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Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample.
Ludwig KU, Schumacher J, Schulte-Körne G, König IR, Warnke A, Plume E, Anthoni H, Peyrard-Janvid M, Meng H, Ziegler A, Remschmidt H, Kere J, Gruen JR, Müller-Myhsok B, Nöthen MM, Hoffmann P. Ludwig KU, et al. Among authors: schumacher j. Psychiatr Genet. 2008 Dec;18(6):310-2. doi: 10.1097/YPG.0b013e3283063a78. Psychiatr Genet. 2008. PMID: 19018237 Free PMC article.
A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25--q26.
Cichon S, Schmidt-Wolf G, Schumacher J, Müller DJ, Hürter M, Schulze TG, Albus M, Borrmann-Hassenbach M, Franzek E, Lanczik M, Fritze J, Kreiner R, Weigelt B, Minges J, Lichtermann D, Lerer B, Kanyas K, Strauch K, Windemuth C, Baur MP, Wienker TF, Maier W, Rietschel M, Propping P, Nöthen MM. Cichon S, et al. Among authors: schumacher j. Mol Psychiatry. 2001 May;6(3):342-9. doi: 10.1038/sj.mp.4000864. Mol Psychiatry. 2001. PMID: 11326307
Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia.
Schulze TG, Schumacher J, Müller DJ, Krauss H, Alfter D, Maroldt A, Ahle G, Maroldt AO, Novo y Fernández A, Weber T, Held T, Propping P, Maier W, Nöthen MM, Rietschel M. Schulze TG, et al. Among authors: schumacher j. Am J Med Genet. 2001 Aug 8;105(6):498-501. doi: 10.1002/ajmg.1472. Am J Med Genet. 2001. PMID: 11496364
A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q.
Cichon S, Schumacher J, Müller DJ, Hürter M, Windemuth C, Strauch K, Hemmer S, Schulze TG, Schmidt-Wolf G, Albus M, Borrmann-Hassenbach M, Franzek E, Lanczik M, Fritze J, Kreiner R, Reuner U, Weigelt B, Minges J, Lichtermann D, Lerer B, Kanyas K, Baur MP, Wienker TF, Maier W, Rietschel M, Propping P, Nöthen MM. Cichon S, et al. Among authors: schumacher j. Hum Mol Genet. 2001 Dec 1;10(25):2933-44. doi: 10.1093/hmg/10.25.2933. Hum Mol Genet. 2001. PMID: 11741836
No association between a putative functional promoter variant in the dopamine beta-hydroxylase gene and schizophrenia.
Jönsson EG, Abou Jamra R, Schumacher J, Flyckt L, Edman G, Forslund K, Mattila-Evenden M, Rylander G, Asberg M, Bjerkenstedt L, Wiesel FA, Propping P, Cichon S, Nöthen MM, Sedvall GC. Jönsson EG, et al. Among authors: schumacher j. Psychiatr Genet. 2003 Sep;13(3):175-8. doi: 10.1097/00041444-200309000-00007. Psychiatr Genet. 2003. PMID: 12960750
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: schumacher j. 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.
1,468 results