(Q46808828)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

title

The functional R620W variant of the PTPN22 gene is associated with celiac disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Izortze Santin

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Juan Carlos Vitoria

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Jose Ramon Bilbao

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

author name string

A Castellanos-Rubio

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

A M Aransay

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

publication date

10 January 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

volume

71

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

page(s)

247-249

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

Prospective population screening for celiac disease: high prevalence in the first 3 years of life.

1 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

Genetics in coeliac disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

C1858T functional variant of PTPN22 gene is not associated with celiac disease genetic predisposition

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

HLA-DQA1 and HLA-DQB1 genetic markers and clinical presentation in celiac disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

Protein tyrosine phosphatase PTPN22 in human autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.01002.X

10.1111/J.1399-0039.2007.01002.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18194365%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference