HumansAnimals
    183. Wood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, Chu AY, Estrada K, Luan J, Amin N, Buchkovich ML, Croteau-Chonka DC, Day FR, Duan Y, Fall T, Fehrmann R, Ferreira T, Jackson AU, Karjalainen J, Lo KS, Locke AE, Mihailov E, Porcu E, Randall JC, Vinkhuyzen AA, Westra HJ, Winkler TW, Workalemahu T, Zhao JH, Absher D, Anderson D, Baron J, Beekman M, Demirkan A, Ehret GB, Feenstra B, Feitosa MF, Fischer K, Fraser RM, Goel A, Gong J, Justice AE, Kanoni S, Kleber ME, Kristiansson K, Lim U, Lotay V, Lui JC, Mangino M, Mateo Leach I, Medina-Gomez C, Nalls MA, Nyholt DR, Palmer CD, Pasko D, Pechlivanis S, Prokopenko I, Ripke S, Strawbridge RJ, Sung YJ, Tanaka T, Teumer A, Trompet S, van der Laan SW, van Setten J, Van Vliet-Ostaptchouk JV, Zhang W, Afzal U, Arscott GM, Bandinelli S, Barrett A, Bellis C, Bennett AJ, Berne C, Bolton JL, Boyd HA, Bruinenberg M, Buckley BM, Buyske S, Caspersen IH, Chines PS, Clarke R, Claudi-Boehm S, Cooper M, Daw EW, De Jong PA, Deelen J, Delgado G, Denny JC, Dhonukshe-Rutten R, Dimitriou M, Doney AS, Eklund N, Folkersen L, Garcia ME, Geller F, Giedraitis V, Go AS, Grammer TB, de Groot LC, Groves CJ, Haessler J, Hall P, Haller T, Hannemann A, Hartman CA, Hassinen M, Hayward C, Heard-Costa NL, Helmer Q, Hemani G, Henders AK, Hillege HL, Hlatky MA, Hoffmann P, Holmen O, Houwing-Duistermaat JJ, Isaacs A, James AL, Jeff J, Johansen B, Jolley J, Juliusdottir T, Junttila J, Kho AN, Kinnunen L, Kocher T, Kratzer W, Lind L, Lorentzon M, Lu Y, Lyssenko V, Magnusson PK, Mahajan A, Maillard M, McArdle WL, McKenzie CA, McLachlan S, Menni C, Merger S, Milani L, Moayyeri A, Monda KL, Morken MA, Musk AW, Narisu N, Nolte IM, Oozageer L, Pilz S, Rayner NW, Robertson NR, Rose LM, Roussel R, Sanna S, Scharnagl H, Scholtens S, Schumacher FR, Scott RA, Sehmi J, Seufferlein T, Shi J, Silventoinen K, Smit JH, Smith AV, Smolonska J, Stanton AV, Stirrups K, Stott DJ, Stringham HM, Swertz MA, Tayo BO, Thorleifsson G, Tyrer JP, van Dijk S, van Schoor NM, van der Velde N, van Heemst D, van Oort FV, Vermeulen SH, Verweij N, Vonk JM, Waite LL, Wennauer R, Wilkens LR, Wojczynski MK, Wong A, Wright AF, Zhang Q, Arveiler D, Bakker SJ, Beilby J, Bergman RN, Bergmann S, Biffar R, Blangero J, Boomsma DI, Bovet P, Brambilla P, Brown MJ, Campbell H, Caulfield MJ, Chakravarti A, Collins R, Collins FS, Crawford DC, Cupples LA, Danesh J, de Faire U, den Ruijter HM, Erbel R, Eriksson JG, Farrall M, Ferrannini E, Ford I, Forouhi NG, Forrester T, Gansevoort RT, Gejman PV, Golay A, Gottesman O, Gudnason V, Gyllensten U, Haas DW, Hall AS, Harris TB, Hattersley AT, Heath AC, Hindorff LA, Hingorani AD, Hofman A, Hovingh GK, Humphries SE, Hunt SC, Hypponen E, Jacobs KB, Jarvelin MR, Jousilahti P, Jula AM, Kaprio J, Kastelein JJ, Kayser M, Kee F, Keinanen-Kiukaanniemi SM, Kiemeney LA, Kooner JS, Kooperberg C, Koskinen S, Kovacs P, Kraja AT, Kumari M, Kuusisto J, Lakka TA, Langenberg C, Le Marchand L, Lupoli S, Madden PA, Matise TC, McKnight B, Moll FL, Montgomery GW, Morris AD, Morris AP, Murray JC, Nelis M, Ohlsson C, Oldehinkel AJ, Ong KK, Ouwehand WH, Pasterkamp G, Price JF, Qi L, Raitakari OT, Rankinen T, Rao DC, Rice TK, Ritchie M, Rudan I, Salomaa V, Samani NJ, Saramies J, Sarzynski MA, Sebert S, Sever P, Shuldiner AR, Sinisalo J, Steinthorsdottir V, Stolk RP, Tremblay A, Virtamo J, Vohl MC, Electronic Medical Records and Genomics (eMEMERGEGE) Consortium, MIGen Consortium, PAGEGE Consortium, LifeLines Cohort Study, Asselbergs FW, Assimes TL, Bochud M, Boehm BO, Boerwinkle E, Bottinger EP, Bouchard C, Chambers JC, Chanock SJ, Cooper RS, de Bakker PI, Dedoussis G, Ferrucci L, Haiman CA, Hamsten A, Hayes MG, Hui J, Hunter DJ, Hveem K, Jukema JW, Kaplan RC, Kivimaki M, Kuh D, Laakso M, Liu Y, Martin NG, Melbye M, Moebus S, Munroe PB, Oostra BA, Palmer CN, Pedersen NL, Perola M, Peters U, Powell JE, Power C, Quertermous T, Rauramaa R, Reinmaa E, Ridker PM, Rivadeneira F, Rotter JI, Saaristo TE, Saleheen D, Schlessinger D, et al. Defining the role of common variation in the genomic and biological architecture of adult human height. Nat Genet. 2014 Nov; 46(11):1173-86. PMID: 25282103; PMCID: PMC4250049.
      Citations: 931     Fields:    Translation:Humans
    184. Horpaopan S, Spier I, Zink AM, Holzapfel S, Laner A, Vogt S, Uhlhaas S, Heilmann S, Stienen D, Pasternack SM, Keppler K, Adam R, Kayser K, Moebus S, Draaken M, Degenhardt F, Engels H, Hofmann A, Steinke V, Perez-Bouza A, Herms S, Holinski-Feder E, Thiele H, Hoffmann P, Aretz S, Altm?ller J, N?then MM, Fr?hlich H. Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis. Int J Cancer. 2015 Mar 15; 136(6):E578-89. PMID: 25219767.
      Citations: 31     Fields:    Translation:Humans
    185. Juraeva D, Treutlein J, Scholz H, Frank J, Degenhardt F, Cichon S, Ridinger M, Mattheisen M, Witt SH, Lang M, Sommer WH, Hoffmann P, Herms S, Wodarz N, Soyka M, Zill P, Maier W, Dahmen N, Scherbaum N, Steffens M, Mann K, Kiefer F, Spanagel R, Brors B, Rietschel M, J?nger E, Gaebel W, Schm?l C, Lucae S, Ising M, Smolka MN, Zimmermann US, M?ller-Myhsok B, N?then MM. XRCC5 as a risk gene for alcohol dependence: evidence from a genome-wide gene-set-based analysis and follow-up studies in Drosophila and humans. Neuropsychopharmacology. 2015 Jan; 40(2):361-71. PMID: 25035082; PMCID: PMC4443948.
      Citations: 6     Fields:    Translation:HumansAnimals
    186. Chen B, Elisei R, Romei C, Cipollini M, Cristaudo A, Bambi F, Paolicchi E, Hoffmann P, Herms S, Kalemba M, Kula D, Pastor S, Marcos R, Jarzab B, Landi S, Hemminki K, Gemignani F, Figlioli G, K?hler A, Vel?zquez A, F?rsti A. Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk. J Clin Endocrinol Metab. 2014 Oct; 99(10):E2084-92. PMID: 25029422.
      Citations: 29     Fields:    Translation:Humans
    187. Ramirez A, van der Flier WM, Herold C, Ramonet D, Heilmann S, Popp J, Drichel D, Louwersheimer E, Kummer MP, Cruchaga C, Hoffmann P, Teunissen C, Holstege H, Naj AC, Chouraki V, Gerrish A, International Genomics of Alzheimer's Project (IGAP), Alzheimer's Disease Neuroimaging Initiative (ADNI), Heun R, Buscemi L, Herms S, Scheltens P, Breteler MM, Goate A, Jessen F, Maier W, Heneka MT, Becker T, Lewczuk P, Lacour A, Kornhuber J, Peters O, Bellenguez C, Fr?lich L, H?ll M, K?lsch H, R?ther E, Wiltfang J, N?then MM. SUCLG2 identified as both a determinator of CSF A?1-42 levels and an attenuator of cognitive decline in Alzheimer's disease. Hum Mol Genet. 2014 Dec 15; 23(24):6644-58. PMID: 25027320; PMCID: PMC4240204.
      Citations: 27     Fields:    Translation:HumansCells
    188. Gockel I, Becker J, Wouters MM, Niebisch S, Gockel HR, Hess T, Ramonet D, Zimmermann J, Trynka G, Kumar V, Franke L, Westra HJ, Drescher D, Kneist W, Marquardt JU, Galle PR, Mattheisen M, Annese V, Latiano A, Fumagalli U, Laghi L, Cuomo R, Sarnelli G, Eckardt AJ, Tack J, Hoffmann P, Herms S, Mangold E, Heilmann S, Kiesslich R, Allescher HD, Schulz HG, Wijmenga C, Heneka MT, Lang H, Hopfner KP, Boeckxstaens GE, de Bakker PI, Knapp M, Schumacher J, Vigo AG, de Le?n AR, de la Serna JP, Urcelay E, M?ller M, von Rahden BH, N?then MM. Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia. Nat Genet. 2014 Aug; 46(8):901-4. PMID: 24997987.
      Citations: 41     Fields:    Translation:Humans
    189. Arking DE, Pulit SL, van der Harst P, Munroe PB, Koopmann TT, Sotoodehnia N, Rossin EJ, Morley M, Wang X, Johnson AD, Lundby A, Noseworthy PA, Eijgelsheim M, Bradford Y, Tarasov KV, Lahtinen AM, Nolte IM, Smith AV, Bis JC, Isaacs A, Newhouse SJ, Evans DS, Post WS, Waggott D, Eisele L, Ellinghaus D, Hayward C, Navarro P, Ulivi S, Tanaka T, Tester DJ, Gustafsson S, Kumari M, Morris RW, Padmanabhan S, Kluttig A, Strohmer B, Panayiotou AG, Knoflach M, Hubacek JA, Slowikowski K, Raychaudhuri S, Kumar RD, Harris TB, Launer LJ, Shuldiner AR, Alonso A, Bader JS, Ehret G, Huang H, Kao WH, Strait JB, Macfarlane PW, Brown M, Caulfield MJ, Samani NJ, Kronenberg F, Willeit J, CARe Consortium, COGENT Consortium, Smith JG, Greiser KH, Meyer Zu Schwabedissen H, Werdan K, Carella M, Zelante L, Heckbert SR, Psaty BM, Rotter JI, Kolcic I, Wright AF, Griffin M, Daly MJ, DCCT/EDIC, Arnar DO, Thorsteinsdottir U, eMERGE Consortium, Denny JC, Roden DM, Zuvich RL, Emilsson V, Plump AS, Larson MG, O'Donnell CJ, Yin X, Bobbo M, D'Adamo AP, Iorio A, Sinagra G, Cummings SR, Nalls MA, Jula A, Kontula KK, Marjamaa A, Oikarinen L, Perola M, Porthan K, Erbel R, Hoffmann P, HRGEN Consortium, den Hoed M, Loos RJ, Thelle DS, Gieger C, de Boer RA, Franke L, van der Vleuten PA, Bardai A, Hofman N, Wilde AA, Behr ER, Dalageorgou C, Giudicessi JR, Medeiros-Domingo A, Ghidoni A, Insolia R, Hamilton RM, Scherer SW, Brandimarto J, Margulies K, Moravec CE, Fuchsberger C, O'Connell JR, Lee WK, Watt GC, Campbell H, Wild SH, El Mokhtari NE, Frey N, Asselbergs FW, Mateo Leach I, Navis G, van den Berg MP, van Veldhuisen DJ, Kellis M, Krijthe BP, Franco OH, Hofman A, Kors JA, Witteman JC, Kedenko L, Lamina C, Oostra BA, Lakatta EG, Mulas A, Schlessinger D, Uda M, Markus MR, Snieder H, Spector TD, Lind L, Kivimaki M, Mononen N, Raitakari OT, Viikari JS, Adamkova V, Kiechl S, Nicolaides AN, Paulweber B, Haerting J, Dominiczak AF, Whincup PH, Hingorani AD, Bezzina CR, Ingelsson E, Ferrucci L, Gasparini P, Wilson JF, Rudan I, Franke A, Paterson AD, Parsa A, Liu Y, van Duijn CM, Siscovick DS, Gudnason V, Jamshidi Y, Salomaa V, Felix SB, Sanna S, Ritchie MD, Stricker BH, Stefansson K, Boyer LA, Cappola TP, Olsen JV, Lage K, Schwartz PJ, Chakravarti A, Ackerman MJ, de Bakker PI, Newton-Cheh C, Crotti L, Gudbjartsson DF, D?rr M, M?ller-Nurasyid M, Lyytik?inen LP, Hicks AA, Chatel S, Naluai ?T, Torres M, Pola?ek O, H?lm H, Carracedo A, J?ckel KH, K?lsch H, N?then MM, Meitinger T, Perz S, Peters A, Prucha H, Sinner MF, Waldenberger M, Beckmann BM, Martens E, Barc J, Kyndt F, Probst V, del Greco M F, Uitterlinden AG, Abecasis GR, Orr? M, V?lker U, ?rnl?v J, Sundstr?m J, Syv?nen AC, K?h?nen M, Brion M, Nyberg F, Schott JJ, M?hleisen TW, Pramstaller PP, Lehtim?ki TJ, K??b S, Pfeufer A. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat Genet. 2014 Aug; 46(8):826-36. PMID: 24952745; PMCID: PMC4124521.
      Citations: 156     Fields:    Translation:HumansCells
    190. Dragano N, Pechlivanis S, Hoffmann P, Erbel R, Moebus S, Schmidt B, Scherag A, N?then MM, J?ckel KH. Exploring genetic variants predisposing to diabetes mellitus and their association with indicators of socioeconomic status. BMC Public Health. 2014 Jun 16; 14:609. PMID: 24935819; PMCID: PMC4071333.
      Citations:    Fields:    Translation:Humans
    191. Reinthaler EM, Lal D, Lebon S, Hildebrand MS, Dahl HH, Regan BM, Feucht M, Neophytou B, Ronen GM, Roche L, Gruber-Sedlmayr U, Haberlandt E, Hoffmann P, Herms S, Franke A, Wittig M, Schoch S, Becker AJ, Hahn A, Toliat MR, 16p11.2 European Consortium, Mefford H, Scheffer IE, Berkovic SF, Beckmann JS, EPICURE Consortium, EuroEPINOMICS Consortium, Sander T, Jacquemont S, Reymond A, Zimprich F, Neubauer BA, Steinb?ck H, Geldner J, Gieger C, Waldenberger M, M?nnik K, Winterer G, Lerche H, N?rnberg P. 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy. Hum Mol Genet. 2014 Nov 15; 23(22):6069-80. PMID: 24939913.
      Citations: 32     Fields:    Translation:HumansCells
    192. Woltmann A, Chen B, Hamann U, Herms S, Hoffmann P, Lascorz J, Johansson R, Eyfj?rd JE, Manjer J, Enquist-Olsson K, Henriksson R, Hemminki K, Lenner P, F?rsti A. Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome. PLoS One. 2014; 9(6):e98229. PMID: 24886783; PMCID: PMC4041745.
      Citations: 11     Fields:    Translation:HumansCells
    193. Hammer C, Degenhardt F, Priebe L, Heilmann S, Waszak SM, Schlattl A, Mangold E, Hoffmann P, Rietschel M, Rappold G, Korbel J, Cichon S, Niesler B, MooDS Consortium, St?tz AM, N?then MM. A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders. Bipolar Disord. 2014 Nov; 16(7):764-8. PMID: 24754353.
      Citations: 1     Fields:    Translation:Humans
    194. Al Chawa T, Ludwig KU, Fier H, Reich RH, Braumann B, Daratsianos N, Schuencke H, Alblas M, Fricker N, Hoffmann P, Knapp M, Lange C, Mangold E, P?tzsch B, Schmidt G, B?hmer AC, N?then MM. Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway. Birth Defects Res A Clin Mol Teratol. 2014 Jun; 100(6):493-8. PMID: 24706492.
      Citations: 12     Fields:    Translation:HumansCells
    195. Leber M, Strohmaier J, Degenhardt F, Treutlein J, Mattheisen M, Forstner AJ, Schumacher J, Meier S, Herms S, Witt SH, Lucae S, Maier W, Schwarz M, Vedder H, Kammerer-Ciernioch J, Pfennig A, Bauer M, Moebus S, Priebe L, Czerski PM, Hauser J, Lissowska J, Szeszenia-Dabrowska N, Brennan P, McKay JD, Wright A, Mitchell PB, Fullerton JM, Schofield PR, Montgomery GW, Medland SE, Gordon SD, Martin NG, Krasnow V, Chuchalin A, Babadjanova G, Pantelejeva G, Abramova LI, Tiganov AS, Polonikov A, Khusnutdinova E, Alda M, Grof P, Turecki G, Rivas F, Mayoral F, Kogevinas M, Grigoroiu-Serbanescu M, Propping P, Becker T, Rietschel M, M?hleisen TW, Schulze TG, Breuer R, Hoffmann P, Lacour A, Reif A, M?ller-Myhsok B, Hautzinger M, Rouleau GA, Laprise C, N?then MM, Cichon S. Genome-wide association study reveals two new risk loci for bipolar disorder. Nat Commun. 2014 Mar 11; 5:3339. PMID: 24618891.
      Citations: 158     Fields:    Translation:Humans
    196. Bisht S, Heukamp LC, Kebschull M, Florin A, Haarmann J, Hoffmann P, Bendas G, Buettner R, Brossart P, Feldmann G, Sch?tte U. Hippo signaling mediates proliferation, invasiveness, and metastatic potential of clear cell renal cell carcinoma. Transl Oncol. 2014 Apr; 7(2):309-21. PMID: 24913676; PMCID: PMC4101344.
      Citations: 44     
    197. Weinhold N, Johnson DC, Rawstron AC, Doughty C, Vijayakrishnan J, Broderick P, Dahir NB, Begum DB, Hosking FJ, Yong K, Walker BA, Hoffmann P, Langer C, Eisele L, Hose D, Davies FE, Goldschmidt H, Morgan GJ, Hemminki K, Houlston RS, F?rsti A, M?hleisen TW, D?rner E, J?ckel KH, N?then MM. Inherited genetic susceptibility to monoclonal gammopathy of unknown significance. Blood. 2014 Apr 17; 123(16):2513-7; quiz 2593. PMID: 24449210.
      Citations: 19     Fields:    Translation:Humans
    198. Yildiz Y, Hoffmann P, Vom Dahl S, Breiden B, Sandhoff R, Niederau C, Horwitz M, Karlsson S, Filocamo M, Elstein D, Beck M, Sandhoff K, Mengel E, Gonzalez MC, Sidransky E, Zimran A, Mattheisen M, N?then MM. Functional and genetic characterization of the non-lysosomal glucosylceramidase 2 as a modifier for Gaucher disease. Orphanet J Rare Dis. 2013 Sep 26; 8:151. PMID: 24070122; PMCID: PMC3850879.
      Citations: 15     Fields:    Translation:AnimalsCells
    199. Becker J, Czamara D, Scerri TS, Talcott JB, Stein J, Morris A, Ludwig KU, Hoffmann P, van der Mark S, Vaessen A, Maurer U, Zucchelli M, Brandeis D, Blomert L, Bruder J, Monaco AP, Landerl K, Paracchini S, Peyrard-Janvid M, Schumacher J, Ramus F, Cs?pe V, Honbolyg? F, T?th D, Fauchereau F, Bogliotti C, Iannuzzi S, Chaix Y, Valdois S, Billard C, George F, Soares-Boucaud I, G?rard CL, Schulz E, Lohvansuu K, Lyytinen H, Lepp?nen PH, M?ller-Myhsok B, Kere J, N?then MM, Schulte-K?rne G. Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. Eur J Hum Genet. 2014 May; 22(5):675-80. PMID: 24022301; PMCID: PMC3992562.
      Citations: 26     Fields:    Translation:Humans
    200. Grimminger T, Pernhorst K, Surges R, Niehusmann P, Priebe L, von Lehe M, Hoffmann P, Cichon S, Schoch S, Becker AJ. Levetiracetam resistance: Synaptic signatures & corresponding promoter SNPs in epileptic hippocampi. Neurobiol Dis. 2013 Dec; 60:115-25. PMID: 24018139.
      Citations: 11     Fields:    Translation:HumansCells
    201. Migliorini G, Fiege B, Hosking FJ, Ma Y, Kumar R, Sherborne AL, da Silva Filho MI, Vijayakrishnan J, Koehler R, Thomsen H, Irving JA, Allan JM, Lightfoot T, Roman E, Kinsey SE, Sheridan E, Thompson P, Hoffmann P, Eisele L, Zimmermann M, Bartram CR, Schrappe M, Greaves M, Stanulla M, Hemminki K, Houlston RS, N?then MM, M?hleisen TW. Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. Blood. 2013 Nov 07; 122(19):3298-307. PMID: 23996088.
      Citations: 87     Fields:    Translation:HumansCells
    202. Nokhbehsaim M, Eick S, Nogueira AV, Hoffmann P, Herms S, Cirelli JA, Deschner J, Fr?hlich H, Jepsen S, J?ger A. Stimulation of MMP-1 and CCL2 by NAMPT in PDL cells. Mediators Inflamm. 2013; 2013:437123. PMID: 24058270; PMCID: PMC3766615.
      Citations: 21     Fields:    Translation:HumansCells
    203. Chubb D, Weinhold N, Broderick P, Chen B, Johnson DC, Vijayakrishnan J, Migliorini G, Dobbins SE, Holroyd A, Hose D, Walker BA, Davies FE, Gregory WA, Jackson GH, Irving JA, Pratt G, Fegan C, Fenton JA, Neben K, Hoffmann P, Eisele L, Ross FM, Langer C, Allan JM, Jauch A, Morgan GJ, Hemminki K, Houlston RS, Goldschmidt H, F?rsti A, N?then MM, M?hleisen TW, Straka C, Einsele H, D?rner E. Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. Nat Genet. 2013 Oct; 45(10):1221-1225. PMID: 23955597; PMCID: PMC5053356.
      Citations: 83     Fields:    Translation:HumansCells
    204. Lemke JR, Lal D, Reinthaler EM, Steiner I, Nothnagel M, Alber M, Geider K, Laube B, Schwake M, Finsterwalder K, Franke A, Schilhabel M, Muhle H, Boor R, Van Paesschen W, Caraballo R, Fejerman N, Weckhuysen S, De Jonghe P, Larsen J, Hjalgrim H, Addis L, Tang S, Hughes E, Pal DK, Veri K, Vaher U, Talvik T, Dimova P, Linnankivi T, Lehesjoki AE, Ruf S, Wolff M, Buerki S, Wohlrab G, Kroell J, Datta AN, Fiedler B, Kurlemann G, Kluger G, Hahn A, Haberlandt DE, Kutzer C, Becker F, Weber YG, Feucht M, Neophythou B, Ronen GM, Gruber-Sedlmayr U, Geldner J, Harvey RJ, Hoffmann P, Herms S, Toliat MR, Thiele H, Wilhelm C, Stephani U, Helbig I, Lerche H, Zimprich F, Neubauer BA, Biskup S, von Spiczak S, J?hn JA, M?ller RS, Guerrero L?pez R, Serratosa JM, Sperner J, Steinb?ck H, Altm?ller J, N?rnberg P. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Nat Genet. 2013 Sep; 45(9):1067-72. PMID: 23933819.
      Citations: 162     Fields:    Translation:HumansCells
    205. Chen B, Gemignani F, Elisei R, Romei C, Figlioli G, Cipollini M, Cristaudo A, Bambi F, Hoffmann P, Herms S, Kalemba M, Kula D, Harris S, Broderick P, Houlston R, Pastor S, Marcos R, Jarzab B, Hemminki K, Landi S, K?hler A, Vel?zquez A, F?rsti A. Genome-wide association study on differentiated thyroid cancer. J Clin Endocrinol Metab. 2013 Oct; 98(10):E1674-81. PMID: 23894154.
      Citations: 56     Fields:    Translation:Humans
    206. Priebe L, Degenhardt F, Strohmaier J, Herms S, Witt SH, Hoffmann P, Kulbida R, Mattheisen M, Moebus S, Meyer-Lindenberg A, Walter H, Nenadic I, Sauer H, Rujescu D, Maier W, Rietschel M, Cichon S, Breuer R, M?ssner R, N?then MM. Copy number variants in German patients with schizophrenia. PLoS One. 2013; 8(7):e64035. PMID: 23843933; PMCID: PMC3699619.
      Citations: 15     Fields:    Translation:Humans
    207. Ellinghaus D, Esparza-Gordillo J, Matanovic A, Marenholz I, Schaarschmidt H, Novak N, Michel S, Maintz L, Werfel T, Meyer-Hoffert U, Hotze M, Prokisch H, Heim K, Herder C, Hirota T, Tamari M, Kubo M, Takahashi A, Nakamura Y, Tsoi LC, Stuart P, Elder JT, Sun L, Zuo X, Yang S, Zhang X, Hoffmann P, Winkelmann J, Illig T, Boehm BO, Duerr RH, Brand S, McAleer MA, Fahy CM, Kabesch M, Brown S, McLean WH, Irvine AD, Schreiber S, Lee YA, Franke A, Weidinger S, Baurecht H, Rodr?guez E, H?bner N, N?then MM, F?lster-Holst R, B?ning C, Glas J. High-density genotyping study identifies four new susceptibility loci for atopic dermatitis. Nat Genet. 2013 Jul; 45(7):808-12. PMID: 23727859; PMCID: PMC3797441.
      Citations: 63     Fields:    Translation:Humans
    208. Pernhorst K, Herms S, Hoffmann P, Cichon S, Schulz H, Sander T, Schoch S, Becker AJ, Grote A. TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue. Seizure. 2013 Oct; 22(8):675-8. PMID: 23706953.
      Citations: 37     Fields:    Translation:HumansCells
    209. Agha-Hosseini F, Jatzwauk M, von Kannen S, Noack B, Eckelt U, Hoffmann P, Shabestari SB, Mehdipour P, Schackert HK, G?rgens H. Complete homozygous deletion of CTSC in an Iranian family with Papillon-Lef?vre syndrome. Int J Dermatol. 2014 Jul; 53(7):885-7. PMID: 23556547.
      Citations: 3     Fields:    Translation:HumansCells
    210. Volckmar AL, Cichon S, Hoffmann P, Schreiber S, Wichmann HE, Faraone SV, Neale BM, Herpertz-Dahlmann B, Lehmkuhl G, Sinzig J, Renner TJ, Romanos M, Warnke A, Lesch KP, Reif A, Schimmelmann BG, Hebebrand J, Hinney A, Psychiatric GWAS Consortium: ADHD Subgroup, Albayrak ?, P?tter C, N?then MM, J?ckel KH, Scherag A. Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet. 2013 Jun; 162B(4):295-305. PMID: 23533005.
      Citations: 44     Fields:    Translation:Humans
    211. Weinhold N, Johnson DC, Chubb D, Chen B, Hosking FJ, Broderick P, Ma YP, Dobbins SE, Hose D, Walker BA, Davies FE, Kaiser MF, Li NL, Gregory WA, Jackson GH, Witzens-Harig M, Neben K, Hoffmann P, Eisele L, Ross FM, Jauch A, Goldschmidt H, Houlston RS, Morgan GJ, Hemminki K, F?rsti A, N?then MM, M?hleisen TW. The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. Nat Genet. 2013 May; 45(5):522-525. PMID: 23502783; PMCID: PMC5056630.
      Citations: 57     Fields:    Translation:HumansCells
    212. Easton AC, Lucchesi W, Lourdusamy A, Lenz B, Solati J, Golub Y, Lewczuk P, Fernandes C, Desrivieres S, Dawirs RR, Moll GH, Kornhuber J, Frank J, Hoffmann P, Soyka M, Kiefer F, GESGA Consortium, Schumann G, Peter Giese K, Treutlein J, Cichon S, Ridinger M, Mattheisen P, Herms S, Wodarz N, Zill P, Maier W, Gaebel W, Dahmen N, Scherbaum N, Steffens M, Lucae S, Ising M, Mann K, Rietschel M, M?ller CP, M?ssner R, Schm?l C, M?ller-Myhsok B, N?then MM. aCaMKII autophosphorylation controls the establishment of alcohol drinking behavior. Neuropsychopharmacology. 2013 Aug; 38(9):1636-47. PMID: 23459588; PMCID: PMC3717547.
      Citations: 33     Fields:    Translation:HumansAnimalsCells
    213. Pechlivanis S, Schadendorf D, Erbel R, Hoffmann P, Moebus S, Heinz Nixdorf Recall Study Investigative Group, M?hleisen TW, M?hlenkamp S, J?ckel KH, N?then MM, Scherag A. Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study. BMC Med Genet. 2013 Feb 08; 14:23. PMID: 23394302; PMCID: PMC3583714.
      Citations: 19     Fields:    Translation:HumansCells
    214. Degenhardt F, Priebe L, Strohmaier J, Herms S, Hoffmann P, Mattheisen M, Nenadic I, Sauer H, Rujescu D, Maier W, Schulze TG, Rietschel M, Cichon S, M?ssner R, N?then MM. No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder. Psychiatr Genet. 2013 Feb; 23(1):45-6. PMID: 23250005.
      Citations: 5     Fields:    Translation:Humans
    215. Nowak M, Haupt M, Papapanou PN, Kebschull J, Hoffmann P, Schmidt-Wolf IG, Brossart P, Perner S, Kebschull M, Kr?mer B, Jepsen S. Activation of invariant NK T cells in periodontitis lesions. J Immunol. 2013 Mar 01; 190(5):2282-91. PMID: 23365081; PMCID: PMC3620697.
      Citations: 15     Fields:    Translation:HumansAnimalsCells
    216. Draaken M, Mughal SS, Pennimpede T, Wolter S, Wittler L, Ebert AK, Stein R, Bartels E, Schmidt D, Boemers TM, Schmiedeke E, Hoffmann P, Moebus S, Herrmann BG, Reutter H, Ludwig M, R?sch W, N?then MM. Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12. Birth Defects Res A Clin Mol Teratol. 2013 Mar; 97(3):133-9. PMID: 23359465.
      Citations: 11     Fields:    Translation:HumansAnimalsCells
    217. Pernhorst K, van Loo KM, von Lehe M, Priebe L, Cichon S, Herms S, Hoffmann P, Helmstaedter C, Sander T, Schoch S, Becker AJ. Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue. Brain Res. 2013 Mar 07; 1499:136-44. PMID: 23333373.
      Citations: 8     Fields:    Translation:HumansCells
    218. Frampton M, da Silva Filho MI, Broderick P, Thomsen H, Vijayakrishnan J, Cooke R, Enciso-Mora V, Hoffmann P, Lloyd A, Holroyd A, Eisele L, Ponader S, von Strandmann EP, Lightfoot T, Roman E, Lake A, Montgomery D, Jarrett RF, Swerdlow AJ, Engert A, Hemminki K, Houlston RS, F?rsti A, N?then MM, J?ckel KH. Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. Nat Commun. 2013; 4:2549. PMID: 24149102; PMCID: PMC5053363.
      Citations: 30     Fields:    Translation:HumansCells
    219. Tsoi LC, Spain SL, Knight J, Ellinghaus E, Stuart PE, Capon F, Ding J, Li Y, Tejasvi T, Gudjonsson JE, Kang HM, Allen MH, McManus R, Novelli G, Samuelsson L, Schalkwijk J, Burden AD, Smith CH, Cork MJ, Estivill X, Bowcock AM, Krueger GG, Weger W, Worthington J, Tazi-Ahnini R, Nestle FO, Hayday A, Hoffmann P, Winkelmann J, Wijmenga C, Langford C, Edkins S, Andrews R, Blackburn H, Strange A, Band G, Pearson RD, Vukcevic D, Spencer CC, Deloukas P, Mrowietz U, Schreiber S, Weidinger S, Koks S, Esko T, Metspalu A, Lim HW, Voorhees JJ, Weichenthal M, Wichmann HE, Chandran V, Rosen CF, Rahman P, Gladman DD, Griffiths CE, Reis A, Kere J, Collaborative Association Study of Psoriasis (CASP), Genetic Analysis of Psoriasis Consortium, Psoriasis Association Genetics Extension, Wellcome Trust Case Control Consortium 2, Nair RP, Franke A, Barker JN, Abecasis GR, Elder JT, Trembath RC, St?hle M, Kingo K. Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nat Genet. 2012 Dec; 44(12):1341-8. PMID: 23143594; PMCID: PMC3510312.
      Citations: 460     Fields:    Translation:HumansCells
    220. Quasdorff M, Vogt A, Tamke A, Yildiz Y, Hoffmann P, Lehmann T, Bartenschlager R, Engels JW, Kullak-Ublick GA, Sauerbruch T, Caselmann WH, Gonz?lez-Carmona MA. Inhibition of hepatitis C virus RNA translation by antisense bile acid conjugated phosphorothioate modified oligodeoxynucleotides (ODN). Antiviral Res. 2013 Jan; 97(1):49-59. PMID: 23142319.
      Citations: 3     Fields:    Translation:HumansCells
    221. Nasser E, Mangold E, Tradowsky DC, Fier H, Becker J, Boehmer AC, Herberz R, Fricker N, Barth S, Wahle P, Nowak S, Reutter H, Reich RH, Lauster C, Braumann B, Kreusch T, Hemprich A, Hoffmann P, Kramer FJ, Knapp M, Lange C, Ludwig KU, P?tzsch B, N?then MM. Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate. Birth Defects Res A Clin Mol Teratol. 2012 Nov; 94(11):925-33. PMID: 23081944.
      Citations: 6     Fields:    Translation:HumansCells
    222. Schulz AC, Mora NW, Pineda-Alvarez DE, Wijers CHW, Marcelis CM, Ritgen J, Schmiedeke E, Mattheisen M, Draaken M, Hoffmann P, Hilger AC, Dworschak GC, Baudisch F, Ludwig M, Bagci S, Gembruch U, Geipel A, Berg C, Bartmann P, van Rooij IALM, Solomon BD, Reutter HM, Bartels E, Stressig R, M?ller A, N?then MM. VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis. Clin Dysmorphol. 2012 Oct; 21(4):191-195. PMID: 22895008; PMCID: PMC4126840.
      Citations: 6     Fields:    Translation:Humans
    223. Mattheisen M, Strohmaier J, Treutlein J, Nenadic I, Alblas M, Meier S, Degenhardt F, Herms S, Hoffmann P, Witt SH, Giegling I, Sauer H, Schulze TG, Rujescu D, Rietschel M, Cichon S, M?hleisen TW, N?then MM. Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia. Schizophr Res. 2012 Nov; 141(2-3):262-5. PMID: 23017826.
      Citations: 8     Fields:    Translation:Humans
    224. Ludwig KU, Mangold E, Herms S, Nowak S, Reutter H, Paul A, Becker J, Herberz R, AlChawa T, Nasser E, Mattheisen M, Alblas MA, Barth S, Kluck N, Lauster C, Braumann B, Reich RH, Hemprich A, Blaumeiser B, Daratsianos N, Kreusch T, Murray JC, Marazita ML, Ruczinski I, Scott AF, Beaty TH, Kramer FJ, Wienker TF, Steegers-Theunissen RP, Rubini M, Mossey PA, Hoffmann P, Lange C, Cichon S, Propping P, Knapp M, B?hmer AC, P?tzsch S, N?then MM. Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nat Genet. 2012 Sep; 44(9):968-71. PMID: 22863734; PMCID: PMC3598617.
      Citations: 161     Fields:    Translation:Humans
    225. Spier I, Horpaopan S, Vogt S, Uhlhaas S, Morak M, Stienen D, Draaken M, Ludwig M, Holinski-Feder E, Hoffmann P, Aretz S, N?then MM. Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis. Hum Mutat. 2012 Jul; 33(7):1045-50. PMID: 22431159.
      Citations: 33     Fields:    Translation:Humans
    226. Mattheisen M, Strohmaier J, Degenhardt F, Priebe L, Schultz CC, Meier S, Hoffmann P, GROUP Investigators, Rivandeneira F, Hofman A, Moebus S, Gieger C, Emeny R, Ladwig KH, Wichmann HE, Schwarz M, Kammerer-Ciernioch J, Nenadic I, Sauer H, Maier W, Rujescu D, Lange C, Ophoff RA, Schulze TG, Rietschel M, Cichon S, M?hleisen TW, Breuer R, Uitterlinden AG, Schl?sser RG, M?ssner R, N?then MM. Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder. Schizophr Res. 2012 Jun; 138(1):69-73. PMID: 22497794.
      Citations: 42     Fields:    Translation:Humans
    227. Thier M, Lakes YB, Gorris R, Herms S, Opitz T, Seiferling D, Quandel T, Hoffmann P, Edenhofer F, W?rsd?rfer P, N?then MM, Br?stle O. Direct conversion of fibroblasts into stably expandable neural stem cells. Cell Stem Cell. 2012 Apr 06; 10(4):473-9. PMID: 22445518.
      Citations: 267     Fields:    Translation:AnimalsCells
    228. Anthoni H, Sucheston LE, Lewis BA, Fan X, Zucchelli M, Taipale M, Stein CM, Hokkanen ME, Pennington BF, Smith SD, Olson RK, Tomblin JB, Schumacher J, Hoffmann P, Gilger JW, Hynd GW, Nopola-Hemmi J, Leppanen PH, Lyytinen H, Schoumans J, Spencer J, Stanic D, Boon WC, Simpson E, Peyrard-Janvid M, Iyengar S, Kere J, Tapia-P?ez I, Castr?n E, Schulte-K?rne G, N?then M, M?ller-Myhsok B, Nordenskj?ld M, M?kel? S, Gustafsson J?. The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language. Behav Genet. 2012 Jul; 42(4):509-27. PMID: 22426781; PMCID: PMC3375077.
      Citations: 32     Fields:    Translation:HumansAnimalsCells
    229. Hilger A, Schramm C, Draaken M, Mughal SS, Dworschak G, Bartels E, Hoffmann P, Reutter H, Ludwig M, N?then MM. Familial occurrence of the VATER/VACTERL association. Pediatr Surg Int. 2012 Jul; 28(7):725-9. PMID: 22422375.
      Citations: 22     Fields:    Translation:Humans
    230. Degenhardt F, Priebe L, Herms S, Mattheisen M, Meier S, Moebus S, Strohmaier J, Lange C, Hoffmann P, Meyer-Lindenberg A, Heinz A, Walter H, Lucae S, Wolf C, Holsboer F, Maier W, Rietschel M, Cichon S, M?hleisen TW, Gro? M, Breuer R, M?ller-Myhsok B, N?then MM. Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample. Am J Med Genet B Neuropsychiatr Genet. 2012 Apr; 159B(3):263-73. PMID: 22344817.
      Citations: 20     Fields:    Translation:HumansCells
    231. Pernhorst K, Raabe A, Niehusmann P, van Loo KM, Grote A, Hoffmann P, Cichon S, Sander T, Schoch S, Becker AJ. Promoter variants determine ?-aminobutyric acid homeostasis-related gene transcription in human epileptic hippocampi. J Neuropathol Exp Neurol. 2011 Dec; 70(12):1080-8. PMID: 22082659.
      Citations: 7     Fields:    Translation:HumansCells
    232. Broderick P, Chubb D, Johnson DC, Weinhold N, Lloyd A, Olver B, Ma Y, Dobbins SE, Walker BA, Davies FE, Gregory WA, Childs JA, Ross FM, Jackson GH, Neben K, Jauch A, Hoffmann P, Moebus S, Tomlinson IP, Goldschmidt H, Hemminki K, Morgan GJ, Houlston RS, F?rsti A, M?hleisen TW, N?then MM. Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. Nat Genet. 2011 Nov 27; 44(1):58-61. PMID: 22120009; PMCID: PMC5108406.
      Citations: 75     Fields:    Translation:HumansCells
    233. Koch P, Breuer P, Peitz M, Jungverdorben J, Kesavan J, Poppe D, Doerr J, Ladewig J, Mertens J, Hoffmann P, Klockgether T, Evert BO, T?ting T, W?llner U, Br?stle O. Excitation-induced ataxin-3 aggregation in neurons from patients with Machado-Joseph disease. Nature. 2011 Nov 23; 480(7378):543-6. PMID: 22113611.
      Citations: 158     Fields:    Translation:HumansCells
    234. Hinney A, Jarick I, Pechlivanis S, Dauvermann MR, Beck S, Weber H, Scherag S, Nguyen TT, Volckmar AL, Knoll N, Faraone SV, Neale BM, Franke B, Cichon S, Hoffmann P, Schreiber S, Wichmann HE, Freitag C, Lempp T, Meyer J, Gilsbach S, Herpertz-Dahlmann B, Sinzig J, Lehmkuhl G, Renner TJ, Warnke A, Romanos M, Lesch KP, Reif A, Schimmelmann BG, Hebebrand J, Psychiatric GWAS Consortium: ADHD subgroup, Scherag A, Albayrak ?, P?tter C, N?then MM, J?ckel KH. Genome-wide association study in German patients with attention deficit/hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet. 2011 Dec; 156B(8):888-97. PMID: 22012869.
      Citations: 46     Fields:    Translation:Humans
    235. Frank J, Cichon S, Treutlein J, Ridinger M, Mattheisen M, Hoffmann P, Herms S, Wodarz N, Soyka M, Zill P, Maier W, Gaebel W, Dahmen N, Scherbaum N, Steffens M, Lucae S, Ising M, Mann K, Kiefer F, Rietschel M, M?ssner R, Schm?l C, M?ller-Myhsok B, N?then MM. Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster. Addict Biol. 2012 Jan; 17(1):171-80. PMID: 22004471; PMCID: PMC3245349.
      Citations: 85     Fields:    Translation:Humans
    236. Ligges C, Burkhardt J, Alexander M, Wolf C, Quente E, Ahnert P, Hoffmann P, Becker A, Cichon S, Boltze J, Kirsten H, Wilcke A, M?ller-Myhsok B. Imaging genetics of FOXP2 in dyslexia. Eur J Hum Genet. 2012 Feb; 20(2):224-9. PMID: 21897444; PMCID: PMC3260915.
      Citations: 27     Fields:    Translation:Humans
    237. Dobbins SE, Broderick P, Melin B, Feychting M, Johansen C, Andersson U, Schramm J, Olver B, Lloyd A, Ma YP, Hosking FJ, Ahlbom A, Henriksson R, Schoemaker MJ, Hepworth SJ, Hoffmann P, Moebus S, Eisele L, Kosteljanetz M, Muir K, Swerdlow A, Simon M, Houlston RS, Br?nnstr?m T, L?nn S, M?hleisen TW, N?then MM. Common variation at 10p12.31 near MLLT10 influences meningioma risk. Nat Genet. 2011 Jul 31; 43(9):825-7. PMID: 21804547; PMCID: PMC5053355.
      Citations: 31     Fields:    Translation:HumansCells
    238. Shi H, Bevier M, Johansson R, Grzybowska E, Chen B, Hamann U, Manjer J, Enquist K, Henriksson R, Carlson J, Brandt A, Butkiewicz D, Pamula-Pilat J, Tecza K, Herms S, Hoffmann P, Hemminki K, Lenner P, Eyfj?rd JE, Lascorz J, F?rsti A. Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome. Breast Cancer Res Treat. 2011 Dec; 130(3):905-16. PMID: 21630024.
      Citations: 21     Fields:    Translation:HumansCells
    239. Schramm C, Draaken M, Bartels E, Boemers TM, Schmiedeke E, Grasshoff-Derr S, Hosie S, Holland-Cunz S, Baudisch F, Priebe L, Hoffmann P, Zink AM, Engels H, Brockschmidt FF, Aretz S, Ludwig M, Reutter H, M?rzheuser S, N?then MM. De novo duplication of 18p11.21-18q12.1 in a female with anorectal malformation. Am J Med Genet A. 2011 Feb; 155A(2):445-9. PMID: 21271671.
      Citations: 7     Fields:    Translation:HumansCells
    240. Vogt A, Heinicke T, Quasdorff M, Hoffmann P, Yildiz Y, Schneider C, Serwe M, Bartenschlager R, Sauerbruch T, Caselmann WH, Gonz?lez-Carmona MA. Inhibition of hepatitis C virus gene expression by adenoviral vectors encoding antisense RNA in vitro and in vivo. J Hepatol. 2011 Jul; 55(1):19-28. PMID: 21145870.
      Citations: 5     Fields:    Translation:AnimalsCells
    241. Czamara D, Bruder J, Becker J, Hoffmann P, Ludwig KU, Bartling J, M?ller-Myhsok B, Schulte-K?rne G. Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia. Behav Genet. 2011 Jan; 41(1):110-9. PMID: 21104116.
      Citations: 27     Fields:    Translation:HumansCells
    242. Schramm C, Draaken M, Tewes G, Bartels E, Schmiedeke E, Grasshoff-Derr S, Hosie S, Holland-Cunz S, Priebe L, Kreiss-Nachtsheim M, Hoffmann P, Aretz S, Reutter H, Ludwig M, M?rzheuser S, N?then MM. Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature. Eur J Pediatr. 2011 Jun; 170(6):741-6. PMID: 21042811.
      Citations: 8     Fields:    Translation:Humans
    243. Schumacher J, Hoffmann P, Ludwig KU, Grimm T, Neuhoff N, Preis M, Roeske D, Warnke A, Propping P, Remschmidt H, Ziegler A, K?nig IR, Kleensang A, N?then MM, M?ller-Myhsok B, Schulte-K?rne G. Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21. Am J Med Genet B Neuropsychiatr Genet. 2011 Jan; 156B(1):36-43. PMID: 21184582.
      Citations: 17     Fields:    Translation:HumansCells
    244. de Assis NA, Nowak S, Ludwig KU, Reutter H, Vollmer J, Heilmann S, Kluck N, Lauster C, Braumann B, Reich RH, Hemprich A, Knapp M, Wienker TF, Kramer FJ, Hoffmann P, Mangold E, N?then MM. SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patients. Int J Pediatr Otorhinolaryngol. 2011 Jan; 75(1):49-52. PMID: 21044801.
      Citations: 3     Fields:    Translation:Humans
    245. Reutter H, Mattheisen M, Draaken M, Bartels E, Hoffmann P, Payabvash S, Saar K, Kajbafzadeh AM, Ludwig M, R?schendorf F, H?bner N, N?then MM. Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family. Birth Defects Res A Clin Mol Teratol. 2010 Sep; 88(9):757-61. PMID: 20672349.
      Citations: 3     Fields:    Translation:HumansCells
    246. Rojas-Martinez A, Reutter H, Chacon-Camacho O, Leon-Cachon RB, Munoz-Jimenez SG, Nowak S, Becker J, Herberz R, Ludwig KU, Paredes-Zenteno M, Raeder S, Herms S, Ortiz-Lopez R, Knapp M, Hoffmann P, Mangold E, Arizpe-Cant? A, N?then MM. Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25. Birth Defects Res A Clin Mol Teratol. 2010 Jul; 88(7):535-7. PMID: 20564431.
      Citations: 18     Fields:    Translation:HumansCells
    247. Nikopensius T, Birnbaum S, Ludwig KU, Saag M, Herms S, Knapp M, Hoffmann P, Metspalu A, Mangold E, Jagom?gi T, N?then MM. Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients. Eur J Oral Sci. 2010 Jun; 118(3):317-9. PMID: 20572868.
      Citations: 9     Fields:    Translation:HumansCells
    248. Pagnamenta AT, Bacchelli E, de Jonge MV, Mirza G, Scerri TS, Minopoli F, Chiocchetti A, Ludwig KU, Hoffmann P, Paracchini S, Lowy E, Harold DH, Chapman JA, Klauck SM, Poustka F, Houben RH, Staal WG, Ophoff RA, O'Donovan MC, Williams J, Deloukas P, Ragoussis J, Bailey AJ, Maestrini E, Monaco AP, International Molecular Genetic Study Of Autism Consortium, N?then MM, Schulte-K?rne G. Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biol Psychiatry. 2010 Aug 15; 68(4):320-8. PMID: 20346443; PMCID: PMC2941017.
      Citations: 76     Fields:    Translation:HumansCells
    249. Ludwig KU, Roeske D, Herms S, Schumacher J, Neuhoff N, Bruder J, Remschmidt H, Hoffmann P, Warnke A, Plume E, Schulte-K?rne G, M?ller-Myhsok B, N?then MM. Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 05; 153B(2):503-511. PMID: 19591125.
      Citations: 18     Fields:    Translation:Humans
    250. Draaken M, Reutter H, Schramm C, Bartels E, Boemers TM, Ebert AK, Stein R, Moebus S, Stienen D, Hoffmann P, Ludwig M, R?sch W, Schr?der A, N?then MM. Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy. Eur J Med Genet. 2010 Mar-Apr; 53(2):55-60. PMID: 20060941.
      Citations: 18     Fields:    Translation:HumansCells
    251. Mangold E, Ludwig KU, Birnbaum S, Baluardo C, Ferrian M, Herms S, Reutter H, de Assis NA, Chawa TA, Mattheisen M, Steffens M, Barth S, Kluck N, Paul A, Becker J, Lauster C, Braumann B, Scheer M, Reich RH, Hemprich A, Blaumeiser B, Moebus S, Krawczak M, Schreiber S, Meitinger T, Wichmann HE, Steegers-Theunissen RP, Kramer FJ, Cichon S, Propping P, Wienker TF, Knapp M, Rubini M, Mossey PA, Hoffmann P, Schmidt G, P?tzsch S, N?then MM. Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. Nat Genet. 2010 Jan; 42(1):24-6. PMID: 20023658.
      Citations: 185     Fields:    Translation:Humans
    252. Birnbaum S, Ludwig KU, Reutter H, Herms S, de Assis NA, Diaz-Lacava A, Barth S, Lauster C, Scheer M, Saffar M, Martini M, Reich RH, Schiefke F, Hemprich A, Wienker TF, Hoffmann P, Knapp M, Kramer FJ, Mangold E, Schmidt G, P?tzsch S, P?tzsch B, N?then MM. IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate. Eur J Oral Sci. 2009 Dec; 117(6):766-9. PMID: 20121942.
      Citations: 18     Fields:    Translation:Humans
    253. Nikopensius T, Ambrozaityte L, Ludwig KU, Birnbaum S, Saag M, Matuleviciene A, Linkeviciene L, Herms S, Knapp M, Hoffmann P, Kucinskas V, Metspalu A, Mangold E, Jagom?gi T, N?then MM. Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients. Am J Med Genet A. 2009 Nov; 149A(11):2551-3. PMID: 19839039.
      Citations: 12     Fields:    Translation:HumansCells
    254. Reutter H, Birnbaum S, Mende M, de Assis NA, Hoffmann P, Lacava AD, Herms S, Braumann B, Scheer M, Lauster C, Schiefke F, Dunsche A, Martini M, Knapp M, Kramer FJ, Mangold E, Schmidt G, N?then MM. Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent. Int J Pediatr Otorhinolaryngol. 2009 Oct; 73(10):1334-8. PMID: 19586667.
      Citations: 2     Fields:    Translation:HumansAnimals
    255. Schumacher J, Laje G, Abou Jamra R, Becker T, Vasilescu C, Mattheisen M, Herms S, Hoffmann P, Hillmer AM, Georgi A, Herold C, Schulze TG, Propping P, Rietschel M, McMahon FJ, Cichon S, M?hleisen TW, N?then MM. The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations. Hum Mol Genet. 2009 Jul 15; 18(14):2719-27. PMID: 19414483; PMCID: PMC2701338.
      Citations: 29     Fields:    Translation:Humans
    256. Birnbaum S, Ludwig KU, Reutter H, Herms S, Steffens M, Rubini M, Baluardo C, Ferrian M, Almeida de Assis N, Alblas MA, Barth S, Freudenberg J, Lauster C, Scheer M, Braumann B, Reich RH, Schiefke F, Hemprich A, Steegers-Theunissen RP, Moebus S, Horsthemke B, Kramer FJ, Wienker TF, Mossey PA, Propping P, Cichon S, Hoffmann P, Knapp M, Mangold E, Schmidt G, Berg? SJ, P?tzsch S, P?tzsch B, N?then MM. Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. Nat Genet. 2009 Apr; 41(4):473-7. PMID: 19270707.
      Citations: 207     Fields:    Translation:HumansCells
    257. Ludwig KU, Schumacher J, Warnke A, Plume E, Anthoni H, Peyrard-Janvid M, Meng H, Ziegler A, Remschmidt H, Kere J, Gruen JR, Hoffmann P, Schulte-K?rne G, K?nig IR, M?ller-Myhsok B, N?then MM. Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample. Psychiatr Genet. 2008 Dec; 18(6):310-2. PMID: 19018237; PMCID: PMC9748830.
      Citations: 32     Fields:    Translation:HumansCells
    258. Rujescu D, Ingason A, Cichon S, Barnes MR, Toulopoulou T, Picchioni M, Vassos E, Ettinger U, Bramon E, Murray R, Ruggeri M, Tosato S, Bonetto C, Steinberg S, Sigurdsson E, Sigmundsson T, Petursson H, Gylfason A, Olason PI, Hardarsson G, Jonsdottir GA, Gustafsson O, Fossdal R, Giegling I, Hartmann AM, Hoffmann P, Crombie C, Fraser G, Walker N, Lonnqvist J, Suvisaari J, Tuulio-Henriksson A, Djurovic S, Melle I, Andreassen OA, Hansen T, Werge T, Kiemeney LA, Franke B, Veltman J, Buizer-Voskamp JE, GROUP Investigators, Sabatti C, Ophoff RA, Rietschel M, Stefansson K, Peltonen L, St Clair D, Stefansson H, Collier DA, Pietil?inen OP, M?ller HJ, N?then MM. Disruption of the neurexin 1 gene is associated with schizophrenia. Hum Mol Genet. 2009 Mar 01; 18(5):988-96. PMID: 18945720; PMCID: PMC2695245.
      Citations: 213     Fields:    Translation:Humans
    259. Ludwig KU, Roeske D, Schumacher J, Warnke A, Plume E, Ziegler A, Remschmidt H, Hoffmann P, Schulte-K?rne G, K?nig IR, M?ller-Myhsok B, N?then MM. Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample. J Neural Transm (Vienna). 2008 Nov; 115(11):1587-9. PMID: 18810304.
      Citations: 23     Fields:    Translation:HumansCells
    260. O'Donovan MC, Craddock N, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, Leung HT, Hartmann AM, Morris DW, Shi Y, Feng G, Hoffmann P, Propping P, Vasilescu C, Maier W, Rietschel M, Zammit S, Schumacher J, Quinn EM, Schulze TG, Williams NM, Giegling I, Iwata N, Ikeda M, Darvasi A, Shifman S, He L, Duan J, Sanders AR, Levinson DF, Gejman PV, Cichon S, Gill M, Corvin A, Rujescu D, Kirov G, Owen MJ, Buccola NG, Mowry BJ, Freedman R, Amin F, Black DW, Silverman JM, Byerley WF, Cloninger CR, Molecular Genetics of Schizophrenia Collaboration, M?ller HJ, N?then MM. Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat Genet. 2008 Sep; 40(9):1053-5. PMID: 18677311.
      Citations: 463     Fields:    Translation:Humans
    261. Schirmbeck F, Georgi A, Strohmaier J, Schmael C, Boesshenz KV, Herms S, Hoffmann P, Jamra RA, Schumacher J, Maier W, Propping P, Cichon S, Rietschel M, Schulze TG, M?hleisen TW, N?then MM. Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin. J Autism Dev Disord. 2008 Nov; 38(10):1977-81. PMID: 18473158.
      Citations:    Fields:    Translation:Humans
    262. Gustafsson L, Oreland S, Hoffmann P, Nylander I. The impact of postnatal environment on opioid peptides in young and adult male Wistar rats. Neuropeptides. 2008 Apr; 42(2):177-91. PMID: 18082882.
      Citations: 15     Fields:    Translation:Animals
    263. Anthoni H, Zucchelli M, Matsson H, Fransson I, Schumacher J, Massinen S, Warnke A, Griesemann H, Hoffmann P, Nopola-Hemmi J, Lyytinen H, Kere J, Peyrard-Janvid M, M?ller-Myhsok B, Onkamo P, Schulte-K?rne G, N?then MM. A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Hum Mol Genet. 2007 Mar 15; 16(6):667-77. PMID: 17309879.
      Citations: 55     Fields:    Translation:HumansAnimalsCells
    264. Schumacher J, Hoffmann P, Schm?l C, Schulte-K?rne G, N?then MM. Genetics of dyslexia: the evolving landscape. J Med Genet. 2007 May; 44(5):289-97. PMID: 17307837; PMCID: PMC2597981.
      Citations: 49     Fields:    Translation:HumansCells
    265. Hoffmann P, Schneider C, Sievers E, Schmidt-Wolf IG, Sauerbruch T, Caselmann WH, Gonz?lez-Carmona MA, M?rten A. Patient-derived dendritic cells transduced with an a-fetoprotein-encoding adenovirus and co-cultured with autologous cytokine-induced lymphocytes induce a specific and strong immune response against hepatocellular carcinoma cells. Liver Int. 2006 Apr; 26(3):369-79. PMID: 16584401.
      Citations: 10     Fields:    Translation:HumansCells
    266. Gonzalez-Carmona MA, Serwe M, Alt M, Sproat BS, Steigerwald R, Hoffmann P, Quasdorff M, Schildgen O, Caselmann WH, Sch?ssler S, Ludwig J. Hammerhead ribozymes with cleavage site specificity for NUH and NCH display significant anti-hepatitis C viral effect in vitro and in recombinant HepG2 and CCL13 cells. J Hepatol. 2006 Jun; 44(6):1017-25. PMID: 16469406.
      Citations: 5     Fields:    Translation:HumansCells
    267. Musch A, Rabe C, Paik MD, Berna MJ, Schmitz V, Hoffmann P, Nischalke HD, Sauerbruch T, Caselmann WH. Altered expression of TGF-beta receptors in hepatocellular carcinoma--effects of a constitutively active TGF-beta type I receptor mutant. Digestion. 2005; 71(2):78-91. PMID: 15775675.
      Citations: 10     Fields:    Translation:HumansCells

    Related

    Topics (821)

    Explore

    Co-Authors (12)

    Explore

    Similar People (60)

    Explore
    © 2022 Next Generation Sequencing Competence Network (NGS-CN) | Imprint | Privacy