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Article

Genetic variants at chromosome 9p21 and risk of first versus subsequent coronary heart disease events: a systematic review and meta-analysis.

Journal of the American College of Cardiology - 3 Jun 2014

Patel Riyaz S, Asselbergs Folkert W, Quyyumi Arshed A, Palmer Tom M, Finan Chris I, Tragante Vinicius, Deanfield John, Hemingway Harry, Hingorani Aroon D, Holmes Michael V

Abstract excerpt

OBJECTIVES: The purpose of this analysis was to compare the association between variants at the chromosome 9p21 locus (Ch9p21) and risk of first versus subsequent coronary heart disease (CHD) events through systematic review and meta-analysis. BACKGROUND: Ch9p21 is a recognized risk factor for a first CHD event. However, its association with risk of subsequent events in patients with established CHD is less...

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Share to Chromosomes, Human, Pair 9
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Associations and Epidemiology

Share to Genetic Predisposition to Disease

Share to Genetic Variation

Share to Genomic variations and chromosomal abnormalities

Share to Polymorphism, Single Nucleotide

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Source

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Identifiers

PMID: 24607648
DOI: 10.1016/j.jacc.2014.01.065
PMCID: PMC4035794

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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