IGR2096a_1 T and IGR2198a_1 C alleles on IBD5 locus of chromosome 5q31 region confer risk for Crohn's disease in Hungarian patients. (Q54494742)

30 May 2018

title

IGR2096a_1 T and IGR2198a_1 C alleles on IBD5 locus of chromosome 5q31 region confer risk for Crohn's disease in Hungarian patients. (English)

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30 May 2018

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Lilla Lakner

1

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30 May 2018

Veronika Csöngei

2

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30 May 2018

Patrícia Sarlós

3

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30 May 2018

Luca Járomi

4

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30 May 2018

Eniko Sáfrány

5

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30 May 2018

Márta Varga

6

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30 May 2018

Péter Orosz

7

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30 May 2018

Lili Magyari

8

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30 May 2018

Judit Bene

9

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30 May 2018

Pál Miheller

10

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30 May 2018

Zsolt Tulassay

11

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30 May 2018

Béla Melegh

12

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30 May 2018

publication date

13 February 2009

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30 May 2018

International Journal of Colorectal Disease

published in

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30 May 2018

volume

24

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30 May 2018

issue

5

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30 May 2018

page(s)

503-507

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30 May 2018

Review article: Inflammatory bowel disease and genetics

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A genome-wide search identifies potential new susceptibility loci for Crohn's disease

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Role of CARD15, DLG5 and OCTN genes polymorphisms in children with inflammatory bowel diseases

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Association between polymorphisms in the Toll-like receptor 4, CD14, and CARD15/NOD2 and inflammatory bowel disease in the Greek population

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IBD5 polymorphisms in inflammatory bowel disease: association with response to infliximab

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Prevalence of SLC22A4, SLC22A5 and CARD15 gene mutations in Hungarian pediatric patients with Crohn's disease

21 January 2018

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Contribution of the IBD5 locus to Crohn's disease in the Swedish population

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Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

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Inflammatory Bowel Disease

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Polymorphisms in the organic cation transporter genes SLC22A4 and SLC22A5 and Crohn's disease in a New Zealand Caucasian cohort

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Variants of OCTN1-2 cation transporter genes are associated with both Crohn's disease and ulcerative colitis

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A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

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Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci

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12 December 2020

DLG5 variants in inflammatory bowel disease

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Mechanisms of Disease: pathogenesis of Crohn's disease and ulcerative colitis

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Single nucleotide polymorphisms of OCTN1, OCTN2, and DLG5 genes in Greek patients with Crohn's disease

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Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

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Comparison of mtDNA haplogroups in Hungarians with four other European populations: a small incidence of descents with Asian origin

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12 December 2020

rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants

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Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci

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The Contribution of OCTN1/2 Variants Within the IBD5 Locus to Disease Susceptibility and Severity in Crohn’s Disease

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Evidence for association of OCTN genes and IBD5 with ulcerative colitis

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Smoking in inflammatory bowel diseases: good, bad or ugly?

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Functional variants of OCTN cation transporter genes are associated with Crohn disease

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12 December 2020

A Nonsynonymous SNP in ATG16L1 Predisposes to Ileal Crohn’s Disease and Is Independent of CARD15 and IBD5

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Refined genomic localization and ethnic differences observed for the IBD5 association with Crohn's disease

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12 December 2020

Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's disease

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12 December 2020

Characterization of genotype-phenotype relationships and stratification by the CARD15 variant genotype for inflammatory bowel disease susceptibility loci using multiple short tandem repeat genetic markers

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Association of Organic Cation Transporter Risk Haplotype With Perianal Penetrating Crohn’s Disease but Not With Susceptibility to IBD

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Direct or indirect association in a complex disease: the role ofSLC22A4 andSLC22A5 functional variants in Crohn disease

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A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease

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12 December 2020

Prevalence of SLC22A4 1672T and SLC22A5 -207C combination defined TC haplotype in Hungarian ulcerative colitis patients.

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12 December 2020

Lack of association between IBD5 and Crohn's disease in Japanese patients demonstrates population-specific differences in inflammatory bowel disease.

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12 December 2020

Population-based controlled study of social support, self-perceived stress, activity and work issues, and access to health care in inflammatory bowel disease.

1 reference

12 December 2020

10.1007/S00384-009-0670-X

Identifiers

DOI

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30 May 2018

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30 May 2018