(Q28943344)

English

Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA

scientific journal article

In more languages

Statements

scholarly article

1 reference

14 March 2017

Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA (English)

1 reference

14 March 2017

genome-wide association study

0 references

Naoyuki Kamatani

5

0 references

6

object named as

Michiaki Kubo

1 reference

14 March 2017

Atsushi Takahashi

2

object named as

Atsushi Takahashi

1 reference

14 March 2017

Yūsuke Nakamura

7

object named as

Yusuke Nakamura

1 reference

14 March 2017

Hitoshi Zembutsu

4

object named as

Hitoshi Zembutsu

1 reference

14 March 2017

3

object named as

Pei-Chieng Cha

1 reference

14 March 2017

1

object named as

Siew-Kee Low

1 reference

14 March 2017

publication date

1 May 2012

1 reference

14 March 2017

Human Molecular Genetics

1 reference

14 March 2017

21

1 reference

14 March 2017

2102–2110

1 reference

14 March 2017

9

1 reference

14 March 2017

describes a project that uses

genome-wide association study

1 reference

based on heuristic

inferred from title

Trends in surgical and management outcomes in patients with aneurysmal subarachnoid hemorrhage in Izumo city, Japan, between 1980-1989 and 1990-1998.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Risk of rupture associated with intact cerebral aneurysms in the Japanese population: a systematic review of the literature from Japan.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Epidemiology of subarachnoid hemorrhage in Finland from 1983 to 1985

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

A multinational comparison of subarachnoid hemorrhage epidemiology in the WHO MONICA stroke study.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Incidence of aneurysmal subarachnoid hemorrhage in Shimokita, Japan, from 1989 to 1998.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Risk factors for subarachnoid hemorrhage: a systematic review

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Risk of harboring an unruptured intracranial aneurysm.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Risk factors for the formation and rupture of intracranial saccular aneurysms in Shimane, Japan

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Genomewide-linkage and haplotype-association studies map intracranial aneurysm to chromosome 7q11

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Search for intracranial aneurysm susceptibility gene(s) using Finnish families

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Susceptibility loci for intracranial aneurysm in European and Japanese populations

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Genome-wide association study of intracranial aneurysm identifies three new risk loci

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Endothelin ETA receptor expression in human cerebrovascular smooth muscle cells

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Association between migraine and endothelin type A receptor (ETA -231 A/G) gene polymorphism.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Association of genetic variants with myocardial infarction in Japanese individuals with metabolic syndrome.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Association of EDNRA, but not WNK4 or FKBP1B, polymorphisms with essential hypertension

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Down-regulation of an inhibitor of cell growth, transmembrane protein 34 (TMEM34), in anaplastic thyroid cancer

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Identification and characterization of PS-GAP as a novel regulator of caspase-activated PAK-2

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Discovery and verification of functional single nucleotide polymorphisms in regulatory genomic regions: current and developing technologies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

New susceptibility locus for coronary artery disease on chromosome 3q22.3.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

A common variant on chromosome 9p21 affects the risk of myocardial infarction

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Chromosome 9p21 and coronary artery disease.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Chromosome 9p21 in ischemic stroke: population structure and meta-analysis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

A high-throughput SNP typing system for genome-wide association studies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Genomic control for association studies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Measuring inconsistency in meta-analyses

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS020

21 January 2018

Identifiers

10.1093/HMG/DDS020

1 reference

14 March 2017

1 reference

14 March 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28943344&oldid=1855813219"