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Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.
Saccone NL, Culverhouse RC, Schwantes-An TH, Cannon DS, Chen X, Cichon S, Giegling I, Han S, Han Y, Keskitalo-Vuokko K, Kong X, Landi MT, Ma JZ, Short SE, Stephens SH, Stevens VL, Sun L, Wang Y, Wenzlaff AS, Aggen SH, Breslau N, Broderick P, Chatterjee N, Chen J, Heath AC, Heliövaara M, Hoft NR, Hunter DJ, Jensen MK, Martin NG, Montgomery GW, Niu T, Payne TJ, Peltonen L, Pergadia ML, Rice JP, Sherva R, Spitz MR, Sun J, Wang JC, Weiss RB, Wheeler W, Witt SH, Yang BZ, Caporaso NE, Ehringer MA, Eisen T, Gapstur SM, Gelernter J, Houlston R, Kaprio J, Kendler KS, Kraft P, Leppert MF, Li MD, Madden PA, Nöthen MM, Pillai S, Rietschel M, Rujescu D, Schwartz A, Amos CI, Bierut LJ. Saccone NL, et al. Among authors: rietschel m. PLoS Genet. 2010 Aug 5;6(8):e1001053. doi: 10.1371/journal.pgen.1001053. PLoS Genet. 2010. PMID: 20700436 Free PMC article.
CNTF and psychiatric disorders.
Nöthen MM, Cichon S, Eggermann K, Propping P, Knapp M, Maier W, Rietschel M. Nöthen MM, et al. Among authors: rietschel m. Nat Genet. 1996 Jun;13(2):142-3; author reply 144. doi: 10.1038/ng0696-142b. Nat Genet. 1996. PMID: 8640216 No abstract available.
Systematic screening for mutations in the 5'-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder.
Cichon S, Nöthen MM, Stöber G, Schroers R, Albus M, Maier W, Rietschel M, Körner J, Weigelt B, Franzek E, Wildenauer D, Fimmers R, Propping P. Cichon S, et al. Among authors: rietschel m. Am J Med Genet. 1996 Jul 26;67(4):424-8. doi: 10.1002/(SICI)1096-8628(19960726)67:4<424::AID-AJMG21>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8837716
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: rietschel m. Psychiatr Genet. 1996 Summer;6(2):75-9. doi: 10.1097/00041444-199622000-00007. Psychiatr Genet. 1996. PMID: 8840393
A gene for universal congenital alopecia maps to chromosome 8p21-22.
Nöthen MM, Cichon S, Vogt IR, Hemmer S, Kruse R, Knapp M, Höller T, Faiyaz ul Haque M, Haque S, Propping P, Ahmad M, Rietschel M. Nöthen MM, et al. Among authors: rietschel m. Am J Hum Genet. 1998 Feb;62(2):386-90. doi: 10.1086/301717. Am J Hum Genet. 1998. PMID: 9463324 Free PMC article.
Familial occurrence of primary premature ejaculation.
Waldinger MD, Rietschel M, Nöthen MM, Hengeveld MW, Olivier B. Waldinger MD, et al. Among authors: rietschel m. Psychiatr Genet. 1998 Spring;8(1):37-40. doi: 10.1097/00041444-199800810-00007. Psychiatr Genet. 1998. PMID: 9564687 No abstract available.
915 results