(Q34461040)

2 August 2017

title

Molecular analysis of RNF213 gene for moyamoya disease in the Chinese Han population (English)

1 reference

2 August 2017

1 reference

Zhiyuan Wu

1

1 reference

2 August 2017

Hanqiang Jiang

2

1 reference

2 August 2017

Lei Zhang

3

1 reference

2 August 2017

Xiao Xu

4

1 reference

2 August 2017

Xinju Zhang

5

1 reference

2 August 2017

Zhihua Kang

6

1 reference

2 August 2017

Donglei Song

7

1 reference

2 August 2017

Jin Zhang

8

1 reference

2 August 2017

Ming Guan

9

1 reference

2 August 2017

Yuxiang Gu

10

1 reference

2 August 2017

language of work or name

English

0 references

publication date

23 October 2012

1 reference

2 August 2017

1 reference

2 August 2017

volume

7

1 reference

2 August 2017

issue

10

1 reference

2 August 2017

page(s)

e48179

1 reference

Creative Commons Attribution 4.0 International

2 August 2017

copyright license

start time

23 October 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

A genome-wide association study identifies RNF213 as the first Moyamoya disease gene.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Moyamoya disease in children

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Polymorphisms in TGFB1 and PDGFRB are associated with Moyamoya disease in European patients

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Moyamoya: epidemiology, presentation, and diagnosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Moyamoya disease: case report and literature review.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Moyamoya disease and moyamoya syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Moyamoya disease: current concepts and future perspectives

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Prevalence and clinicoepidemiological features of moyamoya disease in Japan: findings from a nationwide epidemiological survey

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Moyamoya syndrome associated with Down syndrome: outcome after surgical revascularization

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Epidemiological features of moyamoya disease in Japan: findings from a nationwide survey.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Epidemiological and clinical features of Moyamoya disease in Nanjing, China

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Autosomal dominant moyamoya disease maps to chromosome 17q25.3.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Novel epidemiological features of moyamoya disease

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Familial occurrence of moyamoya disease: a clinical study.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Moyamoya disease in Washington State and California

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

Epidemiological study of moyamoya disease in Taiwan.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3479116

A novel susceptibility locus for moyamoya disease on chromosome 8q23

27 October 2018

1 reference

12 December 2020

Introduction: moyamoya disease

1 reference

12 December 2020

1 reference

12 December 2020

Genetics of Moyamoya disease

1 reference

12 December 2020

Linkage analysis of moyamoya disease on chromosome 6

1 reference

12 December 2020

Linkage of Familial Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis) to Chromosome 17q25

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0048179

Identifiers

DOI

1 reference

2 August 2017

0 references

1 reference

2 August 2017

1 reference