(Q56508282)

Jana V van Vliet-Ostaptchouk

1

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Ronit Shiri-Sverdlov

Ronit Shiri-Sverdlov

6

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Lude Franke

Lude Franke

4

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Yvonne T van der Schouw

Yvonne T van der Schouw

7

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Cisca Wijmenga

Cisca Wijmenga

9

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Clara C Elbers

5

Clara C Elbers

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Timon W van Haeften

3

Timon W van Haeften

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N Charlotte Onland-Moret

2

N Charlotte Onland-Moret

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author name string

Marten H Hofker

European Journal of Human Genetics

8

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publication date

30 January 2008

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published in

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volume

16

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issue

5

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page(s)

652-656

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exact match

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5202008

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cites work

Genetic factors in type 2 diabetes: the end of the beginning?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

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.5202008

7 January 2021

TCF7L2: the biggest story in diabetes genetics since HLA?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

Hex homeobox gene-dependent tissue positioning is required for organogenesis of the ventral pancreas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

Insulin-degrading enzyme regulates the levels of insulin, amyloid beta-protein, and the beta-amyloid precursor protein intracellular domain in vivo

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

TCF7L2 and type 2 diabetes--we WNT to know

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

Heart induction by Wnt antagonists depends on the homeodomain transcription factor Hex.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

A genome-wide scan in type 2 diabetes mellitus provides independent replication of a susceptibility locus on 18p11 and suggests the existence of novel Loci on 2q12 and 19q13.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

Pedigree disequilibrium tests for multilocus haplotypes.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

Sample size requirements for matched case-control studies of gene-environment interaction

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

Association of variants of transcription factor 7-like 2 (TCF7L2) with susceptibility to type 2 diabetes in the Dutch Breda cohort

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202008

7 January 2021