Association between ALMS 1 variants and early-onset coronary artery disease: a case-control study in Chinese population.

doi:10.1042/BSR20193637

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

Community

Back to search

Article

Association between ALMS 1 variants and early-onset coronary artery disease: a case-control study in Chinese population.

Bioscience reports - 30 Sept 2020

Zhang Shao-Yan, Xuan Chao, Wang Yi, Zhang Shao-Qiang, Li Hui, He Guo-Wei, Tian Qing-Wu

Abstract excerpt

BACKGROUND: Genome-wide linkage analysis revealed the polymorphism of rs6748040 and glutamic acid repeat are potential pathogenic factors of early-onset myocardial infarction (MI). The present study was designed to investigate the associations of Alström syndrome 1 (ALMS 1) gene in Chinese populations with early-onset coronary artery disease (CAD). METHODS: The two variants of the ALMS 1 gene were genotyped in...

Read the complete abstract on PubMed

Topics

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

Share to Age of Onset

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Asian People

Share to Case-Control Studies

Share to Cell Cycle Proteins

Share to Coronary Artery Disease

Share to Exons

Share to Gene Frequency

Share to Introns

Source

Open in PubMed Open full text

Identifiers

PMID: 32808654
DOI: 10.1042/BSR20193637
PMCID: PMC7463302

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association between ALMS 1 variants and early-onset coronary artery disease: a case-control study in Chinese population.PMID 32808654Read ↗

Identification of a glutamic acid repeat polymorphism of ALMS1 as a novel genetic risk marker for early-onset myocardial infarction by genome-wide linkage analysis.Semantic proximity Read ↗

Genome-wide analyses of early-onset acute myocardial infarction identify 29 novel loci by whole genome sequencingSemantic proximity Read ↗

[Genetic Predisposition to Early Myocardial Infarction].Semantic proximity Read ↗

Genetic Predisposition to Early Myocardial InfarctionSemantic proximity Read ↗

A common variant on chromosome 9p21 affects the risk of early-onset coronary artery disease.Semantic proximity Read ↗

Impact of the ApoE Genotype on Coronary Artery Disease and the Incidence of Myocardial Infarction: A Clinical Observational StudySemantic proximity Read ↗

[Genetic background of acute coronary syndrome].Semantic proximity Read ↗

Promoter polymorphisms in the lncRNA-MIAT gene associated with acute myocardial infarction in Chinese Han population: a case-control study.Semantic proximity Read ↗

Genetic analysis of the SIRT1 gene promoter in myocardial infarction.Semantic proximity Read ↗

<i>SYNE1</i>gene novel variant is associated with myocardial infarction in young people with a family history of premature atherosclerosisSemantic proximity Read ↗

A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.Semantic proximity Read ↗

Polymorphisms on chromosome 9p21 confer a risk for acute coronary syndrome in a Chinese Han population.Semantic proximity Read ↗

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