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Nature|March 4, 2011
Somatic coding mutations in human induced pluripotent stem cellsAthurva Gore, Zhe Li, Ho-Lim Fung, et al.Plos Genetics|September 15, 2010
The characterization of twenty sequenced human genomesKimberly Pelak, Kevin V Shianna, Dongliang Ge, et al.The American Journal of Psychiatry|October 21, 2015
Comprehensive Versus Usual Community Care for First-Episode Psychosis: 2-Year Outcomes From the NIMH RAISE Early Treatment ProgramJohn M Kane, Delbert G Robinson, Nina R Schooler, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2017
Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseasesLoren D M Pena, Yong-Hui Jiang, Kelly Schoch, et al.Nature Neuroscience|March 18, 2018
Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortiumStephan J Sanders, Benjamin M Neale, Hailiang Huang, et al.Nature|October 9, 2009
Finding the missing heritability of complex diseasesTeri A Manolio, Francis S Collins, Nancy J Cox, et al.The New England Journal of Medicine|March 25, 2011
HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in EuropeansMark McCormack, Ana Alfirevic, Stephane Bourgeois, et al.Nature|April 25, 2014
Guidelines for investigating causality of sequence variants in human diseaseD G MacArthur, T A Manolio, D P Dimmock, et al.The New England Journal of Medicine|September 18, 2014
Ultrasonography versus computed tomography for suspected nephrolithiasisRebecca Smith-Bindman, Chandra Aubin, John Bailitz, et al.American Journal of Human Genetics|September 26, 2017
De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with SeizuresCandace T Myers, Nicholas Stong, Emily I Mountier, et al.Pageof 144