HLA types in celiac disease patients not carrying the DQA105-DQB102 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac Disease (Q28185658)

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scientific article (publication date: April 2003)

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English	HLA types in celiac disease patients not carrying the DQA105-DQB102 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac Disease	scientific article (publication date: April 2003)

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1 November 2019

HLA types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac Disease (English)

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1 November 2019

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Ludvig M Sollid

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Ludvig M Sollid

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1 November 2019

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Kati Karell

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1 November 2019

Andrew S Louka

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Simon J Moodie

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1 November 2019

Henry Ascher

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1 November 2019

Fabienne Clot

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1 November 2019

Paul J Ciclitira

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1 November 2019

European Genetics Cluster on Celiac Disease

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1 April 2003

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Human Immunology

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469-477

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1 November 2019

The first large population based twin study of coeliac disease.

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Evidence for a primary association of celiac disease to a particular HLA-DQ alpha/beta heterodimer

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Molecular basis of celiac disease

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A study of Italian pediatric celiac disease patients confirms that the primary HLA association is to the DQ(alpha 1*0501, beta 1*0201) heterodimer

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HLA-DR and -DQ genotypes of celiac disease patients serologically typed to be non-DR3 or non-DR5/7.

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HLA-DQ2-negative celiac disease in Finland and Spain.

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HLA-DR53 molecules are associated with susceptibility to celiac disease and selectively bind gliadin-derived peptides

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Synergistic effect of two HLA heterodimers in the susceptibility to celiac disease in Tunisia

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The HLA-DRB4 gene does not explain genetic susceptibility in HLA-DQ2-negative celiac disease

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The HLA-DRB4 gene is present in half of the Spanish HLA-DQ2-negative celiac patients

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MICA-A5.1 allele is associated with atypical forms of celiac disease in HLA-DQ2-negative patients

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Celiac patients predominantly inherit HLA-DPB1*0101 positive haplotype from HLA-DQ2 homozygous parent

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Not all HLA DR3 DQ2 haplotypes confer equal susceptibility to coeliac disease: transmission analysis in families

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HLA in coeliac disease families: a novel test of risk modification by the 'other' haplotype when at least one DQA1*05-DQB1*02 haplotype is carried

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HLA-DQB1 and -DQA1 typing by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours

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Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21

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Reevaluation of the relative risk for susceptibility to celiac disease of HLA-DRB1, -DQA1, -DQB1, -DPB1, and -TAP2 alleles in a French population.

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10.1016/S0198-8859(03)00027-2

2 references

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Europe PubMed Central

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1 November 2019

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12651074%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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