Associated Papers
The clinical, molecular, and therapeutic features of patients with IL10/IL10R deficiency: a systematic review.
Sharifinejad N et al.
Clinical and Experimental Immunology, 2022
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
A Novel Rare Missense Variation of the NOD2 Gene: Evidencesof Implication in Crohn's Disease.
Frade-Proud'Hon-Clerc S et al.
International Journal of Molecular Sciences, 2019
Genetic profile of patients with early onset inflammatory bowel disease.
Girardelli M et al.
Gene, 2018
Interleukin-10 receptor mutation presenting with severe nappy ulceration and infantile inflammatory bowel disease.
McDonald BS et al.
Clinical and Experimental Dermatology, 2017
Genetic association and epistatic interaction of the interleukin-10 signaling pathway in pediatric inflammatory bowel disease.
Lin Z et al.
World Journal of Gastroenterology, 2017
Candidate gene association studies and risk of Hodgkin lymphoma: a systematic review and meta-analysis.
Sud A et al.
Hematological Oncology, 2017
Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.
Karageorgos I et al.
Human Genomics, 2015
Novel missense mutation in the NOD2 gene in a patient with early onset ulcerative colitis: causal or chance association?
Girardelli M et al.
International Journal of Molecular Sciences, 2014
Symptom clusters of pain, depressed mood, and fatigue in lung cancer: assessing the role of cytokine genes.
Reyes-Gibby CC et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer, 2013
Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes.
Christodoulou K et al.
Gut, 2013
Genetic variants in inflammation-related genes are associated with radiation-induced toxicity following treatment for non-small cell lung cancer.
Hildebrandt MA et al.
Plos One, 2010
Role of inflammation gene polymorphisms on pain severity in lung cancer patients.
Reyes-Gibby CC et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2009
Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
Ryu GM et al.
Nucleic Acids Research, 2009
The IL-10R1 S138G loss-of-function allele and ulcerative colitis.
Grundtner P et al.
Genes and Immunity, 2009
Antiretroviral therapy immunologic non-response in a Brazilian population: association study using pharmaco- and immunogenetic markers.
Coelho AVC et al.
The Brazilian Journal of Infectious Diseases : an Official Publication of the Brazilian Society of Infectious Diseases, 0
Blau syndrome with a rare mutation in exon 9 of NOD2 gene.
Velickovic J et al.
Autoimmunity, 0