Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

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Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23

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Sorting Out Cholesterol and Coronary Artery Disease

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Liver and Adipose Expression Associated SNPs Are Enriched for Association to Type 2 Diabetes

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Finding the missing heritability of complex diseases

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Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

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Global patterns of cis variation in human cells revealed by high-density allelic expression analysis

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New susceptibility locus for coronary artery disease on chromosome 3q22.3

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Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

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Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease

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Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study

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Common variants at 30 loci contribute to polygenic dyslipidemia

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Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease—A Mendelian Randomisation Study

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