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

A Genomewide Linkage Study of 1,933 Families Affected by Premature Coronary Artery Disease: The British Heart Foundation (BHF) Family Heart Study

7 Nov 2005

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Bioinformatics and Genomic Networks
Share to Cardiovascular Function and Risk Factors
Share to Genetic Associations and Epidemiology

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16380912
DOI: 10.1086/498653

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

A Genomewide Linkage Study of 1,933 Families Affected by Premature Coronary Artery Disease: The British Heart Foundation (BHF) Family Heart StudyPMID 16380912Read ↗

An Investigation of Coronary Heart Disease in Families: The Framingham Offspring StudySemantic proximity Read ↗

NHLBI Family Heart Study: Objectives and DesignSemantic proximity Read ↗

Genetics of the Framingham Heart Study population.Semantic proximity Read ↗

Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients.Semantic proximity Read ↗

Phenome-wide screening for traits causally associated with the risk of coronary artery diseaseSemantic 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 ↗

Family studies: their role in the evaluation of genetic cardiovascular risk factors.Semantic proximity Read ↗

The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports.Semantic proximity Read ↗

Family study designs in the age of genome-wide association studies: experience from the Framingham Heart Study.Semantic proximity Read ↗

Novel Genetic Contributors to Premature Coronary Artery Disease: Insights from Whole-Exome Sequencing in Families with Early Onset DiseaseSemantic proximity Read ↗

Genome scan for loci regulating HDL cholesterol levels in Finnish extended pedigrees with early coronary heart disease.Semantic proximity Read ↗

HapMap and mapping genes for cardiovascular disease.Semantic proximity Read ↗

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