Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.

Associations of the APOC3 rs5128 polymorphism with plasma APOC3 and lipid levels: a meta-analysis.

A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates.

An APOC3 3'UTR variant associated with plasma triglycerides levels and coronary heart disease by creating a functional miR-4271 binding site.

TREM2 rare variant p.R47H is not associated with Parkinson's disease.

Change in LDL particle size is associated with change in plasma triglyceride concentration.

A rare sequence variant in intron 1 of THAP1 is associated with primary dystonia.

P-selectin Plasma Levels and Genetic Variant Associated With Diabetic Retinopathy in African Americans.

A rare variant at 11p13 is associated with tuberculosis susceptibility in the Han Chinese population.

$A common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults.$
A common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults.

Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests.

Decreased levels of BAG3 in a family with a rare variant and in idiopathic dilated cardiomyopathy.

Inactivation of ANGPTL3 reduces hepatic VLDL-triglyceride secretion.

Zinc Finger 259 Gene Polymorphism rs964184 is Associated with Serum Triglyceride Levels and Metabolic Syndrome.

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.

Triglyceride Rich Lipoprotein -LPL-VLDL Receptor and Lp(a)-VLDL Receptor Pathways for Macrophage Foam Cell Formation.

Erratum to: The PNPLA3 Ile148Met interacts with overweight and dietary intakes on fasting triglyceride levels.

A functional polymorphism affecting the APOA5 gene expression is causally associated with plasma triglyceride levels conferring coronary atherosclerosis risk in Han Chinese Population.

Homocysteine is associated with plasma high-sensitivity cardiac troponin T levels in a community-dwelling population.

Hyperhomocysteinaemia is associated with low plasma apolipoprotein AI levels in patients with impaired glucose tolerance.

Elevated serum triglyceride and retinol-binding protein 4 levels associated with fructose-sweetened beverages in adolescents.

Long-term effects of bezafibrate on in vivo VLDL-triglyceride production in the rat.

Plasma HDL cholesterol in epileptics with elevated triglyceride and cholesterol.

A whole-grain cereal-based diet lowers postprandial plasma insulin and triglyceride levels in individuals with metabolic syndrome.

A causal network analysis in an observational study identifies metabolomics pathways influencing plasma triglyceride levels.

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Associations of the APOC3 rs5128 polymorphism with plasma APOC3 and lipid levels: a meta-analysis.

A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates.

An APOC3 3'UTR variant associated with plasma triglycerides levels and coronary heart disease by creating a functional miR-4271 binding site.

TREM2 rare variant p.R47H is not associated with Parkinson's disease.

Change in LDL particle size is associated with change in plasma triglyceride concentration.

A rare sequence variant in intron 1 of THAP1 is associated with primary dystonia.

P-selectin Plasma Levels and Genetic Variant Associated With Diabetic Retinopathy in African Americans.

A rare variant at 11p13 is associated with tuberculosis susceptibility in the Han Chinese population.

A common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults.

Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests.

Decreased levels of BAG3 in a family with a rare variant and in idiopathic dilated cardiomyopathy.

Inactivation of ANGPTL3 reduces hepatic VLDL-triglyceride secretion.

Zinc Finger 259 Gene Polymorphism rs964184 is Associated with Serum Triglyceride Levels and Metabolic Syndrome.

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.

Triglyceride Rich Lipoprotein -LPL-VLDL Receptor and Lp(a)-VLDL Receptor Pathways for Macrophage Foam Cell Formation.

Erratum to: The PNPLA3 Ile148Met interacts with overweight and dietary intakes on fasting triglyceride levels.

A functional polymorphism affecting the APOA5 gene expression is causally associated with plasma triglyceride levels conferring coronary atherosclerosis risk in Han Chinese Population.

Homocysteine is associated with plasma high-sensitivity cardiac troponin T levels in a community-dwelling population.

Hyperhomocysteinaemia is associated with low plasma apolipoprotein AI levels in patients with impaired glucose tolerance.

Elevated serum triglyceride and retinol-binding protein 4 levels associated with fructose-sweetened beverages in adolescents.

Long-term effects of bezafibrate on in vivo VLDL-triglyceride production in the rat.

Plasma HDL cholesterol in epileptics with elevated triglyceride and cholesterol.

A whole-grain cereal-based diet lowers postprandial plasma insulin and triglyceride levels in individuals with metabolic syndrome.

A causal network analysis in an observational study identifies metabolomics pathways influencing plasma triglyceride levels.

Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.

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