Associated Papers
A novel dual histone mark reader ZCWPW2 regulates meiotic recombination through lactylation and transcriptional regulation in humans and mice.
Ruan T et al.
Nucleic Acids Research, 2026
Integrated multi-omics analysis reveals the involvement of the gut-brain axis in children with autism.
Zhong H et al.
Frontiers in Microbiology, 2026
Association of SLC22A4 and TNF-α gene polymorphism with susceptibility to inflammatory bowel disease among patients in the Eastern Province of Saudi Arabia.
AlQahtani SM et al.
Arab Journal of Gastroenterology : the Official Publication of the Pan-arab Association of Gastroenterology, 2025
Multi-omic insights from a multi-ancestry genome-wide meta-analysis of ankylosing spondylitis reveal novel pathways of disease susceptibility.
Brown M et al.
Research Square, 2025
Genetic Mutations and Small Bowel Ulcerating Disease: Role in Diagnosis?
Modi R et al.
Current Gastroenterology Reports, 2025
The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individuals.
Wang LY et al.
Innovation (cambridge (mass.)), 2025
Deciphering the immunocellular regulatory network in inflammatory bowel disease: from susceptibility genes to cellular effectors and toward precision therapies.
Wu Z et al.
Frontiers in Immunology, 2025
Case-control study of IL23R rs76418789 polymorphism, smoking, and ulcerative colitis in Japan.
Miyake Y et al.
Cytokine, 2024
Whole exome sequencing identifies genetic markers of enterovirus susceptibility in East Asians.
Sung CC et al.
Frontiers in Microbiology, 2024
Genetic architecture of the inflammatory bowel diseases across East Asian and European ancestries.
Liu Z et al.
Nature Genetics, 2023
Current Status and Future Prospects of Inflammatory Bowel Disease Genetics.
Kakuta Y et al.
Digestion, 2023
Safety and efficacy of canakinumab treatment for undifferentiated autoinflammatory diseases: the data of a retrospective cohort two-centered study.
Alexeeva E et al.
Frontiers in Medicine, 2023
Clinical significance of genetic variation in hypertrophic cardiomyopathy: comparison of computational tools to prioritize missense variants.
Barbosa P et al.
Frontiers in Cardiovascular Medicine, 2022
Genotype-protein phenotype characterization of NOD2 and IL23R missense variants associated with inflammatory bowel disease: A paradigm from molecular modelling, dynamics, and docking simulations.
Nasser KK et al.
Frontiers in Medicine, 2022
Deep resequencing identifies candidate functional genes in leprosy GWAS loci.
Fava VM et al.
Plos Neglected Tropical Diseases, 2021
Mapping leprosy-associated coding variants of interleukin genes by targeted sequencing.
Zhang DF et al.
Clinical Genetics, 2021
Mutational analyses of novel rat models with targeted modifications in inflammatory bowel disease susceptibility genes.
Men H et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society, 2021
Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease.
Somineni HK et al.
American Journal of Human Genetics, 2021
EBV-induced gene 3 augments IL-23Rα protein expression through a chaperone calnexin.
Mizoguchi I et al.
The Journal of Clinical Investigation, 2020
IL-12 and IL-23-Close Relatives with Structural Homologies but Distinct Immunological Functions.
Floss DM et al.
Cells, 2020
Genetic control of CCL24, POR, and IL23R contributes to the pathogenesis of sarcoidosis.
Meguro A et al.
Communications Biology, 2020
Genetic Analysis of Ulcerative Colitis in Japanese Individuals Using Population-specific SNP Array.
Okamoto D et al.
Inflammatory Bowel Diseases, 2020
An Integrated Genomic and Transcriptomic Analysis Reveals Candidates of Susceptibility Genes for Crohn's Disease in Japanese Populations.
Kakuta Y et al.
Scientific Reports, 2020
Single nucleotide polymorphism rs10889677 in miRNAs Let-7e and Let-7f binding site of IL23R gene is a strong colorectal cancer determinant: Report and meta-analysis.
Mosallaei M et al.
Cancer Genetics, 2019
Behçet's disease: An immunogenetic perspective.
Salmaninejad A et al.
Journal of Cellular Physiology, 2019
Genetic Studies of Inflammatory Bowel Disease-Focusing on Asian Patients.
Park SC et al.
Cells, 2019
A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals.
Kakuta Y et al.
Journal of Crohn's & Colitis, 2019
Association of IL23R Variants With Crohn's Disease in Korean Children.
Hong J et al.
Frontiers in Pediatrics, 2019
Candidate long-range regulatory sites acting on the IL17 pathway genes TRAF3IP2 and IL17RA are associated with psoriasis.
Nititham J et al.
Experimental Dermatology, 2018
Deep Resequencing of Ulcerative Colitis-Associated Genes Identifies Novel Variants in Candidate Genes in the Korean Population.
Moon CM et al.
Inflammatory Bowel Diseases, 2018
Genetic profile of patients with early onset inflammatory bowel disease.
Girardelli M et al.
Gene, 2018
Structural Activation of Pro-inflammatory Human Cytokine IL-23 by Cognate IL-23 Receptor Enables Recruitment of the Shared Receptor IL-12Rβ1.
Bloch Y et al.
Immunity, 2018
Immune Regulatory Genes Are Major Genetic Factors to Behcet Disease: Systematic Review.
Deng Y et al.
The Open Rheumatology Journal, 2018
Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling.
Dand N et al.
Human Molecular Genetics, 2017
Fine-mapping inflammatory bowel disease loci to single-variant resolution.
Huang H et al.
Nature, 2017
Genetics of inflammatory bowel disease: beyond NOD2.
Mirkov MU et al.
The Lancet. Gastroenterology & Hepatology, 2017
The genetic background of inflammatory bowel disease: from correlation to causality.
Uniken Venema WT et al.
The Journal of Pathology, 2017
Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.
Ostrowski J et al.
Scientific Reports, 2016
Fine mapping of the GWAS loci identifies SLC35D1 and IL23R as potential risk genes for leprosy.
Li GD et al.
Journal of Dermatological Science, 2016
Lack of association between polymorphisms in interleukin (IL)-12, IL-12R, IL-23, IL-23R genes and Takayasu arteritis in a Chinese population.
Yang KQ et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [et Al.], 2016
Ankylosing spondylitis: beyond genome-wide association studies.
O'Rielly DD et al.
Current Opinion in Rheumatology, 2016
IL23R (Interleukin 23 Receptor) Variants Protective against Inflammatory Bowel Diseases (IBD) Display Loss of Function due to Impaired Protein Stability and Intracellular Trafficking.
Sivanesan D et al.
The Journal of Biological Chemistry, 2016
Identification of Ten Additional Susceptibility Loci for Ulcerative Colitis Through Immunochip Analysis in Koreans.
Ye BD et al.
Inflammatory Bowel Diseases, 2016
Pooled Resequencing of 122 Ulcerative Colitis Genes in a Large Dutch Cohort Suggests Population-Specific Associations of Rare Variants in MUC2.
Visschedijk MC et al.
Plos One, 2016
The immunogenetics of Behçet's disease: A comprehensive review.
Takeuchi M et al.
Journal of Autoimmunity, 2015
Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans.
Yang SK et al.
Inflammatory Bowel Diseases, 2015