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Page 1
Comprehensive epidemiological and genotype-phenotype analyses in a large European sample with idiopathic achalasia.
Becker J, Niebisch S, Ricchiuto A, Schaich EJ, Lehmann G, Waltgenbach T, Schafft A, Hess T, Lenze F, Venerito M, Hüneburg R, Lingohr P, Matthaei H, Seewald S, Scheuermann U, Kreuser N, Veits L, Wouters MM, Gockel HR, Lang H, Vieth M, Müller M, Eckardt AJ, von Rahden BH, Knapp M, Boeckxstaens GE, Fimmers R, Nöthen MM, Schulz HG, Gockel I, Schumacher J. Becker J, et al. Among authors: schumacher j. Eur J Gastroenterol Hepatol. 2016 Jun;28(6):689-95. doi: 10.1097/MEG.0000000000000602. Eur J Gastroenterol Hepatol. 2016. PMID: 26882171
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.
Haplotype interaction analysis of unlinked regions.
Becker T, Schumacher J, Cichon S, Baur MP, Knapp M. Becker T, et al. Among authors: schumacher j. Genet Epidemiol. 2005 Dec;29(4):313-22. doi: 10.1002/gepi.20096. Genet Epidemiol. 2005. PMID: 16240441
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
Genetics of dyslexia: the evolving landscape.
Schumacher J, Hoffmann P, Schmäl C, Schulte-Körne G, Nöthen MM. Schumacher J, et al. J Med Genet. 2007 May;44(5):289-97. doi: 10.1136/jmg.2006.046516. Epub 2007 Feb 16. J Med Genet. 2007. PMID: 17307837 Free PMC article. Review.
1,502 results