The relation between NOD2/CARD15 mutations and the prevalence and phenotypic heterogeneity of Crohn's disease: lessons from the Israeli Arab Crohn's disease cohort (Q44587691)

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scientific article published in September 2005

Language	Label	Description	Also known as
English	The relation between NOD2/CARD15 mutations and the prevalence and phenotypic heterogeneity of Crohn's disease: lessons from the Israeli Arab Crohn's disease cohort	scientific article published in September 2005

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

The relation between NOD2/CARD15 mutations and the prevalence and phenotypic heterogeneity of Crohn's disease: lessons from the Israeli Arab Crohn's disease cohort (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

0 references

Crohn's disease

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based on heuristic

inferred from title

phenotypic heterogeneity

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based on heuristic

inferred from title

11

object named as

Rami Eliakim

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Europe PubMed Central

PubMed publication ID

4 December 2017

author name string

Amir Karban

1

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Europe PubMed Central

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4 December 2017

Oren Atia

2

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Europe PubMed Central

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4 December 2017

Eran Leitersdorf

3

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Europe PubMed Central

PubMed publication ID

4 December 2017

Azmi Shahbari

4

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Europe PubMed Central

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4 December 2017

Wisam Sbeit

5

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Europe PubMed Central

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4 December 2017

Zvi Ackerman

6

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4 December 2017

Rawia Mualem

7

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Europe PubMed Central

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4 December 2017

Arie Levine

8

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Europe PubMed Central

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4 December 2017

Shula Nesher

9

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Europe PubMed Central

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4 December 2017

Rifaat Safadi

10

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4 December 2017

publication date

1 September 2005

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Europe PubMed Central

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4 December 2017

Digestive Diseases and Sciences

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Europe PubMed Central

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4 December 2017

50

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Europe PubMed Central

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4 December 2017

9

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4 December 2017

1692-1697

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4 December 2017

A prospective epidemiologic study of Crohn's disease in Heraklion, Crete. Incidence over a 5-year period

1 reference

https://api.crossref.org/works/10.1007/S10620-005-2917-X

21 January 2018

Epidemiology of Crohn's disease and ulcerative colitis in a central Canadian province: a population-based study

1 reference

https://api.crossref.org/works/10.1007/S10620-005-2917-X

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inflammatory bowel disease: epidemiology and management in an English general practice population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype- phenotype analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiology of Crohn's disease in southern Israel.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiology of inflammatory bowel disease in Asia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence and prevalence of inflammatory bowel disease in Gijon, Asturias, Spain

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiology of Crohn's disease in Indian migrants and the indigenous population in Leicestershire

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inflammatory bowel disease (2)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of inflammatory bowel disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Crohn's disease in Olmsted County, Minnesota, 1940-1993: incidence, prevalence, and survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Crohn's disease in the Hunter Valley region of Australia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence of inflammatory bowel disease in northern France (1988-1990).

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NOD2 insertion mutation in a cretan Crohn's disease population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence and prevalence of inflammatory bowel disease in Japan: nationwide epidemiological survey during the year 1991

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical relevance of advances in genetics and pharmacogenetics of IBD.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical epidemiology of inflammatory bowel disease: Incidence, prevalence, and environmental influences

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Failure to replicate the association of the novel NOD2/CARD15 haplotype (S268P-JW1) to Crohn's disease in the Jewish Israeli population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Crohn disease: frequency and nature of CARD15 mutations in Ashkenazi and Sephardi/Oriental Jewish families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inflammatory bowel disease (1)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Y-chromosome DNA haplotypes in Jews: comparisons with Lebanese and Palestinians

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Crohn's disease in the Kinneret sub-district, Israel, 1960-1990. Incidence and prevalence in different ethnic subgroups

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Race and genomics

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High incidence of inflammatory bowel disease in The Netherlands: results of a prospective study. The South Limburg IBD Study Group.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial empirical risks for inflammatory bowel disease: differences between Jews and non-Jews

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CARD15 gene and the classification of Crohn's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The incidence of Crohn's disease in the Helsinki metropolitan area during 1975-1985.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NOD2/CARD15 genotype and phenotype differences between Ashkenazi and Sephardic Jews with Crohn's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133971

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10620-005-2917-X

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

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