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Nature|January 28, 2014
De novo mutations in schizophrenia implicate synaptic networksMenachem Fromer, Andrew J Pocklington, David H Kavanagh, et al.
Nature|January 28, 2014
A polygenic burden of rare disruptive mutations in schizophreniaShaun M Purcell, Jennifer L Moran, Menachem Fromer, 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.
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.
Science Translational Medicine|January 22, 2016
Quantifying prion disease penetrance using large population control cohortsEric Vallabh Minikel, Sonia M Vallabh, Monkol Lek, et al.
Nature Genetics|August 20, 2008
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorderManuel A R Ferreira, Michael C O'Donovan, Yan A Meng, et al.
Nature Genetics|February 27, 2019
Identification of common genetic risk variants for autism spectrum disorderJakob Grove, Stephan Ripke, Thomas D Als, et al.
Nature Genetics|November 28, 2018
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorderDitte Demontis, Raymond K Walters, Joanna Martin, et al.
Nature Genetics|August 27, 2013
Genome-wide association analysis identifies 13 new risk loci for schizophreniaStephan Ripke, Colm O'Dushlaine, Kimberly Chambert, et al.
Nature Genetics|May 3, 2019
Genome-wide association study identifies 30 loci associated with bipolar disorderEli A Stahl, Gerome Breen, Andreas J Forstner, et al.
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