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

Haplotypes on 9p21 modify the risk for coronary artery disease among Indians.

DNA and cell biology - 1 Feb 2011

AshokKumar Manickaraj, Emmanuel Cyril, Dhandapany Perundurai S, Rani Deepa Selvi, SaiBabu Ramineni, Cherian Kootturathu Mammen, Thangaraj Kumarasamy

Abstract excerpt

The chromosomal region 9p21 has been reported to be associated with myocardial infarction, coronary artery disease (CAD), diabetes, and many other related multifactorial diseases in humans. Although the genome-wide association studies have identified a limited number of single-nucleotide polymorphisms (SNPs) at 9p21 for CAD risk, the role of flanking SNPs has not been studied so far. Therefore, in the present...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 9
Share to Coronary Artery Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Genetic Loci

Share to Haplotypes

Share to Polymorphism, Single Nucleotide

Share to White People

Source

Identifiers

PMID: 20858033
DOI: 10.1089/dna.2010.1046

Genes

CAD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Haplotypes on 9p21 modify the risk for coronary artery disease among Indians.PMID 20858033Read ↗

Association of polymorphisms in 9p21 region with CAD in North Indian population: replication of SNPs identified through GWAS.Semantic proximity Read ↗

Variant on 9p21 is strongly associated with coronary artery disease but lacks association with myocardial infarction and disease severity in a population in Western India.Semantic proximity Read ↗

Evaluation of association between common genetic variants on chromosome 9p21 and coronary artery disease in Turkish population.Semantic proximity Read ↗

Variants in 9p21 Predicts Severity of Coronary Artery Disease in a Chinese Han Population.Semantic proximity Read ↗

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

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

Genetic analysis of the 9p21.3 CAD risk locus in Asian Indians.Semantic proximity Read ↗

The SNP rs7865618 of 9p21.3 locus emerges as the most promising marker of coronary artery disease in the southern Indian population.Semantic proximity Read ↗

Association of chromosome 9p21 genetic variants with risk of coronary heart disease in the East Asian population: a meta-analysis.Semantic proximity Read ↗

Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations.Semantic proximity Read ↗

Association between 9p21.3 genomic markers and coronary artery disease in East Asians: a meta-analysis involving 9,813 cases and 10,710 controls.Semantic proximity Read ↗

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