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Herrington, David
One or more keywords matched the following items that are connected to
Herrington, David
Item Type
Name
Academic Article
Effect of genetic variations in platelet glycoproteins Ibalpha and VI on the risk for coronary heart disease events in postmenopausal women taking hormone therapy.
Academic Article
Relationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart Study.
Academic Article
Association of scavenger receptor class B type I polymorphisms with subclinical atherosclerosis: the Multi-Ethnic Study of Atherosclerosis.
Academic Article
Common variants in the periostin gene influence development of atherosclerosis in young persons.
Academic Article
Genetic analysis of the soluble epoxide hydrolase gene, EPHX2, in subclinical cardiovascular disease in the Diabetes Heart Study.
Academic Article
Association of arachidonate 12-lipoxygenase genotype variation and glycemic control with albuminuria in type 2 diabetes.
Academic Article
An algorithm for learning maximum entropy probability models of disease risk that efficiently searches and sparingly encodes multilocus genomic interactions.
Concept
Genetic Predisposition to Disease
Academic Article
Dietary macronutrients, genetic variation, and progression of coronary atherosclerosis among women.
Academic Article
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Academic Article
Association of the Lipoprotein Receptor SCARB1 Common Missense Variant rs4238001 with Incident Coronary Heart Disease.
Academic Article
Susceptibility Loci for Clinical Coronary Artery Disease and Subclinical Coronary Atherosclerosis Throughout the Life-Course.
Academic Article
Associations between a Genetic Risk Score for Clinical CAD and Early Stage Lesions in the Coronary Artery and the Aorta.
Academic Article
Asymmetric independence modeling identifies novel gene-environment interactions.
Academic Article
Lp-PLA2, scavenger receptor class B type I gene (SCARB1) rs10846744 variant, and cardiovascular disease.
Search Criteria
Genetic Predisposition to Disease