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Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis.
Gharahkhani P, Fitzgerald RC, Vaughan TL, Palles C, Gockel I, Tomlinson I, Buas MF, May A, Gerges C, Anders M, Becker J, Kreuser N, Noder T, Venerito M, Veits L, Schmidt T, Manner H, Schmidt C, Hess T, Böhmer AC, Izbicki JR, Hölscher AH, Lang H, Lorenz D, Schumacher B, Hackelsberger A, Mayershofer R, Pech O, Vashist Y, Ott K, Vieth M, Weismüller J, Nöthen MM; Barrett's and Esophageal Adenocarcinoma Consortium (BEACON); Esophageal Adenocarcinoma GenEtics Consortium (EAGLE); Wellcome Trust Case Control Consortium 2 (WTCCC2); Attwood S, Barr H, Chegwidden L, de Caestecker J, Harrison R, Love SB, MacDonald D, Moayyedi P, Prenen H, Watson RGP, Iyer PG, Anderson LA, Bernstein L, Chow WH, Hardie LJ, Lagergren J, Liu G, Risch HA, Wu AH, Ye W, Bird NC, Shaheen NJ, Gammon MD, Corley DA, Caldas C, Moebus S, Knapp M, Peters WHM, Neuhaus H, Rösch T, Ell C, MacGregor S, Pharoah P, Whiteman DC, Jankowski J, Schumacher J. Gharahkhani P, et al. Among authors: nothen mm. Lancet Oncol. 2016 Oct;17(10):1363-1373. doi: 10.1016/S1470-2045(16)30240-6. Epub 2016 Aug 12. Lancet Oncol. 2016. PMID: 27527254 Free PMC article.
Systematic search for variation in the human norepinephrine transporter gene: identification of five naturally occurring missense mutations and study of association with major psychiatric disorders.
Stöber G, Nöthen MM, Pörzgen P, Brüss M, Bönisch H, Knapp M, Beckmann H, Propping P. Stöber G, et al. Among authors: nothen mm. Am J Med Genet. 1996 Nov 22;67(6):523-32. doi: 10.1002/(SICI)1096-8628(19961122)67:6<523::AID-AJMG3>3.0.CO;2-I. Am J Med Genet. 1996. PMID: 8950409
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: nothen mm. Psychiatr Genet. 2005 Sep;15(3):195-8. doi: 10.1097/00041444-200509000-00010. Psychiatr Genet. 2005. PMID: 16094254
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: nothen mm. 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. 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.
1,029 results