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Common variants conferring risk of schizophrenia.
Stefansson H, Ophoff RA, Steinberg S, Andreassen OA, Cichon S, Rujescu D, Werge T, Pietiläinen OP, Mors O, Mortensen PB, Sigurdsson E, Gustafsson O, Nyegaard M, Tuulio-Henriksson A, Ingason A, Hansen T, Suvisaari J, Lonnqvist J, Paunio T, Børglum AD, Hartmann A, Fink-Jensen A, Nordentoft M, Hougaard D, Norgaard-Pedersen B, Böttcher Y, Olesen J, Breuer R, Möller HJ, Giegling I, Rasmussen HB, Timm S, Mattheisen M, Bitter I, Réthelyi JM, Magnusdottir BB, Sigmundsson T, Olason P, Masson G, Gulcher JR, Haraldsson M, Fossdal R, Thorgeirsson TE, Thorsteinsdottir U, Ruggeri M, Tosato S, Franke B, Strengman E, Kiemeney LA; Genetic Risk and Outcome in Psychosis (GROUP); Melle I, Djurovic S, Abramova L, Kaleda V, Sanjuan J, de Frutos R, Bramon E, Vassos E, Fraser G, Ettinger U, Picchioni M, Walker N, Toulopoulou T, Need AC, Ge D, Yoon JL, Shianna KV, Freimer NB, Cantor RM, Murray R, Kong A, Golimbet V, Carracedo A, Arango C, Costas J, Jönsson EG, Terenius L, Agartz I, Petursson H, Nöthen MM, Rietschel M, Matthews PM, Muglia P, Peltonen L, St Clair D, Goldstein DB, Stefansson K, Collier DA. Stefansson H, et al. Among authors: nothen mm. Nature. 2009 Aug 6;460(7256):744-7. doi: 10.1038/nature08186. Epub 2009 Jul 1. Nature. 2009. PMID: 19571808 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. Nat Genet. 1996 Jun;13(2):142-3; author reply 144. doi: 10.1038/ng0696-142b. Nat Genet. 1996. PMID: 8640216 No abstract available.
5HT 2a receptor T102C polymorphism and schizophrenia.
Jönsson E, Nöthen MM, Bunzel R, Propping P, Sedvall G. Jönsson E, et al. Among authors: nothen mm. Lancet. 1996 Jun 29;347(9018):1831. Lancet. 1996. PMID: 8667938 No abstract available.
Lack of imprinting of the human dopamine D4 receptor (DRD4) gene.
Cichon S, Nöthen MM, Wolf HK, Propping P. Cichon S, et al. Among authors: nothen mm. Am J Med Genet. 1996 Apr 9;67(2):229-31. doi: 10.1002/(SICI)1096-8628(19960409)67:2<229::AID-AJMG17>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8723054
1,027 results