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Psychiatric Genetics|December 23, 1998
Schizophrenia and the serotonin transporter geneD Rao, E G Jönsson, S Paus, et al.
Molecular and Cellular Probes|May 25, 2015
Recurrent null mutation in SPG20 leads to Troyer syndromeHasan Tawamie, Eva Wohlleber, Steffen Uebe, et al.
Human Heredity|April 7, 2005
Computer-assisted phenotype characterization for genetic research in psychiatryHeiner Fangerau, Stephanie Ohlraun, Ralf O Granath, et al.
Brain Research. Molecular Brain Research|September 5, 1998
Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brainR Bunzel, I Blümcke, S Cichon, et al.
Molecular Membrane Biology|July 1, 1997
Assignment of the human serotonin 1F receptor gene (HTR1F) to the short arm of chromosome 3 (3p13-p14.1)J Erdmann, D Shimron-Abarbanell, V Shridhar, et al.
Annals of Human Genetics|July 1, 1996
The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3G Dewald, S Cichon, S P Bryant, et al.
Human Genetics|February 1, 1996
Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunctionT Eggermann, M M Nöthen, B Eiben, et al.
Human Heredity|November 2, 2011
Missing heritability in the tails of quantitative traits? A simulation study on the impact of slightly altered true genetic modelsCarolin Pütter, Sonali Pechlivanis, Markus M Nöthen, et al.
Human Genetics|October 1, 1993
Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome)M M Nöthen, T Eggermann, J Erdmann, et al.
Bioinformatics (Oxford, England)|July 31, 2014
FARVAT: a family-based rare variant association testSungkyoung Choi, Sungyoung Lee, Sven Cichon, et al.
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