CAD exome chip analysis

Publications

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators, et al.

N Engl J Med. 2016 Mar 24;374(12):1134-44. doi: 10.1056/NEJMoa1507652

 

Dataset phenotypes

  • myocardial infarction

Dataset subjects

Cases Controls Cohort Ancestry
2,833 5,912 British Heart Foundation Family Heart Study (BHF-FHS) European
704 1,729 Charles Bronfman Institute for Personalized Medicine (IPM) BioMe Biobank Mixed
660 515 Duke European
392 777 Estonian Genome Centre, University of Tartu (EGCUT) European
1,386 7,037 European Prospective Study into Cancer and Nutrition (EPIC) CAD European
2,473 2,047 First-time incidence of myocardial infarction in the AC county 3 (FIA3) European
1,568 2,772 Genetics of Diabetes Audit and Research in Tayside Scotland (GoDARTS) CAD European
4,464 2,886 German CAD North European
5,255 2,921 German CAD South European
1,428 1,069 Italian Atherosclerosis, Thrombosis, and Vascular Biology Study (ATVB) European
2,283 4,511 Malmo Diet and Cancer Study-Cardiovascular Cohort (MDC) European
3,990 6,585 Montreal Heart Institute Study (MHI) European
2,351 2,348 Nord-Trøndelag health study (HUNT) European
1,024 2,267 Ottawa Heart Study (OHS) European
2,490 2,220 Precocious Coronary Artery Disease Study (PROCARDIS) European
728 808 Premature Atherosclerosis Study at Academic Medical Center Amsterdam (PAS-AMC) European
683 156 University of Pennsylvania Catheterization Study (PennCath) European
4,587 16,556 Vanderbilt University Medical Center Biorepository (BioVU) European
176 164 Verona Heart Study (VHS) European
2,860 14,960 Women’s Health Initiative (WHI) European
Total: 42,335 cases | 78,240 controls  

Project

Myocardial Infarction Genetics Consortium
The Myocardial Infarction Genetics Consortium (MIGen) investigates the genetics of coronary artery disease and early-onset heart attack.

Experiment summary

CAD exome chip analysis is a study of 42,335 patients with coronary artery disease and 78,240 controls, from 20 individual studies. Samples were genotyped using the Illumina Human-Exome BeadChip array or the Illumina OmniExome array.

Dataset ID
ExChip_MICAD