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

Variants within HNF1α and ANGPTL4 genes and acute coronary syndrome in Czech population. The GENDEMIP study.

Neuro endocrinology letters - 1 Jan 2012

Dlouha Dana, Pitha Jan, Adámkova Vera, Lanska Vera, Hubacek Jaroslav A

Abstract excerpt

BACKGROUND: Atherosclerosis is a complex arterial disease involving interactions between multiple genetic and environmental factors. A large number of genetic polymorphisms associated with atherosclerotic diseases have been identified in recent years. We investigated the possible association between hepatic nuclear factor (HNF1-α) and angiopoietin-like 4 (ANGPTL4) single nucleotide polymorphisms and the risk of...

Read the complete abstract on PubMed

Topics

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

Share to Acute Coronary Syndrome
Share to Angiopoietins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Czech Republic

Share to Genetic Predisposition to Disease

Share to Genetic Variation

Share to Hepatocyte Nuclear Factor 1-alpha

Share to Polymorphism, Single Nucleotide

Share to Risk Factors

Source

Identifiers

PMID: 23183503

Genes

ANGPTL4

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

Variants within HNF1α and ANGPTL4 genes and acute coronary syndrome in Czech population. The GENDEMIP study.PMID 23183503Read ↗

Common coding variants of the HNF1A gene are associated with multiple cardiovascular risk phenotypes in community-based samples of younger and older European-American adults: the Coronary Artery Risk Development in Young Adults Study and The Cardiovascular Health Study.Semantic proximity Read ↗

Association of the HNF1A polymorphisms and serum lipid traits, the risk of coronary artery disease and ischemic stroke.Semantic proximity Read ↗

Association of NFKB1 gene polymorphism (rs28362491)with cardiometabolic risk factor in patients undergoing coronary angiographySemantic proximity Read ↗

Association of a genetic variant in Angiopoietin-like 3 with HDL-C and risk of cardiovascular disease: MASHAD cohort study over 10 yearsSemantic proximity Read ↗

NPAS4 Polymorphisms Contribute to Coronary Heart Disease (CHD) RiskSemantic proximity Read ↗

The Link between ANRIL Gene RS4977574 Polymorphism and Common Atherosclerosis Cardiovascular Complications: A Hospital-Based Case-Control Study in Ukrainian Population.Semantic proximity Read ↗

A molecular case-control study of association of HNF1A gene polymorphisms (rs2259816 and rs7310409) with risk of coronary artery disease in Iranian patients.Semantic proximity Read ↗

Single nucleotide polymorphism rs3774261 in the AdipoQ gene is associated with the risk of coronary heart disease (CHD) in Northeast Han Chinese population: a case-control study.Semantic proximity Read ↗

A new susceptibility locus for myocardial infarction, hypertension, type 2 diabetes mellitus, and dyslipidemia on chromosome 12q24.Semantic proximity Read ↗

Angiopoietin-like protein 4 serum levels and gene polymorphisms are associated with large artery atherosclerotic stroke.Semantic proximity Read ↗

A case-control study of the interaction of the eNOS gene polymorphisms rs1799983 and rs1800780 with acute coronary syndrome (ACS) risk factorsSemantic proximity Read ↗

The relationship between plasma angiopoietin-like protein 4 levels, angiopoietin-like protein 4 genotype, and coronary heart disease risk.Semantic proximity Read ↗

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