Next Generation Sequencing Competence Network

Next Generation Sequencing Competence Network

e.g. CCGA
(min 2 characters)

Stefan Herms

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University of Bonn
Human Genetics
Venusberg-Campus Buld. 76, 53127 Bonn, Germany
Bonn 53127
+49 228 6885411
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    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.
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    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. 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
    2. 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:    
    3. 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:    
    4. 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
    5. 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
    6. 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:    
    7. 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
    8. 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
    9. 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
    10. Diebold M, Galli E, Kopf A, Sanderson NSR, Callegari I, Benkert P, Ingelfinger F, Herms S, Cichon S, Kappos L, Kuhle J, Becher B, Derfuss T, Gonzalo N??ez N, Claassen M. High-dimensional immune profiling identifies a biomarker to monitor dimethyl fumarate response in multiple sclerosis. Proc Natl Acad Sci U S A. 2022 08 02; 119(31):e2205042119. PMID: 35881799; PMCID: PMC9351505.
      Citations: 7     Fields:    Translation:HumansCells
    11. 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:    
    12. Stefani A, Bachmann CG, Herms S, Tilch E, Schormair B, Zhao C, H?gl B, Berger K, Trenkwalder C, Hornyak M, Fietze I, M?ller-Nurasyid M, Peters A, N?then MM, M?ller-Myhsok B, Oexle K, Winkelmann J. ExomeChip-based rare variant association study in restless legs syndrome. Sleep Med. 2022 06; 94:26-30. PMID: 35489115.
      Citations:    Fields:    Translation:Humans
    13. 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, Yu X, 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
    14. 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
    15. 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:    
    16. 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
    17. 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
    18. 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     
    19. Watson HJ, Thornton LM, Yilmaz Z, Baker JH, Coleman JRI, Adan RAH, Alfredsson L, Andreassen OA, Ask H, Berrettini WH, Boehnke M, Boehm I, Boni C, Buehren K, Bulant J, Burghardt R, Chang X, Cichon S, Cone RD, Courtet P, Crow S, Crowley JJ, Danner UN, de Zwaan M, Dedoussis G, DeSocio JE, Dick DM, Dikeos D, Dina C, Djurovic S, Dmitrzak-Weglarz M, Docampo-Martinez E, Duriez P, Egberts K, Ehrlich S, Eriksson JG, Escaram?s G, Esko T, Estivill X, Farmer A, Fern?ndez-Aranda F, Fichter MM, F?cker M, Foretova L, Forstner AJ, Frei O, Gallinger S, Giegling I, Giuranna J, Gonidakis F, Gorwood P, Gratac?s M, Guillaume S, Guo Y, Hakonarson H, Hauser J, Havdahl A, Hebebrand J, Helder SG, Herms S, Herpertz-Dahlmann B, Herzog W, Hinney A, H?bel C, Hudson JI, Imgart H, Jamain S, Janout V, Jim?nez-Murcia S, Jones IR, Juli? A, Kalsi G, Kaminsk? D, Kaprio J, Karhunen L, Kas MJH, Keel PK, Kennedy JL, Keski-Rahkonen A, Kiezebrink K, Klareskog L, Klump KL, Knudsen GPS, La Via MC, Le Hellard S, Leboyer M, Li D, Lilenfeld L, Lin B, Lissowska J, Luykx J, Magistretti P, Maj M, Marsal S, Marshall CR, Mattingsdal M, Meulenbelt I, Micali N, Mitchell KS, Monteleone AM, Monteleone P, Myers R, Navratilova M, Ntalla I, O'Toole JK, Ophoff RA, Padyukov L, Pantel J, Pape?ov? H, Pinto D, Raevuori A, Ramoz N, Reichborn-Kjennerud T, Ricca V, Ripatti S, Ripke S, Ritschel F, Roberts M, Rotondo A, Rujescu D, Rybakowski F, Scherag A, Scherer SW, Schmidt U, Scott LJ, Seitz J, Sil?n Y, ?lachtov? L, Slagboom PE, Slof-Op 't Landt MCT, Slopien A, Sorbi S, Swiatkowska B, Tortorella A, Tozzi F, Treasure J, Tsitsika A, Tyszkiewicz-Nwafor M, Tziouvas K, van Elburg AA, van Furth EF, Walton E, Widen E, Zerwas S, Zipfel S, Bergen AW, Boden JM, Brandt H, Crawford S, Halmi KA, Horwood LJ, Johnson C, Kaplan AS, Kaye WH, Mitchell JE, Olsen CM, Pearson JF, Pedersen NL, Strober M, Werge T, Whiteman DC, Woodside DB, Gordon S, Maguire S, Larsen JT, Parker R, Petersen LV, Jordan J, Kennedy M, Wade TD, Birgeg?rd A, Lichtenstein P, Land?n M, Martin NG, Mortensen PB, Breen G, Bulik CM. Common Genetic Variation and Age of Onset of Anorexia Nervosa. Biol Psychiatry Glob Open Sci. 2022 Oct; 2(4):368-378. PMID: 36324647; PMCID: PMC9616394.
      Citations: 5     
    20. Schierbaum LM, Schneider S, Herms S, Sivalingam S, Fabian J, Reutter H, Weber S, Merz WM, Miklaszewska M, Sikora P, Szmigielska A, Krzemien G, Zachwieja K, Szczepanska M, Taranta-Janusz K, Kroll P, Hilger AC, Tkaczyk M, Polok M, Zaniew M. Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO). Genes (Basel). 2021 09 20; 12(9). PMID: 34573432; PMCID: PMC8468665.
      Citations: 2     Fields:    Translation:Humans
    21. 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
    22. Herms S, Ziegler GC, Radtke F, Vitale MR, Preu?e A, Klopocki E, Lesch KP. Generation of multiple human iPSC lines from peripheral blood mononuclear cells of two SLC2A3 deletion and two SLC2A3 duplication carriers. Stem Cell Res. 2021 10; 56:102526. PMID: 34492570.
      Citations:    Fields:    Translation:HumansCells
    23. 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
    24. 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
    25. 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
    26. 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
    27. 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
    28. 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
    29. Mehrjardi NZ, Molcanyi M, Hatay FF, Timmer M, Shahbazi E, Ackermann JP, Herms S, Heilmann-Heimbach S, Wunderlich TF, Prochnow N, Haghikia A, Lampert A, Neugebauer EAM, Baharvand H, Hescheler J, ?aric T. Acquisition of chromosome 1q duplication in parental and genome-edited human-induced pluripotent stem cell-derived neural stem cells results in their higher proliferation rate in vitro and in vivo. Cell Prolif. 2020 Oct; 53(10):e12892. PMID: 32918782; PMCID: PMC7574866.
      Citations: 4     Fields:    Translation:HumansCells
    30. 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
    31. 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
    32. 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
    33. Grasby KL, Jahanshad N, Painter JN, Bralten J, Hibar DP, Lind PA, Pizzagalli F, Ching CRK, McMahon MAB, Shatokhina N, Zsembik LCP, Thomopoulos SI, Zhu AH, Strike LT, Agartz I, Alhusaini S, Almeida MAA, Amlien IK, Andersson M, Ard T, Armstrong NJ, Ashley-Koch A, Atkins JR, Bernard M, Brouwer RM, Buimer EEL, Cannon DM, Chakravarty M, Chen Q, Cheung JW, Couvy-Duchesne B, Dale AM, Dalvie S, de Zubicaray GI, de Zwarte SMC, den Braber A, Doan NT, Dohm K, Ehrlich S, Engelbrecht HR, Erk S, Fan CC, Fedko IO, Foley SF, Ford JM, Fukunaga M, Garrett ME, Ge T, Giddaluru S, Goldman AL, Green MJ, Groenewold NA, Grotegerd D, Gurholt TP, Gutman BA, Hansell NK, Harris MA, Harrison MB, Haswell CC, Hauser M, Herms S, Heslenfeld DJ, Ho NF, Hoehn D, Hoffmann P, Holleran L, Hoogman M, Hottenga JJ, Ikeda M, Janowitz D, Jansen IE, Jia T, Jockwitz C, Kanai R, Karama S, Kasperaviciute D, Kaufmann T, Kelly S, Kikuchi M, Klein M, Knapp M, Knodt AR, Lam M, Lancaster TM, Lee PH, Lett TA, Lewis LB, Lopes-Cendes I, Luciano M, Macciardi F, Marquand AF, Mathias SR, Melzer TR, Milaneschi Y, Mirza-Schreiber N, Moreira JCV, Najt P, Nakahara S, Nho K, Olde Loohuis LM, Orfanos DP, Pearson JF, Pitcher TL, Ragothaman A, Rashid FM, Reay WR, Redlich R, Repple J, Riedel BC, Risacher SL, Rocha CS, Mota NR, Salminen L, Saremi A, Saykin AJ, Schlag F, Schmaal L, Schofield PR, Secolin R, Shapland CY, Shen L, Shin J, Shumskaya E, Sprooten E, Tansey KE, Teumer A, Thalamuthu A, Turner JA, Uhlmann A, Vallerga CL, van der Meer D, van Donkelaar MMJ, van Eijk L, van Erp TGM, van Haren NEM, van Rooij D, Veldink JH, Verhoef E, Walton E, Wang M, Wang Y, Wardlaw JM, Wen W, Westlye LT, Whelan CD, Witt SH, Wittfeld K, Wolf C, Wolfers T, Wu JQ, Yasuda CL, Zaremba D, Zhang Z, Zwiers MP, Artiges E, Assareh AA, Ayesa-Arriola R, Belger A, Brandt CL, Brown GG, Cichon S, Curran JE, Davies GE, Degenhardt F, Dennis MF, Dietsche B, Djurovic S, Doherty CP, Espiritu R, Garijo D, Gil Y, Gowland PA, Green RC, Heindel W, Ho BC, Hoffmann WU, Holsboer F, Homuth G, Hosten N, Jack CR, Jang M, Jansen A, Kimbrel NA, Koops S, Krug A, Lim KO, Luykx JJ, Mathalon DH, Mather KA, Mattay VS, Matthews S, Mayoral Van Son J, McEwen SC, Melle I, Morris DW, Mueller BA, Nauck M, Nordvik JE, O'Leary DS, Opel N, Pike GB, Preda A, Quinlan EB, Rasser PE, Ratnakar V, Reppermund S, Steen VM, Tooney PA, Veltman DJ, Voyvodic JT, Whelan R, White T, Yamamori H, Adams HHH, Bis JC, Debette S, Decarli C, Fornage M, Gudnason V, Hofer E, Ikram MA, Launer L, Longstreth WT, Lopez OL, Mazoyer B, Mosley TH, Roshchupkin GV, Satizabal CL, Schmidt R, Seshadri S, Yang Q, CHARGE Consortium, EPIGEN Consortium, IMAGEN Consortium, SYS Consortium, Alvim MKM, Ames D, Anderson TJ, Andreassen OA, Arias-Vasquez A, Bastin ME, Baune BT, Beckham JC, Blangero J, Boomsma DI, Brodaty H, Brunner HG, Buckner RL, Buitelaar JK, Bustillo JR, Cahn W, Cairns MJ, Calhoun V, Carr VJ, Caseras X, Caspers S, Cavalleri GL, Cendes F, Corvin A, Crespo-Facorro B, Dalrymple-Alford JC, Dannlowski U, de Geus EJC, Deary IJ, Delanty N, Depondt C, Donohoe G, Espeseth T, Fisher SE, Flor H, Forstner AJ, Francks C, Franke B, Glahn DC, Gollub RL, Grabe HJ, Gruber O, Hariri AR, Hartman CA, Hashimoto R, Heinz A, Henskens FA, Hillegers MHJ, Hoekstra PJ, Holmes AJ, Hong LE, Hopkins WD, Hulshoff Pol HE, Jernigan TL, Kennedy MA, Kircher TTJ, Kochunov P, Kwok JBJ, Le Hellard S, Loughland CM, Martin NG, Martinot JL, McDonald C, McMahon KL, Meyer-Lindenberg A, Michie PT, Morey RA, Mowry B, Nyberg L, Oosterlaan J, Ophoff RA, Pantelis C, Paus T, Pausova Z, Penninx BWJH, Polderman TJC, Posthuma D, Rietschel M, Roffman JL, Rowland LM, Sachdev PS, Schall U, Schumann G, Scott RJ, Sim K, Sisodiya SM, Smoller JW, Sommer IE, St Pourcain B, Stein DJ, Toga AW, Trollor JN, Van der Wee NJA, van 't Ent D, Walter H, Weber B, Weinberger DR, Wright MJ, Zhou J, Stein JL, Thompson PM, Medland SE, Colodro-Conde L, Aln?s D, B?low R, B?rger C, de Araujo TK, Kr?mer B, M?hleisen TW, M?ller-Myhsok B, et al. The genetic architecture of the human cerebral cortex. Science. 2020 03 20; 367(6484). PMID: 32193296; PMCID: PMC7295264.
      Citations: 237     Fields:    Translation:Humans
    34. 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.
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    36. 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.
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    37. Grigoroiu-Serbanescu M, Giaroli G, Thygesen JH, Shenyan O, Bigdeli TB, Bass NJ, Diaconu CC, Neagu AI, Forstner AJ, Degenhardt F, Herms S, McQuillin A, N?then MM. Predictive power of the ADHD GWAS 2019 polygenic risk scores in independent samples of bipolar patients with childhood ADHD. J Affect Disord. 2020 03 15; 265:651-659. PMID: 31791676.
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    38. 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.
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    39. 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.
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    40. Watson HJ, Yilmaz Z, Thornton LM, Coleman JRI, Bryois J, Hinney A, Mattheisen M, Medland SE, Ripke S, Yao S, Anorexia Nervosa Genetics Initiative, Hanscombe KB, Purves KL, Eating Disorders Working Group of the Psychiatric Genomics Consortium, Adan RAH, Alfredsson L, Ando T, Andreassen OA, Baker JH, Berrettini WH, Boni C, Perica VB, 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, Mayora MG, 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, Kaprio J, Karhunen L, Karwautz A, Kas MJH, Kennedy JL, Keski-Rahkonen A, Kiezebrink K, Kim YR, Klareskog L, 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, Munn-Chernoff MA, 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 JE, Olsen CM, Pearson JF, Pedersen NL, Strober M, Werge T, Whiteman DC, Woodside DB, Stuber GD, Gordon S, Grove J, Henders AK, Kirk KM, Larsen JT, Parker R, Petersen L, Jordan J, Kennedy M, Montgomery GW, Wade TD, Lichtenstein P, Norring C, Martin NG, Mortensen PB, Sullivan PF, Breen G, Bulik CM, 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, F?cker M, Guillaume S, Jim?nez-Murcia S, Juli? A, Kaminsk? D, Rabionet R, Ritschel F, Scherag A, Walton E, Jur?us A, Birgeg?rd A, Land?n M. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nat Genet. 2019 08; 51(8):1207-1214. PMID: 31308545; PMCID: PMC6779477.
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    43. Heilbronner U, Schlattmann P, Bschor T, Steinacher B, Herms S, Lang UE, Bopp SK, M?hleisen TW, Richter C, Stamm TJ, Merkl A, K?hler S, Sterzer P, Hellweg R, Heinz A, Cichon S, Schulze TG, Adli M, Ricken R. Leptin gene polymorphisms are associated with weight gain during lithium augmentation in patients with major depression. Eur Neuropsychopharmacol. 2019 12; 29(2):211-221. PMID: 30554862.
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    44. 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
    45. Mattheisen M, Frank J, Krumm B, Treutlein J, Kassem L, Strohmaier J, Herms S, Degenhardt F, Cichon S, Karypis G, Kelsoe J, Greenwood T, Nievergelt C, Shilling P, Shekhtman T, Edenberg H, Craig D, Szelinger S, Nurnberger J, Gershon E, Alliey-Rodriguez N, Zandi P, Goes F, Schork N, Smith E, Koller D, Zhang P, Badner J, Berrettini W, Bloss C, Byerley W, Coryell W, Foroud T, Guo Y, Hipolito M, Keating B, Lawson W, Liu C, Mahon P, McInnis M, Murray S, Nwulia E, Potash J, Rice J, Scheftner W, McMahon FJ, Rietschel M, Schulze TG, Breuer R, M?hleisen TW, N?then MM, Z?llner S. Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics. Int J Bipolar Disord. 2018 Nov 11; 6(1):24. PMID: 30415424; PMCID: PMC6230336.
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    46. 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
    47. 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
    48. 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.
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    49. 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.
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    50. Spoerri I, Herms S, Eytan O, Sarig O, Heinimann K, Sprecher E, Itin PH, Burger B. Immune-regulatory genes as possible modifiers of familial pityriasis rubra pilaris - lessons from a family with PRP and psoriasis. J Eur Acad Dermatol Venereol. 2018 Oct; 32(10):e389-e392. PMID: 29704870.
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    51. 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
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      Citations: 685     Fields:    Translation:Humans
    53. 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.
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    54. 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
    55. 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
    56. Biscaldi M, Degenhardt F, Herms S, Cichon S, Koch I, Klauck SM, Chiocchetti AG, Yousaf A, Bour HS, Haslinger D, Waltes R, Duketis E, Jarczok T, Sachse M, Ackermann J, Freitag CM. Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities. J Neural Transm (Vienna). 2018 02; 125(2):259-271. PMID: 29147782.
      Citations: 5     Fields:    Translation:Humans
    57. 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
    58. 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.
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    59. 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.
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    60. 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
    61. Witt SH, Streit F, Jungkunz M, Frank J, Reinbold CS, Treutlein J, Degenhardt F, Forstner AJ, Heilmann-Heimbach S, Schwarze CE, Schendel D, Strohmaier J, Abdellaoui A, Air TM, Akil H, Alda M, Alliey-Rodriguez N, Andreassen OA, Babadjanova G, Bass NJ, Bauer M, Baune BT, Bergen S, Bethell A, Biernacka JM, Blackwood DHR, Boks MP, Boomsma DI, Borrmann-Hassenbach M, Brennan P, Byrne EM, Cervantes P, Clarke TK, Craddock N, Cruceanu C, Curtis D, Czerski PM, Dannlowski U, Davis T, de Geus EJC, Di Florio A, Edenberg HJ, Fischer SB, Forty L, Fraser C, Frye MA, Fullerton JM, Gershon ES, Giegling I, Gordon SD, Gordon-Smith K, Grabe HJ, Green EK, Greenwood TA, Grigoroiu-Serbanescu M, Hall LS, Hamshere M, Hauser J, Heilbronner U, Herms S, Hitturlingappa S, Hoffmann P, Holmans P, Hottenga JJ, Jones I, Jones LA, Kahn RS, Kammerer-Ciernioch J, Kirov G, Kittel-Schneider S, Kloiber S, Knott SV, Kogevinas M, Leber M, Li QS, Lissowska J, Lucae S, Martin NG, McElroy SL, McIntosh AM, McKay JD, McQuillin A, Medland SE, Middeldorp CM, Milaneschi Y, Mitchell PB, Montgomery GW, Morken G, Mors O, Myers RM, Nievergelt CM, Nurnberger JI, O'Donovan MC, Loohuis LMO, Ophoff R, Oruc L, Owen MJ, Paciga SA, Penninx BWJH, Perry A, Pfennig A, Potash JB, Preisig M, Reif A, Rouleau GA, Schofield PR, Schulze TG, Schwarz M, Scott L, Sinnamon GCB, Stahl EA, Strauss J, Turecki G, Van der Auwera S, Vedder H, Vincent JB, Willemsen G, Witt CC, Wray NR, Xi HS, Bipolar Disorders Working Group of the Psychiatric Genomics Consortium, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Tadic A, Dahmen N, Cichon S, Mobascher A, Rujescu D, Lieb K, Schmahl C, Bohus M, Rietschel M, Awasthi S, Dietl L, Adolfsson R, Bellivier F, B?rglum AD, Budde M, Buttensch?n HN, Djurovic S, Domenici E, Etain B, Gade K, Guzman-Parra J, Hautzinger M, Jamain S, Jur?us A, Land?n M, Leboyer M, Mayoral-Cleries F, M?hleisen TW, M?ller-Myhsok B, Rivas F, Schott BH, N?then MM, Ripke S, Roepke S. Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. Transl Psychiatry. 2017 06 20; 7(6):e1155. PMID: 28632202; PMCID: PMC5537640.
      Citations: 59     Fields:    Translation:Humans
    62. Kurzwelly D, Wagner H, Tao F, Peitz M, Rehbach K, Pyle A, Thiele H, Timmann D, Karaca I, Lennarz M, Baets J, Feely S, Kennerson M, Gonzalez MA, Roeske S, Jung J, Herms S, Heilmann-Heimbach S, Nicholson G, Mahanjah M, Sharkia R, Mathews KD, Shy ME, de Jonghe P, Chinnery PF, Horvath R, Schmitt I, Wolf M, Greschus S, Maier W, Zuchner S, Klockgether T, Ramirez A, Minnerop M, Soehn AS, Reichbauer J, Rattay TW, Giorgetti A, Altm?ller J, Hengel H, Synofzik M, Atasu B, Stendel C, Lindig T, Stirnberg R, Sturm M, Bauer P, Lohmann E, Carloni P, Br?stle O, Klopstock T, Kohlhase J, Amunts K, Sch?ls L, N?rnberg P, Sch?le R. Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia. Brain. 2017 06 01; 140(6):1561-1578. PMID: 28459997; PMCID: PMC6402316.
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      Citations: 53     Fields:    Translation:HumansCells
    64. Bigdeli TB, Ripke S, Peterson RE, Trzaskowski M, Bacanu SA, Abdellaoui A, Andlauer TF, Beekman AT, Blackwood DH, Boomsma DI, Breen G, Byrne EM, Cichon S, Clarke TK, Couvy-Duchesne B, Craddock N, de Geus EJ, Degenhardt F, Dunn EC, Edwards AC, Fanous AH, Forstner AJ, Frank J, Gill M, Gordon SD, Grabe HJ, Hamilton SP, Hardiman O, Hayward C, Heath AC, Henders AK, Herms S, Hickie IB, Hoffmann P, Homuth G, Hottenga JJ, Ising M, Jansen R, Kloiber S, Knowles JA, Lang M, Li QS, Lucae S, MacIntyre DJ, Madden PA, Martin NG, McGrath PJ, McGuffin P, McIntosh AM, Medland SE, Mehta D, Middeldorp CM, Milaneschi Y, Montgomery GW, Mors O, Nauck M, Nyholt DR, Owen MJ, Penninx BW, Pergadia ML, Perlis RH, Peyrot WJ, Porteous DJ, Potash JB, Rice JP, Rietschel M, Riley BP, Rivera M, Schoevers R, Schulze TG, Shi J, Shyn SI, Smit JH, Smoller JW, Streit F, Strohmaier J, Teumer A, Treutlein J, Van der Auwera S, van Grootheest G, van Hemert AM, Webb BT, Weissman MM, Willemsen G, Witt SH, Levinson DF, Lewis CM, Wray NR, Flint J, Sullivan PF, Kendler KS, Berger K, Buttensch?n HN, M?ller-Myhsok B, N?then MM, V?lzke H, Wellmann J. Genetic effects influencing risk for major depressive disorder in China and Europe. Transl Psychiatry. 2017 03 28; 7(3):e1074. PMID: 28350396; PMCID: PMC5404611.
      Citations: 34     Fields:    Translation:Humans
    65. Barnholtz-Sloan JS, Wrensch MR, Johansen C, Il'yasova D, Kinnersley B, Ostrom QT, Labreche K, Chen Y, Armstrong G, Liu Y, Eckel-Passow JE, Decker PA, Broderick P, Gousias K, Schramm J, Schoemaker MJ, Fleming SJ, Herms S, Heilmann S, Wichmann HE, Schreiber S, Swerdlow A, Simon M, Rajaraman P, Chanock S, Linet M, Wang Z, Yeager M, GliomaScan Consortium, Wiencke JK, Hansen H, McCoy L, Rice T, Kosel ML, Sicotte H, Amos CI, Bernstein JL, Davis F, Lachance D, Lau C, Merrell RT, Shildkraut J, Ali-Osman F, Sadetzki S, Scheurer M, Shete S, Lai RK, Claus EB, Olson SH, Jenkins RB, Houlston RS, Bondy ML, Melin BS, Labussi?re M, Idbaih A, Hoang-Xuan K, Di Stefano AL, Mokhtari K, Delattre JY, Galan P, N?then MM, Lathrop M, Sanson M, Andersson U. Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Nat Genet. 2017 May; 49(5):789-794. PMID: 28346443; PMCID: PMC5558246.
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    66. 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
    67. 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.
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    68. 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
    69. Tompkins VS, Sompallae R, Rosean TR, Walsh S, Acevedo M, Kovalchuk AL, Han SS, Jing X, Holman C, Rehg JE, Herms S, Sunderland JS, Morse HC, Janz S. Transgenic mouse model of IgM+ lymphoproliferative disease mimicking Waldenstr?m macroglobulinemia. Blood Cancer J. 2016 11 04; 6(11):e488. PMID: 27813533; PMCID: PMC5148059.
      Citations: 2     Fields:    Translation:HumansAnimals
    70. Johnson EC, Bjelland DW, Howrigan DP, Abdellaoui A, Breen G, Borglum A, Cichon S, Degenhardt F, Forstner AJ, Frank J, Genovese G, Heilmann-Heimbach S, Herms S, Hoffman P, Maier W, Mattheisen M, Morris D, Mowry B, Neale B, Nenadic I, O'Dushlaine C, Rietschel M, Ruderfer DM, Rujescu D, Schulze TG, Simonson MA, Stahl E, Strohmaier J, Witt SH, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Sullivan PF, Keller MC, M?ller-Mhysok B, N?then MM. No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. PLoS Genet. 2016 Oct; 12(10):e1006343. PMID: 27792727; PMCID: PMC5085024.
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    71. Zayats T, Jacobsen KK, Kleppe R, Kittel-Schneider S, Mota NR, Grevet EH, Klein M, Corominas J, Bralten J, Galesloot T, Vasquez AA, Herms S, Forstner AJ, Larsson H, Breen G, Asherson P, Cichon S, Gabrielsen MB, Holmen OL, Bau CH, Buitelaar J, Kiemeney L, Faraone SV, Franke B, Reif A, Haavik J, Johansson S, Jacob CP, Ribas?s M, Ramos-Quiroga JA, Richarte V, Casas M, Gross-Lesch S, Lesch KP, Cormand B. Exome chip analyses in adult attention deficit hyperactivity disorder. Transl Psychiatry. 2016 10 18; 6(10):e923. PMID: 27754487; PMCID: PMC5315553.
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    72. Gade K, Herms S, Strohmaier J, Lang M, Rietschel M, Schulze TG, Degenhardt F, Heilbronner U, N?then MM. Effect of copy number variant burden on Global Assessment of Functioning in schizophrenia. Psychiatr Genet. 2016 08; 26(4):184-5. PMID: 27096220.
      Citations:    Fields:    Translation:Humans
    73. 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
    74. 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
    75. Andlauer TF, Buck D, Antony G, Bayas A, Bechmann L, Berthele A, Chan A, Gasperi C, Gold R, Graetz C, Hecker M, Knop M, Linker RA, Loleit V, Luessi F, Nischwitz S, Salmen A, Stangel M, Stellmann JP, Then Bergh F, Tumani H, Weber F, Wildemann B, Zettl UK, Zipp F, Weber P, Bettecken T, Czamara D, Carrillo-Roa T, Binder EB, Franke A, Herms S, Homuth G, Ising M, Kacprowski T, Kloiber S, Laudes M, Lieb W, Lucae S, Moebus S, Petersmann A, Schminke U, Porcu E, Pitzalis M, Sidore C, Zara I, Hemmer B, Haas J, Infante-Duarte C, K?mpfel T, Limmroth V, Meuth SG, M?hlau M, Paul F, P?tz M, Ruck T, St?rner KH, Tackenberg B, Warnke C, Wiendl H, Ziemann U, Arloth J, Radivojkov-Blagojevic M, Scheinhardt MO, Dankowski T, Lichtner P, Berger K, Bertram L, Gieger C, J?ckel KH, Lill CM, Meitinger T, M?ller-Nurasyid M, N?then MM, Rawal R, Strauch K, V?lzke H, Waldenberger M, Wellmann J, Mulas A, Cucca F, Zoledziewska M, Ziegler A, M?ller-Myhsok B. Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. Sci Adv. 2016 06; 2(6):e1501678. PMID: 27386562; PMCID: PMC4928990.
      Citations: 72     Fields:    Translation:Humans
    76. 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
    77. 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
    78. Kuehnle E, Herms S, Kohls F, Kundu S, Hillemanns P, Staboulidou I. Correlation of fetal scalp blood sampling pH with neonatal outcome umbilical artery pH value. Arch Gynecol Obstet. 2016 10; 294(4):763-70. PMID: 26969647.
      Citations: 2     Fields:    Translation:Humans
    79. 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
    80. Fatima A, Ivanyuk D, Herms S, Heilmann-Heimbach S, O'Shea O, Chapman C, Farr M, Izsv?k Z, Hescheler J, ?aric T. Generation of human induced pluripotent stem cell line from a patient with a long QT syndrome type 2. Stem Cell Res. 2016 Mar; 16(2):304-7. PMID: 27345990.
      Citations: 3     Fields:    Translation:HumansCells
    81. 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
    82. Forstner AJ, Hofmann A, Maaser A, Sumer S, Khudayberdiev S, Leber M, Schulze TG, Strohmaier J, Degenhardt F, Treutlein J, Mattheisen M, Schumacher J, Breuer R, Meier S, Herms S, Hoffmann P, Lacour A, Witt SH, Reif A, Lucae S, Maier W, Schwarz M, Vedder H, Kammerer-Ciernioch J, Pfennig A, Bauer M, Moebus S, Priebe L, Sivalingam S, Verhaert A, Schulz H, 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, Propping P, Becker T, Rietschel M, Cichon S, Schratt G, M?hleisen TW, M?ller-Myhsok B, Hautzinger M, Laprise C, N?then MM. Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. Transl Psychiatry. 2015 Nov 10; 5:e678. PMID: 26556287; PMCID: PMC5068755.
      Citations: 34     Fields:    Translation:HumansAnimals
    83. Antony G, Bayas A, Bechmann L, Chan A, Franke A, Gold R, Graetz C, Hecker M, Herms S, Knop M, Lill CM, Linker RA, Moebus S, Nischwitz S, Salmen A, Stangel M, Stellmann JP, Then Bergh F, Tumani H, Weber F, Wildemann B, Zettl UK, Zipp F, German Competence Network for Multiple Sclerosis (KKNMS), Dankowski T, Buck D, Andlauer TF, Berthele A, Bettecken T, Haas J, Infante-Duarte C, J?ckel KH, Kieseier BC, Knier B, K?mpfel T, Lichtner P, Lieb W, Limmroth V, Loleit V, Meuth SG, M?ller-Myhsok B, N?then MM, Paul F, P?tz M, Ruck T, Strauch K, St?rner KH, Tackenberg B, Waldenberger M, Wiendl H, Ziemann U, Hemmer B, Ziegler A. Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array. Genet Epidemiol. 2015 Dec; 39(8):601-8. PMID: 26497834.
      Citations: 6     Fields:    Translation:Humans
    84. Kinnersley B, Holroyd A, Broderick P, Vijayakrishnan J, Schoemaker MJ, Fleming SJ, Herms S, Heilmann S, Swerdlow A, Bondy M, Houlston RS, Labussi?re M, Di Stefano AL, Mokhtari K, Delattre JY, Gousias K, Schramm J, Schreiber S, Wichmann HE, N?then MM, Lathrop M, Simon M, Sanson M. Genome-wide association study identifies multiple susceptibility loci for glioma. Nat Commun. 2015 Oct 01; 6:8559. PMID: 26424050; PMCID: PMC4600760.
      Citations: 67     Fields:    Translation:Humans
    85. 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
    86. Fischer A, Ellinghaus D, Nutsua M, Hofmann S, Montgomery CG, Iannuzzi MC, Rybicki BA, Petrek M, Mrazek F, Pabst S, Grunewald J, Ronninger M, Eklund A, Padyukov L, Mihailovic-Vucinic V, Jovanovic D, Sterclova M, Homolka J, Herms S, Gieger C, Strauch K, Winkelmann J, Boehm BO, Brand S, Ellinghaus E, Lieb W, Nebel A, Franke A, Schreiber S, GenPhenReSa Consortium, Groh? C, N?then MM, B?ning C, Sch?rmann M, Baurecht H, M?ller-Quernheim J. Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk. Am J Respir Crit Care Med. 2015 Sep 15; 192(6):727-36. PMID: 26051272; PMCID: PMC4595678.
      Citations: 49     Fields:    Translation:Humans
    87. Kinnersley B, Kamatani Y, Wang Y, Gousias K, Schramm J, Schoemaker MJ, Swerdlow A, Fleming SJ, Herms S, Heilmann S, Simon M, Lathrop M, Houlston RS, Labussi?re M, Galan P, Mokhtari K, Delattre JY, N?then MM, Sanson M. Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis. Eur J Hum Genet. 2016 May; 24(5):717-24. PMID: 26264438; PMCID: PMC4677454.
      Citations: 7     Fields:    Translation:Humans
    88. Aung T, Ozaki M, Mizoguchi T, Allingham RR, Li Z, Haripriya A, Nakano S, Uebe S, Harder JM, Chan AS, Lee MC, Burdon KP, Astakhov YS, Abu-Amero KK, Zenteno JC, Zarnowski T, Pakravan M, Safieh LA, Jia L, Wang YX, Williams S, Paoli D, Schlottmann PG, Huang L, Sim KS, Foo JN, Nakano M, Ikeda Y, Kumar RS, Ueno M, Manabe S, Hayashi K, Kazama S, Ideta R, Mori Y, Miyata K, Sugiyama K, Higashide T, Chihara E, Inoue K, Ishiko S, Yoshida A, Yanagi M, Kiuchi Y, Aihara M, Ohashi T, Sakurai T, Sugimoto T, Chuman H, Matsuda F, Yamashiro K, Gotoh N, Miyake M, Astakhov SY, Osman EA, Al-Obeidan SA, Owaidhah O, Al-Jasim L, Shahwan SA, Fogarty RA, Leo P, Yetkin Y, Kanavi MR, Beni AN, Yazdani S, Akopov EL, Toh KY, Howell GR, Orr AC, Goh Y, Meah WY, Peh SQ, Kosior-Jarecka E, Lukasik U, Krumbiegel M, Vithana EN, Wong TY, Liu Y, Koch AE, Challa P, Rautenbach RM, Mackey DA, Hewitt AW, Mitchell P, Wang JJ, Ziskind A, Carmichael T, Ramakrishnan R, Narendran K, Venkatesh R, Vijayan S, Zhao P, Chen X, Guadarrama-Vallejo D, Cheng CY, Perera SA, Husain R, Ho SL, Welge-Luessen UC, Mardin C, Schloetzer-Schrehardt U, Hillmer AM, Herms S, Moebus S, Weisschuh N, Shetty R, Ghosh A, Teo YY, Brown MA, Lischinsky I, Blue Mountains Eye Study GWAS Team, Wellcome Trust Case Control Consortium 2, Crowston JG, Coote M, Zhao B, Sang J, Zhang N, You Q, Vysochinskaya V, Founti P, Chatzikyriakidou A, Lambropoulos A, Anastasopoulos E, Coleman AL, Wilson MR, Rhee DJ, Kang JH, May-Bolchakova I, Heegaard S, Mori K, Alward WL, Jonas JB, Xu L, Liebmann JM, Chowbay B, Schaeffeler E, Schwab M, Lerner F, Wang N, Yang Z, Frezzotti P, Kinoshita S, Fingert JH, Inatani M, Tashiro K, Edward DP, Pasquale LR, Kubota T, Wiggs JL, Pasutto F, Topouzis F, Dubina M, Craig JE, Yoshimura N, Sundaresan P, John SW, Ritch R, Hauser MA, Khor CC, Nilg?n Y, Oguz ?, N?then MM, Reis A. Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Nat Genet. 2015 Jun; 47(6):689. PMID: 26018902.
      Citations: 1     Fields:    
    89. 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
    90. 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
    91. Ibrahim-Verbaas CA, Bressler J, Debette S, Schuur M, Smith AV, Bis JC, Davies G, Trompet S, Smith JA, Wolf C, Chibnik LB, Liu Y, Vitart V, Kirin M, Petrovic K, Polasek O, Zgaga L, Fawns-Ritchie C, Hoffmann P, Karjalainen J, Lahti J, Llewellyn DJ, Schmidt CO, Mather KA, Sun Q, Resnick SM, Rose LM, Oldmeadow C, Stewart M, Smith BH, Gudnason V, Yang Q, Mirza SS, Jukema JW, deJager PL, Harris TB, Liewald DC, Amin N, Coker LH, Lopez OL, Schmidt R, Teumer A, Ford I, Karbalai N, Becker JT, Jonsdottir MK, Au R, Fehrmann R, Herms S, Nalls M, Zhao W, Turner ST, Yaffe K, Lohman K, van Swieten JC, Kardia S, Knopman DS, Meeks WM, Heiss G, Holliday EG, Schofield PW, Tanaka T, Stott DJ, Wang J, Ridker P, Gow AJ, Pattie A, Starr JM, Hocking LJ, Armstrong NJ, McLachlan S, Shulman JM, Pilling LC, Eiriksdottir G, Scott RJ, Kochan NA, Palotie A, Hsieh YC, Penman A, Gottesman RF, Oostra BA, Yu L, DeStefano AL, Beiser A, Garcia M, Rotter JI, Hofman A, Slagboom PE, Westendorp R, Buckley BM, Wolf PA, Uitterlinden AG, Psaty BM, Grabe HJ, Bandinelli S, Chasman DI, Grodstein F, Porteous DJ, Generation Scotland, Price JF, Sachdev PS, Ferrucci L, Attia JR, Rudan I, Hayward C, Wright AF, Wilson JF, Cichon S, Franke L, Schmidt H, Ding J, de Craen A, Fornage M, Bennett DA, Deary IJ, Ikram MA, Launer LJ, Fitzpatrick AL, Seshadri S, van Duijn CM, Mosley TH, Chouraki V, Stegle O, Eriksson JG, N?then MM, R?ikk?nen K, Lambert JC. GWAS for executive function and processing speed suggests involvement of the CADM2 gene. Mol Psychiatry. 2016 Feb; 21(2):189-197. PMID: 25869804; PMCID: PMC4722802.
      Citations: 72     Fields:    Translation:Humans
    92. 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
    93. Aung T, Ozaki M, Mizoguchi T, Allingham RR, Li Z, Haripriya A, Nakano S, Harder JM, Chan AS, Lee MC, Burdon KP, Astakhov YS, Abu-Amero KK, Zarnowski T, Pakravan M, Safieh LA, Jia L, Wang YX, Williams S, Paoli D, Huang L, Sim KS, Foo JN, Nakano M, Ikeda Y, Kumar RS, Ueno M, Manabe S, Hayashi K, Kazama S, Ideta R, Mori Y, Miyata K, Sugiyama K, Higashide T, Chihara E, Inoue K, Ishiko S, Yoshida A, Yanagi M, Kiuchi Y, Aihara M, Ohashi T, Sakurai T, Sugimoto T, Chuman H, Matsuda F, Yamashiro K, Gotoh N, Miyake M, Astakhov SY, Osman EA, Al-Obeidan SA, Owaidhah O, Al-Jasim L, Al Shahwan S, Fogarty RA, Leo P, Yetkin Y, Kanavi MR, Beni AN, Yazdani S, Akopov EL, Toh KY, Howell GR, Orr AC, Goh Y, Meah WY, Peh SQ, Kosior-Jarecka E, Lukasik U, Vithana EN, Wong TY, Liu Y, Koch AE, Challa P, Rautenbach RM, Mackey DA, Hewitt AW, Mitchell P, Wang JJ, Ziskind A, Carmichael T, Ramakrishnan R, Narendran K, Venkatesh R, Vijayan S, Zhao P, Chen X, Cheng CY, Perera SA, Husain R, Ho SL, Hillmer AM, Herms S, Moebus S, Shetty R, Ghosh A, Teo YY, Brown MA, Blue Mountains Eye Study GWAS Team, Wellcome Trust Case Control Consortium 2, Crowston JG, Coote M, Zhao B, Sang J, Zhang N, You Q, Vysochinskaya V, Founti P, Chatzikyriakidou A, Lambropoulos A, Anastasopoulos E, Coleman AL, Wilson MR, Rhee DJ, Kang JH, May-Bolchakova I, Heegaard S, Mori K, Alward WL, Jonas JB, Xu L, Liebmann JM, Chowbay B, Schaeffeler E, Wang N, Yang Z, Frezzotti P, Kinoshita S, Fingert JH, Inatani M, Tashiro K, Edward DP, Pasquale LR, Kubota T, Wiggs JL, Topouzis F, Dubina M, Craig JE, Yoshimura N, Sundaresan P, John SW, Ritch R, Hauser MA, Khor CC, Uebe S, Zenteno JC, Nilg?n Y, Schlottmann PG, Oguz ?, Krumbiegel M, Guadarrama-Vallejo D, Welge-Luessen UC, Mardin C, Schloetzer-Schrehardt U, N?then MM, Weisschuh N, Lischinsky I, Schwab M, Lerner F, Reis A, Pasutto F. A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Nat Genet. 2015 Apr; 47(4):387-92. PMID: 25706626; PMCID: PMC4605818.
      Citations: 41     Fields:    Translation:HumansAnimalsCells
    94. 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
    95. 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
    96. Thomsen H, da Silva Filho MI, Fuchs M, Ponader S, von Strandmann EP, Eisele L, Herms S, Hofmann P, Sundquist J, Engert A, F?rsti A, Hemminki K. Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach. Eur J Hum Genet. 2015 Jun; 23(6):824-30. PMID: 25227146; PMCID: PMC4795060.
      Citations: 4     Fields:    Translation:HumansCells
    97. Christoforou A, Espeseth T, Davies G, Fernandes CP, Giddaluru S, Mattheisen M, Tenesa A, Harris SE, Liewald DC, Payton A, Ollier W, Horan M, Pendleton N, Haggarty P, Djurovic S, Herms S, Hoffman P, Cichon S, Starr JM, Lundervold A, Reinvang I, Steen VM, Deary IJ, Le Hellard S. GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. Genes Brain Behav. 2014 Sep; 13(7):663-74. PMID: 24975275; PMCID: PMC4261989.
      Citations: 11     Fields:    Translation:Humans
    98. 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
    99. 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
    100. 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
    101. Grigoroiu-Serbanescu M, Rietschel M, Hauser J, Czerski PM, Herms S, Sun X, Wickramaratne P, Elston RC. Commingling analysis of age-of-onset in bipolar I disorder and the morbid risk for major psychoses in first degree relatives of bipolar I probands. J Affect Disord. 2014 Oct; 168:197-204. PMID: 25063958.
      Citations: 9     Fields:    Translation:Humans
    102. 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
    103. 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
    104. 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
    105. Draaken M, Baudisch F, Timmermann B, Kuhl H, Kerick M, Proske J, Wittler L, Pennimpede T, Ebert AK, Stein R, Bartels E, von Lowtzow C, Boemers TM, Herms S, Gearhart JP, Lakshmanan Y, Kockum CC, Holmdahl G, Boyadjiev SA, Herrmann BG, Ludwig M, Reutter H, R?sch W, L?ckgren G, Nordenskj?ld A, N?then MM. Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region. Birth Defects Res A Clin Mol Teratol. 2014 Jun; 100(6):512-7. PMID: 24764164.
      Citations: 12     Fields:    Translation:HumansAnimalsCells
    106. Haenisch B, Herms S, Molderings GJ, Fr?hlich H. Evidence for contribution of epigenetic mechanisms in the pathogenesis of systemic mast cell activation disease. Immunogenetics. 2014 May; 66(5):287-97. PMID: 24622794.
      Citations: 6     Fields:    Translation:HumansCells
    107. 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
    108. Ludwig KU, Rubini M, Mossey PA, Herms S, Nowak S, Reutter H, Alblas MA, Lippke B, Barth S, Paredes-Zenteno M, Ortiz-Lopez R, Kreusch T, Hemprich A, Martini M, Braumann B, Molloy A, Peterlin B, Hoffmann P, Rojas-Martinez A, Knapp M, Steegers-Theunissen RP, Mangold E, B?hmer AC, Mu?oz-Jimenez SG, J?ger A, P?tzsch B, N?then MM. Strong association of variants around FOXE1 and orofacial clefting. J Dent Res. 2014 Apr; 93(4):376-81. PMID: 24563486.
      Citations: 25     Fields:    Translation:Humans
    109. Boraska V, Franklin CS, Floyd JA, Thornton LM, Huckins LM, Southam L, Rayner NW, Tachmazidou I, Klump KL, Treasure J, Lewis CM, Schmidt U, Tozzi F, Kiezebrink K, Gorwood P, Adan RA, Kas MJ, Favaro A, Santonastaso P, Rybakowski F, Dmitrzak-Weglarz M, Kaprio J, Keski-Rahkonen A, Raevuori A, Van Furth EF, Slof-Op 't Landt MC, Hudson JI, Reichborn-Kjennerud T, Knudsen GP, Monteleone P, Kaplan AS, Karwautz A, Hakonarson H, Berrettini WH, Guo Y, Li D, Schork NJ, Komaki G, Ando T, Inoko H, Esko T, Fischer K, Metspalu A, Baker JH, Cone RD, Dackor J, DeSocio JE, Hilliard CE, O'Toole JK, Pantel J, Szatkiewicz JP, Taico C, Zerwas S, Trace SE, Davis OS, Helder S, de Zwaan M, Ehrlich S, Herpertz-Dahlmann B, Herzog W, Imgart H, Boni C, Ramoz N, Versini A, Brandys MK, Danner UN, de Kovel C, Hendriks J, Koeleman BP, Ophoff RA, Strengman E, van Elburg AA, Bruson A, Clementi M, Degortes D, Forzan M, Tenconi E, Lissowska J, Rajewski A, Szeszenia-Dabrowska N, Slopien A, Hauser J, Karhunen L, Meulenbelt I, Slagboom PE, Tortorella A, Maj M, Dedoussis G, Dikeos D, Gonidakis F, Tziouvas K, Tsitsika A, Papezova H, Slachtova L, Martaskova D, Kennedy JL, Levitan RD, Yilmaz Z, Huemer J, Koubek D, Merl E, Wagner G, Lichtenstein P, Breen G, Cohen-Woods S, Farmer A, McGuffin P, Herms S, Schreiber S, Dina C, Sladek R, Gambaro G, Soranzo N, Julia A, Marsal S, Gaborieau V, Dick DM, Palotie A, Ripatti S, Andreassen OA, Espeseth T, Reinvang I, Steen VM, Le Hellard S, Mattingsdal M, Ntalla I, Bencko V, Foretova L, Janout V, Navratilova M, Gallinger S, Pinto D, Scherer SW, Aschauer H, Carlberg L, Schosser A, Alfredsson L, Ding B, Klareskog L, Padyukov L, Finan C, Kalsi G, Roberts M, Logan DW, Peltonen L, Ritchie GR, Barrett JC, Wellcome Trust Case Control Consortium 3, Sullivan PF, Collier DA, Zeggini E, Bulik CM, Hebebrand J, Fern?ndez-Aranda F, Gratacos M, M?nnik K, B?hren K, Burghardt R, Egberts K, Scherag A, Scherag S, Zipfel S, Docampo E, Escaram?s G, Jim?nez-Murcia S, Cichon S, Giegling I, Rujescu D, Wichmann HE, Rabionet R, Wid?n E, Lundervold A, Courtet P, Guillaume S, Jaussent I, Estivill X, Hinney A. A genome-wide association study of anorexia nervosa. Mol Psychiatry. 2014 Oct; 19(10):1085-94. PMID: 24514567; PMCID: PMC4325090.
      Citations: 119     Fields:    Translation:Humans
    110. 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
    111. 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
    112. Cross-Disorder Group of the Psychiatric Genomics Consortium, Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, Andreassen OA, Anjorin A, Anney R, Anttila V, Arking DE, Asherson P, Azevedo MH, Backlund L, Badner JA, Bailey AJ, Banaschewski T, Barchas JD, Barnes MR, Barrett TB, Bass N, Battaglia A, Bauer M, Bellivier F, Bergen SE, Berrettini W, Betancur C, Bettecken T, Biederman J, Binder EB, Black DW, Blackwood DH, Bloss CS, Boehnke M, Boomsma DI, Breen G, Bruggeman R, Cormican P, Buccola NG, Buitelaar JK, Bunney WE, Buxbaum JD, Byerley WF, Byrne EM, Caesar S, Cahn W, Cantor RM, Casas M, Chakravarti A, Chambert K, Choudhury K, Cichon S, Cloninger CR, Collier DA, Cook EH, Coon H, Cormand B, Corvin A, Coryell WH, Craig DW, Craig IW, Crosbie J, Cuccaro ML, Curtis D, Czamara D, Datta S, Dawson G, Day R, De Geus EJ, Degenhardt F, Djurovic S, Donohoe GJ, Doyle AE, Duan J, Dudbridge F, Duketis E, Ebstein RP, Edenberg HJ, Elia J, Ennis S, Etain B, Fanous A, Farmer AE, Ferrier IN, Flickinger M, Fombonne E, Foroud T, Frank J, Franke B, Fraser C, Freedman R, Freimer NB, Freitag CM, Friedl M, Gallagher L, Gejman PV, Georgieva L, Gershon ES, Geschwind DH, Giegling I, Gill M, Gordon SD, Gordon-Smith K, Green EK, Greenwood TA, Grice DE, Gross M, Grozeva D, Guan W, Gurling H, De Haan L, Haines JL, Hakonarson H, Hallmayer J, Hamilton SP, Hamshere ML, Hansen TF, Hartmann AM, Hautzinger M, Heath AC, Henders AK, Herms S, Hickie IB, Hipolito M, Hoefels S, Holmans PA, Holsboer F, Hoogendijk WJ, Hottenga JJ, Hultman CM, Hus V, Ising M, Jones EG, Jones I, Jones L, Tzeng JY, Kandaswamy R, Keller MC, Kennedy JL, Kenny E, Kent L, Kim Y, Kirov GK, Klauck SM, Klei L, Knowles JA, Kohli MA, Koller DL, Konte B, Korszun A, Krabbendam L, Krasucki R, Kuntsi J, Kwan P, Lathrop M, Lawrence J, Lawson WB, Leboyer M, Ledbetter DH, Lee PH, Lencz T, Lesch KP, Levinson DF, Lewis CM, Li J, Lichtenstein P, Lieberman JA, Lin DY, Linszen DH, Liu C, Lohoff FW, Loo SK, Lord C, Lowe JK, Lucae S, MacIntyre DJ, Madden PA, Maestrini E, Magnusson PK, Mahon PB, Maier W, Malhotra AK, Mane SM, Martin CL, Martin NG, Mattheisen M, Matthews K, Mattingsdal M, McCarroll SA, McGhee KA, McGough JJ, McGrath PJ, McGuffin P, McInnis MG, McIntosh A, McKinney R, McLean AW, McMahon FJ, McMahon WM, McQuillin A, Medeiros H, Medland SE, Meier S, Melle I, Meng F, Meyer J, Middeldorp CM, Middleton L, Milanova V, Miranda A, Monaco AP, Montgomery GW, Moran JL, Moreno-De-Luca D, Morken G, Morris DW, Morrow EM, Moskvina V, Muglia P, Muir WJ, Murtha M, Myers RM, Myin-Germeys I, Neale MC, Nelson SF, Nievergelt CM, Nikolov I, Nimgaonkar V, Nolen WA, Nurnberger JI, Nwulia EA, Nyholt DR, O'Dushlaine C, Oades RD, Olincy A, Oliveira G, Olsen L, Ophoff RA, Osby U, Owen MJ, Palotie A, Parr JR, Paterson AD, Pato CN, Pato MT, Penninx BW, Pergadia ML, Pericak-Vance MA, Pickard BS, Pimm J, Piven J, Posthuma D, Potash JB, Poustka F, Propping P, Puri V, Quested DJ, Quinn EM, Ramos-Quiroga JA, Rasmussen HB, Raychaudhuri S, Reif A, Rice JP, Rietschel M, Roeder K, Roeyers H, Rossin L, Rothenberger A, Rouleau G, Ruderfer D, Rujescu D, Sanders AR, Sanders SJ, Santangelo SL, Sergeant JA, Schachar R, Schalling M, Schatzberg AF, Scheftner WA, Schellenberg GD, Scherer SW, Schork NJ, Schulze TG, Schumacher J, Schwarz M, Scolnick E, Scott LJ, Shi J, Shilling PD, Shyn SI, Silverman JM, Slager SL, Smalley SL, Smit JH, Smith EN, Sonuga-Barke EJ, St Clair D, State M, Steffens M, Steinhausen HC, Strauss JS, Strohmaier J, Stroup TS, Sutcliffe JS, Szatmari P, Szelinger S, Thirumalai S, Thompson RC, Todorov AA, Tozzi F, Treutlein J, Uhr M, van den Oord EJ, Van Grootheest G, Van Os J, Vicente AM, Vieland VJ, Vincent JB, Visscher PM, Walsh CA, Wassink TH, Watson SJ, Weissman MM, Werge T, Wienker TF, Wijsman EM, Willemsen G, Williams N, Willsey AJ, Witt SH, Xu W, Young AH, Yu TW, Zammit S, Zandi PP, Zhang P, Zitman FG, Devlin B, et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet. 2013 Sep; 45(9):984-94. PMID: 23933821; PMCID: PMC3800159.
      Citations: 1013     Fields:    Translation:Humans
    113. 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
    114. 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
    115. 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
    116. Haenisch B, Herms S, Molderings GJ. The transcriptome of the human mast cell leukemia cells HMC-1.2: an approach to identify specific changes in the gene expression profile in KitD816V systemic mastocytosis. Immunol Res. 2013 May; 56(1):155-62. PMID: 23504229.
      Citations: 3     Fields:    Translation:HumansCells
    117. Liu JZ, Hov JR, Folseraas T, Ellinghaus E, Rushbrook SM, Doncheva NT, Andreassen OA, Weersma RK, Eksteen B, Invernizzi P, Hirschfield GM, Gotthardt DN, Pares A, Ellinghaus D, Shah T, Juran BD, Milkiewicz P, Rust C, Schramm C, Srivastava B, Dalekos G, Herms S, Winkelmann J, Mitrovic M, Braun F, Ponsioen CY, Croucher PJ, Sterneck M, Teufel A, Mason AL, Saarela J, Leppa V, Dorfman R, Alvaro D, Floreani A, Onengut-Gumuscu S, Rich SS, Thompson WK, Schork AJ, Thomsen I, Mayr G, Hveem K, Cleynen I, Gutierrez-Achury J, van Heel D, Sandford RN, Durie PR, Melum E, Vatn MH, Silverberg MS, Duerr RH, Padyukov L, Brand S, Sans M, Annese V, Achkar JP, Boberg KM, Marschall HU, Bowlus CL, Wijmenga C, Schrumpf E, Vermeire S, Albrecht M, UK-PSCSC Consortium, Rioux JD, Alexander G, Bergquist A, Cho J, Schreiber S, Manns MP, Dale AM, Chapman RW, Lazaridis KN, International PSC Study Group, Franke A, Anderson CA, Karlsen TH, International IBD Genetics Consortium, Weism?ller TJ, M?ller T, N?then MM, N?ss S, K?nig IR, Rica?o-Ponce I, Bj?rnsson E, Chazouill?res O, F?rkkil? M. Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Nat Genet. 2013 Jun; 45(6):670-5. PMID: 23603763; PMCID: PMC3667736.
      Citations: 179     Fields:    Translation:Humans
    118. 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
    119. 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
    120. 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
    121. 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
    122. Haenisch B, Herms S, Mattheisen M, Steffens M, Breuer R, Strohmaier J, Degenhardt F, Lucae S, Maier W, Rietschel M, Cichon S, Schm?l C, N?then MM. Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder. J Affect Disord. 2013 Apr 25; 146(3):438-40. PMID: 22921522.
      Citations: 7     Fields:    Translation:Humans
    123. Mangold E, Reutter H, Ludwig KU, Herms S, Paredes-Zenteno M, Nowak S, Kramer FJ, Wienker TF, Knapp M, Le?n-Cach?n RB, Chac?n-Camacho ?, Ortiz-L?pez R, Arizpe-Cant? A, Mu?oz-Jim?nez SG, N?then MM, Rojas-Mart?nez A. Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate. Eur J Oral Sci. 2012 Oct; 120(5):373-7. PMID: 22984993.
      Citations: 3     Fields:    Translation:Humans
    124. 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
    125. Redler S, Brockschmidt FF, Tazi-Ahnini R, Drichel D, Birch MP, Dobson K, Giehl KA, Herms S, Refke M, Kluck N, Kruse R, Lutz G, Wolff H, Becker T, Messenger AG, Betz RC, B?hm M, N?then MM. Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss. Br J Dermatol. 2012 Jun; 166(6):1314-8. PMID: 22309448.
      Citations: 11     Fields:    Translation:HumansCells
    126. Ladewig J, Mertens J, Kesavan J, Doerr J, Poppe D, Glaue F, Herms S, Wernet P, Koch P, K?gler G, M?ller FJ, Br?stle O. Small molecules enable highly efficient neuronal conversion of human fibroblasts. Nat Methods. 2012 Jun; 9(6):575-8. PMID: 22484851.
      Citations: 176     Fields:    Translation:HumansCells
    127. Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium, Ripke S, Wray NR, Lewis CM, Hamilton SP, Weissman MM, Breen G, Byrne EM, Blackwood DH, Boomsma DI, Cichon S, Heath AC, Holsboer F, Lucae S, Madden PA, Martin NG, McGuffin P, Muglia P, Noethen MM, Penninx BP, Pergadia ML, Potash JB, Rietschel M, Lin D, Shi J, Steinberg S, Grabe HJ, Lichtenstein P, Magnusson P, Perlis RH, Preisig M, Smoller JW, Stefansson K, Uher R, Kutalik Z, Tansey KE, Teumer A, Viktorin A, Barnes MR, Bettecken T, Binder EB, Castro VM, Churchill SE, Coryell WH, Craddock N, Craig IW, Czamara D, De Geus EJ, Degenhardt F, Farmer AE, Fava M, Frank J, Gainer VS, Gallagher PJ, Gordon SD, Goryachev S, Gross M, Guipponi M, Henders AK, Herms S, Hickie IB, Hoefels S, Hoogendijk W, Hottenga JJ, Iosifescu DV, Ising M, Jones I, Jones L, Jung-Ying T, Knowles JA, Kohane IS, Kohli MA, Korszun A, Landen M, Lawson WB, Lewis G, Macintyre D, Maier W, Mattheisen M, McGrath PJ, McIntosh A, McLean A, Middeldorp CM, Middleton L, Montgomery GM, Murphy SN, Nauck M, Nolen WA, Nyholt DR, O'Donovan M, Pedersen N, Scheftner WA, Schulz A, Schulze TG, Shyn SI, Sigurdsson E, Slager SL, Smit JH, Stefansson H, Steffens M, Thorgeirsson T, Tozzi F, Treutlein J, Uhr M, van den Oord EJ, Van Grootheest G, Weilburg JB, Willemsen G, Zitman FG, Neale B, Daly M, Levinson DF, Sullivan PF, M?ller-Myhsok B, Breuer R, Oskarsson H, V?lzke H. A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry. 2013 Apr; 18(4):497-511. PMID: 22472876; PMCID: PMC3837431.
      Citations: 550     Fields:    Translation:Humans
    128. 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
    129. 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
    130. 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
    131. Rietschel M, Mattheisen M, Degenhardt F, Genetic Risk and Outcome in Psychosis (GROUP Investigators), Kirsch P, Esslinger C, Herms S, Demontis D, Steffens M, Strohmaier J, Haenisch B, Breuer R, Czerski PM, Giegling I, Strengman E, Schmael C, Mors O, Mortensen PB, Hougaard DM, Kapelski P, Priebe L, Basmanav FF, Forstner AJ, Hoffman P, Meier S, Nikitopoulos J, Moebus S, Alexander M, Wichmann H-, Schreiber S, Rivandeneira F, Hofman A, Uitterlinden AG, Wienker TF, Schumacher J, Hauser J, Maier W, Cantor RM, Erk S, Schulze TG, SGENE-plus Consortium, Craddock N, Owen MJ, O'Donovan MC, Rujescu D, Walter H, Meyer-Lindenberg A, Ophoff RA, Cichon S, M?hleisen TW, ?rntoft T, M?ssner R, B?rglum AD, N?then NM. Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Mol Psychiatry. 2012 Sep; 17(9):906-17. PMID: 21747397.
      Citations: 57     Fields:    Translation:HumansCells
    132. 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
    133. Pabst S, Golebiewski M, Herms S, Karpushova A, Walier M, Zimmer S, Cichon S, Wienker TF, Nickenig G, Meyer R, Skowasch D, D?az-Lacava A, N?then MM, Groh? C. Caspase recruitment domain 15 gene haplotypes in sarcoidosis. Tissue Antigens. 2011 Apr; 77(4):333-7. PMID: 21388357.
      Citations: 1     Fields:    Translation:Humans
    134. Priebe L, Degenhardt FA, Herms S, Haenisch B, Mattheisen M, Nieratschker V, Weingarten M, Witt S, Breuer R, Paul T, Alblas M, Moebus S, Lathrop M, Leboyer M, Schreiber S, Grigoroiu-Serbanescu M, Maier W, Propping P, Rietschel M, Cichon S, N?then MM, M?hleisen TW. Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder. Mol Psychiatry. 2012 Apr; 17(4):421-32. PMID: 21358712.
      Citations: 33     Fields:    Translation:Humans
    135. Cichon S, Degenhardt FA, Mattheisen M, Strohmaier J, Steffens M, Meesters C, Herms S, Weingarten M, Priebe L, Haenisch B, Alexander M, Vollmer J, Tessmann P, Moebus S, Wichmann HE, Schreiber S, Lucae S, Leboyer M, Bellivier F, Etain B, Henry C, Kahn JP, Heath S, Bipolar Disorder Genome Study (BiGS) Consortium, Hamshere M, O'Donovan MC, Owen MJ, Craddock N, Schwarz M, Vedder H, Kammerer-Ciernioch J, Reif A, Sasse J, Bauer M, Hautzinger M, Wright A, Mitchell PB, Schofield PR, Montgomery GW, Medland SE, Gordon SD, Martin NG, Gustafsson O, Andreassen O, Djurovic S, Sigurdsson E, Steinberg S, Stefansson H, Stefansson K, Kapur-Pojskic L, Oruc L, Rivas F, Chuchalin A, Babadjanova G, Tiganov AS, Pantelejeva G, Abramova LI, Grigoroiu-Serbanescu M, Diaconu CC, Czerski PM, Hauser J, Zimmer A, Lathrop M, Schulze TG, Wienker TF, Schumacher J, Maier W, Propping P, Rietschel M, M?hleisen TW, Mir? X, Breuer R, Schm?l C, M?ller-Myhsok B, Jamain S, Mayoral F, N?then MM. Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Am J Hum Genet. 2011 Mar 11; 88(3):372-81. PMID: 21353194; PMCID: PMC3059436.
      Citations: 136     Fields:    Translation:HumansAnimals
    136. Basmanav FB, Forstner AJ, Mattheisen M, Priebe L, Herms S, Breuer R, Moebus S, Nenadic I, Sauer H, Maier W, Rujescu D, Ludwig M, Rietschel M, Cichon S, M?hleisen TW, M?ssner R, N?then MM. Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients. Schizophr Res. 2011 Apr; 127(1-3):35-40. PMID: 21288692.
      Citations: 5     Fields:    Translation:Humans
    137. Rietschel M, Mattheisen M, Frank J, Treutlein J, Degenhardt F, Steffens M, Mier D, Esslinger C, Walter H, Kirsch P, Erk S, Schnell K, Herms S, Wichmann HE, Schreiber S, Strohmaier J, Roeske D, Haenisch B, Gross M, Hoefels S, Lucae S, Binder EB, Wienker TF, Schulze TG, Zimmer A, Juraeva D, Brors B, Bettecken T, Meyer-Lindenberg A, Maier W, Cichon S, Breuer R, J?ckel KH, Schm?l C, M?ller-Myhsok B, N?then MM. Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression. Biol Psychiatry. 2010 Sep 15; 68(6):578-85. PMID: 20673876.
      Citations: 89     Fields:    Translation:Humans
    138. Nieratschker V, Frank J, Strohmaier J, Wendland JR, Schumacher J, Treutlein J, Abou Jamra R, Mattheisen M, Herms S, Maier W, Cichon S, Rietschel M, Schulze TG, M?hleisen TW, Breuer R, Schm?l C, N?then MM. The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: findings from a large German case-control and family-based sample. Schizophr Res. 2010 Sep; 122(1-3):24-30. PMID: 20643532.
      Citations: 8     Fields:    Translation:Humans
    139. 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
    140. 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
    141. Steffens M, Becker T, Sander T, Fimmers R, Herold C, Holler DA, Leu C, Herms S, Cichon S, Bohn B, Gerstner T, Griebel M, Wienker TF, Baur MP, N?then MM. Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests. Hum Hered. 2010; 69(4):268-84. PMID: 20357478.
      Citations: 10     Fields:    Translation:Humans
    142. Grigoroiu-Serbanescu M, Herms S, Diaconu CC, Jamra RA, Meier S, Bleotu C, Neagu AI, Prelipceanu D, Sima D, Gherghel M, Mihailescu R, Rietschel M, Cichon S, N?then MM, M?hleisen TW. Possible association of different G72/G30 SNPs with mood episodes and persecutory delusions in bipolar I Romanian patients. Prog Neuropsychopharmacol Biol Psychiatry. 2010 May 30; 34(4):657-63. PMID: 20230869.
      Citations: 3     Fields:    Translation:Humans
    143. 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
    144. Strohmaier J, Frank J, Wendland JR, Schumacher J, Jamra RA, Treutlein J, Nieratschker V, Mattheisen M, Herms S, Maier W, Cichon S, Rietschel M, Schulze TG, Breuer R, M?hleisen TW, N?then MM. A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry. Schizophr Res. 2010 May; 118(1-3):98-105. PMID: 20083391; PMCID: PMC2856768.
      Citations: 11     Fields:    Translation:Humans
    145. 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
    146. 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
    147. 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
    148. Grigoroiu-Serbanescu M, Herms S, Georgi A, Diaconu CC, Strohmaier J, Czerski P, Hauser J, Leszczynska-Rodziewicz A, Jamra RA, Babadjanova G, Tiganov A, Krasnov V, Kapiletti S, Neagu AI, Vollmer J, Rietschel M, Cichon S, Propping P, M?hleisen TW, Breuer R, N?then MM. Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 05; 150B(7):1017-21. PMID: 19330776.
      Citations: 21     Fields:    Translation:Humans
    149. Pabst S, Karpushova A, Diaz-Lacava A, Herms S, Walier M, Zimmer S, Cichon S, Nickenig G, Wienker TF, N?then MM, Groh? C. VEGF gene haplotypes are associated with sarcoidosis. Chest. 2010 Jan; 137(1):156-63. PMID: 19741061.
      Citations: 14     Fields:    Translation:Humans
    150. 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
    151. 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
    152. Hillmer AM, Freudenberg J, Myles S, Herms S, Tang K, Hughes DA, Brockschmidt FF, Ruan Y, Stoneking M, N?then MM. Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness. Hum Genet. 2009 Aug; 126(2):255-64. PMID: 19373488; PMCID: PMC3774421.
      Citations: 14     Fields:    Translation:HumansCells
    153. Treutlein J, Frank J, Mattheisen M, Herms S, Ludwig KU, Treutlein T, Schmael C, Strohmaier J, Paul T, Witt SH, Schulze TG, Nenadic I, Sauer H, Becker T, Maier W, Cichon S, Rietschel M, M?hleisen TW, B?sshenz KV, Breuer R, Schl?sser RG, N?then MM. Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter. Schizophr Res. 2009 Jun; 111(1-3):123-30. PMID: 19346103.
      Citations: 39     Fields:    Translation:HumansCells
    154. Birnbaum S, Reutter H, Mende M, de Assis NA, Diaz-Lacava A, Herms S, Scheer M, Lauster C, Braumann B, Martini M, Hemprich A, Knapp M, Kramer FJ, Mangold E, Schmidt G, P?tzsch S, N?then MM. Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate. Eur J Oral Sci. 2009 Apr; 117(2):200-3. PMID: 19320731.
      Citations: 13     Fields:    Translation:Humans
    155. 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
    156. Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, Herms S, Becker T, Nyholt DR, Zhao ZZ, Montgomery GW, Martin NG, Alblas MA, Moebus S, Erbel R, Reinartz R, Betz RC, Cichon S, Propping P, Baur MP, Wienker TF, Kruse R, Kort?m AK, M?hleisen TW, J?ckel KH, Br?cker-Preuss M, N?then MM. Susceptibility variants for male-pattern baldness on chromosome 20p11. Nat Genet. 2008 Nov; 40(11):1279-81. PMID: 18849994.
      Citations: 32     Fields:    Translation:HumansCells
    157. Grigoroiu-Serbanescu M, Diaconu CC, Herms S, Bleotu C, Vollmer J, Prelipceanu D, Priebe L, Mihailescu R, Georgescu MJ, Sima D, Grimberg M, Cichon S, M?hleisen TW, N?then MM. Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population. Psychiatr Genet. 2008 Oct; 18(5):240-7. PMID: 18797398.
      Citations: 7     Fields:    Translation:Humans
    158. 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
    159. Herms S, Seehaus K, Koehle H, Conrath U. A strobilurin fungicide enhances the resistance of tobacco against tobacco mosaic virus and Pseudomonas syringae pv tabaci. Plant Physiol. 2002 Sep; 130(1):120-7. PMID: 12226492; PMCID: PMC166545.
      Citations: 17     Fields:    Translation:Cells
    160. Adam U, Herms S, Werner U, Strubelt H, Makowiec F, Hopt UT, Drewelow B. The penetration of ciprofloxacin into human pancreatic and peripancreatic necroses in acute necrotizing pancreatitis. Infection. 2001 Dec; 29(6):326-31. PMID: 11787833.
      Citations: 5     Fields:    Translation:Humans

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