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Paper Details

Rare, Damaging DNA Variants in and Risk of Coronary Artery Disease: Insights From Functional Genomics and Large-Scale Sequencing Analyses.
Circulation. Genomic and precision medicine
8
2021
CAD, CAD-21, CORIN, CORIN variants, Corin, Coronary Artery Disease, LOF, LOF variants, cardiomyocytes, coronary artery disease, missense mutations, participants, proatrial natriuretic peptide, rare, rare missense variants
Author NameAffiliation
Hong-Hee WonSamsung Advanced Institute for Health Sciences and Technology (SAIHST), Sungkyunkwan University, Samsung Medical Center
Olle MelanderLund University
Olle MelanderSkane University Hospital
Daniel J RaderCardiovascular Institute, Perelman School of Medicine, University of Pennsylvania
Pradeep NatarajanBroad Institute of MIT and Harvard
Pradeep NatarajanBroad Institute of MIT and Harvard
Pradeep NatarajanCenter for Genomic Medicine (M.W., Massachusetts General Hospital
Pradeep NatarajanMassachusetts General Hospital
Sekar KathiresanCenter for Genomic Medicine (M.W., Massachusetts General Hospital
Sekar KathiresanMassachusetts General Hospital
Sekar Kathiresan
Virendar K KaushikBroad Institute of MIT and Harvard
Amit KheraBroad Institute of MIT and Harvard
Amit KheraCenter for Genomic Medicine (M.W., Massachusetts General Hospital
Amit KheraMassachusetts General Hospital
Rajat M GuptaBroad Institute of MIT and Harvard
Rajat M GuptaBroad Institute of MIT and Harvard
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