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Biological Psychiatry|January 29, 2019
Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective CasesAlexander W Charney, Eli A Stahl, Elaine K Green, et al.Molecular Psychiatry|October 28, 2015
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorderJ Song, S E Bergen, A Di Florio, et al.Science (New York, N.Y.)|February 21, 2012
A systematic survey of loss-of-function variants in human protein-coding genesDaniel G MacArthur, Suganthi Balasubramanian, Adam Frankish, et al.Nature Genetics|November 20, 2019
Comparative genetic architectures of schizophrenia in East Asian and European populationsMax Lam, Chia-Yen Chen, Zhiqiang Li, et al.Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophreniaRunjia Li, Sarah A Gagliano Taliun, Kevin Liao, et al.Nature|November 22, 2019
Genetic predisposition to mosaic Y chromosome loss in bloodDeborah J Thompson, Giulio Genovese, Jonatan Halvardson, et al.HGG Advances|August 31, 2025
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophreniaRunjia Li, Sarah A Gagliano Taliun, Kevin Liao, et al.Nature|February 5, 2011
Mapping copy number variation by population-scale genome sequencingRyan E Mills, Klaudia Walter, Chip Stewart, et al.Nature Neuroscience|March 15, 2016
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disordersTarjinder Singh, Mitja I Kurki, David Curtis, et al.Science Translational Medicine|January 22, 2016
Quantifying prion disease penetrance using large population control cohortsEric Vallabh Minikel, Sonia M Vallabh, Monkol Lek, et al.Pageof 88