(Q46878243)

26 December 2017

title

Evaluating the role of the 620W allele of protein tyrosine phosphatase PTPN22 in Crohn's disease and multiple sclerosis (English)

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26 December 2017

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11

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26 December 2017

Alastair Compston

9

object named as

Alastair Compston

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26 December 2017

10

David A Hafler

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26 December 2017

Stephen Sawcer

2

object named as

Stephen Sawcer

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26 December 2017

Philip L. De Jager

1

object named as

Philip L De Jager

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26 December 2017

author name string

Alicja Waliszewska

3

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26 December 2017

Lisa Farwell

4

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26 December 2017

Gary Wild

5

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26 December 2017

Albert Cohen

6

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26 December 2017

Diane Langelier

7

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26 December 2017

Alain Bitton

8

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26 December 2017

publication date

1 March 2006

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26 December 2017

European Journal of Human Genetics

published in

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26 December 2017

volume

14

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26 December 2017

issue

3

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26 December 2017

page(s)

317-321

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26 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201548

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

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/10.1038%2FSJ.EJHG.5201548

The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

PEST domain-enriched tyrosine phosphatase (PEP) regulation of effector/memory T cells

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

Inflammatory bowel disease: autoimmune or immune-mediated pathogenesis?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

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/10.1038%2FSJ.EJHG.5201548

Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: evidence for epistasis between 1p and IBD1.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group

21 January 2018

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A second-generation genomic screen for multiple sclerosis

21 January 2018

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Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs

21 January 2018

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A high-density screen for linkage in multiple sclerosis

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

Protein tyrosine phosphatase gene (PTPN22) polymorphism in multiple sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

Association between the PTPN22 gene and rheumatoid arthritis and juvenile idiopathic arthritis in a UK population: further support that PTPN22 is an autoimmunity gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

A case-control study of tyrosine phosphatase (PTPN22) confirms the lack of association with Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

New diagnostic criteria for multiple sclerosis: guidelines for research protocols

21 January 2018

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CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure

21 January 2018

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Calculating confidence intervals for relative risks (odds ratios) and standardised ratios and rates

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

21 January 2018

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Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

inferred from DOI database lookup

7 January 2021

based on heuristic

A meta-analysis of whole genome linkage screens in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

inferred from DOI database lookup

7 January 2021

based on heuristic

Classification of inflammatory bowel disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201548

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5201548

1 reference

26 December 2017

1 reference

26 December 2017