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- 2022
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Mark
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis
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- Contribution to journal › Article
- 2021
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Mark
The power of genetic diversity in genome-wide association studies of lipids
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- Contribution to journal › Article
- 2019
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Mark
Effects of the coronary artery disease associated LPA and 9p21 loci on risk of aortic valve stenosis
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- Contribution to journal › Article
- 2018
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Mark
Genome-wide analysis yields new loci associating with aortic valve stenosis
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- Contribution to journal › Article
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Mark
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
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- Contribution to journal › Article
- 2017
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Mark
Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk
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- Contribution to journal › Article
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Mark
A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors
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- Contribution to journal › Article
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Mark
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 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
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
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
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- Contribution to journal › Article
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Mark
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk.
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- Contribution to journal › Article
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Mark
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
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- Contribution to journal › Article
- 2015
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Mark
New genetic loci link adipose and insulin biology to body fat distribution.
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- Contribution to journal › Article
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Mark
Genetic studies of body mass index yield new insights for obesity biology.
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- Contribution to journal › Article
- 2014
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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
Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
(
- Contribution to journal › Article
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Mark
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
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- Contribution to journal › Article
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Mark
Defining the role of common variation in the genomic and biological architecture of adult human height.
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- Contribution to journal › Article
- 2013
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Mark
Large-scale association analysis identifies new risk loci for coronary artery disease
(
- Contribution to journal › Article