Associated Papers
Pharmacogenomic landscape of TNF inhibitors in the Middle Eastern Qatari population.
Jan Z et al.
Frontiers in Immunology, 2025
The Role of Genetics on Psoriasis Susceptibility, Comorbidities, and Treatment Response.
Bui A et al.
Dermatologic Clinics, 2024
The Association between Genetics and Response to Treatment with Biologics in Patients with Psoriasis, Psoriatic Arthritis, Rheumatoid Arthritis, and Inflammatory Bowel Diseases: A Systematic Review and Meta-Analysis.
Al-Sofi RF et al.
International Journal of Molecular Sciences, 2024
TNFRSF1B Gene Variants in Clinicopathological Aspects and Prognosis of Patients with Cutaneous Melanoma.
Carvalho BF et al.
International Journal of Molecular Sciences, 2024
Novel NARS2 variants in a patient with early-onset status epilepticus: case study and literature review.
Yang N et al.
Bmc Pediatrics, 2024
Evolutionary history of adenomas to colorectal cancer in FAP families.
Yang C et al.
Frontiers in Genetics, 2024
Impact of Gene Modifiers on Cystic Fibrosis Phenotypic Profiles: A Systematic Review.
Ward A et al.
Human Mutation, 2024
Lung Inflammatory Genes in Cystic Fibrosis and Their Relevance to Cystic Fibrosis Transmembrane Conductance Regulator Modulator Therapies.
Carbone A et al.
Genes, 2023
Genetics of Familial Combined Hyperlipidemia (FCHL) Disorder: An Update.
Taghizadeh E et al.
Biochemical Genetics, 2022
Genetic Variants of the NF-κB Pathway: Unraveling the Genetic Architecture of Psoriatic Disease.
Queiro R et al.
International Journal of Molecular Sciences, 2021
Pharmacogenetics of Biological Agents Used in Inflammatory Bowel Disease: A Systematic Review.
Lauro R et al.
Biomedicines, 2021
Tumor necrosis factor receptor II and PTPN22 genes polymorphisms and the risk of systemic lupus erythematosus in Egyptian children.
Eid R et al.
Lupus, 2021
Homozygous variant p. Arg90His in NCF1 is associated with early-onset Interferonopathy: a case report.
Schnappauf O et al.
Pediatric Rheumatology Online Journal, 2021
Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis.
Heng AHS et al.
Bmc Medical Genomics, 2021
A bioinformatic approach to investigating cytokine genes and their receptor variants in relation to COVID-19 progression.
Karakas Celik S et al.
International Journal of Immunogenetics, 2021
Pharmacogenetics of trough serum anti-TNF levels in paediatric inflammatory bowel disease.
Salvador-Martín S et al.
British Journal of Clinical Pharmacology, 2021
Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.
Sebate B et al.
Plos One, 2021
Cystic Fibrosis: Systems Biology Analysis from Homozygous p.Phe508del Variant Patients' Samples Reveals Perturbations in Tissue-Specific Pathways.
de Faria Poloni J et al.
Biomed Research International, 2021
TNFα -857 C/T and TNFR2 +587 T/G polymorphisms are associated with cystic fibrosis in Iranian patients.
Hassanzad M et al.
European Journal of Medical Genetics, 2019
Genetic predictors of long-term response and trough levels of infliximab in crohn's disease.
Salvador-Martín S et al.
Pharmacological Research, 2019
What does acne genetics teach us about disease pathogenesis?
Common JEA et al.
The British Journal of Dermatology, 2019
Host genetic variants in sepsis risk: a field synopsis and meta-analysis.
Lu H et al.
Critical Care (london, England), 2019
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family.
Khan MJ et al.
Scientific Reports, 2018
New polymorphisms associated with response to anti-TNF drugs in patients with moderate-to-severe plaque psoriasis.
Prieto-Pérez R et al.
The Pharmacogenomics Journal, 2018
Association of TNFRSF1B Promoter Polymorphisms with Human Disease: Further Studies Examining T-Regulatory Cells Are Required.
Li H et al.
Frontiers in Immunology, 2018
Polymorphic Variants of TNFR2 Gene in Schizophrenia and Its Interaction with -308G/A TNF-α Gene Polymorphism.
Suchanek-Raif R et al.
Mediators of Inflammation, 2018
Genetic architecture of acne vulgaris.
Lichtenberger R et al.
Journal of the European Academy of Dermatology and Venereology : Jeadv, 2017
Brief Report: Deficiency of Complement 1r Subcomponent in Early-Onset Systemic Lupus Erythematosus: The Role of Disease-Modifying Alleles in a Monogenic Disease.
Demirkaya E et al.
Arthritis & Rheumatology (hoboken, N.j.), 2017
FCGR3A-V158F polymorphism is a disease-specific pharmacogenetic marker for the treatment of psoriasis with Fc-containing TNFα inhibitors.
Mendrinou E et al.
The Pharmacogenomics Journal, 2017
Modulators of the extracellular matrix and risk of anterior cruciate ligament ruptures.
Rahim M et al.
Journal of Science and Medicine in Sport, 2017
Genetic Contributions of Inflammation to Depression.
Barnes J et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology, 2017
Genetic Susceptibility in Acute Pancreatitis: Genotyping of GSTM1, GSTT1, GSTP1, CASP7, CASP8, CASP9, CASP10, LTA, TNFRSF1B, and TP53 Gene Variants.
Dʼ Oliveira Martins F et al.
Pancreas, 2017
Susceptibility to pulmonary tuberculosis: host genetic deficiency in tumor necrosis factor alpha (TNF-α) gene and tumor necrosis factor receptor 2 (TNFR2).
Ghamari E et al.
International Journal of Mycobacteriology, 2016
Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.
Maguire SL et al.
The Journal of Pathology, 2016
Spontaneous preterm birth and single nucleotide gene polymorphisms: a recent update.
Sheikh IA et al.
Bmc Genomics, 2016
Glycidamide genotoxicity modulated by Caspases genes polymorphisms.
de Lima JP et al.
Toxicology in Vitro : an International Journal Published in Association With Bibra, 2016
Val/Val glutathione-S-transferase P1 polymorphism predicts nonresponders in psoriasis patients treated with fumaric acid esters.
Gambichler T et al.
Pharmacogenetics and Genomics, 2016
Genetic polymorphisms associated with heart failure: A literature review.
Guo M et al.
The Journal of International Medical Research, 2016
Comparison of single nucleotide polymorphisms [SNP] at TNF-α promoter region with TNF receptor 2 (TNFR2) in susceptibility to pulmonary tuberculosis; using PCR-RFLP technique.
Ghamari E et al.
American Journal of Clinical and Experimental Immunology, 2016
Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing.
Samorodnitsky E et al.
Human Mutation, 2015