Gene-gene interactions lead to higher risk for development of type 2 diabetes in an Ashkenazi Jewish population (Q33548779)

28 July 2017

Gene-gene interactions lead to higher risk for development of type 2 diabetes in an Ashkenazi Jewish population (English)

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28 July 2017

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1 reference

Benjamin Glaser

9

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Nir Barzilai

7

object named as

Nir Barzilai

1 reference

28 July 2017

4

Julio Wainstein

1 reference

28 July 2017

Rosalind J Neuman

1

1 reference

28 July 2017

Jon Wasson

2

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28 July 2017

Gil Atzmon

3

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28 July 2017

Yair Yerushalmi

5

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28 July 2017

Joseph Cohen

6

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28 July 2017

Ilana Blech

8

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28 July 2017

M Alan Permutt

10

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28 July 2017

language of work or name

English

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publication date

26 March 2010

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28 July 2017

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28 July 2017

5

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28 July 2017

e9903

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28 July 2017

3

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Creative Commons Attribution 4.0 International

28 July 2017

start time

26 March 2010

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Genetic architecture of type 2 diabetes: recent progress and clinical implications

21 June 2018

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The emerging genetic architecture of type 2 diabetes

21 June 2018

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Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies

21 June 2018

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Adiponectin levels and genotype: a potential regulator of life span in humans

21 June 2018

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

21 June 2018

1 reference

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Evidence of interaction between PPARG2 and HNF4A contributing to variation in insulin sensitivity in Mexican Americans

21 June 2018

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Testing of diabetes-associated WFS1 polymorphisms in the Diabetes Prevention Program

21 June 2018

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Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

21 June 2018

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The importance of TCF7L2.

21 June 2018

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Common variants in WFS1 confer risk of type 2 diabetes

21 June 2018

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A generalized combinatorial approach for detecting gene-by-gene and gene-by-environment interactions with application to nicotine dependence

21 June 2018

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Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene

21 June 2018

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

21 June 2018

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Three-locus and four-locus QTL interactions influence mouse insulin-like growth factor-I.

21 June 2018

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

21 June 2018

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Lipoprotein genotype and conserved pathway for exceptional longevity in humans

21 June 2018

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A flexible computational framework for detecting, characterizing, and interpreting statistical patterns of epistasis in genetic studies of human disease susceptibility

21 June 2018

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Gene-environment interactions in human diseases

21 June 2018

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Unique lipoprotein phenotype and genotype associated with exceptional longevity

21 June 2018

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A perspective on epistasis: limits of models displaying no main effect

21 June 2018

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Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer

21 June 2018

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Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association

21 June 2018

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Lifestyle intervention, glucose tolerance, and risk of developing type 2 diabetes mellitus.

31 October 2018

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Genetic study of Saudi diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes

31 October 2018

1 reference

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A balanced accuracy function for epistasis modeling in imbalanced datasets using multifactor dimensionality reduction.

31 October 2018

1 reference

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Mice conditionally lacking the Wolfram gene in pancreatic islet beta cells exhibit diabetes as a result of enhanced endoplasmic reticulum stress and apoptosis.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845632

Analysis of separate and combined effects of common variation in KCNJ11 and PPARG on risk of type 2 diabetes

31 October 2018

1 reference

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Multifactor-dimensionality reduction shows a two-locus interaction associated with Type 2 diabetes mellitus.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845632

Young-onset type 2 diabetes families are the major contributors to genetic loci in the Diabetes UK Warren 2 genome scan and identify putative novel loci on chromosomes 8q21, 21q22, and 22q11.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845632

E23K single nucleotide polymorphism in the islet ATP-sensitive potassium channel gene (Kir6.2) contributes as much to the risk of Type II diabetes in Caucasians as the PPARgamma Pro12Ala variant.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845632

Multifactor dimensionality reduction software for detecting gene-gene and gene-environment interactions.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845632

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845632

K(IR)6.2 polymorphism predisposes to type 2 diabetes by inducing overactivity of pancreatic beta-cell ATP-sensitive K(+) channels

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845632

Combined analysis of 19 common validated type 2 diabetes susceptibility gene variants shows moderate discriminative value and no evidence of gene–gene interaction

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845632

Gene-gene interactions betweenHNF4AandKCNJ11in predicting Type 2 diabetes in women

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845632

Evaluation of Common Variants in the Six Known Maturity-Onset Diabetes of the Young (MODY) Genes for Association With Type 2 Diabetes

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2845632

Assessing allele frequencies of single nucleotide polymorphisms in DNA pools by pyrosequencing technology

31 October 2018

1 reference

12 December 2020

Association Studies of Genetic Variation in the WFS1 Gene and Type 2 Diabetes in U.K. Populations

1 reference

12 December 2020

Candidate gene studies reveal that the WFS1 gene joins the expanding list of novel type 2 diabetes genes

1 reference

12 December 2020

A Genome Scan for Type 2 Diabetes Susceptibility Loci in a Genetically Isolated Population

1 reference

12 December 2020

Commentary: facing the challenge of gene-environment interaction: the two-by-four table and beyond

1 reference

12 December 2020

Epistasis and the evolutionary dynamics of measured genotypic values during simulated serial bottlenecks

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0009903

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DOI

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28 July 2017

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28 July 2017

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