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- 2023
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Mark
Genetic modification of inflammation- and clonal hematopoiesis-associated cardiovascular risk
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- Contribution to journal › Article
- 2022
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Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
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- Contribution to journal › Article
- 2017
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Mark
Exome-wide association study of plasma lipids in >300,000 individuals
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- Contribution to journal › Article
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Mark
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
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- Contribution to journal › Article
- 2016
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Mark
Association of Exome Sequences with Cardiovascular Traits among Blacks in the Jackson Heart Study
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- Contribution to journal › Article
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Mark
Genetic variants in CETP increase risk of intracerebral hemorrhage
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- Contribution to journal › Article
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Mark
Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease
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- Contribution to journal › Article
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Mark
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease
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- Contribution to journal › Article
- 2015
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Mark
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
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- Contribution to journal › Article
- 2014
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Mark
Multiple Associated Variants Increase the Heritability Explained for Plasma Lipids and Coronary Artery Disease.
(
- Contribution to journal › Article
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Mark
Meta-analysis of gene-level tests for rare variant association.
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- Contribution to journal › Article
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Mark
Association of Low-Density Lipoprotein Cholesterol-Related Genetic Variants With Aortic Valve Calcium and Incident Aortic Stenosis.
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- Contribution to journal › Article
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Mark
Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
(
- Contribution to journal › Article
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Mark
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
(
- Contribution to journal › Article
- 2013
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Mark
Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia.
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- Contribution to journal › Article
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Mark
Genetic Associations with Valvular Calcification and Aortic Stenosis
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- Contribution to journal › Article
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Mark
Discovery and refinement of loci associated with lipid levels
(
- Contribution to journal › Article
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Mark
Common variants associated with plasma triglycerides and risk for coronary artery disease
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- Contribution to journal › Article
- 2012
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Mark
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
(
- Contribution to journal › Article
- 2010
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Mark
Biological, clinical and population relevance of 95 loci for blood lipids
(
- Contribution to journal › Article
- 2009
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Mark
Common variants at 30 loci contribute to polygenic dyslipidemia
(
- Contribution to journal › Article
- 2007
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Mark
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study
(
- Contribution to journal › Article