Showing results (1951-1960 of 2,222) with videos related to

Sort By:
Pageof 223
Human Molecular Genetics|February 25, 2016
Testing the role of predicted gene knockouts in human anthropometric trait variationSamuel Lessard, Alisa K Manning, Cécile Low-Kam, et al.
Neurology|January 24, 2016
Multiplex families with epilepsy: Success of clinical and molecular genetic characterizationZaid Afawi, Karen L Oliver, Sara Kivity, et al.
Heart Rhythm|June 15, 2017
Genome-wide association study of heart rate and its variability in Hispanic/Latino cohortsKathleen F Kerr, Christy L Avery, Henry J Lin, et al.
Bioinformatics (Oxford, England)|August 20, 2013
Imputation of coding variants in African Americans: better performance using data from the exome sequencing projectQing Duan, Eric Yi Liu, Paul L Auer, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 28, 2013
Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemiaNathan O Stitziel, Sigrid W Fouchier, Barbara Sjouke, et al.
Cell Reports|September 13, 2024
Key roles of C2/GAP domains in SYNGAP1-related pathophysiologyDanai Katsanevaki, Sally M Till, Ingrid Buller-Peralta, et al.
Circulation. Genomic and Precision Medicine|March 24, 2023
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine ProgramAmanda A Seyerle, Cecelia A Laurie, Brandon J Coombes, et al.
Human Molecular Genetics|October 11, 2019
Inherited variants at 3q13.33 and 3p24.1 are associated with risk of diffuse large B-cell lymphoma and implicate immune pathwaysGeffen Kleinstern, Huihuang Yan, Michelle A T Hildebrandt, et al.
Pageof 223