(Q35684093)

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The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations

scientific article published on 6 July 2015

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scholarly article

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Europe PubMed Central

PubMed publication ID

9 August 2017

The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Crohn's disease

0 references

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

Christiane Wolf

3

object named as

Christiane Wolf

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

author name string

Fabian Schnitzler

1

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Matthias Friedrich

2

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Johannes Stallhofer

4

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Marianne Angelberger

5

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Julia Diegelmann

6

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Torsten Olszak

7

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Cornelia Tillack

8

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Florian Beigel

9

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Burkhard Göke

10

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Jürgen Glas

11

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Peter Lohse

12

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Europe PubMed Central

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9 August 2017

Stephan Brand

13

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Europe PubMed Central

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9 August 2017

language of work or name

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publication date

6 July 2015

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Europe PubMed Central

PubMed publication ID

9 August 2017

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Europe PubMed Central

PubMed publication ID

9 August 2017

10

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Europe PubMed Central

PubMed publication ID

9 August 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

e0116044

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

copyright license

Creative Commons Attribution 4.0 International

6 July 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

The prognostic power of the NOD2 genotype for complicated Crohn's disease: a meta-analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

Inflammatory bowel disease: cause and immunobiology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

Unravelling the complex genetics of inflammatory bowel disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

Classification of inflammatory bowel disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

27 July 2018

Moving the genetics of inflammatory bowel diseases from bench to bedside: first steps towards personalised medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

25 September 2018

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

25 September 2018

Novel CARD15/NOD2 mutations in Finnish patients with Crohn's disease and their relation to phenotypic variation in vitro and in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

25 September 2018

Predictive value of the CARD15 variant 1007fs for the diagnosis of intestinal stenoses and the need for surgery in Crohn's disease in clinical practice: results of a prospective study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

25 September 2018

Eight novel CARD15 variants detected by DNA sequence analysis of the CARD15 gene in 111 patients with inflammatory bowel disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

25 September 2018

Toward an integrated clinical, molecular and serological classification of inflammatory bowel disease: report of a Working Party of the 2005 Montreal World Congress of Gastroenterology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

25 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

25 September 2018

Long-term evolution of disease behavior of Crohn's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

25 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4493062

25 September 2018

Crohn's disease

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0116044

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0116044

21 January 2018

Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype: results from the IBDchip European Project

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0116044

21 January 2018

TheATG16L1Gene Variants rs2241879 and rs2241880 (T300A) Are Strongly Associated With Susceptibility to Crohn's Disease in the German Population

1 reference

https://pubmed.ncbi.nlm.nih.gov/26147989

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominant disease-causing effect of NOD2 mutations in a family with all family members affected by Crohn's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/26147989

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The c-insertion mutation of the NOD2 gene is associated with fistulizing and fibrostenotic phenotypes in Crohn's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/26147989

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity for the CARD15 frameshift mutation 1007fs is predictive of early onset of Crohn's disease with ileal stenosis, entero-enteral fistulas, and frequent need for surgical intervention with high risk of re-stenosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/26147989

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0116044

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

2015PLoSO..1016044S

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

ResearchGate publication ID

0 references

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