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Page 1
Polygenic risk for depression and the neural correlates of working memory in healthy subjects.
Yüksel D, Dietsche B, Forstner AJ, Witt SH, Maier R, Rietschel M, Konrad C, Nöthen MM, Dannlowski U, Baune BT, Kircher T, Krug A. Yüksel D, et al. Among authors: nothen mm. Prog Neuropsychopharmacol Biol Psychiatry. 2017 Oct 3;79(Pt B):67-76. doi: 10.1016/j.pnpbp.2017.06.010. Epub 2017 Jun 15. Prog Neuropsychopharmacol Biol Psychiatry. 2017. PMID: 28624581
A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: no role in the genetic predisposition to bipolar affective disorder.
Rietschel M, Nöthen MM, Lannfelt L, Sokoloff P, Schwartz JC, Lanczik M, Fritze J, Cichon S, Fimmers R, Körner J, et al. Rietschel M, et al. Among authors: nothen mm. Psychiatry Res. 1993 Mar;46(3):253-9. doi: 10.1016/0165-1781(93)90093-v. Psychiatry Res. 1993. PMID: 8493294
[Genetic counseling in psychiatric diseases].
Körner J, Rietschel M, Nöthen MM, Propping P. Körner J, et al. Among authors: nothen mm. Nervenarzt. 1996 Jan;67(1):3-14. Nervenarzt. 1996. PMID: 8676986 Review. German.
Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia.
Shimron-Abarbanell D, Harms H, Erdmann J, Albus M, Maier W, Rietschel M, Körner J, Weigelt B, Franzek E, Sander T, Knapp M, Propping P, Nöthen MM. Shimron-Abarbanell D, et al. Among authors: nothen mm. Am J Med Genet. 1996 Apr 9;67(2):225-8. doi: 10.1002/(SICI)1096-8628(19960409)67:2<225::AID-AJMG16>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8723053
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: nothen mm. 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
1,057 results