(Q33511546)

27 July 2017

title

Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer (English)

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27 July 2017

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7

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27 July 2017

19

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27 July 2017

5

Bence Sipos

0 references

Clemens Schafmayer

18

Clemens Schafmayer

0 references

Witigo von Schönfels

2

Witigo von Schönfels

0 references

Mario Brosch

Mario Brosch

9

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Michael Krawczak

14

Michael Krawczak

1 reference

27 July 2017

15

Stefan Schreiber

1 reference

27 July 2017

8

Andre Franke

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27 July 2017

Nikolaus Möckelmann

1

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27 July 2017

Stephan Buch

3

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27 July 2017

Oliver von Kampen

4

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27 July 2017

Jan Hendrik Egberts

6

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27 July 2017

Sebastian Hinz

10

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27 July 2017

Christian Röder

11

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27 July 2017

Holger Kalthoff

12

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27 July 2017

Ulrich R Fölsch

13

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27 July 2017

Clemens Dieter Bröring

16

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27 July 2017

Jürgen Tepel

17

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27 July 2017

publication date

20 October 2009

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27 July 2017

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27 July 2017

volume

9

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27 July 2017

page(s)

79

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Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer

27 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

Innate immunity in inflammatory bowel disease.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

Common NOD2/CARD15 variants are not associated with susceptibility or the clinicopathologic characteristics of sporadic colorectal cancer in Hungarian patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

NOD-like receptors and human diseases.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

No association between the functional CARD4 insertion/deletion polymorphism and inflammatory bowel diseases in the German population

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

TUCAN (CARD8) genetic variants and inflammatory bowel disease.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

PopGen: population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

A haplotype map of the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

Efficiency and power in genetic association studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

Genome-wide association studies for common diseases and complex traits

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

Random-effects Cox proportional hazards model: general variance components methods for time-to-event data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

Haploview: analysis and visualization of LD and haplotype maps

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

Familial risk for colorectal cancers are mainly due to heritable causes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

Review article: the incidence and prevalence of colorectal cancer in inflammatory bowel disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

21 June 2018

Inflammation and cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

Chronic inflammation and cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

The NOD: a signaling module that regulates apoptosis and host defense against pathogens

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

Inflammation and cancer: back to Virchow?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776017

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

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

The NOD2 3020insC mutation and the risk of colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

No evidence for association of NOD2 R702W and G908R with colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

Pedigree disequilibrium tests for multilocus haplotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

NOD1 gene E266K polymorphism is associated with disease susceptibility but not with disease phenotype or NOD2/CARD15 in Hungarian patients with Crohn's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

NOD23020insC Alone Is Not Sufficient for Colorectal Cancer Predisposition

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

An integrated system for high throughput TaqManTM based SNP genotyping

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

Investigation of the colorectal cancer susceptibility region on chromosome 8q24.21 in a large German case-control sample

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

Association between a complex insertion/deletion polymorphism in NOD1 (CARD4) and susceptibility to inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-9-79

Inflammation and colorectal cancer: IBD-associated and sporadic cancer compared

21 January 2018

1 reference

12 December 2020

Colorectal cancer mortality in first-degree relatives of early-onset colorectal cancer cases

1 reference

12 December 2020

Familial relative risk of colorectal cancer: a population-based study

1 reference

12 December 2020

Age at onset as an indicator of familial risk of breast cancer

1 reference

12 December 2020

Association between mutations in the CARD15/NOD2 gene and colorectal cancer in a Greek population

1 reference

12 December 2020

Investigation of NOD1/CARD4 variation in inflammatory bowel disease using a haplotype-tagging strategy

1 reference

12 December 2020

Caspase Recruitment Domain-Containing Protein 15 Mutations in Patients with Colorectal Cancer

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-230X-9-79

1 reference

release_zugge5e7cvevbpmri6ifmttkcm

27 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/zugge5e7cvevbpmri6ifmttkcm

24 November 2022

mapped directly with Wikidata item

PMC publication ID

2776017

1 reference

27 July 2017

1 reference