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CARDIoGRAMplusC4D Consortium

Publications

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.

Effect of Bile Acid Sequestrants on the Risk of Cardiovascular Events: A Mendelian Randomization Analysis.

Genetically determined height and coronary artery disease.

Common variants associated with plasma triglycerides and risk for coronary artery disease.

Multiethnic meta-analysis of genome-wide association studies in 100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.

Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.

The shared allelic architecture of adiponectin levels and coronary artery disease.

A systems biology framework identifies molecular underpinnings of coronary heart disease.

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.

Overlap between common genetic polymorphisms underpinning kidney traits and cardiovascular disease phenotypes: the CKDGen consortium.

Genetic predisposition to higher blood pressure increases coronary artery disease risk.

Loci influencing blood pressure identified using a cardiovascular gene-centric array.

Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.

 

Large-scale association analysis identifies new risk loci for coronary artery disease.

Genetic variants from lipid-related pathways and risk for incident myocardial infarction.

Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation.

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study.

Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.

A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.

Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.

TGFB1 genetic polymorphisms and coronary heart disease risk: a meta-analysis.

Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.

Blood pressure loci identified with a gene-centric array.

Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1.

Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.

Human metabolic individuality in biomedical and pharmaceutical research.

Large-scale gene-centric analysis identifies novel variants for coronary artery disease.

A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease.

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

Genetic variants influencing circulating lipid levels and risk of coronary artery disease.

Biological, clinical and population relevance of 95 loci for blood lipids.

Involvement of two protein factors and ATP in in vitro DNA synthesis catalyzed by DNA polymerase 3 of Escherichia coli.

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.

No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis.

Loss of Cardio-Protective Effects at the ADAMTS7 Locus Due to Gene-Smoking Interactions.

Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits.

Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease.

Identifying systematic heterogeneity patterns in genetic association meta-analysis studies.

Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.

Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease.

Association analyses based on false discovery rate implicate new loci for coronary artery disease.

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