Associated Papers
Association of PCSK9 Loss-of-Function Variants With Risk of Heart Failure.
Trudsø LC et al.
Jama Cardiology, 2023
Association of Common and Rare Genetic Variation in the 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Gene and Cataract Risk.
Ghouse J et al.
Journal of the American Heart Association, 2022
Population specific genetic heterogeneity of familial hypercholesterolemia in South Africa.
Smyth N et al.
Current Opinion in Lipidology, 2018
Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemia.
Rimbert A et al.
Atherosclerosis, 2016
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