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

Genetic variants in loci 1p13 and 9p21 and fatal coronary heart disease in a Norwegian case-cohort study.

Molecular biology reports - 1 May 2014

Jansen Mona Dverdal, Knudsen Gun Peggy, Myhre Ronny, Høiseth Gudrun, Mørland Jørg, Næss Øyvind, Tambs Kristian, Magnus Per

Abstract excerpt

Single nucleotide polymorphisms (SNPs) in loci 1p13 and 9p21 have previously been found to be associated with incident coronary heart disease (CHD). This study aimed to investigate whether these SNPs show associations with fatal CHD in a population-based cohort study after adjustment for socioeco...

Read the complete abstract on PubMed

Topics

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

Share to Aged, 80 and over
Share to Chromosomes, Human, Pair 1
Share to Chromosomes, Human, Pair 9

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Coronary Disease

Share to Genetic Loci

Share to Genome-Wide Association Study

Share to Norway

Share to White People

Source

Identifiers

PMID: 24728607
DOI: 10.1007/s11033-014-3096-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24728607-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic variants in loci 1p13 and 9p21 and fatal coronary heart disease in a Norwegian case-cohort study.PMID 24728607Read ↗

The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts.Semantic proximity Read ↗

Associations between single nucleotide polymorphisms on chromosome 9p21 and risk of coronary heart disease in Chinese Han population.Semantic proximity Read ↗

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

Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study.Semantic proximity Read ↗

Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men.Semantic proximity Read ↗

Genomic risk variants at 1p13.3, 1q41, and 3q22.3 are associated with subsequent cardiovascular outcomes in healthy controls and in established coronary artery disease.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 ↗

Association of Common Variants of APOE, CETP, and the 9p21.3 Chromosomal Region with the Risk of Myocardial Infarction: A Prospective Study.Semantic proximity Read ↗

Independent association of the variant rs1333049 at the 9p21 locus and coronary heart disease.Semantic proximity Read ↗

Lack of association between genetic variants in the 19q13.32 region and CHD risk in the Algerian population: a population-based nested case-control study.Semantic proximity Read ↗

9p21 Locus Polymorphism Is A Strong Predictor of Metabolic Syndrome and Cardiometabolic Risk Phenotypes Regardless of Coronary Heart Disease.Semantic proximity Read ↗

Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study.Semantic proximity Read ↗

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