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Page 1
Haplotype-based systematic association studies of ATP1A2 in migraine with aura.
Netzer C, Todt U, Heinze A, Freudenberg J, Zumbroich V, Becker T, Goebel I, Ohlraun S, Goebel H, Kubisch C. Netzer C, et al. Among authors: ohlraun s. Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):257-60. doi: 10.1002/ajmg.b.30283. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16508935
The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease.
Van Den Bogaert A, Schumacher J, Schulze TG, Otte AC, Ohlraun S, Kovalenko S, Becker T, Freudenberg J, Jönsson EG, Mattila-Evenden M, Sedvall GC, Czerski PM, Kapelski P, Hauser J, Maier W, Rietschel M, Propping P, Nöthen MM, Cichon S. Van Den Bogaert A, et al. Among authors: ohlraun s. Am J Hum Genet. 2003 Dec;73(6):1438-43. doi: 10.1086/379928. Epub 2003 Nov 14. Am J Hum Genet. 2003. PMID: 14618545 Free PMC article.
Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depression.
Schumacher J, Jamra RA, Becker T, Ohlraun S, Klopp N, Binder EB, Schulze TG, Deschner M, Schmäl C, Höfels S, Zobel A, Illig T, Propping P, Holsboer F, Rietschel M, Nöthen MM, Cichon S. Schumacher J, et al. Among authors: ohlraun s. Biol Psychiatry. 2005 Aug 15;58(4):307-14. doi: 10.1016/j.biopsych.2005.04.006. Biol Psychiatry. 2005. PMID: 16005437
Family-based association studies of alpha-adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder.
Abou Jamra R, Schumacher J, Golla A, Richter C, Otte AC, Schulze TG, Ohlraun S, Maier W, Rietschel M, Cichon S, Propping P, Nöthen MM. Abou Jamra R, et al. Among authors: ohlraun s. Am J Med Genet B Neuropsychiatr Genet. 2004 Apr 1;126B(1):79-81. doi: 10.1002/ajmg.b.20145. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15048653
The power of sample size and homogenous sampling: association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder.
Hoefgen B, Schulze TG, Ohlraun S, von Widdern O, Höfels S, Gross M, Heidmann V, Kovalenko S, Eckermann A, Kölsch H, Metten M, Zobel A, Becker T, Nöthen MM, Propping P, Heun R, Maier W, Rietschel M. Hoefgen B, et al. Among authors: ohlraun s. Biol Psychiatry. 2005 Feb 1;57(3):247-51. doi: 10.1016/j.biopsych.2004.11.027. Biol Psychiatry. 2005. PMID: 15691525
Genotype-phenotype studies in bipolar disorder showing association between the DAOA/G30 locus and persecutory delusions: a first step toward a molecular genetic classification of psychiatric phenotypes.
Schulze TG, Ohlraun S, Czerski PM, Schumacher J, Kassem L, Deschner M, Gross M, Tullius M, Heidmann V, Kovalenko S, Jamra RA, Becker T, Leszczynska-Rodziewicz A, Hauser J, Illig T, Klopp N, Wellek S, Cichon S, Henn FA, McMahon FJ, Maier W, Propping P, Nöthen MM, Rietschel M. Schulze TG, et al. Among authors: ohlraun s. Am J Psychiatry. 2005 Nov;162(11):2101-8. doi: 10.1176/appi.ajp.162.11.2101. Am J Psychiatry. 2005. PMID: 16263850
European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset.
Mathieu F, Dizier MH, Etain B, Jamain S, Rietschel M, Maier W, Albus M, McKeon P, Roche S, Blackwood D, Muir WJ, Henry C, Malafosse A, Preisig M, Ferrero F, Cichon S, Schumacher J, Ohlraun S, Propping P, Abou Jamra R, Schulze TG, Zelenica D, Charon C, Marusic A, Dernovsek MC, Gurling H, Nöthen M, Lathrop M, Leboyer M, Bellivier F. Mathieu F, et al. Among authors: ohlraun s. Am J Med Genet B Neuropsychiatr Genet. 2010 Dec 5;153B(8):1425-33. doi: 10.1002/ajmg.b.31121. Epub 2010 Sep 30. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20886542 Free article.
42 results