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

Meta-analysis of genotype and phenotype studies to confirm the predictive role of the RNF213 p.R4810K variant for moyamoya disease.

European journal of neurology - 1 Mar 2021

Wang Yue, Yang Luping, Wang Xiaotong, Zeng Fanxin, Zhang Kaili, Zhang Qian, Liu Mengwei, Liu Shan, Shang Mengke, Li Qian, Yang Yuetian, Liang Man, Liu Wanyang

Abstract excerpt

BACKGROUND AND PURPOSE: The aim of this meta-analysis study was to assess the predictive effects of RNF213 p.R4810K on phenotype in moyamoya disease (MMD). METHODS: Electronic databases (e.g., Pubmed and EMBASE) were searched, and relevant articles published up to August 2020 were retrieved. Review Manager 5.3 and Stata 12.0 were used for all statistical analyses. Pooled odds ratios, with 95% confidence...

Read the complete abstract on PubMed

Topics

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

Share to Adenosine Triphosphatases
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Genotype

Share to Moyamoya Disease

Share to Moyamoya disease diagnosis and treatment

Share to Phenotype

Share to Ubiquitin-Protein Ligases

Source

Identifiers

PMID: 33175469
DOI: 10.1111/ene.14635

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Meta-analysis of genotype and phenotype studies to confirm the predictive role of the RNF213 p.R4810K variant for moyamoya disease.PMID 33175469Read ↗

Association of Genetic Variants With Moyamoya Disease in 13 000 Individuals: A Meta-Analysis.Semantic proximity Read ↗

Validation and Extension Study Exploring the Role of RNF213 p.R4810K in 2,877 Chinese Moyamoya Disease Patients.Semantic proximity Read ↗

RNF213 polymorphism and Moyamoya disease: A systematic review and meta-analysis.Semantic proximity Read ↗

Importance of RNF213 polymorphism on clinical features and long-term outcome in moyamoya disease.Semantic proximity Read ↗

Meta-analysis of the association between RNF213 polymorphisms and clinical features of moyamoya disease in Asian population.Semantic proximity Read ↗

RNF213 p.Arg4810Lys Heterozygosity in Moyamoya Disease Indicates Early Onset and Bilateral Cerebrovascular Events.Semantic proximity Read ↗

RNF213 in moyamoya disease: Genotype-phenotype association and the underlying mechanism.Semantic proximity Read ↗

RNF213 p.Arg4810Lys Wild Type is Associated with De Novo Hemorrhage in Asymptomatic Hemispheres with Moyamoya Disease.Semantic proximity Read ↗

The RNF213 rs112735431 polymorphism might influence predisposition to moyamoya disease and exhibit different clinical features in Asian populationSemantic proximity Read ↗

RNF213 p.R4810K Polymorphism and the Risk of Moyamoya Disease, Intracranial Major Artery Stenosis/Occlusion, and Quasi-Moyamoya Disease: A Meta-Analysis.Semantic proximity Read ↗

Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya disease.Semantic proximity Read ↗

Familial Moyamoya disease associated with dual RNF213 variants (R4810K and T1727M): A case report and genetic investigation.Semantic proximity Read ↗

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