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

PHACTR1 and APOC1 genetic variants are associated with multi-vessel coronary artery disease.

Lipids in health and disease - 12 Oct 2024

Al Hageh Cynthia, O'Sullivan Siobhán, Henschel Andreas, Abchee Antoine, Hantouche Mireille, Iakovidou Nantia, Issa Taly, Chacar Stephanie, Nader Moni, Zalloua Pierre A

Abstract excerpt

BACKGROUND: Severe coronary artery disease (CAD) represents an advanced arterial narrowing, often associated with critical complications like myocardial infarction and angina. This study aimed to comprehensively investigate determinants of severe and multi-vessel CAD manifestations. METHODS: One thousand nine hundred patients with severe and multivessel CAD (stenosis > 70%) were recruited along with 1,056...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Apolipoprotein C-I

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to Coronary Artery Disease

Share to Genetic Predisposition to Disease

Share to Genotype

Share to Microfilament Proteins

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 39395990
DOI: 10.1186/s12944-024-02327-2
PMCID: PMC11471027

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PHACTR1 and APOC1 genetic variants are associated with multi-vessel coronary artery disease.PMID 39395990Read ↗

Pathogenesis of coronary artery disease: focus on genetic risk factors and identification of genetic variantsSemantic proximity Read ↗

Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.Semantic proximity Read ↗

Common and distinct genetic features of three atherosclerotic cardiovascular diseases.Semantic proximity Read ↗

Etiologic Puzzle of Coronary Artery Disease: How Important Is Genetic Component?Semantic proximity Read ↗

Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.Semantic proximity Read ↗

Genetics: Implications for Prevention and Management of Coronary Artery Disease.Semantic proximity Read ↗

Genomic risk prediction of coronary artery disease in nearly 500,000 adults: implications for early screening and primary preventionSemantic proximity Read ↗

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

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.Semantic proximity Read ↗

Clinical and Genomic Prediction of Coronary Artery Disease Subtypes.Semantic proximity Read ↗

Coronary Heart Disease, Peripheral Arterial Disease, and Stroke in Familial Hypercholesterolaemia: Insights From the SAFEHEART Registry (Spanish Familial Hypercholesterolaemia Cohort Study).Semantic proximity Read ↗

Genome-wide association studies of cardiovascular disease.Semantic proximity Read ↗

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