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Page 1
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
No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder.
Abou Jamra R, Schumacher J, Becker T, Dahdouh F, Ohlraun S, Suliman H, Schulze TG, Tullius M, Kovalenko S, Maier W, Rietschel M, Propping P, Nöthen MM, Cichon S. Abou Jamra R, et al. Among authors: ohlraun s. Psychiatr Genet. 2005 Sep;15(3):195-8. doi: 10.1097/00041444-200509000-00010. Psychiatr Genet. 2005. PMID: 16094254
Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.
Schumacher J, Kaneva R, Jamra RA, Diaz GO, Ohlraun S, Milanova V, Lee YA, Rivas F, Mayoral F, Fuerst R, Flaquer A, Windemuth C, Gay E, Sanz S, González MJ, Gil S, Cabaleiro F, del Rio F, Perez F, Haro J, Kostov C, Chorbov V, Nikolova-Hill A, Stoyanova V, Onchev G, Kremensky I, Strauch K, Schulze TG, Nürnberg P, Gaebel W, Klimke A, Auburger G, Wienker TF, Kalaydjieva L, Propping P, Cichon S, Jablensky A, Rietschel M, Nöthen MM. Schumacher J, et al. Among authors: ohlraun s. Am J Hum Genet. 2005 Dec;77(6):1102-11. doi: 10.1086/498619. Epub 2005 Nov 2. Am J Hum Genet. 2005. PMID: 16380920 Free PMC article.
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
Family history influences age of onset in bipolar I disorder in females but not in males.
Grigoroiu-Serbanescu M, Nöthen MM, Ohlraun S, Propping P, Maier W, Wickramaratne P, Georgescu MJ, Prelipceanu D, Grimberg M, Sima D, Rietschel M. Grigoroiu-Serbanescu M, et al. Among authors: ohlraun s. Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):6-11. doi: 10.1002/ajmg.b.30133. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15635595
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.
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.
42 results