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

APOL1 polymorphisms are not influencing acute coronary syndrome risk in Czech males.

Molecular genetics & genomic medicine - 1 Aug 2024

Hubacek Jaroslav A, Adamkova Vera, Lanska Vera, Stanek Vladimir, Mrazkova Jolana, Gebauerova Marie, Kettner Jiri, Kautzner Josef, Pitha Jan

Abstract excerpt

BACKGROUND: The highest mortality and morbidity worldwide is associated with atherosclerotic cardiovascular disease (ASCVD), which has in background both environmental and genetic risk factors. Apolipoprotein L1 (APOL1) variability influences the risk of ASCVD in Africans, but little is known about the APOL1 and ASCVD in other ethnic groups. METHODS: To investigate the role of APOL1 and ASCVD, we have genotyped...

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 Apolipoprotein L1

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Apolipoproteins

Share to Case-Control Studies

Share to Czech Republic

Share to Haplotypes

Share to Lipoproteins, HDL

Share to White People

Source

Open in PubMed Open full text

Identifiers

PMID: 39171649
DOI: 10.1002/mgg3.2449
PMCID: PMC11339648

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

APOL1 polymorphisms are not influencing acute coronary syndrome risk in Czech males.PMID 39171649Read ↗

Cholesterol associated genetic risk score and acute coronary syndrome in Czech males.Semantic proximity Read ↗

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

Toll-like receptor 4 gene polymorphisms and acute coronary syndrome: no association in a Mexican population.Semantic proximity Read ↗

Single nucleotide polymorphisms in IL1B and the risk of acute coronary syndrome: a Danish case-cohort study.Semantic proximity Read ↗

Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD.Semantic proximity Read ↗

APOL1 Gene Variants and Risk for Cardiovascular Disease.Semantic proximity Read ↗

The MCP-1 -2518 (A to G) single nucleotide polymorphism is not associated with myocardial infarction in the Czech population.Semantic proximity Read ↗

Genetic variants within the interleukin-1 gene cluster, and risk of incident myocardial infarction, and ischemic stroke: a nested case-control approach.Semantic proximity Read ↗

The C766T low-density lipoprotein receptor related protein polymorphism and coronary artery disease, plasma lipoproteins, and longevity in the Czech population.Semantic proximity Read ↗

Common genetic variants do not predict recurrent events in coronary heart disease patients.Semantic proximity Read ↗

TLR4 Asp299Gly polymorphism is not associated with coronary artery stenosis.Semantic proximity Read ↗

Association of soluble endothelial protein C receptor plasma levels and PROCR rs867186 with cardiovascular risk factors and cardiovascular events in coronary artery disease patients: the Athero Gene study.Semantic proximity Read ↗

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