Associated Papers
Utilization of the All of Us Research Program in a study of genetics in Yao syndrome.
Wu S et al.
The Journal of Allergy and Clinical Immunology, 2025
Identifying functional dysregulation of NOD2 variant Q902K in patients with Yao syndrome.
Zhang J et al.
Arthritis Research & Therapy, 2024
Clinical phenotype, NOD2 genotypes, and treatment observations in Yao syndrome: a retrospective case series.
Williamson KA et al.
Frontiers in Immunology, 2024
Genetic Landscape of Rare Autoinflammatory Disease Variants in Qatar and Middle Eastern Populations Through the Integration of Whole-Genome and Exome Datasets.
Sharma P et al.
Frontiers in Genetics, 2021
34054914 (PubMed )
Supplement: Data_Sheet_1.zip › Table_4.XLSX › Sheet1
Genetic profile of patients with early onset inflammatory bowel disease.
Girardelli M et al.
Gene, 2018
Mutational profile of rare variants in inflammasome-related genes in Behçet disease: A Next Generation Sequencing approach.
Burillo-Sanz S et al.
Scientific Reports, 2017
NOD2 genetic variants and sarcoidosis-associated uveitis.
Davoudi S et al.
American Journal of Ophthalmology Case Reports, 2016
Novel CARD15/NOD2 mutations in Finnish patients with Crohn's disease and their relation to phenotypic variation in vitro and in vivo.
Lappalainen M et al.
Inflammatory Bowel Diseases, 2008
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease.
Hugot JP et al.
Nature, 2001
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