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

Significant Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease.

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association - 1 Nov 2016

Morimoto Takaaki, Mineharu Yohei, Kobayashi Hatasu, Harada Kouji H, Funaki Takeshi, Takagi Yasushi, Sakai Nobuyuki, Miyamoto Susumu, Koizumi Akio

Abstract excerpt

BACKGROUND: Quasi-moyamoya disease is an angiographical moyamoya disease equivalent accompanied by known underlying diseases. Mysterin/RNF213 is a major susceptibility gene for moyamoya disease, of which the p.R4810K variant is a founder polymorphism. The genetics of quasi-moyamoya disease is poorly understood, therefore, this study investigated a potential association between the p.R4810K polymorphism and...

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 Cerebral Angiography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Logistic Models

Share to Magnetic Resonance Angiography

Share to Moyamoya Disease

Share to Odds Ratio

Share to Ubiquitin-Protein Ligases

Source

Identifiers

PMID: 27476341
DOI: 10.1016/j.jstrokecerebrovasdis.2016.07.004

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Significant Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease.PMID 27476341Read ↗

The Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease and a Review of the Pertinent Literature.Semantic proximity Read ↗

RNF213 p.R4810K Variant and Intracranial Arterial Stenosis or Occlusion in Relatives of Patients with Moyamoya Disease.Semantic 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 ↗

Frequency of RNF213 p.R4810K, a susceptibility variant for moyamoya disease, and health characteristics of carriers in the Japanese population.Semantic proximity Read ↗

Rare variants of RNF213 and moyamoya/non-moyamoya intracranial artery stenosis/occlusion disease risk: a meta-analysis and systematic review.Semantic proximity Read ↗

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

The Role of RNF213 4810G>A and 4950G>A Variants in Patients with Moyamoya Disease in Korea.Semantic proximity Read ↗

Frequency of the moyamoya-related RNF213 p.Arg4810Lys variant in 1,516 Korean individualsSemantic proximity Read ↗

Systematic Validation of RNF213 Coding Variants in Japanese Patients With Moyamoya Disease.Semantic proximity Read ↗

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

Distribution of moyamoya disease susceptibility polymorphism p.R4810K in RNF213 in East and Southeast Asian populations.Semantic proximity Read ↗

Significant association of RNF213 p.R4810K, a moyamoya susceptibility variant, with coronary artery disease.Semantic proximity Read ↗

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