Discover Community Create You

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

No association of chromosome 9p21.3 variation with clinical and angiographic outcomes after placement of drug-eluting stents.

JACC. Cardiovascular interventions - 1 Nov 2009

Hoppmann Petra, Erl Anna, Türk Serin, Tiroch Klaus, Mehilli Julinda, Schömig Albert, Kastrati Adnan, Koch Werner

Abstract excerpt

OBJECTIVES: After novel findings from genomewide association studies that sequence variation on chromosome 9p21.3 is a genetic factor for coronary heart disease, we investigated whether this locus influenced the clinical and angiographic outcomes after implantation of drug-eluting stents in coronary arteries. BACKGROUND: Recently, genomewide association studies have identified a locus on chromosome 9...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Angioplasty, Balloon, Coronary
Share to Cardiovascular Agents

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 9

Share to Coronary Angiography

Share to Coronary Restenosis

Share to Paclitaxel

Share to Sirolimus

Share to Thrombosis

Source

Identifiers

PMID: 19926059
DOI: 10.1016/j.jcin.2009.08.021

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

No association of chromosome 9p21.3 variation with clinical and angiographic outcomes after placement of drug-eluting stents.PMID 19926059Read ↗

Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarction.Semantic proximity Read ↗

The association of 9p21-3 locus with coronary atherosclerosis: a systematic review and meta-analysis.Semantic proximity Read ↗

Exploration of a hypothesized independent association of a common 9p21.3 gene variant and ischemic stroke in patients with and without angiographic coronary artery disease.Semantic proximity Read ↗

Evaluation of the association of genetic variants on the chromosomal loci 9p21.3, 6q25.1, and 2q36.3 with angiographically characterized coronary artery disease.Semantic proximity Read ↗

Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease.Semantic proximity Read ↗

Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.Semantic proximity Read ↗

Association between 1p13.3 genomic markers and coronary artery disease: a meta-analysis involving patients and controls.Semantic proximity Read ↗

Polymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarction.Semantic proximity Read ↗

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

Chromosome 9p21 polymorphism is associated with myocardial infarction but not with clinical outcome in Han Chinese.Semantic proximity Read ↗

Genetic risk of restenosis after percutaneous coronary interventions in the era of drug-eluting stents.Semantic proximity Read ↗

A common variant at chromosome 9P21.3 is associated with age of onset of coronary disease but not subsequent mortality.Semantic proximity Read ↗

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