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Paper Details

Association of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History.
JAMA Netw Open
61
2020
DNA variants, Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, Lynch Syndrome, Lynch syndrome, Participants, Pathogenic DNA variants, Rare Pathogenic DNA Variants, atherosclerotic cardiovascular disease, breast and ovarian cancer syndrome, breast or ovarian cancer, cancer, cancers, colorectal or uterine cancer, familial hypercholesterolemia, genomic conditions, hereditary breast and, hereditary breast and ovarian cancer syndrome, ovarian cancer syndrome, participants
Author NameAffiliation
Sami S AmrHarvard Medical School
Sami S Amr
Sami S AmrBrigham and Women's Hospital
Anthony A PhilippakisBroad Institute of MIT and Harvard
Anthony A PhilippakisBroad Institute of MIT and Harvard
Patrick T EllinorDivision of Cardiology and Center for Genomic Medicine, Massachusetts General Hospital
Patrick T EllinorHarvard Medical School
Patrick T EllinorBroad Institute of MIT and Harvard
Patrick T EllinorDivision of Cardiology and Center for Genomic Medicine, Massachusetts General Hospital
Patrick T EllinorBroad Institute of MIT and Harvard
Patrick T EllinorHarvard Medical School
Sekar KathiresanHarvard Medical School
Sekar Kathiresan
Kenney NgCenter for Computational Health
Matthew S LeboHarvard Medical School
Matthew S Lebo
Matthew S LeboBrigham and Women's Hospital
Amit KheraDivision of Cardiology and Center for Genomic Medicine, Massachusetts General Hospital
Amit KheraBroad Institute of MIT and Harvard
Amit KheraHarvard Medical School
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