Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease.
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Reduced risk of recurrent myocardial infarction in homozygous carriers of the chromosome 9p21 rs1333049 C risk allele in the contemporary percutaneous coronary intervention era: a prospective observational studyIdentification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studiesTwo chromosome 9p21 haplotype blocks distinguish between coronary artery disease and myocardial infarction risk.Genetic variants at chromosome 9p21 and risk of first versus subsequent coronary heart disease events: a systematic review and meta-analysis.Genetics of coronary artery disease: an updateA variant at chromosome 9p21 is associated with recurrent myocardial infarction and cardiac death after acute coronary syndrome: the GRACE Genetics StudyThe association between variants on chromosome 9p21 and inflammatory biomarkers in ethnically diverse women with coronary heart disease: a pilot study.Polymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarctionThe effect of chromosome 9p21 variants on cardiovascular disease may be modified by dietary intake: evidence from a case/control and a prospective study.Joint effects of common genetic variants from multiple genes and pathways on the risk of premature coronary artery diseaseAdvances in the genetics of endometriosisHeterogeneity of the phenotypic definition of coronary artery disease and its impact on genetic association studies.Interaction of type 2 diabetes mellitus with chromosome 9p21 rs10757274 polymorphism on the risk of myocardial infarction: a case-control study in Chinese population.Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease.The relationship between polymorphisms on chromosome 9p21 and age of onset of coronary heart disease in black and white women.The 9p21 locus is associated with coronary artery disease and cardiovascular events in the presence (but not in the absence) of coronary calcificationGenome-wide association study of perioperative myocardial infarction after coronary artery bypass surgeryThe rs12526453 Polymorphism in an Intron of the PHACTR1 Gene and Its Association with 5-Year Mortality of Patients with Myocardial Infarction.Value of Chromosome 9p21 Polymorphism for Prediction of Cardiovascular Mortality in Han Chinese Without Coronary Lesions: An Observational StudyEffect of 9p21 genetic variation on coronary heart disease is not modified by other risk markers. The Atherosclerosis Risk in Communities (ARIC) StudyAssociation of a genetic risk score with prevalent and incident myocardial infarction in subjects undergoing coronary angiography.Genome-wide association studies in myocardial infarction and coronary artery disease.Two-marker association tests yield new disease associations for coronary artery disease and hypertensionAssociation between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis.Association of arterial stiffness with single nucleotide polymorphism rs1333049 and metabolic risk factors.9p21 locus rs10757278 is associated with advanced carotid atherosclerosis in a gender-specific manner.Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery diseaseGenetics of coronary artery disease: focus on genome-wide association studies.Predictive genetic testing for coronary artery disease.Variants in ANRIL gene correlated with its expression contribute to myocardial infarction risk.Genetic mechanisms mediating atherosclerosis susceptibility at the chromosome 9p21 locus.The role of genetic risk factors in coronary artery disease."Desert" gene (Chr9p21) variants as novel markers for coronary artery disease.Enhanced Megakaryopoiesis and Platelet Activity in Hypercholesterolemic, B6-Ldlr-/-, Cdkn2a-Deficient Mice.The 9p21 polymorphism is linked with atrial fibrillation during acute phase of ST-segment elevation myocardial infarction.An association between the endothelial nitric oxide synthase gene G894T polymorphism and premature coronary artery disease: a meta-analysis.Variant at 9p21 rs1333049 is associated with age of onset of coronary artery disease in a Western Indian population: a case control association study.
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P2860
Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on December 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Association of variation in th ...... ronic coronary artery disease.
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Association of variation in th ...... ronic coronary artery disease.
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type
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Association of variation in th ...... ronic coronary artery disease.
@en
Association of variation in th ...... ronic coronary artery disease.
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prefLabel
Association of variation in th ...... ronic coronary artery disease.
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Association of variation in th ...... ronic coronary artery disease.
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P2093
P2860
P1476
Association of variation in th ...... ronic coronary artery disease.
@en
P2093
Benjamin D Horne
Jeffrey L Anderson
John F Carlquist
Joseph B Muhlestein
Tami L Bair
P2860
P356
10.1161/CIRCGENETICS.108.793158
P577
2008-12-01T00:00:00Z