Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Two chromosome 9p21 haplotype blocks distinguish between coronary artery disease and myocardial infarction risk.

Circulation. Cardiovascular genetics - 1 Aug 2013

Fan Meng, Dandona Sonny, McPherson Ruth, Allayee Hooman, Hazen Stanley L, Wells George A, Roberts Robert, Stewart Alexandre F R

Abstract excerpt

BACKGROUND: Variants at the 9p21 locus associate with the risk of coronary artery disease (CAD) or myocardial infarction (MI). However, atherosclerotic plaque deposition is distinct from MI (plaque rupture and thrombosis), and recent studies showed no association between these variants and MI in patients with preexisting CAD. We performed haplotype analysis at the 9p21 locus to test whether haplotypes at distinct...

Topics

Join the communities discussing this publication.

Age Factors
Chromosomes, Human, Pair 9
Coronary Artery Disease
Genetic Loci
Haplotypes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Linkage Disequilibrium

Myocardial Infarction

Source

Open in PubMed Open full text

Identifiers

PMID: 23729007
DOI: 10.1161/CIRCGENETICS.113.000104
PMCID: PMC3839299

Genes

CAD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Two chromosome 9p21 haplotype blocks distinguish between coronary artery disease and myocardial infarction risk.PMID 23729007Read ↗

Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease.Semantic proximity Read ↗

Genetics of premature myocardial infarction.Semantic proximity Read ↗

The chromosome 9p21 region and myocardial infarction in a European population.Semantic proximity Read ↗

Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis.Semantic proximity Read ↗

Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease.Semantic proximity Read ↗

9p21 and the genetic revolution for coronary artery disease.Semantic proximity Read ↗

Genomics in coronary artery disease: past, present and future.Semantic proximity Read ↗

Haplotypes on 9p21 modify the risk for coronary artery disease among Indians.Semantic proximity Read ↗

Genetics of myocardial infarction: a progress reportSemantic proximity Read ↗

Progress in unraveling the genetics of coronary artery disease and myocardial infarction.Semantic proximity Read ↗

9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population.Semantic proximity Read ↗

Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.