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Works
11
Genetic implication of a novel thiamine transporter in human hypertension
Adrenergic polymorphism and the human stress response
Catecholamine release-inhibitory peptide catestatin (chromogranin A(352-372)): naturally occurring amino acid variant Gly364Ser causes profound changes in human autonomic activity and alters risk for hypertension
Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study
Genetic risks and clinical rewards
Cancer Diagnosis, Polygenic Risk, and Longevity-Associated Variants
All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs
The VA Hypertension Primary Care Longitudinal Cohort: Electronic medical records in the post-genomic era.
A comprehensive literature review of haplotyping software and methods for use with unrelated individuals
Powerful designs for genetic association studies that consider twins and sibling pairs with discordant genotypes.