Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus. (Q34677297)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27181629%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

title

Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27181629%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

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1 April 2020

Rieko Okada

8

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1 April 2020

3

Hirofumi Nakaoka

1 reference

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1 April 2020

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Sayo Kawai

1 reference

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1 April 2020

1

Masayuki Sakiyama

1 reference

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1 April 2020

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Nariyoshi Shinomiya

1 reference

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1 April 2020

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Hiroshi Ooyama

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1 April 2020

author name string

Hirotaka Matsuo

2

1 reference

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1 April 2020

Ken Yamamoto

4

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1 April 2020

Takahiro Nakamura

6

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1 April 2020

Toru Shimizu

10

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1 April 2020

language of work or name

English

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publication date

16 May 2016

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1 April 2020

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1 April 2020

volume

6

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1 April 2020

page(s)

25360

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Creative Commons Attribution 4.0 International

1 April 2020

copyright license

start time

16 May 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867610

ABCG2 dysfunction causes hyperuricemia due to both renal urate underexcretion and renal urate overload

7 July 2018

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Common variant of leucine-rich repeat-containing 16A (LRRC16A) gene is associated with gout susceptibility

7 July 2018

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Common dysfunctional variants in ABCG2 are a major cause of early-onset gout

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867610

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

7 July 2018

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Fate-restricted neural progenitors in the mammalian cerebral cortex.

7 July 2018

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Decreased extra-renal urate excretion is a common cause of hyperuricemia

7 July 2018

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1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data

7 July 2018

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Identification of low-frequency variants associated with gout and serum uric acid levels

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867610

Identification of high-quality cancer prognostic markers and metastasis network modules

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867610

Baseline data of Shizuoka area in the Japan Multi-Institutional Collaborative Cohort Study (J-MICC Study).

7 July 2018

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Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867610

Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867610

Cux2 (Cutl2) integrates neural progenitor development with cell-cycle progression during spinal cord neurogenesis

7 July 2018

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PLINK: a tool set for whole-genome association and population-based linkage analyses

7 July 2018

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The International HapMap Project

7 July 2018

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Distribution of ADH2 and ALDH2 genotypes in different populations.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867610

Preliminary criteria for the classification of the acute arthritis of primary gout

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4867610

Common defects of ABCG2, a high-capacity urate exporter, cause gout: a function-based genetic analysis in a Japanese population

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSREP25360

Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSREP25360

Alcohol Dehydrogenase 2 His47Arg Polymorphism Influences Drinking Habit Independently of Aldehyde Dehydrogenase 2 Glu487Lys Polymorphism: Analysis of 2,299 Japanese Subjects

21 January 2018

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Crossref

https://api.crossref.org/works/10.1038%2FSREP25360

Analysis of the Genotypes for Aldehyde Dehydrogenase 2 in Japanese Patients with Primary Gout

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27181629

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The Japan Multi-Institutional Collaborative Cohort Study (J-MICC Study) to detect gene-environment interactions for cancer

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27181629

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Confirmation of ALDH2 as a Major locus of drinking behavior and of its variants regulating multiple metabolic phenotypes in a Japanese population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27181629

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/SREP25360

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27181629%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

1 April 2020

0 references

1 reference

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1 April 2020

PubMed publication ID

27181629

1 reference