Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31 (Q57436278)

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28 January 2020

title

Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31 (English)

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28 January 2020

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linkage disequilibrium

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5

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28 January 2020

Alastair Forbes

6

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28 January 2020

Cathryn Lewis

8

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28 January 2020

Christopher G. Mathew

9

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28 January 2020

author name string

Onnie C

1

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28 January 2020

Fisher SA

2

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28 January 2020

King K

3

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28 January 2020

Mirza M

4

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28 January 2020

Sanderson J

7

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28 January 2020

publication date

18 May 2006

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28 January 2020

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28 January 2020

volume

7

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28 January 2020

issue

5

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28 January 2020

page(s)

359-365

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https://scigraph.springernature.com/pub.10.1038/sj.gene.6364307

28 January 2020

exact match

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

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Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

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Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease.

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IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis

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High-resolution haplotype structure in the human genome

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

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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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Understanding Association and Causality in the Genetic Studies of Inflammatory Bowel Disease

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Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter

21 January 2018

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An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis

21 January 2018

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Variation in conserved non-coding sequences on chromosome 5q and susceptibility to asthma and atopy.

21 January 2018

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Evidence for common genetic control in pathways of inflammation for Crohn's disease and psoriatic arthritis

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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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Genetic Variation at the Chromosome 16 Chemokine Gene Cluster: Development of a Strategy for Association Studies in Complex Disease

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Genetic association between EPHX1 and Crohn's disease: population stratification, genotyping error, or random chance?

21 January 2018

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No association of the NFKB1 promoter polymorphism with ulcerative colitis in a British case control cohort.

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