(Q28246013)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

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)

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

Association of CARD15 polymorphisms with atopy-related traits in a population-based cohort of Caucasian adults

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

Comparative phenotypic and CARD15 mutational analysis among African American, Hispanic, and White children with Crohn's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

The emergence of inflammatory bowel disease in the Asian Pacific region.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

CARD15 gene polymorphisms in patients with spondyloarthropathies identify a specific phenotype previously related to Crohn's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

Both donor and recipient NOD2/CARD15 mutations associate with transplant-related mortality and GvHD following allogeneic stem cell transplantation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

CARD15: a pleiotropic autoimmune gene that confers susceptibility to psoriatic arthritis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

CARD15 mutations in Blau syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

The genetics of complex autoimmune diseases: non-MHC susceptibility genes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype-phenotype analysis in Danish and Portuguese patients and controls

29 September 2017

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3673

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/10.3748%2FWJG.V12.I23.3673

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3673

Analysis of the three common mutations in the CARD15 gene (R702W, G908R and 1007fs) in South African colored patients with inflammatory bowel disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3673

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3673

Analysis of CARD15/NOD2 haplotypes fails to identify common variants associated with rheumatoid arthritis susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3673

CARD 15 gene mutations in sarcoidosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3673

Conserved noncoding sequences are selectively constrained and not mutation cold spots

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3673

Polymorphisms of CARD15/NOD2 and CD14 genes in New Zealand Crohn's disease patients

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3673

Evidence for common genetic control in pathways of inflammation for Crohn's disease and psoriatic arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3673

CARD15 single nucleotide polymorphisms 8, 12 and 13 are not increased in ethnic Danes with sarcoidosis

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

NOD2/CARD15 gene polymorphisms in idiopathic pulmonary fibrosis.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

Crohn’s disease associated CARD15 (NOD2) variants are not involved in the susceptibility to type 1 diabetes

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

[NOD2/CARD15 gene polymorphisms and susceptibility to Crohn's disease in Chinese Han population].

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087459

Prevalence of the NOD2 3020insC mutation in aggregations of breast and lung cancer

27 November 2018

1 reference

12 December 2020

Crohn's disease is associated with polymorphism of CARD15/NOD2 gene in a Hungarian population

1 reference

12 December 2020

CARD15/NOD2 is not a predisposing factor for necrotizing enterocolitis

1 reference

12 December 2020

CARD15 polymorphisms in Behçet's disease

1 reference

12 December 2020

NOD2/CARD15 gene mutation is not associated with susceptibility to Wegener's granulomatosis

1 reference

12 December 2020

The three most common CARD15 mutations associated with Crohn's disease and the chromosome 16 susceptibility locus for systemic lupus erythematosus

1 reference

12 December 2020

NOD2/CARD15 mutation analysis and genotype-phenotype correlation in Jewish pediatric patients compared with adults with Crohn's disease

1 reference

12 December 2020

Association of NOD2/CARD15 variants with Crohn's disease in a Greek population

1 reference

12 December 2020