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The American Journal of Psychiatry|April 3, 2009
Genomewide association studies: history, rationale, and prospects for psychiatric disorders, Sven Cichon, Nick Craddock, et al.Alcoholism, Clinical and Experimental Research|February 15, 2011
Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sampleKenneth S Kendler, Gursharan Kalsi, Peter A Holmans, et al.American Journal of Human Genetics|August 27, 2004
Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophreniaJubao Duan, Maria Martinez, Alan R Sanders, et al.Plos Genetics|April 19, 2012
Runs of homozygosity implicate autozygosity as a schizophrenia risk factorMatthew C Keller, Matthew A Simonson, Stephan Ripke, et al.Nature Communications|September 17, 2014
A sequence variant in human KALRN impairs protein function and coincides with reduced cortical thicknessTheron A Russell, Katherine D Blizinsky, Derin J Cobia, et al.Plos One|June 23, 2012
Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samplesThomas E Gladwin, Eske M Derks, , et al.Scientific Reports|December 9, 2017
Genome-Wide Association Study of Male Sexual OrientationAlan R Sanders, Gary W Beecham, Shengru Guo, et al.Cell Stem Cell|August 15, 2017
Open Chromatin Profiling in hiPSC-Derived Neurons Prioritizes Functional Noncoding Psychiatric Risk Variants and Highlights Neurodevelopmental LociMarc P Forrest, Hanwen Zhang, Winton Moy, et al.American Journal of Human Genetics|August 20, 2013
Additive genetic variation in schizophrenia risk is shared by populations of African and European descentTeresa R de Candia, S Hong Lee, Jian Yang, et al.American Journal of Human Genetics|August 5, 2022
Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neuronsAlena Kozlova, Siwei Zhang, Alex V Kotlar, et al.Pageof 8