(Q57232739)

inflammatory bowel diseases

inferred from title

1 reference

J Kere

9

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David A. Hafler

8

object named as

D A Hafler

0 references

Timothy Vyse

10

object named as

T J Vyse

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author name string

P L De Jager

1

0 references

R Graham

2

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L Farwell

3

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S Sawcer

4

0 references

A Richardson

5

0 references

T W Behrens

6

0 references

A Compston

7

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J D Rioux

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

11

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publication date

27 April 2006

0 references

published in

Genes and Immunity

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volume

7

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issue

4

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page(s)

327-334

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

CARD15/NOD2 risk alleles in the development of Crohn's disease in the Australian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Transmission of CARD15 (NOD2) variants within families of patients with inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Analysis of the IBD5 locus and potential gene-gene interactions in Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Genotype-phenotype analysis of the Crohn's disease susceptibility haplotype on chromosome 5q31.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Functional variants of OCTN cation transporter genes are associated with Crohn disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Genetic variation in DLG5 is associated with inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Association of DLG5 R30Q variant with inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

The epidemiology and the pathogenesis of inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Familial occurrence of autoimmune diseases and autoantibodies in a Caucasian population of patients with systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Concurrence of inflammatory bowel disease and multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

The clustering of other chronic inflammatory diseases in inflammatory bowel disease: a population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Increased risk for demyelinating diseases in patients with inflammatory bowel disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

HLA-DR and -DQ phenotypes in inflammatory bowel disease: a meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

A high-density screen for linkage in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

A genome-wide search for susceptibility genes in human systemic lupus erythematosus sib-pair families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Genome screening in human systemic lupus erythematosus: results from a second Minnesota cohort and combined analyses of 187 sib-pair families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Genome-wide screen for systemic lupus erythematosus susceptibility genes in multiplex families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Crohn's associated NOD2 gene variants are not involved in determining susceptibility to multiple sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

A haplotype map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

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.GENE.6364303

NOD2 and Crohn's disease: loss or gain of function?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

CARD15: a pleiotropic autoimmune gene that confers susceptibility to psoriatic arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Both donor and recipient NOD2/CARD15 mutations associate with transplant-related mortality and GvHD following allogeneic stem cell transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

CARD15 mutations in Blau syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Signalling pathways and molecular interactions of NOD1 and NOD2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

The frameshift mutation in Nod2 results in unresponsiveness not only to Nod2- but also Nod1-activating peptidoglycan agonists

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Muramyl dipeptide and toll-like receptor sensitivity in NOD2-associated Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

PTPN22 and autoimmune disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

The 1982 revised criteria for the classification of systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Common NOD2 polymorphisms in Hong Kong Chinese patients with systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Role ofNOD2 variants in spondylarthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

Association of NOD2 with Crohn's Disease in a homogenous Irish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

Association between mutations in the CARD15 (NOD2) gene and Crohn's disease in Israeli Jewish patients

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

Analysis of the CARD15 variants R702W, G908R and L1007fs in Italian IBD patients

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

The frame-shift mutation of the NOD2/CARD15 gene is significantly increased in ulcerative colitis: an *IG-IBD study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

Possible familial association of multiple sclerosis and inflammatory bowel disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

Multiple sclerosis and systemic lupus erythematosus. Occurrence in two generations of the same family

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

MS and SLE in twins of successive generations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

Familial occurrence of multiple sclerosis with thyroid disease and systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

Association of ulcerative colitis with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

Autoimmune disease in first-degree relatives of patients with multiple sclerosis. A UK survey

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

The genetic epidemiology of multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

The three most common CARD15 mutations associated with Crohn's disease and the chromosome 16 susceptibility locus for systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021

Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364303

7 January 2021