(Q79634107)

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24 December 2019

title

TCF7L2 polymorphisms are associated with type 2 diabetes in northern Sweden (English)

1 reference

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24 December 2019

1 reference

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1

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24 December 2019

author name string

Kurt Lackovic

2

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24 December 2019

Petter Lindgren

3

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24 December 2019

Karin Ruikka

4

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24 December 2019

Asa Agren

5

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24 December 2019

Mats Eliasson

6

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24 December 2019

Dan Holmberg

7

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24 December 2019

publication date

24 January 2007

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European Journal of Human Genetics

24 December 2019

published in

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24 December 2019

volume

15

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24 December 2019

issue

3

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24 December 2019

page(s)

342-346

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201773

24 December 2019

exact match

0 references

cites work

Genetics of type 2 diabetes mellitus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

Candidate genes for type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

Missense mutations in the pancreatic islet beta cell inwardly rectifying K+ channel gene (KIR6.2/BIR): a meta-analysis suggests a role in the polygenic basis of Type II diabetes mellitus in Caucasians

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

Association studies of variants in promoter and coding regions of beta-cell ATP-sensitive K-channel genes SUR1 and Kir6.2 with Type 2 diabetes mellitus (UKPDS 53).

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

Linkage but Not Association of Calpain-10 to Type 2 Diabetes Replicated in Northern Sweden

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

A haplotype map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

TCF7L2 variation predicts hyperglycemia incidence in a French general population: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: replication and evidence for a role in both insulin secretion and insulin resistance.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201773

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201773

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17245407%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

1 reference