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Paper Details

Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease risk.
Am J Hum Genet
4
2022
Asian haplogroups, CHD, MtDNAcns, RNA, blood, cardiac, cardiac defects, cardiac disease, cardiac mitochondrial DNA, cardiovascular tissue samples, child, congenital heart disease, heteroplasmic variants, mitochondrial DNA, mitochondrial RNA, mitochondrial cardiomyopathy, mtDNA, mtDNAcns, nuclear genome, people, variant allele
Author NameAffiliation
Sarah U MortonHarvard Medical School, Boston Children's Hospital
Steven R DePalmaHarvard Medical School
Daniel BernsteinStanford University
Martina BruecknerYale University School of Medicine
Wendy K ChungColumbia University Medical Center
Wendy K ChungColumbia University Medical Center
Alessandro GiardiniGreat Ormond Street Hospital
Elizabeth GoldmuntzThe Perelman School of Medicine, University of Pennsylvania
Richard KimChildren's Hospital Los Angeles
Jane W NewburgerBoston Children's Hospital
Jane W NewburgerBoston Children's Hospital
Yufeng ShenColumbia University Medical Center
Deepak SrivastavaGladstone Institute of Cardiovascular Disease
Deepak SrivastavaGladstone Institute of Cardiovascular Disease
Martin Tristani-FirouziNora Eccles Harrison Cardiovascular Research and Training Institute, University of Utah
George A PorterUniversity of Rochester Medical Center
Jonathan G SeidmanHarvard Medical School
Jonathan G SeidmanHarvard Medical School
Christine E SeidmanHarvard Medical School, Brigham and Women's Hospital, USA Howard Hughes Medical Institute, Harvard University
Christine E SeidmanHarvard Medical School, Brigham and Women's Hospital, USA Howard Hughes Medical Institute, Harvard University
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Datasets

Release 1.2