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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: nothen mm. Eur J Gastroenterol Hepatol. 2016 Jun;28(6):689-95. doi: 10.1097/MEG.0000000000000602. Eur J Gastroenterol Hepatol. 2016. PMID: 26882171
The use of microsatellites in zygosity diagnosis of twins.
Erdmann J, Nöthen MM, Stratmann M, Fimmers R, Franzek E, Propping P. Erdmann J, et al. Among authors: nothen mm. Acta Genet Med Gemellol (Roma). 1993;42(1):45-51. doi: 10.1017/s0515283600042281. Acta Genet Med Gemellol (Roma). 1993. PMID: 8191861
Apolipoprotein E genotype distribution in schizophrenia.
Zhu S, Nöthen MM, Uhlhaas S, Rietschel M, Körner J, Lanczik M, Fimmers R, Propping P. Zhu S, et al. Among authors: nothen mm. Psychiatr Genet. 1996 Summer;6(2):75-9. doi: 10.1097/00041444-199622000-00007. Psychiatr Genet. 1996. PMID: 8840393
Investigation of complement C4B deficiency in schizophrenia.
Schroers R, Nöthen MM, Rietschel M, Albus M, Maier W, Schwab S, Wildenauer D, Fimmers R, Propping P, Dewald G. Schroers R, et al. Among authors: nothen mm. Hum Hered. 1997 Sep-Oct;47(5):279-82. doi: 10.1159/000154424. Hum Hered. 1997. PMID: 9358016
Genetics of dyslexia: the evolving landscape.
Schumacher J, Hoffmann P, Schmäl C, Schulte-Körne G, Nöthen MM. Schumacher J, et al. Among authors: nothen mm. 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.
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.
Schumacher J, Laje G, Abou Jamra R, Becker T, Mühleisen TW, Vasilescu C, Mattheisen M, Herms S, Hoffmann P, Hillmer AM, Georgi A, Herold C, Schulze TG, Propping P, Rietschel M, McMahon FJ, Nöthen MM, Cichon S. Schumacher J, et al. Among authors: nothen mm. Hum Mol Genet. 2009 Jul 15;18(14):2719-27. doi: 10.1093/hmg/ddp204. Epub 2009 May 4. Hum Mol Genet. 2009. PMID: 19414483 Free PMC article.
Achalasia: will genetic studies provide insights?
Gockel HR, Schumacher J, Gockel I, Lang H, Haaf T, Nöthen MM. Gockel HR, et al. Among authors: nothen mm. Hum Genet. 2010 Oct;128(4):353-64. doi: 10.1007/s00439-010-0874-8. Epub 2010 Aug 11. Hum Genet. 2010. PMID: 20700745 Review.
1,049 results