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

Contribution of WNT2B Genetic Variants to Ischemic Stroke Occurrence in a Chinese Han Population.

Journal of cardiovascular pharmacology - 1 Jul 2021

Yuan Haozheng, Fan Pei, Yao Li, Lv Yuying, Wei Haidong, Zheng Juan, Han Xinsheng

Abstract excerpt

ABSTRACT: Wnt signaling pathway-related WNT2B gene was upregulated in ischemic brain damage. We aimed to assess the contribution of WNT2B genetic variant to ischemic stroke (IS) susceptibility in the Chinese Han population. Five polymorphisms including rs3790606, rs351364, rs3790608, rs12037987, and rs10776752 in WNT2B were genotyped using Agena MassARRAY platform in 476 healthy controls and 501 patients with IS....

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Case-Control Studies
Share to China
Share to Genetic Association Studies
Share to Glycoproteins
Share to Ischemic Stroke
Share to Risk Assessment
Share to Wnt Proteins

Source

Identifiers

PMID: 34009855
DOI: 10.1097/FJC.0000000000001032

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

Contribution of WNT2B Genetic Variants to Ischemic Stroke Occurrence in a Chinese Han Population.PMID 34009855Read ↗

Effects of CASZ1, WNT2B and PTPRG SNPs on stroke susceptibility in the Chinese Han population.Semantic proximity Read ↗

Genetic Variants and Alteration in<i>Transcription Factor 7-Like 2 (TCF7L2)</i>mRNA level in Ischemic Stroke Patients: An Indian ScenarioSemantic proximity Read ↗

CYP1B1 Genetic Variants (rs10916 and rs2855658) Are Associated with Increased Risk of Ischemic Stroke in Chinese Han Population.Semantic proximity Read ↗

CYP2B6 Polymorphisms Are Associated with Ischemic Stroke Risk in a Chinese Han Population.Semantic proximity Read ↗

<i>TTC7B</i> Emerges as a Novel Risk Factor for Ischemic Stroke Through the Convergence of Several Genome-Wide ApproachesSemantic proximity Read ↗

Impact of miR-200b and miR-495 variants on the risk of large-artery atherosclerosis stroke.Semantic proximity Read ↗

Novel CD137 Gene Polymorphisms and Susceptibility to Ischemic Stroke in the Northern Chinese Han Population.Semantic proximity Read ↗

Association between ischemic stroke, hemorrhagic stroke, dementia, and rs201118034 among general Taiwanese population.Semantic proximity Read ↗

Variants of WNT7A and GPR124 are associated with hemorrhagic transformation following intravenous thrombolysis in ischemic stroke.Semantic proximity Read ↗

Association of genetic variations in the Wnt signaling pathway genes with myocardial infarction susceptibility in Chinese Han population.Semantic proximity Read ↗

Genetic Variants and Alteration in Transcription Factor 7-Like 2 (TCF7L2) mRNA Level in Ischemic Stroke Patients Among Bengali and Gujarati Population from India.Semantic proximity Read ↗

Significant Association between OPG/TNFRSF11B Variant and Common Complex Ischemic Stroke.Semantic proximity Read ↗

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