Varaico: Literature-Extracted Genetic Variants

Gene:TNFRSF1A
Variant:p.P12P
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TNFRSF1A

NM_001065.4:p.P12P

Associated Papers

Pharmacogenomic landscape of TNF inhibitors in the Middle Eastern Qatari population.

Jan Z et al.

Frontiers in Immunology, 2025

41346622 (PubMed )
Supplement: Table2.xlsx › Supplementary_Table_8

Gene polymorphisms in odontogenic keratocysts and ameloblastomas: A systematic review.

Andric M et al.

Oral Diseases, 2022

Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.

Chen W et al.

Frontiers in Neurology, 2022

36619910 (PubMed )
Supplement: Data_Sheet_6.ZIP › case2-C › 3.________ › CA2275B________.____Exonic_Variants.xlsx › sheet1

Pharmacogenetics of Biological Agents Used in Inflammatory Bowel Disease: A Systematic Review.

Lauro R et al.

Biomedicines, 2021

Clinical Significance of TNFRSF1A36T/C Polymorphism in Cachectic Patients with Chronic Heart Failure.

Sobieszek G et al.

Journal of Clinical Medicine, 2021

The association of tumor necrosis factor alpha, lymphotoxin alpha, tumor necrosis factor receptor 1 and tumor necrosis factor receptor 2 gene polymorphisms and serum levels with periodontitis and type 2 diabetes in Serbian population.

Petrovic SM et al.

Archives of Oral Biology, 2020

Association of polymorphisms in TNF-α, IL-1β, GSTM and GSTT genes with apical periodontitis: is there a link with herpesviral infection?

Jakovljevic A et al.

International Endodontic Journal, 2020

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

Novel Genetic Risk Variants Can Predict Anti-TNF Agent Response in Patients With Inflammatory Bowel Disease.

Wang MH et al.

Journal of Crohn's & Colitis, 2019

Single nucleotide polymorphisms of cytokine-related genes and association with clinical outcome in a Chagas disease case-control study from Brazil.

Alvarado-Arnez LE et al.

Memorias Do Instituto Oswaldo Cruz, 2018

Frequency of TNFR1 36 A/G gene polymorphism in azoospermic infertile men: A case-control study.

Ashrafzadeh HR et al.

International Journal of Reproductive Biomedicine, 2017

TNF-α (-308G>A) and TNF-R1 (36A>G) single nucleotide polymorphisms are strong risk factors for odontogenic keratocystic tumor development.

Ilic B et al.

Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2017

Genes of tumor necrosis factors and their receptors and the primary open angle glaucoma in the population of Central Russia.

Tikunova E et al.

International Journal of Ophthalmology, 2017

Associations between functional TNFR2 196 M/R polymorphisms and susceptibility to rheumatoid arthritis: a meta-analysis.

Song GG et al.

Rheumatology International, 2014

Advances in IBD genetics.

Van Limbergen J et al.

Nature Reviews. Gastroenterology & Hepatology, 2014

Identification of a new exon 2-skipped TNFR1 transcript: regulation by three functional polymorphisms of the TNFR-associated periodic syndrome (TRAPS) gene.

Rittore C et al.

Annals of the Rheumatic Diseases, 2014

TNF-α -857C>T genotype is predictive of clinical response after treatment with definitive 5-fluorouracil/cisplatin-based chemoradiotherapy in Japanese patients with esophageal squamous cell carcinoma.

Omatsu H et al.

International Journal of Medical Sciences, 2013

Effects of polymorphisms in TRAILR1 and TNFR1A on the response to anti-TNF therapies in patients with rheumatoid and psoriatic arthritis.

Morales-Lara MJ et al.

Joint Bone Spine, 2012

-383 A/C tumor necrosis factor receptor 1 polymorphism and ankylosing spondylitis in Mexicans: a preliminary study.

Corona-Sanchez EG et al.

Rheumatology International, 2012

Pharmacogenetic analysis of TNF, TNFRSF1A, and TNFRSF1B gene polymorphisms and prediction of response to anti-TNF therapy in psoriasis patients in the Greek population.

Vasilopoulos Y et al.

Molecular Diagnosis & Therapy, 2012

Genetic variation in the TNF gene is associated with susceptibility to severe sepsis, but not with mortality.

Song Z et al.

Plos One, 2012

Human lymphatic filariasis: genetic polymorphism of endothelin-1 and tumor necrosis factor receptor II correlates with development of chronic disease.

Panda AK et al.

The Journal of Infectious Diseases, 2011

A regulatory polymorphism in promoter region of TNFR1 gene is associated with Kawasaki disease in Chinese individuals.

Wang GB et al.

Human Immunology, 2011

TNFRSF1B A1466G genotype is predictive of clinical efficacy after treatment with a definitive 5-fluorouracil/cisplatin-based chemoradiotherapy in Japanese patients with esophageal squamous cell carcinoma.

Kuwahara A et al.

Journal of Experimental & Clinical Cancer Research : Cr, 2010

Lack of association between tumour necrosis factor receptor types 1 and 2 gene polymorphism and severe acute alcoholic hepatitis.

Nguyen-Khac E et al.

European Journal of Gastroenterology & Hepatology, 2010

Tumor necrosis factor-alpha gene polymorphisms are associated with severity of acute graft-versus-host disease following matched unrelated donor bone marrow transplantation in children: a Pediatric Blood and Marrow Transplant Consortium study.

Goyal RK et al.

Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation, 2010

Association of IL23R, TNFRSF1A, and HLA-DRB1*0103 allele variants with inflammatory bowel disease phenotypes in the Finnish population.

Lappalainen M et al.

Inflammatory Bowel Diseases, 2008

A potential role of TNFR gene polymorphisms in autoimmune thyroid diseases in the Tunisian population.

Kammoun-Krichen M et al.

Cytokine, 2008

Tumour necrosis factor-alpha receptor 1 polymorphisms and serum soluble TNFR1 in early spontaneous miscarriage.

Yu XW et al.

Cell Biology International, 2007

The TNFRSF1A R92Q mutation is frequent in rheumatoid arthritis but shows no evidence for association or linkage with the disease.

Dieudé P et al.

Annals of the Rheumatic Diseases, 2007

TNF polymorphisms in psoriasis: association of psoriatic arthritis with the promoter polymorphism TNF*-857 independent of the PSORS1 risk allele.

Reich K et al.

Arthritis and Rheumatism, 2007

Polymorphism A36G of the tumor necrosis factor receptor 1 gene is associated with PAI-1 levels in obese women.

Mavri A et al.

Thrombosis and Haemostasis, 2007

Association study of the tumor necrosis factor-alpha gene and its 1A receptor gene with methamphetamine dependence.

Nomura A et al.

Annals of the New York Academy of Sciences, 2006

Physical function and its response to exercise: associations with cytokine gene variation in older adults with knee osteoarthritis.

Nicklas BJ et al.

The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 2005

Anemia in rheumatoid arthritis: association with polymorphism in the tumor necrosis factor receptor I and II genes.

Glossop JR et al.

The Journal of Rheumatology, 2005

Polymorphism in the tumour necrosis factor receptor II gene is associated with circulating levels of soluble tumour necrosis factor receptors in rheumatoid arthritis.

Glossop JR et al.

Arthritis Research & Therapy, 2005

Tumour necrosis factor-alpha receptor 1 and 2 polymorphisms in inflammatory bowel disease and their association with response to infliximab.

Pierik M et al.

Alimentary Pharmacology & Therapeutics, 2004

A TNFR1 genotype with a protective role in familial rheumatoid arthritis.

Dieudé P et al.

Arthritis and Rheumatism, 2004

No association of polymorphisms in the tumor necrosis factor receptor I and receptor II genes with disease severity in rheumatoid arthritis.

Glossop JR et al.

The Journal of Rheumatology, 2003

TNF receptor I polymorphism is associated with persistent palindromic rheumatism.

Lu LY et al.

Scandinavian Journal of Rheumatology, 0

The role of tumor necrosis factor (TNF)-alpha and TNF receptor polymorphisms in susceptibility to ankylosing spondylitis.

Chatzikyriakidou A et al.

Clinical and Experimental Rheumatology, 0

Blau syndrome with a rare mutation in exon 9 of NOD2 gene.

Velickovic J et al.

Autoimmunity, 0

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