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Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry

By Thomas Scheffold, Silke Kullmann, Andreas Huge, Priska Binner, Hermann R Ochs, Wolfgang Schöls, Joachim Thale, Wolfgang Motz, Franz Josef Hegge, Christoph Stellbrink, Thomas Dorsel, Hartmut Gülker, Hubertus Heuer, Wilfried Dinh, Monika Stoll and Georg Haltern
Topics: Research Article
Publisher: BioMed Central
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Provided by: PubMed Central

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  1. (2007). A common allele on chromosome 9 associated with coronary heart disease. Science
  2. (2009). A common variant on chromosome 9p21 affects the risk of early-onset coronary artery disease. Mol Biol Rep
  3. (2007). al: A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science
  4. al: Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. BMC Med Genet 2007, 8(Suppl 1):S5.
  5. (2007). al: Genomewide association analysis of coronary artery disease.
  6. (2005). Daly MJ: Genome-wide association studies for common diseases and complex traits. Nat Rev Genet
  7. (1989). Diabetes mellitus and hypertension in the elderly: concomitant hyperlipidemia and coronary heart disease risk.
  8. (2008). et al: Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.
  9. (2004). et al: Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study. Lancet
  10. (2010). et al: Gene dosage of the common variant 9p21 predicts severity of coronary artery disease.
  11. (2009). et al: Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet
  12. (2008). et al: Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease. Circulation
  13. (2008). et al: Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations.
  14. (2008). et al: Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multiethnic ADVANCE study. Hum Mol Genet
  15. (2008). et al: The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet
  16. (2007). Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature
  17. (2008). Humphries SE: Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men. Clin Chem
  18. (2008). Identifying the susceptibility genes for coronary artery disease: from hyperbole through doubt to cautious optimism.
  19. (1976). Menopause and risk of cardiovascular disease: the Framingham study. Ann Intern Med
  20. (2008). Meschia JF: Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21. Stroke
  21. (2008). QK: Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest). Ann Hum Genet
  22. (2008). Risk factors for myocardial infarction in women and men: insights from the INTERHEART study. Eur Heart J
  23. (1998). WB: Prediction of coronary heart disease using risk factor categories. Circulation