Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Strong association of common variants in the CDKN2A/CDKN2B region with type 2 diabetes in French Europids.

Diabetologia - 1 May 2008

Duesing K, Fatemifar G, Charpentier G, Marre M, Tichet J, Hercberg S, Balkau B, Froguel P, Gibson F

Abstract excerpt

AIMS/HYPOTHESIS: Genome-wide association studies (GWASs) recently identified common variants in the CDKN2A/CDKN2B region on chromosome 9p as being strongly associated with type 2 diabetes. Since these association signals were not picked up by the French-Canadian GWAS, we sought to replicate these findings in the French Europid population and to further characterise the susceptibility variants at this novel locus....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to 5' Untranslated Regions
Share to Cyclin-Dependent Kinase Inhibitor p15

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cyclin-Dependent Kinase Inhibitor p16

Share to Diabetes Mellitus, Type 2

Share to France

Share to Introns

Share to Linkage Disequilibrium

Share to White People

Source

Identifiers

PMID: 18368387
DOI: 10.1007/s00125-008-0973-4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Strong association of common variants in the CDKN2A/CDKN2B region with type 2 diabetes in French Europids.PMID 18368387Read ↗

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.Semantic proximity Read ↗

Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study).Semantic proximity Read ↗

Type 2 diabetes-associated genetic variants discovered in the recent genome-wide association studies are related to gestational diabetes mellitus in the Korean population.Semantic proximity Read ↗

Investigation of type 2 diabetes risk alleles support CDKN2A/B, CDKAL1, and TCF7L2 as susceptibility genes in a Han Chinese cohort.Semantic proximity Read ↗

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.Semantic proximity Read ↗

Common variants in CDKAL1, CDKN2A/B, IGF2BP2, SLC30A8, and HHEX/IDE genes are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population.Semantic proximity Read ↗

The relationship between five widely-evaluated variants in CDKN2A/B and CDKAL1 genes and the risk of type 2 diabetes: a meta-analysis.Semantic proximity Read ↗

Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population.Semantic proximity Read ↗

Variants of the PPARG, IGF2BP2, CDKAL1, HHEX, and TCF7L2 genes confer risk of type 2 diabetes independently of BMI in the German KORA studies.Semantic proximity Read ↗

Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value.Semantic proximity Read ↗

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.Semantic proximity Read ↗

Impact of common variants of PPARG, KCNJ11, TCF7L2, SLC30A8, HHEX, CDKN2A, IGF2BP2, and CDKAL1 on the risk of type 2 diabetes in 5,164 Indians.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.