Coronary Heart Disease
[PMID 4021556] Analysis of common and coding variants with cardiovascular disease in the diabetes heart study.
[PMID 3584137] Improvement in Prediction of Coronary Heart Disease Risk over Conventional Risk Factors Using SNPs Identified in Genome-Wide Association Studies.
[PMID 3583714] Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study
[PMID 3266236
] Genetic Profiling Using Genome-Wide Significant Coronary Artery Disease Risk Variants Does Not Improve the Prediction of Subclinical Atherosclerosis: The Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey – A Meta-Analysis of Three Independent Studies
[PMID 3179381] Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.
[PMID 3178591] Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease.
[PMID 24573017] Associations between the CDKN2A/B, ADTRP and PDGFD Polymorphisms and the Development of Coronary Atherosclerosis in Japanese Patients.
[PMID 23202125] Large-scale association analysis identifies new risk loci for coronary artery disease.
| GWAS snp
|
| PMID
|
[PMID 24262325]
|
| Trait
|
Coronary artery disease
|
| Title
|
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
|
| Risk Allele
|
G
|
| P-val
|
2E-6
|
| Odds Ratio
|
1.08 [1.05-1.12]
|
| GWAS snp
|
| PMID
|
[PMID 21378990]
|
| Trait
|
Coronary heart disease
|
| Title
|
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
|
| Risk Allele
|
G
|
| P-val
|
4E-9
|
| Odds Ratio
|
1.0700 [1.05-1.09]
|
] Genetic Profiling Using Genome-Wide Significant Coronary Artery Disease Risk Variants Does Not Improve the Prediction of Subclinical Atherosclerosis: The Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey – A Meta-Analysis of Three Independent Studies
