Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study (Q34739104)

4 August 2017

Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study (English)

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4 August 2017

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11

Philippe Froguel

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Hélène Choquet

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Hélène Choquet

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Michel Marre

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Michel Marre

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David Meyre

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David Meyre

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Stéphane Cauchi

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4 August 2017

Christine Proença

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Stefan Gaget

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Franck De Graeve

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Beverley Balkau

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Jean Tichet

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Martine Vaxillaire

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D.E.S.I.R. Study Group

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22 January 2008

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Journal of Molecular Medicine

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86

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3

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341-348

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https://scigraph.springernature.com/pub.10.1007/s00109-007-0295-x

4 August 2017

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

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ENPP1 K121Q polymorphism and obesity, hyperglycaemia and type 2 diabetes in the prospective DESIR Study

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12 December 2020

A Search for Variants Associated With Young-Onset Type 2 Diabetes in American Indians in a 100K Genotyping Array

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12 December 2020

[An epidemiologic survey from a network of French Health Examination Centres, (D.E.S.I.R.): epidemiologic data on the insulin resistance syndrome]

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12 December 2020

Genome-wide association studies provide new insights into type 2 diabetes aetiology

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12 December 2020

Polymorphisms within novel risk loci for type 2 diabetes determine beta-cell function

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12 December 2020

Whole-genome patterns of common DNA variation in three human populations

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12 December 2020

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

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12 December 2020

K-value and low insulin secretion in a non-obese white population: predicted glucose tolerance after 25 years

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12 December 2020

What makes a good genetic association study?

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12 December 2020

Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

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Studies of association of variants near the HHEX, CDKN2A/B, and IGF2BP2 genes with type 2 diabetes and impaired insulin release in 10,705 Danish subjects: validation and extension of genome-wide association studies.

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

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

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

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

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American Diabetes Association: clinical practice recommendations 1997

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Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF.

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Common variants of the novel type 2 diabetes genes CDKAL1 and HHEX/IDE are associated with decreased pancreatic beta-cell function

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Beta-catenin regulates the gene of MMP-26, a novel metalloproteinase expressed both in carcinomas and normal epithelial cells

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Cdk5-dependent regulation of glucose-stimulated insulin secretion.

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IA1 is NGN3-dependent and essential for differentiation of the endocrine pancreas

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Variation in the HHEX–IDE gene region predisposes to type 2 diabetes in the prospective, population-based EPIC-Potsdam cohort

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Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies

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12 December 2020

10.1007/S00109-007-0295-X

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4 August 2017

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