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Cell Reports. Medicine|February 21, 2024
Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferationValeria Lo Faro, Arjun Bhattacharya, Wei Zhou, et al.
Science (New York, N.Y.)|May 5, 2007
A common variant on chromosome 9p21 affects the risk of myocardial infarctionAnna Helgadottir, Gudmar Thorleifsson, Andrei Manolescu, et al.
Scientific Reports|January 3, 2024
Clinical correlates of CT imaging-derived phenotypes among lean and overweight patients with hepatic steatosisIsabel Song, Elizabeth W Thompson, Anurag Verma, et al.
International Journal of Molecular Epidemiology and Genetics|September 15, 2011
Prospective study of insulin-like growth factor-I, insulin-like growth factor-binding protein 3, genetic variants in the IGF1 and IGFBP3 genes and risk of coronary artery diseaseSally L Ricketts, Katrijn L Rensing, Jeff M Holly, et al.
Cell Metabolism|August 11, 2016
Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and RodentsSumeet A Khetarpal, Katrine T Schjoldager, Christina Christoffersen, et al.
Circulation. Cardiovascular Genetics|February 10, 2012
A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complexRobert W Davies, George A Wells, Alexandre F R Stewart, et al.
Lancet (London, England)|January 18, 2011
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studiesMuredach P Reilly, Mingyao Li, Jing He, et al.
Science Translational Medicine|August 24, 2012
Niacin lipid efficacy is independent of both the niacin receptor GPR109A and free fatty acid suppressionBrett Lauring, Andrew K P Taggart, James R Tata, et al.
Atherosclerosis|October 29, 2017
Health disparities among adult patients with a phenotypic diagnosis of familial hypercholesterolemia in the CASCADE-FH™ patient registryStephen M Amrock, P Barton Duell, Thomas Knickelbine, et al.
Nature Genetics|April 8, 2025
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
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