(Q56968957)

1

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Alienke J Monsuur

2

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María Luisa Mearin

3

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Chris Mulder

European Journal of Human Genetics

4

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publication date

14 June 2006

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published in

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volume

14

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issue

10

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page(s)

1120-1124

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cites work

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The interferon gamma gene in celiac disease: augmented expression correlates with tissue damage but no evidence for genetic susceptibility.

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Coeliac disease: dissecting a complex inflammatory disorder

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Meta and pooled analysis of European coeliac disease data

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A major non-HLA locus in celiac disease maps to chromosome 191 1This study is dedicated to the memory of Lodewijk Sandkuijl (1953–2002), who died shortly after its completion. He was an inspiration to us and was a world expert on biostatistics

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Molecular basis of celiac disease

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Constitutive activation of the signal transducer and activator of transcription pathway in celiac disease lesions

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Interferon-alpha drives T cell-mediated immunopathology in the intestine

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Regulation of the T helper cell type 1 transcription factor T-bet in coeliac disease mucosa

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Cytokine gene polymorphisms and genetic association with coeliac disease in the Finnish population.

21 January 2018

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Genomewide search and association studies in a Finnish celiac disease population: Identification of a novel locus and replication of the HLA and CTLA4 loci

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CTLA-4 in autoimmune diseases--a general susceptibility gene to autoimmunity?

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CTLA4 +49 A/G and CT60 polymorphisms in Dutch coeliac disease patients

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CTLA4 is differentially associated with autoimmune diseases in the Dutch population

21 January 2018

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Variation in the CTLA4/CD28 gene region confers an increased risk of coeliac disease

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A common CTLA4 haplotype associated with coeliac disease

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CTLA-4 gene polymorphism is associated with predisposition to coeliac disease

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Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations.

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CTLA-4/CD28 gene region is associated with genetic susceptibility to coeliac disease in UK families.

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Analysis of the CTLA4 gene in Swedish coeliac disease patients

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Genetic analysis of the CD28/CTLA4/ICOS (CELIAC3) region in coeliac disease

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Genetic association of coeliac disease susceptibility to polymorphisms in the ICOS gene on chromosome 2q33

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Regulation of JAK-STAT signalling in the immune system

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A point mutation in PTPRC is associated with the development of multiple sclerosis

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Revised criteria for diagnosis of coeliac disease. Report of Working Group of European Society of Paediatric Gastroenterology and Nutrition

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7 January 2021

The CTLA4/CD28 gene region on chromosome 2q33 confers susceptibility to celiac disease in a way possibly distinct from that of type 1 diabetes and other chronic inflammatory disorders

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7 January 2021

CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association study

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7 January 2021

Coeliac disease: investigation of proposed causal variants in the CTLA4 gene region

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7 January 2021

CTLA-4 +49 A/G dimorphism in Italian patients with celiac disease

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7 January 2021

No association of CTLA4 gene with celiac disease in the Basque population

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7 January 2021