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Paper Details

Genomic analyses implicate noncoding de novo variants in congenital heart disease.
Nat Genet
82
2020
CHD, DNV, DNVs, RNA-binding-protein regulatory sites, coding de novo variants, congenital heart disease, enhancers, genome sequences, noncoding DNVs, patients, regulatory noncoding DNVs
Author NameAffiliation
Sarah U MortonHarvard Medical School
Sarah U MortonBoston Children's Hospital
Kathleen M ChenFlatiron Institute, Simons Foundation
Steven R DePalmaHarvard Medical School
Michael ParfenovHarvard Medical School
Michael ParfenovHarvard Medical School
Andrew FarrellUtah Center for Genetic Discovery, University of Utah School of Medicine
Eric E SchadtIcahn School of Medicine at Mount Sinai
Eric E SchadtIcahn Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai
Eric E Schadt
Eric E SchadtIcahn School of Medicine at Mount Sinai
Eric E Schadt
Eric E SchadtIcahn Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai
Jane W NewburgerBoston Children's Hospital
Jane W NewburgerBoston Children's Hospital
Alessandro GiardiniGreat Ormond Street Hospital
Elizabeth GoldmuntzChildren's Hospital of Philadelphia
Elizabeth GoldmuntzThe Perelman School of Medicine, University of Pennsylvania
Martina BruecknerYale University School of Medicine
Richard KimChildren's Hospital Los Angeles
George A PorterUniversity of Rochester
Daniel BernsteinStanford University
Wendy K ChungColumbia University Medical Center
Wendy K ChungColumbia University Medical Center
Deepak SrivastavaGladstone Institute of Cardiovascular Disease and University of California San Francisco
Deepak SrivastavaGladstone Institute of Cardiovascular Disease and University of California San Francisco
Martin Tristani-FirouziUniversity of Utah School of Medicine
Olga G TroyanskayaFlatiron Institute, Simons Foundation
Olga G TroyanskayaPrinceton University
Olga G TroyanskayaLewis-Sigler Institute for Integrative Genomics, Princeton University
Olga G TroyanskayaFlatiron Institute, Simons Foundation
Olga G TroyanskayaLewis-Sigler Institute for Integrative Genomics, Princeton University
Olga G TroyanskayaPrinceton University
Diane E Dickel
Yufeng ShenColumbia University
Jonathan G SeidmanHarvard Medical School
Jonathan G SeidmanHarvard Medical School
Christine E SeidmanHarvard Medical School
Christine E SeidmanBrigham and Women's Hospital
Christine E SeidmanHarvard Medical School
Christine E SeidmanBrigham and Women's Hospital
Bruce D GelbIcahn School of Medicine at Mount Sinai
Bruce D GelbMindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai
Bruce D GelbIcahn School of Medicine at Mount Sinai
Bruce D GelbIcahn School of Medicine at Mount Sinai
Bruce D GelbMindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai
Bruce D GelbIcahn School of Medicine at Mount Sinai
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