Chromosome 9p21 genetic variation explains 13% of cardiovascular disease incidence but does not improve risk prediction
Author:
Affiliation:
1. Department of Internal Medicine; Skåne University Hospital Malmö; Malmö Sweden
2. Department of Clinical Sciences; Lund University; Malmö Sweden
Publisher
Wiley
Subject
Internal Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/joim.12063/fullpdf
Reference25 articles.
1. A common variant on chromosome 9p21 affects the risk of myocardial infarction;Helgadottir;Science,2007
2. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants;Kathiresan;Nat Genet,2009
3. A common allele on chromosome 9 associated with coronary heart disease;McPherson;Science,2007
4. Genome wide association analysis of coronary artery disease;Samani;N Engl J Med,2007
5. Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke;Gschwendtner;Ann Neurol,2009
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