(Q37105918)

18 August 2017

FitSNPs: highly differentially expressed genes are more likely to have variants associated with disease (English)

1 reference

18 August 2017

8

Atul J Butte

1 reference

18 August 2017

Rong Chen

1

1 reference

18 August 2017

Alex A Morgan

2

1 reference

18 August 2017

Joel Dudley

3

1 reference

18 August 2017

Tarangini Deshpande

4

1 reference

18 August 2017

Li Li

5

1 reference

18 August 2017

Keiichi Kodama

6

1 reference

18 August 2017

Annie P Chiang

7

1 reference

18 August 2017

5 December 2008

1 reference

18 August 2017

1 reference

18 August 2017

9

1 reference

18 August 2017

R170

1 reference

18 August 2017

12

1 reference

https://scigraph.springernature.com/pub.10.1186/gb-2008-9-12-r170

18 August 2017

0 references

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

14 September 2017

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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

14 September 2017

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Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk

14 September 2017

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Natural selection on genes that underlie human disease susceptibility

14 September 2017

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ENDEAVOUR update: a web resource for gene prioritization in multiple species

14 September 2017

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Association of calpain-10 polymorphisms with type 2 diabetes in the Tunisian population

14 September 2017

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Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians

14 September 2017

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Network-based global inference of human disease genes

14 September 2017

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Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies

14 September 2017

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Evaluation of the association of IGF2BP2 variants with type 2 diabetes in French Caucasians

14 September 2017

1 reference

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Prediction of human disease genes by human-mouse conserved coexpression analysis

14 September 2017

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A gene expression network model of type 2 diabetes links cell cycle regulation in islets with diabetes susceptibility

14 September 2017

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Variations in DNA elucidate molecular networks that cause disease

14 September 2017

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Genetics of gene expression and its effect on disease

14 September 2017

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Multiple loci identified in a genome-wide association study of prostate cancer

14 September 2017

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

14 September 2017

1 reference

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

14 September 2017

1 reference

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Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

14 September 2017

1 reference

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Candidate gene identification approach: progress and challenges

14 September 2017

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AILUN: reannotating gene expression data automatically

14 September 2017

1 reference

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Association of TCF7L2 gene polymorphisms with reduced acute insulin response in Hispanic Americans

14 September 2017

1 reference

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Variations in the HHEX gene are associated with increased risk of type 2 diabetes in the Japanese population.

14 September 2017

1 reference

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Association of polymorphisms in the insulin-degrading enzyme gene with type 2 diabetes in the Korean population.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Identification of pathways for atherosclerosis in mice: integration of quantitative trait locus analysis and global gene expression data

14 September 2017

1 reference

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A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

14 September 2017

1 reference

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

14 September 2017

1 reference

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Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

14 September 2017

1 reference

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

14 September 2017

1 reference

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Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

14 September 2017

1 reference

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Identification of Abcc6 as the major causal gene for dystrophic cardiac calcification in mice through integrative genomics

14 September 2017

1 reference

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

14 September 2017

1 reference

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A computational system to select candidate genes for complex human traits

14 September 2017

1 reference

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The modular nature of genetic diseases.

14 September 2017

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A comprehensive analysis of common copy-number variations in the human genome

14 September 2017

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NCBI GEO: mining tens of millions of expression profiles--database and tools update

14 September 2017

1 reference

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CGI: a new approach for prioritizing genes by combining gene expression and protein-protein interaction data

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Reverse engineering gene networks to identify key drivers of complex disease phenotypes

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

A haplotype map of the human genome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

G2D: a tool for mining genes associated with disease

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

GeneSeeker: extraction and integration of human disease-related information from web-based genetic databases

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

GFINDer: genetic disease and phenotype location statistical analysis and mining of dynamically annotated gene lists

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Integration of text- and data-mining using ontologies successfully selects disease gene candidates

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Speeding disease gene discovery by sequence based candidate prioritization

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Genome-wide identification of genes likely to be involved in human genetic disease

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

The genetic association database

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

A gene atlas of the mouse and human protein-encoding transcriptomes

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

The human genome browser at UCSC

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Significance analysis of microarrays applied to the ionizing radiation response

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

dbSNP: the NCBI database of genetic variation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Medicine. The ultimate model organism

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

TOM: a web-based integrated approach for identification of candidate disease genes

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Effect of 3-acetylpyridine on serotonin uptake and release from rat cerebellar slices

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

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).

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Quantitative trait analysis of type 2 diabetes susceptibility loci identified from whole genome association studies in the Insulin Resistance Atherosclerosis Family Study

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

KCNJ11 E23K polymorphism and diabetes mellitus with adult onset in Czech patients.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Gene expression profiling of peripheral blood from patients with untreated new-onset systemic juvenile idiopathic arthritis reveals molecular heterogeneity that may predict macrophage activation syndrome.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

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.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Replication and identification of novel variants at TCF7L2 associated with type 2 diabetes in Hong Kong Chinese

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

A novel 111/121 diplotype in the Calpain-10 gene is associated with type 2 diabetes.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Predicting disease genes using protein-protein interactions.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

High-density haplotype structure and association testing of the insulin-degrading enzyme (IDE) gene with type 2 diabetes in 4,206 people

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

The functional Thr130Ile and Val255Met polymorphisms of the hepatocyte nuclear factor-4alpha (HNF4A): gene associations with type 2 diabetes or altered beta-cell function among Danes.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Using literature-based discovery to identify disease candidate genes.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Association of Pro12Ala polymorphism of PPARgamma gene with insulin resistance and related diseases

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Polymorphisms in both promoters of hepatocyte nuclear factor 4-alpha are associated with type 2 diabetes in the Amish

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Gene expression in juvenile arthritis and spondyloarthropathy: pro-angiogenic ELR+ chemokine genes relate to course of arthritis.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Human Gene Mutation Database (HGMD): 2003 update.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Association of the Pro12Ala polymorphism in the PPAR-gamma2 gene with 3-year incidence of type 2 diabetes and body weight change in the Finnish Diabetes Prevention Study

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

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

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Studies in 3,523 Norwegians and Meta-Analysis in 11,571 Subjects Indicate That Variants in the Hepatocyte Nuclear Factor 4 (HNF4A) P2 Region Are Associated With Type 2 Diabetes in Scandinavians

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646274

Polymorphisms in the IDE-KIF11-HHEX gene locus are reproducibly associated with type 2 diabetes in a Japanese population

4 December 2018

1 reference

12 December 2020

Association of TCF7L2 polymorphisms with susceptibility to type 2 diabetes in 4,087 Japanese subjects

1 reference

12 December 2020

Type 2 diabetes susceptibility loci in the Ashkenazi Jewish population

1 reference

12 December 2020

Aldehyde dehydrogenase 2 genotype in type 1 diabetes mellitus

1 reference

12 December 2020

Common Variants of the Hepatocyte Nuclear Factor-4 P2 Promoter Are Associated With Type 2 Diabetes in the U.K. Population

1 reference

12 December 2020

Association of the Pro12Ala variant in the peroxisome proliferator-activated receptor-gamma2 gene with obesity in two Caucasian populations

1 reference

12 December 2020

P2 Promoter Variants of the Hepatocyte Nuclear Factor 4 Gene Are Associated With Type 2 Diabetes in Mexican Americans

1 reference

12 December 2020

Common variants in the TCF7L2 gene and predisposition to type 2 diabetes in UK European Whites, Indian Asians and Afro-Caribbean men and women

1 reference

12 December 2020

10.1186/GB-2008-9-12-R170

Identifiers

DOI

1 reference

Dimensions Publication ID

18 August 2017

0 references

1 reference

18 August 2017

1 reference