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Article

Lack of association of MYO9B genetic variants with coeliac disease in a British cohort.

Gut - 1 Jul 2006

Hunt K A, Monsuur A J, McArdle W L, Kumar P J, Travis S P L, Walters J R F, Jewell D P, Strachan D P, Playford R J, Wijmenga C, van Heel D A

Abstract excerpt

BACKGROUND AND AIMS: Development of coeliac disease involves an interaction between environmental factors (especially dietary wheat, rye, and barley antigens) and genetic factors (there is strong inherited disease susceptibility). The known human leucocyte antigen (HLA)-DQ2 and -DQ8 association explains only a minority of disease heritability. A recent study in the Dutch population suggested that genetic...

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Identifiers

PMID: 16423886
DOI: 10.1136/gut.2005.086769
PMCID: PMC1856329

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Lack of association of MYO9B genetic variants with coeliac disease in a British cohort.PMID 16423886Read ↗

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Lack of Association between MYO9B Gene Polymorphisms and Susceptibility to Coeliac Disease in Caucasians: Evidence from a Meta-Analysis.Semantic proximity Read ↗

Association analysis of MYO9B gene polymorphisms and inflammatory bowel disease in a Norwegian cohort.Semantic proximity Read ↗

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Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect.Semantic proximity Read ↗

Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis.Semantic proximity Read ↗

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