(Q57606742)

John D Rioux

15

0 references

Jerome I Rotter

9

Jerome I Rotter

0 references

Mark Joseph Daly

16

Mark J Daly

0 references

Kent D Taylor

12

Kent D Taylor

0 references

Steven R. Brant

4

Steven R Brant

0 references

Mark S. Silverberg

1

Mark S Silverberg

0 references

Judy H. Cho

14

Judy H Cho

0 references

A Hillary Steinhart

11

A Hillary Steinhart

0 references

Lisa Wu Datta

6

Lisa W Datta

0 references

L Philip Schumm

10

L Philip Schumm

0 references

Huiying Yang

13

Huiying Yang

0 references

Gillian P Bromfield

5

Gillian Bromfield

0 references

Sunanda Kane

8

Sunanda V Kane

0 references

author name string

Niraj Jani

European Journal of Human Genetics

7

0 references

publication date

10 January 2007

0 references

published in

0 references

volume

15

0 references

issue

3

0 references

page(s)

328-335

0 references

exact match

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201756

0 references

cites work

Inflammatory Bowel Disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

21 January 2018

Indeterminate colitis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Update in inflammatory bowel disease pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Ulcerative colitis and Crohn's disease in an unselected population of monozygotic and dizygotic twins. A study of heritability and the influence of smoking

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Genetics versus environment in inflammatory bowel disease: results of a British twin study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Inflammatory bowel disease in a Swedish twin cohort: a long-term follow-up of concordance and clinical characteristics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Familial occurrence of inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Mapping of a susceptibility locus for Crohn's disease on chromosome 16

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

A genome-wide search identifies potential new susceptibility loci for Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

High-density genome scan in Crohn disease shows confirmed linkage to chromosome 14q11-12

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

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.EJHG.5201756

Differential effects of NOD2 variants on Crohn's disease risk and phenotype in diverse populations: a metaanalysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Lack of common NOD2 variants in Japanese patients with Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Linkage disequilibrium patterns of the human genome across populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

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.EJHG.5201756

High-resolution haplotype structure in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

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.EJHG.5201756

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.EJHG.5201756

Further evidence of IBD5/CARD15 (NOD2) epistasis in the susceptibility to ulcerative colitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

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.EJHG.5201756

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.EJHG.5201756

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

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.EJHG.5201756

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.EJHG.5201756

Association of Organic Cation Transporter Risk Haplotype With Perianal Penetrating Crohn’s Disease but Not With Susceptibility to IBD

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Evidence for association of OCTN genes and IBD5 with ulcerative colitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

New approaches to gene hunting in IBD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Parental phenotypes in family-based association analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Perinuclear antineutrophil cytoplasmic antibodies in patients with Crohn's disease define a clinical subgroup

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

inferred from DOI database lookup

7 January 2021

based on heuristic

The Contribution of OCTN1/2 Variants Within the IBD5 Locus to Disease Susceptibility and Severity in Crohn’s Disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756

inferred from DOI database lookup

7 January 2021

based on heuristic

Variants of OCTN1-2 cation transporter genes are associated with both Crohn's disease and ulcerative colitis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201756