Next Generation Sequencing Competence Network

Next Generation Sequencing Competence Network

e.g. CCGA
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André Heimbach

Dr.
University of Bonn
NGS Core Facility, Human Genetics
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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. Ishorst N, Henschel L, Thieme F, Drichel D, Sivalingam S, Mehrem SL, Fechtner AC, Fazaal J, Welzenbach J, Heimbach A, Maj C, Borisov O, Hausen J, Raff R, Hoischen A, Dixon M, Rada-Iglesias A, Bartusel M, Rojas-Martinez A, Aldhorae K, Braumann B, Kruse T, Kirschneck C, Spanier G, Reutter H, Nowak S, G?lz L, Knapp M, Buness A, Krawitz P, N?then MM, Nothnagel M, Becker T, Ludwig KU, Mangold E. Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores. Mol Genet Genomic Med. 2023 03; 11(3):e2109. PMID: 36468602; PMCID: PMC10009911.
      Citations: 1     Fields:    Translation:Humans
    2. Vennin C, Hewel C, Todorov H, Wendelmuth M, Radyushkin K, Heimbach A, Horenko I, Ayash S, M?ller MB, Schweiger S, Gerber S, Lutz B. A Resilience Related Glial-Neurovascular Network Is Transcriptionally Activated after Chronic Social Defeat in Male Mice. Cells. 2022 Oct 27; 11(21). PMID: 36359800; PMCID: PMC9655779.
      Citations: 1     Fields:    Translation:Animals
    3. Zillich L, Poisel E, Frank J, Foo JC, Friske MM, Streit F, Sirignano L, Heilmann-Heimbach S, Hoffmann P, Degenhardt F, Hansson AC, Bakalkin G, Rietschel M, Spanagel R, Witt SH, Heimbach A, N?then MM. Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum. Transl Psychiatry. 2022 05 06; 12(1):190. PMID: 35523767; PMCID: PMC9076849.
      Citations: 7     Fields:    Translation:Humans
    4. Hauke J, Harter P, Ernst C, Schmidt S, Reuss A, Borde J, Dietrich D, El-Balat A, Kayali M, Gevensleben H, Hilpert F, Schoemig-Markiefka B, Thiele H, Kimmig R, Richters L, Schmutzler RK, Hahnen E, Burges A, De Gregorio N, Altm?ller J, Heimbach A, Meier W, N?rnberg P, Kast K, Sehouli J. Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883). J Med Genet. 2022 03; 59(3):248-252. PMID: 33273034; PMCID: PMC8867275.
      Citations: 1     Fields:    Translation:HumansCells
    5. Jamil MA, Sharma A, Nuesgen N, Pezeshkpoor B, Pavlova A, Oldenburg J, El-Maarri O, Heimbach A. F8 Inversions at Xq28 Causing Hemophilia A Are Associated With Specific Methylation Changes: Implication for Molecular Epigenetic Diagnosis. Front Genet. 2019; 10:508. PMID: 31191618; PMCID: PMC6548806.
      Citations: 9     
    6. Hauke J, Hahnen E, Schneider S, Reuss A, Richters L, Kommoss S, Schmidt S, Prieske K, Gevensleben H, Borde J, El-Balat A, Thiele H, Hilpert F, Meier W, Dietrich D, Kimmig R, Schoemig-Markiefka B, Jackisch C, Park-Simon TW, Ernst C, Pfisterer J, Schnelzer A, du Bois A, Schmutzler RK, Harter P, Heimbach A, Marm? F, Burges A, De Gregorio N, N?rnberg P, Altm?ller J, Kast K, Braicu E, Baumann K, Hanker L. Deleterious somatic variants in 473 consecutive individuals with ovarian cancer: results of the observational AGO-TR1 study (NCT02222883). J Med Genet. 2019 09; 56(9):574-580. PMID: 30979843.
      Citations: 18     Fields:    Translation:HumansCells
    7. Lackner P, Hoffmann P, Stanzial F, Parmeggiani L, Benedicenti F, Pellegrin S, Casara G, Domingues FS, K?nig E, Schwienbacher C, Volpato CB, Picard A, Cantaloni C, Mascalzoni D, Heimbach A, Hicks AA, Pramstaller PP. Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly. Seizure. 2019 Mar; 66:81-85. PMID: 30818181.
      Citations: 9     Fields:    Translation:Humans
    8. Spinell T, Hoffmann P, Enkling N, Renvert S, Schwarz F, Demmer RT, Papapanou PN, Kebschull M, Kr?ger A, H?lsmann C, Fickl S, H?ttig F, Kaufmann F, Heimbach A, Jepsen S. The severity of human peri-implantitis lesions correlates with the level of submucosal microbial dysbiosis. J Clin Periodontol. 2018 12; 45(12):1498-1509. PMID: 30341964.
      Citations: 15     Fields:    Translation:HumansPHPublic Health
    9. Harter P, Hauke J, Heitz F, Reuss A, Prieske K, Richters L, Neidhardt G, de Gregorio N, El-Balat A, Hilpert F, Meier W, Kimmig R, Baumann K, Jackisch C, Park-Simon TW, Pfisterer J, Gevensleben H, Schnelzer A, Dietrich D, Thiele H, Lamla J, Elser G, du Bois A, Hahnen E, Schmutzler R, Kommoss S, Marm? F, Heimbach A, Burges A, Kast K, Sehouli J, Hanker L, Kr?ber S, Neunh?ffer T, Krockenberger M, Brucker SY, N?rnberg P, Altm?ller J. Prevalence of deleterious germline variants in risk genes including BRCA1/2 in consecutive ovarian cancer patients (AGO-TR-1). PLoS One. 2017; 12(10):e0186043. PMID: 29053726; PMCID: PMC5650145.
      Citations: 53     Fields:    Translation:Humans
    10. Brockschmidt A, Chung B, Weber S, Fischer DC, Kolatsi-Joannou M, Christ L, Shtiza D, Simonetti GD, Konrad M, Winyard P, Haffner D, Schaefer F, Weber RG, Heimbach A, Klaus G. CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT). Nephrol Dial Transplant. 2012 Jun; 27(6):2355-64. PMID: 22146311.
      Citations: 15     Fields:    Translation:HumansCells
    11. Park JS, Mehta P, Cooper AA, Veivers D, Stiller B, Kubisch C, Fung VS, Krainc D, Mackay-Sim A, Sue CM, Heimbach A. Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism. Hum Mutat. 2011 Aug; 32(8):956-64. PMID: 21542062.
      Citations: 50     Fields:    Translation:HumansAnimalsCells
    12. Ramirez A, Stiller B, Hampshire D, Cid LP, Goebel I, Mubaidin AF, Wriekat AL, Roeper J, Al-Din A, Hillmer AM, Karsak M, Liss B, Woods CG, Behrens MI, Kubisch C, Heimbach A, Gr?ndemann J. Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase. Nat Genet. 2006 Oct; 38(10):1184-91. PMID: 16964263.
      Citations: 470     Fields:    Translation:HumansCells
    13. Wilhelm AM, Heimbach A, Kuntz BM, Br?ster HT. [Immunogenetic disposition in HIV infection. Consequences for transfusion medicine?]. Beitr Infusionther Klin Ernahr. 1987; 18:17-20. PMID: 3439967.
      Citations:    Fields:    Translation:Humans

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