(Q28246016)

5

0 references

Natalie J. Prescott

Natalie J Prescott

6

0 references

John D. Rioux

John D Rioux

17

0 references

Christopher G. Mathew

Christopher G Mathew

16

0 references

Alastair Forbes

Alastair Forbes

7

0 references

Cathryn Lewis

Cathryn M Lewis

14

0 references

Mark Joseph Daly

1

Mark J Daly

0 references

Sheila A Fisher

4

Sheila A Fisher

0 references

Jeremy Sanderson

9

Jeremy Sanderson

0 references

author name string

Alexandra V Pearce

2

0 references

Lisa Farwell

3

0 references

John Mansfield

8

0 references

Diane Langelier

10

0 references

Albert Cohen

11

0 references

Alain Bitton

12

0 references

Gary Wild

European Journal of Human Genetics

13

0 references

language of work or name

English

0 references

publication date

July 2005

0 references

published in

0 references

volume

13

0 references

page(s)

835-9

0 references

issue

7

0 references

cites work

Genetic variation in DLG5 is associated with inflammatory bowel disease

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201403

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201403

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201403

Haploview: analysis and visualization of LD and haplotype maps

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.EJHG.5201403

Genome scan analyses and positional cloning strategy in IBD: successes and limitations

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201403

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.5201403

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201403

Inflammatory bowel disease (1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201403

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201403

Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201403

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.EJHG.5201403

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.5201403

Classification of inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201403

inferred from DOI database lookup

7 January 2021

based on heuristic

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201403