The TCF7L2 rs7903146 (C/T) polymorphism is associated with risk to type 2 diabetes mellitus in Southern-Brazil. (Q53626875)

http://europepmc.org/abstract/MED/25627047

16 May 2018

title

The TCF7L2 rs7903146 (C/T) polymorphism is associated with risk to type 2 diabetes mellitus in Southern-Brazil. (English)

1 reference

http://europepmc.org/abstract/MED/25627047

16 May 2018

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6

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25627047%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

author name string

Taís S Assmann

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25627047%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Guilherme C K Duarte

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25627047%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Jakeline Rheinheimer

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25627047%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Lavínia A Cruz

4

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25627047%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Luís H Canani

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25627047%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

publication date

1 December 2014

1 reference

http://europepmc.org/abstract/MED/25627047

16 May 2018

published in

Arquivos Brasileiros de Endocrinologia e Metabologia

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25627047%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

volume

58

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25627047%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

issue

9

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25627047%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

page(s)

918-925

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25627047%20AND%20SRC:MED&resulttype=core&format=json

Type 2 diabetes: principles of pathogenesis and therapy

1 June 2020

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Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

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Association of variants of the TCF7L2 gene with increases in the risk of type 2 diabetes and the proinsulin:insulin ratio in the Spanish population.

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Variants of transcription factor 7-like 2 (TCF7L2) gene and incident glucose intolerance in Japanese-Brazilians

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Association of the rs7903146 single nucleotide polymorphism at the Transcription Factor 7-like 2 (TCF7L2) locus with type 2 diabetes in Brazilian subjects.

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The fatty acid-binding protein-2 A54T polymorphism is associated with renal disease in patients with type 2 diabetes.

21 January 2018

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The A allele of the rs1990760 polymorphism in the IFIH1 gene is associated with protection for arterial hypertension in type 1 diabetic patients and with expression of this gene in human mononuclear cells.

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The presence of the -866A/55Val/Ins haplotype in the uncoupling protein 2 (UCP2) gene is associated with decreased UCP2 gene expression in human retina.

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Association of TCF7L2 gene polymorphisms with T2DM in the population of Hyderabad, India

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TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups: a global meta-analysis

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TCF7L2 is not a major susceptibility gene for type 2 diabetes in Pima Indians: analysis of 3,501 individuals

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Association of genetic variations in TCF7L2, SLC30A8, HHEX, LOC387761, and EXT2 with Type 2 diabetes mellitus in Tunisia.

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Impact of common type 2 diabetes risk gene variants on future type 2 diabetes in the non-diabetic population in Korea

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Association of type 2 diabetes susceptibility genes (TCF7L2, SLC30A8, PCSK1 and PCSK2) and proinsulin conversion in a Chinese population.

21 January 2018

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Meta-analysis of the association between SNPs in TCF7L2 and type 2 diabetes in East Asian population.

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Association of rs7903146 (IVS3C/T) and rs290487 (IVS3C/T) polymorphisms in TCF7L2 with type 2 diabetes in 9,619 Han Chinese population

21 January 2018

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21 January 2018

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TCF7L2 variant genotypes and type 2 diabetes risk in Brazil: significant association, but not a significant tool for risk stratification in the general population

21 January 2018

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21 January 2018

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21 January 2018

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Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant

21 January 2018

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Transcription Factor TCF7L2 Genetic Study in the French Population: Expression in Human -Cells and Adipose Tissue and Strong Association With Type 2 Diabetes

21 January 2018

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21 January 2018

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25627047%20AND%20SRC:MED&resulttype=core&format=json

release_mfig52wv7rdbxkojvhses7ytuu

1 June 2020

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mapped directly with Wikidata item

24 November 2022

based on heuristic

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