Genetic Variation at the Phospholipid Transfer Protein Locus Affects Its Activity and High-Density Lipoprotein Size and Is a Novel Marker of Cardiovascular Disease Susceptibility

High-Density Lipoprotein Particle Size and Concentration and Coronary Risk

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Update on strategies to increase HDL quantity and function

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Variants in the coagulation factor 2 receptor (F2R) gene influence the risk of myocardial infarction in men through an interaction with interleukin 6 serum levels

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Elevation of systemic PLTP, but not macrophage-PLTP, impairs macrophage reverse cholesterol transport in transgenic mice

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Correlation between Genetic and Geographic Structure in Europe

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Common variants in mismatch repair genes and risk of colorectal cancer

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Time to rethink high-density lipoprotein?

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Association of Loss-of-Function Mutations in the ABCA1 Gene With High-Density Lipoprotein Cholesterol Levels and Risk of Ischemic Heart Disease

(2008) Ruth Frikke-Schmidt   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

PLTP activity is a risk factor for subsequent cardiovascular events in CAD patients under statin therapy: the AtheroGeneStudy

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Genetic variation in phospholipid transfer protein modulates lipoprotein profiles in hyperalphalipoproteinemia

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Genes mirror geography within Europe

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Common variants at 30 loci contribute to polygenic dyslipidemia

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Newly identified loci that influence lipid concentrations and risk of coronary artery disease

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Genome-Wide Analysis of Single Nucleotide Polymorphisms Uncovers Population Structure in Northern Europe

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Low phospholipid transfer protein (PLTP) is a risk factor for peripheral atherosclerosis

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