A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. (Q34147943)

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15 January 2020

title

A genome-wide association study identifies RNF213 as the first Moyamoya disease gene (English)

1 reference

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genome-wide association study

15 January 2020

main subject

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4

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Naoto Ishii

10

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author name string

Fumiaki Kamada

1

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15 January 2020

Yoko Aoki

2

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15 January 2020

Ayumi Narisawa

3

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15 January 2020

Shoko Komatsuzaki

5

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Atsuo Kikuchi

6

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Junko Kanno

7

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Tetsuya Niihori

8

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Masao Ono

9

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Yuji Owada

11

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Miki Fujimura

12

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15 January 2020

Yoichi Mashimo

13

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Yoichi Suzuki

14

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Shigeru Tsuchiya

16

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Teiji Tominaga

17

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Yoichi Matsubara

18

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15 January 2020

Shigeo Kure

19

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Akira Hata

15

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publication date

4 November 2010

1 reference

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Journal of Human Genetics

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published in

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volume

56

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page(s)

34-40

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issue

1

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describes a project that uses

15 January 2020

genome-wide association study

1 reference

https://scigraph.springernature.com/pub.10.1038/jhg.2010.132

inferred from title

exact match

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cites work

Cerebrovascular "moyamoya" disease. Disease showing abnormal net-like vessels in base of brain.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

Pathophysiology and genetic factors in moyamoya disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

Moyamoya disease and moyamoya syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

Clinical features of familial moyamoya disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

Systemic vascular changes in spontaneous occlusion of the circle of Willis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

Vascular repair by endothelial progenitor cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

Increased levels of circulating endothelial progenitor cells in patients with Moyamoya disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

Increase in circulating CD34-positive cells in patients with angiographic evidence of moyamoya-like vessels

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

7 January 2021

inferred from DOI database lookup

A novel susceptibility locus for moyamoya disease on chromosome 8q23

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

7 January 2021

inferred from DOI database lookup

Linkage analysis of moyamoya disease on chromosome 6

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.132

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/JHG.2010.132

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21048783%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

1 reference