Polymorphisms on chromosome 9p21 confer a risk for acute coronary syndrome in a Chinese Han population.

[1]  D. Atar,et al.  ESC Guidelines for the Management of Acute Myocardial Infarction in Patients Presenting With ST-Segment Elevation , 2013 .

[2]  H. Heuer,et al.  Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry , 2011, BMC cardiovascular disorders.

[3]  Simon C. Potter,et al.  Association of the 9p21.3 Locus With Risk of First-Ever Myocardial Infarction in Pakistanis: Case-Control Study in South Asia and Updated Meta-Analysis of Europeans , 2010, Arteriosclerosis, thrombosis, and vascular biology.

[4]  F. Van de Werf,et al.  A variant at chromosome 9p21 is associated with recurrent myocardial infarction and cardiac death after acute coronary syndrome: the GRACE Genetics Study. , 2010, European heart journal.

[5]  Yu-yu Yao,et al.  A common variant on chromosome 9p21 affects the risk of early-onset coronary artery disease , 2009, Molecular Biology Reports.

[6]  Michael Weis,et al.  Management of acute myocardial infarction in patients presenting with persistent ST-segment elevation: the Task Force on the Management of ST-Segment Elevation Acute Myocardial Infarction of the European Society of Cardiology. , 2008, European heart journal.

[7]  Florian Kronenberg,et al.  Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study. , 2008, Journal of the American College of Cardiology.

[8]  A. Singleton,et al.  Whole Genome Analyses Suggest Ischemic Stroke and Heart Disease Share an Association With Polymorphisms on Chromosome 9p21 , 2008, Stroke.

[9]  Ludwig A Hothorn,et al.  Data Supplement (unedited) at: , 2007 .

[10]  Stefan Lorkowski,et al.  Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p. , 2008, Human molecular genetics.

[11]  S. Humphries,et al.  Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men. , 2008, Clinical chemistry.

[12]  J. Alpert,et al.  Joint ESC/ACCF/AHA/WHF Task Force for the Redefinition of Myocardial Infarction , 2008 .

[13]  Kristian Thygesen,et al.  Uniwersalna definicja zawału serca , 2008 .

[14]  Jeroen J. Bax,et al.  Universal definition of myocardial infarction. , 2007 .

[15]  C. Gieger,et al.  Genomewide association analysis of coronary artery disease. , 2007, The New England journal of medicine.

[16]  A. Gylfason,et al.  A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction , 2007, Science.

[17]  Simon C. Potter,et al.  Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.

[18]  Jonathan C. Cohen,et al.  A Common Allele on Chromosome 9 Associated with Coronary Heart Disease , 2007, Science.

[19]  [Guideline for diagnosis and treatment of patients with unstable angina and non-ST-segment elevation myocardial infarction]. , 2007, Zhonghua xin xue guan bing za zhi.

[20]  S. Lowe,et al.  Tumor suppression by Ink4a-Arf: progress and puzzles. , 2003, Current opinion in genetics & development.

[21]  C. Granger Genetics of coronary heart disease: current understanding and future prospects. , 2000, American heart journal.

[22]  M. Pericak-Vance,et al.  Genetic analysis for common complex disease. , 2000, American heart journal.

[23]  H. Koeffler,et al.  Role of the cyclin-dependent kinase inhibitors in the development of cancer. , 1995, Blood.

[24]  Gregory J. Hannon,et al.  pl5INK4B is a potentia| effector of TGF-β-induced cell cycle arrest , 1994, Nature.