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Paper Details

Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results.
Circ Genom Precis Med
2
2023
CHD, FH, FH variant, FH-associated variant, FH-associated variants, Familial Hypercholesterolemia, actionable genes, cholesterol, coronary heart disease, familial hypercholesterolemia, hypercholesterolemia, low-density lipoprotein cholesterol, monogenic FH, participants, premature CHD
Author NameAffiliation
David C KochanMayo Clinic
Kenneth C AndersonVanderbilt University Medical Center
Kenneth C AndersonVanderbilt University Medical Center
Wendy K ChungColumbia University Irving Medical Center
Wendy K ChungColumbia University Irving Medical Center
Scott J HebbringCenter for Human Genetics, Marshfield Clinic
Richard R SharpBiomedical Ethics Research Program (R.R.S.), Mayo Clinic
Amy C SturmGenomic Medicine Institute
Richard A GibbsBaylor College of Medicine
Richard A GibbsBaylor College of Medicine
Eric VennerBaylor College of Medicine
Jodell E LinderVanderbilt University Medical Center
Josh F PetersonVanderbilt University Medical Center
Gail P JarvikUniversity of Washington Medical Center
Gail P JarvikUniversity of Washington Medical Center
Heidi L Rehm
Heidi L Rehm
Dan M RodenVanderbilt University Medical Center
Marc S WilliamsGenomic Medicine Institute
Teri A ManolioNational Human Genome Research Institute
Teri A ManolioNational Human Genome Research Institute
Iftikhar J KulloMayo Clinic
Iftikhar J KulloMayo Clinic
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Release 1.2