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A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
Effect of the PPARG2 Pro12Ala Polymorphism on Associations of Physical Activity and Sedentary Time with Markers of Insulin Sensitivity in Those with an Elevated Risk of Type 2 Diabetes
Apolipoprotein C-lll gene variation and dyslipidaemia
The UK10K project identifies rare variants in health and disease
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9
Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk
Plasma urate concentration and risk of coronary heart disease: a Mendelian randomisation analysis
