1 – 80 of 80
- show: 100
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2021
-
Mark
Rare, Damaging DNA Variants in CORIN and Risk of Coronary Artery Disease : Insights From Functional Genomics and Large-Scale Sequencing Analyses
(
- Contribution to journal › Article
- 2020
-
Mark
Genome-Wide Polygenic Score, Clinical Risk Factors, and Long-Term Trajectories of Coronary Artery Disease
(
- Contribution to journal › Article
-
Mark
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
(
- Contribution to journal › Article
-
Mark
Genetically Elevated LDL Associates with Lower Risk of Intracerebral Hemorrhage
(
- Contribution to journal › Article
- 2019
-
Mark
Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery
(
- Contribution to journal › Article
- 2018
-
Mark
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
(
- Contribution to journal › Article
- 2017
-
Mark
Heritability of Atrial Fibrillation
(
- Contribution to journal › Article
-
Mark
Genetic Risk Prediction of Atrial Fibrillation
(
- Contribution to journal › Article
-
Mark
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
(
- Contribution to journal › Article
- 2016
-
Mark
Genetic risk, adherence to a healthy lifestyle, and coronary disease
(
- Contribution to journal › Article
-
Mark
Association of Exome Sequences with Cardiovascular Traits among Blacks in the Jackson Heart Study
(
- Contribution to journal › Article
-
Mark
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits
(
- Contribution to journal › Article
-
Mark
Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease
(
- Contribution to journal › Article
-
Mark
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease
(
- Contribution to journal › Article
-
Mark
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
(
- Contribution to journal › Article
-
Mark
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
(
- Contribution to journal › Article
- 2015
-
Mark
Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history.
2015) In European Heart Journal(
- Contribution to journal › Article
-
Mark
Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials.
(
- Contribution to journal › Article
-
Mark
Association of exome sequences with plasma C-reactive protein levels in >9000 participants.
(
- Contribution to journal › Article
-
Mark
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease
(
- Contribution to journal › Article
-
Mark
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis
(
- Contribution to journal › Article
-
Mark
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
(
- Contribution to journal › Article
-
Mark
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
(
- Contribution to journal › Article
-
Mark
Genetic studies of body mass index yield new insights for obesity biology.
(
- Contribution to journal › Article
- 2014
-
Mark
Multiple Associated Variants Increase the Heritability Explained for Plasma Lipids and Coronary Artery Disease.
(
- Contribution to journal › Article
-
Mark
Twelve-Single Nucleotide Polymorphism Genetic Risk Score Identifies Individuals at Increased Risk for Future Atrial Fibrillation and Stroke.
(
- Contribution to journal › Article
-
Mark
Meta-analysis of gene-level tests for rare variant association.
(
- Contribution to journal › Article
-
Mark
Association of Low-Density Lipoprotein Cholesterol-Related Genetic Variants With Aortic Valve Calcium and Incident Aortic Stenosis.
(
- Contribution to journal › Article
-
Mark
Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes.
(
- Contribution to journal › Article
-
Mark
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population.
(
- Contribution to journal › Article
-
Mark
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
(
- Contribution to journal › Article
-
Mark
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
(
- 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
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
(
- Contribution to journal › Article
- 2013
-
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
Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia.
(
- Contribution to journal › Article
-
Mark
Genetic Associations with Valvular Calcification and Aortic Stenosis
(
- Contribution to journal › Article
-
Mark
Large-scale association analysis identifies new risk loci for coronary artery disease
(
- Contribution to journal › Article
-
Mark
Discovery and refinement of loci associated with lipid levels
(
- Contribution to journal › Article
-
Mark
Common variants associated with plasma triglycerides and risk for coronary artery disease
(
- Contribution to journal › Article
-
Mark
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits
(
- Contribution to journal › Article
-
Mark
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
(
- Contribution to journal › Article
- 2012
-
Mark
Hypothesis-Based Analysis of Gene-Gene Interactions and Risk of Myocardial Infarction
(
- Contribution to journal › Article
-
Mark
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
(
- Contribution to journal › Article
-
Mark
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
(
- Contribution to journal › Article
-
Mark
FTO genotype is associated with phenotypic variability of body mass index
(
- Contribution to journal › Article
-
Mark
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci
(
- Contribution to journal › Article
- 2011
-
Mark
The mouse QTL map helps interpret human genome-wide association studies for HDL cholesterol
(
- Contribution to journal › Article
-
Mark
Testing for an Unusual Distribution of Rare Variants
(
- Contribution to journal › Article
-
Mark
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction
(
- Contribution to journal › Article
-
Mark
Power in the Phenotypic Extremes: A Simulation Study of Power in Discovery and Replication of Rare Variants
(
- Contribution to journal › Article
-
Mark
A Genome-Wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease
(
- Contribution to journal › Article
-
Mark
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
(
- Contribution to journal › Article
-
Mark
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
(
- Contribution to journal › Article
- 2010
-
Mark
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses
(
- Contribution to journal › Article
-
Mark
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
(
- Contribution to journal › Article
-
Mark
Genome-Wide Association Study of Blood Pressure Extremes Identifies Variant near UMOD Associated with Hypertension
(
- Contribution to journal › Article
-
Mark
Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies
(
- Contribution to journal › Article
-
Mark
Biological, clinical and population relevance of 95 loci for blood lipids
(
- Contribution to journal › Article
-
Mark
Hundreds of variants clustered in genomic loci and biological pathways affect human height
(
- Contribution to journal › Article
-
Mark
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
(
- Contribution to journal › Article
- 2009
-
Mark
Ion Mobility Analysis of Lipoprotein Subfractions Identifies 3 Independent Axes of Cardiovascular Risk
2009) Joint Nutrition, Physical Activity and Metabolism Conference/49th Cardiovascular Disease Epidemiology and Prevention, 2009 In Circulation 119(10). p.282-283(
- Contribution to journal › Published meeting abstract
-
Mark
Polymorphisms at newly identified lipid-associated loci are associated with blood lipids and cardiovascular disease in an Asian Malay population
(
- Contribution to journal › Article
-
Mark
Ion Mobility Analysis of Lipoprotein Subfractions Identifies Three Independent Axes of Cardiovascular Risk.
(
- Contribution to journal › Article
-
Mark
Association between glucokinase regulatory protein (GCKR) and apolipoprotein A5 (APOA5) gene polymorphisms and triacylglycerol concentrations in fasting, postprandial, and fenofibrate-treated states
(
- Contribution to journal › Article
-
Mark
Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure
(
- Contribution to journal › Article
-
Mark
New susceptibility locus for coronary artery disease on chromosome 3q22.3
(
- Contribution to journal › Article
-
Mark
Common variants at 30 loci contribute to polygenic dyslipidemia
(
- Contribution to journal › Article
-
Mark
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies eight loci associated with blood pressure
(
- Contribution to journal › Article
- 2008
-
Mark
Defining the spectrum of alleles that contribute to blood lipid concentrations in humans
(
- Contribution to journal › Scientific review
-
Mark
Cholesterol gene polymorphisms and cardiovascular events - Reply
(
- Contribution to journal › Letter
-
Mark
Using the mouse model to confirm genes identified by genomewide association studies for the complex trait HDL cholesterol
2008) Arteriosclerosis, Thrombosis, and Vascular Biology Annual Conference 2008Back In Arteriosclerosis, Thrombosis, and Vascular Biology 28(6). p.36-36(
- Contribution to journal › Published meeting abstract
-
Mark
Polymorphism associated with cholesterol and risk of cardiovascular events
(
- Contribution to journal › Article
-
Mark
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
(
- Contribution to journal › Article
-
Mark
Common Missense Variant in the Glucokinase Regulatory Protein Gene Is Associated With Increased Plasma Triglyceride and C-Reactive Protein but Lower Fasting Glucose Concentrations
(
- Contribution to journal › Article
- 2007
-
Mark
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study
(
- Contribution to journal › Article
-
Mark
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
(
- Contribution to journal › Article