1 – 40 of 40
- show: 100
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2021
-
Mark
Plasma Protein Profile of Carotid Artery Atherosclerosis and Atherosclerotic Outcomes : Meta-Analyses and Mendelian Randomization Analyses
(
- Contribution to journal › Article
- 2020
-
Mark
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
(
- Contribution to journal › Article
-
Mark
Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids with Aortic Stenosis
(
- Contribution to journal › Article
- 2018
-
Mark
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes
2018) In Nature Communications(
- Contribution to journal › Article
- 2016
-
Mark
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease
(
- 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
Distinct metabolomic signatures are associated with longevity in humans.
(
- Contribution to journal › Article
-
Mark
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease
(
- Contribution to journal › Article
-
Mark
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
(
- Contribution to journal › Article
- 2014
-
Mark
Association of Low-Density Lipoprotein Cholesterol-Related Genetic Variants With Aortic Valve Calcium and Incident Aortic Stenosis.
(
- 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
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
-
Mark
Metabolite Profiling Identifies Pathways Associated With Metabolic Risk in Humans
(
- Contribution to journal › Article
-
Mark
Identification of the BCAR1-CFDP1-TMEM170A Locus as a Determinant of Carotid Intima-Media Thickness and Coronary Artery Disease Risk
(
- Contribution to journal › Article
-
Mark
Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies
(
- Contribution to journal › Article
-
Mark
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
(
- Contribution to journal › Article
- 2011
-
Mark
Post-Genomic Update on a Classical Candidate Gene for Coronary Artery Disease: ESR1
(
- Contribution to journal › Article
-
Mark
Metabolite profiles and the risk of developing diabetes
(
- 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
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
(
- Contribution to journal › Article
-
Mark
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
(
- Contribution to journal › Article
- 2010
-
Mark
Genome-wide meta-analyses identify multiple loci associated with smoking behavior
(
- 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
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
- 2007
-
Mark
The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts
(
- Contribution to journal › Article