(Q36453347)

14 August 2017

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title

Identifying susceptibility genes for immunological disorders: patterns, power, and proof (English)

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14 August 2017

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John D Rioux

2

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author name string

Robert Plenge

series ordinal

1

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14 August 2017

publication date

1 April 2006

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14 August 2017

published in

Immunological Reviews

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14 August 2017

volume

210

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14 August 2017

page(s)

40-51

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

14 August 2017

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21 January 2018

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21 January 2018

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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

21 January 2018

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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

21 January 2018

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IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis

21 January 2018

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A gene-environment interaction between smoking and shared epitope genes in HLA-DR provides a high risk of seropositive rheumatoid arthritis

21 January 2018

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'Racial' differences in genetic effects for complex diseases

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

21 January 2018

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Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

21 January 2018

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21 January 2018

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An autoimmune disease-associated CTLA-4 splice variant lacking the B7 binding domain signals negatively in T cells

21 January 2018

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The role of the DR4 shared epitope in selection and commitment of autoreactive T cells in rheumatoid arthritis.

21 January 2018

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Cutting edge: the conversion of arginine to citrulline allows for a high-affinity peptide interaction with the rheumatoid arthritis-associated HLA-DRB1*0401 MHC class II molecule

21 January 2018

1 reference

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Role of Nod2 in the Response of Macrophages to Toll-Like Receptor Agonists

21 January 2018

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NOD2 is a negative regulator of Toll-like receptor 2-mediated T helper type 1 responses

21 January 2018

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Nod2-dependent regulation of innate and adaptive immunity in the intestinal tract

21 January 2018

1 reference

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Nod2 mutation in Crohn's disease potentiates NF-kappaB activity and IL-1beta processing

21 January 2018

1 reference

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NOD2 mutation and mice: no Crohn's disease but many lessons to learn.

21 January 2018

1 reference

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Allelic Variation in Human Gene Expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0105-2896.2006.00372.X

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.0105-2896.2006.00372.X

10.1111/J.0105-2896.2006.00372.X

21 January 2018

Identifiers

DOI

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release_sb3meqhlkjaqzdg7h7wfvthh4q

14 August 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/sb3meqhlkjaqzdg7h7wfvthh4q

mapped directly with Wikidata item

24 November 2022

based on heuristic

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