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The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language.
Anthoni H, Sucheston LE, Lewis BA, Tapia-Páez I, Fan X, Zucchelli M, Taipale M, Stein CM, Hokkanen ME, Castrén E, Pennington BF, Smith SD, Olson RK, Tomblin JB, Schulte-Körne G, Nöthen M, Schumacher J, Müller-Myhsok B, Hoffmann P, Gilger JW, Hynd GW, Nopola-Hemmi J, Leppanen PH, Lyytinen H, Schoumans J, Nordenskjöld M, Spencer J, Stanic D, Boon WC, Simpson E, Mäkelä S, Gustafsson JÅ, Peyrard-Janvid M, Iyengar S, Kere J. Anthoni H, et al. Among authors: schumacher j. Behav Genet. 2012 Jul;42(4):509-27. doi: 10.1007/s10519-012-9532-3. Epub 2012 Mar 17. Behav Genet. 2012. PMID: 22426781 Free PMC 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: 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.
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: schumacher j. Psychiatr Genet. 2005 Sep;15(3):195-8. doi: 10.1097/00041444-200509000-00010. Psychiatr Genet. 2005. PMID: 16094254
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
Schumacher J, Anthoni H, Dahdouh F, König IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H, Hülsmann J, Cichon S, Lindgren CM, Propping P, Zucchelli M, Ziegler A, Peyrard-Janvid M, Schulte-Körne G, Nöthen MM, Kere J. Schumacher J, et al. Am J Hum Genet. 2006 Jan;78(1):52-62. doi: 10.1086/498992. Epub 2005 Nov 17. Am J Hum Genet. 2006. PMID: 16385449 Free PMC article.
Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder.
Jamra RA, Klein K, Villela AW, Becker T, Schulze TG, Schmael C, Deschner M, Klopp N, Illig T, Propping P, Cichon S, Rietschel M, Nöthen MM, Schumacher J. Jamra RA, et al. Among authors: schumacher j. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):663-5. doi: 10.1002/ajmg.b.30358. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16823801
No evidence for association between NOTCH4 and schizophrenia in a large family-based and case-control association analysis.
Ivo R, Schulze TG, Schumacher J, Kesper K, Müller DJ, Kremer I, Dobrusin M, Mujaheed M, Murad I, Blanaru M, Bannoura I, Reshef A, Bachner-Melman R, Ebstein RP, Propping P, Belmaker RH, Maier W, Rietschel M, Nöthen MM, Cichon S. Ivo R, et al. Among authors: schumacher j. Psychiatr Genet. 2006 Oct;16(5):197-203. doi: 10.1097/01.ypg.0000218619.50386.7c. Psychiatr Genet. 2006. PMID: 16969274
Interrelationship and familiality of dyslexia related quantitative measures.
Schulte-Körne G, Ziegler A, Deimel W, Schumacher J, Plume E, Bachmann C, Kleensang A, Propping P, Nöthen MM, Warnke A, Remschmidt H, König IR. Schulte-Körne G, et al. Among authors: schumacher j. Ann Hum Genet. 2007 Mar;71(Pt 2):160-75. doi: 10.1111/j.1469-1809.2006.00312.x. Epub 2006 Oct 13. Ann Hum Genet. 2007. PMID: 17038000
1,496 results