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One or more keywords matched the following items that are connected to Herrington, David
Item TypeName
Academic Article Pharmacogenomics--10 years of progress: a cardiovascular perspective.
Academic Article Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.
Academic Article Associations between NOS1AP single nucleotide polymorphisms (SNPs) and QT interval duration in four racial/ethnic groups in the Multi-Ethnic Study of Atherosclerosis (MESA).
Academic Article An algorithm for learning maximum entropy probability models of disease risk that efficiently searches and sparingly encodes multilocus genomic interactions.
Academic Article Review of the Diabetes Heart Study (DHS) family of studies: a comprehensively examined sample for genetic and epidemiological studies of type 2 diabetes and its complications.
Academic Article Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium.
Academic Article Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.
Concept Genome-Wide Association Study
Academic Article Methylomics of gene expression in human monocytes.
Academic Article Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins.
Grant Machine Learning to Identify Complex Interactions in Genome-Wide Association Data
Grant Metabolomic Signatures of CAD Associated Genotypes
Grant SNPs and Extent of Atherosclerosis (SEA) Study
Academic Article Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons.
Academic Article Transcriptome-Wide Analysis Identifies Novel Associations With Blood Pressure.
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
  • Genome Wide Association Study