(Q36935212)

17 August 2017

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

1 reference

17 August 2017

23

Nobuyuki Hamajima

1 reference

17 August 2017

14

Kenji Wakai

1 reference

17 August 2017

12

Mariko Naito

1 reference

17 August 2017

13

Asahi Hishida

1 reference

17 August 2017

4

Akiyoshi Nakayama

1 reference

17 August 2017

7

Yusuke Kawamura

1 reference

17 August 2017

16

Seiko Shimizu

1 reference

17 August 2017

29

Nariyoshi Shinomiya

1 reference

17 August 2017

17

Masayuki Sakiyama

1 reference

17 August 2017

18

Toshinori Chiba

1 reference

17 August 2017

3

Tappei Takada

1 reference

17 August 2017

10

Hiroki Inoue

1 reference

17 August 2017

25

Yoshikatsu Kanai

1 reference

17 August 2017

26

Yutaka Sakurai

1 reference

17 August 2017

2

Kimiyoshi Ichida

1 reference

17 August 2017

22

Atsuyoshi Mori

1 reference

17 August 2017

19

Hiraku Ogata

1 reference

17 August 2017

27

Tatsuo Hosoya

1 reference

17 August 2017

11

Yuji Oikawa

1 reference

17 August 2017

20

Kazuki Niwa

1 reference

17 August 2017

21

Makoto Hosoyamada

1 reference

17 August 2017

Hirotaka Matsuo

1

1 reference

17 August 2017

Hiroshi Nakashima

5

1 reference

17 August 2017

Takahiro Nakamura

6

1 reference

17 August 2017

Yuzo Takada

8

1 reference

17 August 2017

Ken Yamamoto

9

1 reference

17 August 2017

Chisa Okada

15

1 reference

17 August 2017

Hiroshi Suzuki

24

1 reference

17 August 2017

Toru Shimizu

28

1 reference

17 August 2017

language of work or name

English

0 references

publication date

1 January 2013

1 reference

17 August 2017

1 reference

17 August 2017

3

1 reference

17 August 2017

2014

1 reference

Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported

17 August 2017

start time

18 June 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1038/srep02014

0 references

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

The rs2231142 variant of the ABCG2 gene is associated with uric acid levels and gout among Japanese people

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Genome-wide association study of hematological and biochemical traits in a Japanese population

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

New insights into the epidemiology of gout

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Genomewide association studies of stroke

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Uric acid and insulin sensitivity and risk of incident hypertension

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

A HapMap harvest of insights into the genetics of common disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Hypoxanthine-guanine phosophoribosyltransferase (HPRT) deficiency: Lesch-Nyhan syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Genomewide association analysis of coronary artery disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

GATA2 is associated with familial early-onset coronary artery disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

New developments in the epidemiology and genetics of gout

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Genetic factors associated with gout and hyperuricemia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Genomewide scan for gout in taiwanese aborigines reveals linkage to chromosome 4q25.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Molecular identification of a renal urate anion exchanger that regulates blood urate levels

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Localization of a gene for familial juvenile hyperuricemic nephropathy causing underexcretion-type gout to 16p12 by genome-wide linkage analysis of a large family

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Generation of cDNA probes directed by amino acid sequence: cloning of urate oxidase.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

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

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

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

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Gouty arthritis in acute cerebrovascular disease.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Rapid diagnosis of MEN2B using unlabeled probe melting analysis and the LightCycler 480 instrument

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

The effect of mild hyperuricemia on urinary transforming growth factor beta and the progression of chronic kidney disease

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Apolipoprotein E epsilon4 count affects age at onset of Alzheimer disease, but not lifetime susceptibility: The Cache County Study

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

Familial paroxysmal dystonic choreoathetosis: clinical findings in a large Japanese family and genetic linkage to 2q.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3684804

A strong role for the ABCG2 gene in susceptibility to gout in New Zealand Pacific Island and Caucasian, but not Māori, case and control sample sets

4 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSREP02014

Purine overproduction in man associated with increased phosphoribosylpyrophosphate synthetase activity

21 January 2018

1 reference

12 December 2020

Sex differences in uric acid and risk factors for coronary artery disease

1 reference

12 December 2020

Younger age of onset of gout in Taiwan

1 reference

12 December 2020

Hyperuricemia in primary and renal hypertension

1 reference

12 December 2020

Uric acid and cardiovascular risk

1 reference

12 December 2020

Common variants at 30 loci contribute to polygenic dyslipidemia

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSREP02014

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/SREP02014

1 reference

Dimensions Publication ID

17 August 2017

0 references

1 reference

17 August 2017

1 reference