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JAMA Network Open|May 8, 2023
Perspectives of Rare Disease Experts on Newborn Genome SequencingNina B Gold, Sophia M Adelson, Nidhi Shah, et al.
European Journal of Human Genetics : EJHG|July 4, 2024
Burden re-analysis of neurodevelopmental disorder cohorts for prioritization of candidate genesNoor Smal, Fatma Majdoub, Katrien Janssens, et al.
The New England Journal of Medicine|October 15, 2010
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemiaKiran Musunuru, James P Pirruccello, Ron Do, et al.
Cell Stem Cell|April 8, 2017
Induced Pluripotent Stem Cell Differentiation Enables Functional Validation of GWAS Variants in Metabolic DiseaseCurtis R Warren, John F O'Sullivan, Max Friesen, et al.
Journal of the American College of Cardiology|April 8, 2017
ANGPTL3 Deficiency and Protection Against Coronary Artery DiseaseNathan O Stitziel, Amit V Khera, Xiao Wang, et al.
Cell Stem Cell|December 19, 2012
A TALEN genome-editing system for generating human stem cell-based disease modelsQiurong Ding, Youn-Kyoung Lee, Esperance A K Schaefer, et al.
Plos One|May 26, 2012
Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe projectKiran Musunuru, Simon P R Romaine, Guillaume Lettre, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 16, 2025
Systemic delivery of biotherapeutic RNA to the myocardium transiently modulates cardiac contractility in vivoVladimir V Shuvaev, Ying K Tam, Benjamin W Lee, et al.
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