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

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

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

http://www.wikidata.org/entity/Q44210447

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Systematic association mapping identifies NELL1 as a novel IBD disease gene Inflammatory bowel disease in Asia: A systematic review Crohn's disease risk alleles on the NOD2 locus have been maintained by natural selection on standing variation Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease The SPINK gene family and celiac disease susceptibility Patterns of linkage disequilibrium and haplotype distribution in disease candidate genes Association of the T allele of an intronic single nucleotide polymorphism in the colony stimulating factor 1 receptor with Crohn's disease: a case-control study Chronic Inflammation Links Cancer and Parkinson's Disease Nod2: A Critical Regulator of Ileal Microbiota and Crohn's Disease Role of discs large homolog 5 Assessing genetic contributions to phenotypic differences among 'racial' and 'ethnic' groups Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility Genotypes and phenotypes in Crohn's disease: do they help in clinical management?Role of NOD2/CARD15 in coronary heart disease.Tolllike receptor 4 (TLR4) polymorphisms in Tunisian patients with Crohn's disease: genotype-phenotype correlation.Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer.Prediction of Crohn's disease aggression through NOD2/CARD15 gene sequencing in an Australian cohort.NOD2, IL23R and ATG16L1 polymorphisms in Lithuanian patients with inflammatory bowel disease Synthetic associations are unlikely to account for many common disease genome-wide association signals Familial aggregation of inflammatory bowel disease in patients with ulcerative colitis No association between microsomal triglyceride transfer protein (MTP) haplotype and longevity in humans Inflammatory bowel disease in Korea: epidemiological, genomic, clinical, and therapeutic characteristics.The association between race and Crohn's disease phenotype in the Western Cape population of South Africa, defined by the Montreal Classification System Crohn's disease in Korea: past, present, and future.Prevalence of CARD15/NOD2 mutations in Caucasian healthy people.Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans.Review article: the expanding role of biological agents in the treatment of inflammatory bowel disease - focus on selective adhesion molecule inhibition.Review article: exploration of the genetic aetiology of inflammatory bowel disease--implications for diagnosis and therapy.Contributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohn's disease risk in a population-based case-control study: evidence of gene-gene interactions.NOD2 mutations and anti-Saccharomyces cerevisiae antibodies are risk factors for Crohn's disease in African Americans Clinical implications of inflammatory bowel disease genetics on phenotype.Common NOD2 risk variants in African Americans with Crohn's disease are due exclusively to recent Caucasian admixture Genetics of Crohn disease, an archetypal inflammatory barrier disease.Mutations in pattern recognition receptor genes modulate seroreactivity to microbial antigens in patients with inflammatory bowel disease Genetic variants and the risk of Crohn's disease: what does it mean for future disease management?Clinical outcomes and predictive factors for response after the first course of corticosteroid therapy in patients with Crohn's disease Genetics of inflammatory bowel disease: current status and future directions.Management consensus of inflammatory bowel disease for the Asia-Pacific region.Variable responses of formyl peptide receptor haplotypes toward bacterial peptides.

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

http://www.wikidata.org/entity/Q44210447

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Haplotype structure and associ ...... nically divergent populations.

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Haplotype structure and associ ...... nically divergent populations.

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Haplotype structure and associ ...... nically divergent populations.

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SJ.EJHG.5200897

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European Journal of Human Genetics

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Haplotype structure and associ ...... hnically divergent populations

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Henning Frenzel

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Michael Krawczak

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Monika Stoll

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Peter J P Croucher

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Silvia Mascheretti

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Stefan Schreiber

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Suk-Kyun Yang

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Susanna Nikolaus

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Tim Lu

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P2860

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)

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

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

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

Median-joining networks for inferring intraspecific phylogenies

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

Mapping of a susceptibility locus for Crohn's disease on chromosome 16

Linkage disequilibrium in the human genome

International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16.

Haplotype variation and linkage disequilibrium in 313 human genes.

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