(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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scholarly article

1 reference

Europe PubMed Central

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)

1 reference

Europe PubMed Central

2 August 2017

Adebowale A. Adeyemo

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Adebowale Adeyemo

4

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5

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Charles Rotimi

1 reference

Europe PubMed Central

2 August 2017

Carl D. Langefeld

6

object named as

Carl D Langefeld

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Europe PubMed Central

2 August 2017

7

object named as

Barry I Freedman

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Europe PubMed Central

2 August 2017

Donald W Bowden

9

object named as

Donald W Bowden

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Europe PubMed Central

2 August 2017

Nicholette D Palmer

1

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Nicholette D Palmer

1 reference

Europe PubMed Central

2 August 2017

author name string

Jessica M Hester

2

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Europe PubMed Central

2 August 2017

S Sandy An

3

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Europe PubMed Central

2 August 2017

Maggie C Y Ng

8

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Europe PubMed Central

2 August 2017

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publication date

27 October 2010

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Europe PubMed Central

2 August 2017

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Europe PubMed Central

2 August 2017

60

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Europe PubMed Central

2 August 2017

2

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Europe PubMed Central

2 August 2017

662-668

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Europe PubMed Central

2 August 2017

copyright license

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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Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease

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1 reference

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1 reference

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Common variants in WFS1 confer risk of type 2 diabetes

1 reference

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

1 reference

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

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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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1 reference

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1 reference

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Wnt signaling: physiology and pathology

1 reference

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1 reference

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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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Identifiers

10.2337/DB10-0134

1 reference

Europe PubMed Central

2 August 2017

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pubmed-PMC3028368

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1 reference

Europe PubMed Central

2 August 2017

1 reference

Europe PubMed Central

2 August 2017

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