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Plos One|August 11, 2011
The genetic structure of the Swedish populationKeith Humphreys, Alexander Grankvist, Monica Leu, et al.Nature Genetics|December 20, 2016
Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traitsJacqueline M Lane, Jingjing Liang, Irma Vlasac, et al.Journal of the American Heart Association|December 12, 2023
Causal Association Between Subtypes of Excessive Daytime Sleepiness and Risk of Cardiovascular DiseasesMatthew O Goodman, Hassan S Dashti, Jacqueline M Lane, et al.European Journal of Human Genetics : EJHG|January 17, 2013
Mosaic copy number variation in schizophreniaDouglas M Ruderfer, Kim Chambert, Jennifer Moran, et al.American Journal of Human Genetics|December 3, 2014
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseasesAlexander Gusev, S Hong Lee, Gosia Trynka, et al.Nature Human Behaviour|November 17, 2020
Macro and micro sleep architecture and cognitive performance in older adultsIna Djonlagic, Sara Mariani, Annette L Fitzpatrick, et al.JCI Insight|January 26, 2018
Mutations in Hnrnpa1 cause congenital heart defectsZhe Yu, Paul Lf Tang, Jing Wang, et al.The Lancet Regional Health. Western Pacific|April 16, 2025
Twelve-month prevalence of DSM-5 mental disorders and the psychosocial correlates- a child and adolescent psychiatric epidemiologic survey in Hong Kong SARSandra S M Chan, Oscar W H Wong, Samara Hussain, et al.Translational Psychiatry|February 19, 2020
Effects of a patient-derived de novo coding alteration of CACNA1I in mice connect a schizophrenia risk gene with sleep spindle deficitsAyan Ghoshal, David S Uygun, Lingling Yang, et al.Genome Medicine|December 22, 2017
Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disordersHoang T Nguyen, Julien Bryois, April Kim, et al.Pageof 33