(Q55052166)

16 June 2018

title

Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort. (English)

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16 June 2018

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S Nilsson

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16 June 2018

author name string

S S Amundsen

1

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16 June 2018

J Rundberg

2

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S Adamovic

3

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A H Gudjónsdóttir

4

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H Ascher

5

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J Ek

6

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B A Lie

8

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A T Naluai

9

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L M Sollid

10

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publication date

20 August 2009

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16 June 2018

published in

Genes and Immunity

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volume

11

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issue

1

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page(s)

79-86

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https://scigraph.springernature.com/pub.10.1038/gene.2009.67

exact match

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cites work

Haplotype structure and linkage disequilibrium in chemokine and chemokine receptor genes

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Concordance, disease progression, and heritability of coeliac disease in Italian twins

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Coeliac disease: dissecting a complex inflammatory disorder

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The first large population based twin study of coeliac disease.

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Autoimmune diseases: insights from genome-wide association studies

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A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

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7 January 2021

Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases

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7 January 2021

Association study of IL2/IL21 and FcgRIIa: significant association with the IL2/IL21 region in Scandinavian coeliac disease families

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7 January 2021

Six new coeliac disease loci replicated in an Italian population confirm association with coeliac disease.

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https://api.crossref.org/works/10.1038%2FGENE.2009.67

7 January 2021

Newly identified genetic risk variants for celiac disease related to the immune response

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The risk of celiac disease in 107 families with at least two affected siblings.

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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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Management of infantile gastroenteritis

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Haploview: analysis and visualization of LD and haplotype maps

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The structure of haplotype blocks in the human genome

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The 32-base pair deletion of the chemokine receptor 5 gene (CCR5-Delta32) is not associated with primary sclerosing cholangitis in 363 Scandinavian patients

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Pedigree disequilibrium tests for multilocus haplotypes.

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The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene

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7 January 2021

Association study of the IL18RAP locus in three European populations with coeliac disease

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Mechanism of transdominant inhibition of CCR5-mediated HIV-1 infection by ccr5delta32.

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Negative association between the chemokine receptor CCR5-Delta32 polymorphism and rheumatoid arthritis: a meta-analysis

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Lack of association between the chemokine receptor 5 polymorphism CCR5delta32 in rheumatoid arthritis and juvenile idiopathic arthritis

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7 January 2021

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

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7 January 2021

CCL3L1 gene-containing segmental duplications and polymorphisms in CCR5 affect risk of systemic lupus erythaematosus

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7 January 2021

Shared and distinct genetic variants in type 1 diabetes and celiac disease

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7 January 2021

Identifiers

DOI

10.1038/GENE.2009.67

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16 June 2018

Dimensions Publication ID

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16 June 2018