{"id":"W2054153086","doi":"10.1038/ng.327","title":"Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1096,"is_retracted":false,"has_abstract":false,"ca_institutions":"McGill University; Population Health Research Institute; McMaster University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources; National Institute of Environmental Health Sciences; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; Economic and Social Research Council; British Heart Foundation; Wellcome Trust","keywords":"Single-nucleotide polymorphism; Biology; Genetics; Copy-number variation; Locus (genetics); Genome-wide association study; Allele; Myocardial infarction; Genome; Gene; Genotype; Medicine; Internal medicine","routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":null,"machine_scores":{"provisional":true,"baseline":true,"maturity_gate_passed":false,"score_opus":0.003726246391652467,"score_gpt":0.2031098602042561,"score_spread":0.1993836138126037,"validation_status":"score_only:v0-immature-baseline","note":"Baseline scores from an immature model (maturity gate not passed). Scores rank; they never assert a category."}}