(Q28287727)

22

0 references

Marc Prentki

17

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Beverley Balkau

11

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Christian Dina

4

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Thomas J. Hudson

Thomas J Hudson

14

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Robert Sladek

Robert Sladek

1

0 references

Barbara Heude

Barbara Heude

12

0 references

David J. Balding

David J Balding

19

0 references

Constantin Polychronakos

Constantin Polychronakos

21

0 references

David Meyre

20

David Meyre

0 references

Alexey V Pshezhetsky

16

Alexey V Pshezhetsky

0 references

author name string

Ghislain Rocheleau

2

0 references

Johan Rung

3

0 references

Lishuang Shen

5

0 references

David Serre

6

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Philippe Boutin

7

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Daniel Vincent

8

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Alexandre Belisle

9

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Samy Hadjadj

10

0 references

Guillaume Charpentier

13

0 references

Barry I Posner

describes a project that uses

18

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language of work or name

English

0 references

publication date

22 February 2007

0 references

published in

Nature

0 references

volume

445

0 references

page(s)

881-5

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issue

7130

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genome-wide association study

1 reference

Genetic epidemiology of diabetes

inferred from title

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

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%2FNATURE05616

7 January 2021

Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

A common polymorphism in the upstream promoter region of the hepatocyte nuclear factor-4 alpha gene on chromosome 20q is associated with type 2 diabetes and appears to contribute to the evidence for linkage in an ashkenazi jewish population.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels and contribute to the genetic risk for type 2 diabetes in French Caucasians

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

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%2FNATURE05616

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%2FNATURE05616

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%2FNATURE05616

7 January 2021

Variant of Transcription Factor 7-Like 2 (TCF7L2) Gene and the Risk of Type 2 Diabetes in Large Cohorts of U.S. Women and Men

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

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%2FNATURE05616

7 January 2021

Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Association Analysis of 6,736 U.K. Subjects Provides Replication and ConfirmsTCF7L2as a Type 2 Diabetes Susceptibility Gene With a Substantial Effect on Individual Risk

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

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%2FNATURE05616

7 January 2021

Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

A fat attack occurred in fat city

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Limited role for SREBP-1c in defective glucose-induced insulin secretion from Zucker diabetic fatty rat islets: a functional and gene profiling analysis

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

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%2FNATURE05616

7 January 2021

Combining information from common type 2 diabetes risk polymorphisms improves disease prediction

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Increasing the power and efficiency of disease-marker case-control association studies through use of allele-sharing information

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

A haplotype map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Demonstrating stratification in a European American population

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

In vivo expression and functional characterization of the zinc transporter ZnT8 in glucose-induced insulin secretion

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Linkage of type 2 diabetes mellitus and of age at onset to a genetic location on chromosome 10q in Mexican Americans

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

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%2FNATURE05616

7 January 2021

Hex homeobox gene controls the transition of the endoderm to a pseudostratified, cell emergent epithelium for liver bud development

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

An insulin-degrading enzyme inhibitor decreases amylin degradation, increases amylin-induced cytotoxicity, and increases amyloid formation in insulinoma cell cultures

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

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%2FNATURE05616

7 January 2021

Association and haplotype analysis of the insulin-degrading enzyme (IDE) gene, a strong positional and biological candidate for type 2 diabetes susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Polymorphisms in the insulin-degrading enzyme gene are associated with type 2 diabetes in men from the NHLBI Framingham Heart Study

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Sonic hedgehog directs specialised mesoderm differentiation in the intestine and pancreas

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Hedgehog signaling regulation of insulin production by pancreatic beta-cells

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Genetic interaction between Lef1 and Alx4 is required for early embryonic development.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

An evolutionary framework for common diseases: the ancestral-susceptibility model

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Are rare variants responsible for susceptibility to complex diseases?

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

A null mutation of Hhex results in abnormal cardiac development, defective vasculogenesis and elevated Vegfa levels

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

From genotypes to genes: doubling the sample size

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Population structure, differential bias and genomic control in a large-scale, case-control association study

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Genomic control for association studies

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Detecting association in a case-control study while correcting for population stratification

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Case-control association tests correcting for population stratification

1 reference

https://api.crossref.org/works/10.1038%2FNATURE05616

7 January 2021

Identifiers

DOI

10.1038/NATURE05616

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

188007

1022931325

0 references

188007

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference