Our Publications

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. Read more
#Our Publications

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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Polymorphisms associated with cholesterol and risk of cardiovascular events Read more
#Our Publications

Polymorphisms associated with cholesterol and risk of cardiovascular events

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Exome sequencing, mutations in ANGPTL3, and familial combined hypolipidemia Read more
#Our Publications

Exome sequencing, mutations in ANGPTL3, and familial combined hypolipidemia

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Biological, clinical, and population relevance of 95 loci for blood lipids Read more
#Our Publications

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 Read more
#Our Publications

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 Read more
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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 Read more
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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 Read more
#Our Publications

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 Read more
#Our Publications

Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia

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Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigator Read more
#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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