(Q57532982)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18273036%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

title

Variant form of STAT4 is associated with primary Sjögren's syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18273036%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

1 reference

8

1 reference

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2 January 2020

author name string

B D Korman

1

1 reference

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2 January 2020

M I Alba

2

1 reference

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2 January 2020

J M Le

3

1 reference

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2 January 2020

I Alevizos

4

1 reference

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2 January 2020

J A Smith

5

1 reference

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2 January 2020

N P Nikolov

6

1 reference

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2 January 2020

D L Kastner

7

1 reference

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2 January 2020

G G Illei

9

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2 January 2020

publication date

14 February 2008

1 reference

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2 January 2020

1 reference

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2 January 2020

volume

9

1 reference

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2 January 2020

page(s)

267-270

1 reference

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2 January 2020

issue

3

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https://scigraph.springernature.com/pub.10.1038/gene.2008.1

2 January 2020

exact match

0 references

cites work

Anti-Ro (SS-A) and anti-La (SS-B) in patients with Sjögren's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

Gene interaction at HLA-DQ enhances autoantibody production in primary Sjögren's syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

No evidence for association between 1858 C/T single-nucleotide polymorphism of PTPN22 gene and primary Sjögren's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

Influence of CTLA4 haplotypes on susceptibility and some extraglandular manifestations in primary Sjögren's syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

CTLA-4 +49A/G and CT60 gene polymorphisms in primary Sjögren syndrome

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

Classification criteria for Sjögren's syndrome: a revised version of the European criteria proposed by the American-European Consensus Group

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

Signaling by IL-12 and IL-23 and the immunoregulatory roles of STAT4.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

Association of STAT4 with rheumatoid arthritis in the Korean population

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

Association of an IRF5 gene functional polymorphism with Sjögren's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2008.1

7 January 2021

Identifiers

DOI

10.1038/GENE.2008.1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18273036%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

1 reference