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

Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction.

Circulation - 27 Nov 2001

Topol E J, McCarthy J, Gabriel S, Moliterno D J, Rogers W J, Newby L K, Freedman M, Metivier J, Cannata R, O'Donnell C J, Kottke-Marchant K, Murugesan G, Plow E F, Stenina O, Daley G Q

Abstract excerpt

BACKGROUND: Recent advances in high-throughput genomics technology have expanded our ability to catalogue allelic variants in large sets of candidate genes related to premature coronary artery disease. METHODS AND RESULTS: A total of 398 families were identified in 15 participating medical centers; they fulfilled the criteria of myocardial infarction, revascularization, or a significant coronary artery lesion...

Read the complete abstract on PubMed

Topics

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

Share to Coronary Angiography
Share to Coronary Artery Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Coronary Stenosis

Share to Demography

Share to Myocardial Infarction

Share to Oxidoreductases Acting on CH-NH Group Donors

Share to Thrombospondin 1

Share to Thrombospondins

Source

Identifiers

PMID: 11723011
DOI: 10.1161/hc4701.100910

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction.PMID 11723011Read ↗

Coronary artery disease and the thrombospondin single nucleotide polymorphisms.Semantic proximity Read ↗

Thrombospondin-2 polymorphism is associated with a reduced risk of premature myocardial infarction.Semantic proximity Read ↗

Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes.Semantic proximity Read ↗

Genetics of premature myocardial infarction.Semantic proximity Read ↗

Genomics of premature atherosclerotic vascular disease.Semantic proximity Read ↗

Identification of 187 single nucleotide polymorphisms (SNPs) among 41 candidate genes for ischemic heart disease in the Japanese population.Semantic proximity Read ↗

Association between single nucleotide polymorphisms in thrombospondins genes and coronary artery disease: A meta-analysis.Semantic proximity Read ↗

Polymorphisms in thrombospondin genes and myocardial infarction: a case-control study and a meta-analysis of available evidence.Semantic proximity Read ↗

An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.Semantic proximity Read ↗

Genetic variants in SUSD2 are associated with the risk of ischemic heart disease.Semantic proximity Read ↗

Decreased frequency of the 3'UTR T>G single nucleotide polymorphism of thrombospondin-2 gene in sudden death due to plaque erosion.Semantic proximity Read ↗

Thrombospondins, their polymorphisms, and cardiovascular disease.Semantic proximity Read ↗

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