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Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants. Nat Genet 2009;41: 334-341.
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Our Publications
Polymorphisms associated with cholesterol and risk of cardiovascular events
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Exome sequencing, mutations in ANGPTL3, and familial combined hypolipidemia
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Biological, clinical, and population relevance of 95 loci for blood lipids
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Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
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Common variants associated with plasma triglycerides and risk for coronary artery disease
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Loss-of-function mutations in APOC3, Triglycerides, and Coronary Disease
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Inactivating mutations in NPC1L1 and protection from coronary heart disease
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Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia
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Our Publications
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigator
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