(Q82627169)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16493449%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations (English)

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17 January 2020

5

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17 January 2020

10

Bjorn Moum

1 reference

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17 January 2020

9

Jorgen Jahnsen

1 reference

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17 January 2020

12

Morten H Vatn

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17 January 2020

author name string

Valentina Medici

1

1 reference

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17 January 2020

Silvia Mascheretti

2

1 reference

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17 January 2020

Peter J P Croucher

3

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17 January 2020

Monika Stoll

4

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17 January 2020

Jochen Grebe

6

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17 January 2020

Giacomo C Sturniolo

7

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17 January 2020

Camilla Solberg

8

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17 January 2020

Stefan Schreiber

11

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17 January 2020

publication date

1 April 2006

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European Journal of Human Genetics

17 January 2020

published in

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17 January 2020

volume

14

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17 January 2020

issue

4

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17 January 2020

page(s)

459-468

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201576

17 January 2020

exact match

0 references

cites work

Incidence of Crohn's Disease in Four Counties in Southeastern Norway, 1990–93 A Prospective Population-Based Study

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7 January 2021

Incidence of ulcerative colitis and indeterminate colitis in four counties of southeastern Norway, 1990-93. A prospective population-based study. The Inflammatory Bowel South-Eastern Norway (IBSEN) Study Group of Gastroenterologists.

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7 January 2021

Incidence of inflammatory bowel disease across Europe: is there a difference between north and south? Results of the European Collaborative Study on Inflammatory Bowel Disease (EC-IBD)

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7 January 2021

Familial occurrence of inflammatory bowel disease

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7 January 2021

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

1 reference

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7 January 2021

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

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7 January 2021

Genetics of inflammatory bowel disease: scientific and clinical implications

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

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

1 reference

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7 January 2021

Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-kappaB

1 reference

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7 January 2021

Host recognition of bacterial muramyl dipeptide mediated through NOD2. Implications for Crohn's disease

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7 January 2021

Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

The molecular classification of the clinical manifestations of Crohn's disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease

1 reference

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7 January 2021

NOD2/CARD15 gene polymorphisms and Crohn's disease in the Chinese population.

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

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

1 reference

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7 January 2021

NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

Subclinical intestinal inflammation: an inherited abnormality in Crohn’s disease relatives?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

Genetic variation in DLG5 is associated with inflammatory bowel disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

Identification of a novel human homolog of the Drosophila dlg, P-dlg, specifically expressed in the gland tissues and interacting with p55

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

Interaction of lp-dlg/KIAA0583, a membrane-associated guanylate kinase family protein, with vinexin and beta-catenin at sites of cell-cell contact

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study

1 reference

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7 January 2021

Inflammatory bowel disease: re-evaluation of the diagnosis in a prospective population based study in south eastern Norway

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7 January 2021

Inflammatory bowel disease (1)

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7 January 2021

A simple classification of Crohn's disease: report of the Working Party for the World Congresses of Gastroenterology, Vienna 1998.

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7 January 2021

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

1 reference

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7 January 2021

The Nod2 gene in Crohn's disease: implications for future research into the genetics and immunology of Crohn's disease

1 reference

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7 January 2021

Frequency of NOD2/CARD15 variants in both sporadic and familial cases of Crohn's disease across Italy. An Italian Group for Inflammatory Bowel Disease Study.

1 reference

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7 January 2021

Prevalence of mutations of the NOD2/CARD15 gene and relation to phenotype in Spanish patients with Crohn disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

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

1 reference

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7 January 2021

DLG5 variants do not influence susceptibility to inflammatory bowel disease in the Scottish population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

Crohn's disease: ethnic variation in CARD15 genotypes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

Association of DLG5 R30Q variant with inflammatory bowel disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201576

7 January 2021

Association of DLG5 and inflammatory bowel disease across populations

1 reference

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7 January 2021

Understanding Association and Causality in the Genetic Studies of Inflammatory Bowel Disease

1 reference

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7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201576

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16493449%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1 reference