11 – 20 of 40
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2014
-
Mark
Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
(
- Contribution to journal › Article
-
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
-
Mark
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
(
- Contribution to journal › Article
-
Mark
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins.
(
- Contribution to journal › Article
-
Mark
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
(
- Contribution to journal › Article
- 2013
-
Mark
2-Aminoadipic acid is a biomarker for diabetes risk
(
- Contribution to journal › Article
-
Mark
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes
(
- Contribution to journal › Article
-
Mark
Genetic Associations with Valvular Calcification and Aortic Stenosis
(
- Contribution to journal › Article
-
Mark
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
(
- Contribution to journal › Article
- 2012
-
Mark
Hypothesis-Based Analysis of Gene-Gene Interactions and Risk of Myocardial Infarction
(
- Contribution to journal › Article