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

Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations.

Diabetes research and clinical practice - 1 Mar 2016

Prabhanjan Manasa, Suresh Raviraj V, Murthy Megha N, Ramachandra Nallur B

Abstract excerpt

AIMS: To identify the role of copy number variations (CNVs) on disease risk genes and its effect on disease phenotypes in type 2 diabetes mellitus (T2DM) in 12 random populations using high throughput arrays. METHODS: CNV analysis was carried out on a total of 1715 individuals from 12 populations, from ArrayExpress Archive of the European Bioinformatics Institute along with our subjects using Affymetrix Genome...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Aged
Share to Computational Biology

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Diabetes Mellitus, Type 2

Share to DNA Copy Number Variations

Share to Genetic Predisposition to Disease

Share to Genome-Wide Association Study

Share to Young Adult

Source

Identifiers

PMID: 26830856
DOI: 10.1016/j.diabres.2015.12.015

Genes

EGFR
TSPAN8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations.PMID 26830856Read ↗

Association analysis of copy number variations in type 2 diabetes-related susceptible genes in a Chinese population.Semantic proximity Read ↗

The genetic effect of copy number variations on the risk of type 2 diabetes in a Korean population.Semantic proximity Read ↗

Analyses of copy number variation of GK rat reveal new putative type 2 diabetes susceptibility loci.Semantic proximity Read ↗

Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjects.Semantic proximity Read ↗

[Copy number variation: markers and predictors for type 2 diabetes].Semantic proximity Read ↗

CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan Subpopulations.Semantic proximity Read ↗

Implications of gene copy-number variation in health and diseases.Semantic proximity Read ↗

[Association of common copy number variations with diseases].Semantic proximity Read ↗

Divergent patterns of genic copy number variation in KCNIP1 gene reveal risk locus of type 2 diabetes in Chinese population.Semantic proximity Read ↗

Genome-wide analysis of copy number variation in type 1 diabetes.Semantic proximity Read ↗

Genome-wide copy number variation study reveals KCNIP1 as a modulator of insulin secretion.Semantic proximity Read ↗

Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.Semantic proximity Read ↗

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