(Q34527242)

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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

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Europe PubMed Central

PubMed publication ID

2 August 2017

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

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Europe PubMed Central

PubMed publication ID

2 August 2017

Adebowale A. Adeyemo

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Adebowale Adeyemo

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Charles Rotimi

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Europe PubMed Central

PubMed publication ID

2 August 2017

Carl D. Langefeld

6

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Carl D Langefeld

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2 August 2017

7

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Barry I Freedman

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Europe PubMed Central

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2 August 2017

Donald W Bowden

9

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Donald W Bowden

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Europe PubMed Central

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2 August 2017

Nicholette D Palmer

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Nicholette D Palmer

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Europe PubMed Central

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2 August 2017

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Jessica M Hester

2

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Europe PubMed Central

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2 August 2017

S Sandy An

3

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2 August 2017

Maggie C Y Ng

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2 August 2017

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27 October 2010

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Europe PubMed Central

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2 August 2017

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Europe PubMed Central

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2 August 2017

60

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Europe PubMed Central

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2 August 2017

2

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Europe PubMed Central

PubMed publication ID

2 August 2017

662-668

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Europe PubMed Central

PubMed publication ID

2 August 2017

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Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported

30 August 2021

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April 2022 Public Data File from Crossref

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Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study

1 reference

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Rare variants create synthetic genome-wide associations

1 reference

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1 reference

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Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes

1 reference

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Common variants in WFS1 confer risk of type 2 diabetes

1 reference

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7 July 2018

Variants of the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in an African-American population enriched for nephropathy

1 reference

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Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

1 reference

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

1 reference

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1 reference

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A variant in CDKAL1 influences insulin response and risk of type 2 diabetes

1 reference

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A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

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A genome-wide association study identifies novel risk loci for type 2 diabetes

1 reference

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7 July 2018

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

1 reference

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Carnosine as a protective factor in diabetic nephropathy: association with a leucine repeat of the carnosinase gene CNDP1.

1 reference

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A note on exact tests of Hardy-Weinberg equilibrium

1 reference

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TCF-4 mediates cell type-specific regulation of proglucagon gene expression by beta-catenin and glycogen synthase kinase-3beta

1 reference

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1 reference

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1 reference

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12 December 2020

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10.2337/DB10-0134

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Europe PubMed Central

PubMed publication ID

2 August 2017

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pubmed-PMC3028368

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PMC publication ID

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Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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