Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 382 Records) |
| Query Trace: Disease and PTPN22[original query] |
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| Evaluation of NLRP3 (rs10754558) and PTPN22 (1858C/T) (rs2476601) Functional Polymorphisms in Psoriasis Susceptibility in Egypt. The application of clinical genetics 2021 14 331-339. ALrefai Abeer, Dawood Ashraf, Shehata Wafaa, Elhelbawy Mohammed, Elhelbawy Nesre |
| Modulation of PTPN2/22 Function by Spermidine in CRISPR-Cas9-Edited T-Cells Associated with Crohn's Disease and Rheumatoid Arthritis. International journal of molecular sciences 2021 8 22 (16): . Shaw Ameera M, Qasem Ahmad, Naser Saleh |
| Tumor necrosis factor receptor II and PTPN22 genes polymorphisms and the risk of systemic lupus erythematosus in Egyptian children. Lupus 2021 Jun 9612033211020359. Eid Riham, Hammad Ayman, Abdelsalam Maha, Fathy Aya Ahmed, Abd-El Ghafaar Dena M, Elmarghany Eman B, El-Hanafy Aya A, Mostafa Nora, Niazey Nermeen A, Korkor Mai S, Hamdy Nash |
| Genetic Factors of Predisposition and Clinical Characteristics of Rheumatoid Arthritis in Russian Patients. Journal of personalized medicine 2021 May 11 (6): . Vetchinkina Ekaterina A, Mikhaylenko Dmitry S, Kuznetsova Ekaterina B, Deryagina Tatiana A, Alekseeva Ekaterina A, Bure Irina V, Zamyatnin Andrey A, Nemtsova Marina |
| Genome-wide association study identifies five risk loci for pernicious anemia. Nature communications 2021 6 12 (1): 3761. Laisk Triin, Lepamets Maarja, Koel Mariann, Abner Erik, , Mägi Reed |
| Genetic and immunologic findings in children with recurrent aphthous stomatitis with systemic inflammation. Pediatric rheumatology online journal 2021 May 19 (1): 70. Girardelli Martina, Valencic Erica, Moressa Valentina, Margagliotta Roberta, Tesser Alessandra, Pastore Serena, Spadola Ottavia, Athanasakis Emmanouil, Severini Giovanni Maria, Taddio Andrea, Tommasini Alber |
| Recurrence of Graves' Disease: What Genetics of HLA and PTPN22 Can Tell Us. Frontiers in endocrinology 2021 12 12 761077. Vejrazkova Daniela, Vcelak Josef, Vaclavikova Eliska, Vankova Marketa, Zajickova Katerina, Vrbikova Jana, Duskova Michaela, Pacesova Petra, Novak Zdenek, Bendlova Be |
| [Association of polymorphic markers rs7947461 of the TRIM21 gene and rs33996649 of the PTPN22 gene with the risk of developing exogenous dry eye syndrome]. Vestnik oftalmologii 2021 137 (5. Vyp. 2): 217-223. Safonova T N, Zaitseva G V, Burdennyy A M, Loginov V |
GWAS of Chronic Spontaneous Urticaria Reveals Genetic Overlap with Autoimmune Diseases, Not Atopic Diseases.
The Journal of investigative dermatology 2022 Aug . Zhang Liming, Qiu Li, Wu Jian, Qi Yumeng, Gao Xinghua, He Chundi, Qi Ruiqun, Wang Hexiao, Yao Xu, Zhu Hong, Li Yuzhen, Hao Siyu, Lu Qianjin, Long Hai, Lian Shi, Zhu Wei, Zhang Haiping, Lai Wei, Su Xiangyang, Lu Rongbiao, Guo Zaipei, Li Jingyi, Li Mengmeng, Liu Quanzhong, Wang Huiping, He Li, Nong Xiang, Li Fuqiu, Li Yang, Yao Chunli, Xu Jinhua, Tang Hui, Wang Duoqin, Li Zhenlu, Yu Huiqian, Xiao Shengxiang, An Jingang, Pu Xiongming, Yu Shirong, Zhang Jianzhong, Chen Xue, Wang Haifeng, Huang Wei, Chen Hongduo, Xiao Ti |
| Non-HLA Gene Polymorphisms in the Pathogenesis of Type 1 Diabetes: Phase and Endotype Specific Effects. Frontiers in immunology 2022 13 909020. Laine Antti-Pekka, Valta Milla, Toppari Jorma, Knip Mikael, Veijola Riitta, Ilonen Jorma, Lempainen Johan |
| Polymorphism of protein tyrosine phosphatase non-receptor type 22 and protein arginine deiminase 4 gene among Ghanaian rheumatoid arthritis patients: A case-control study. International journal of rheumatic diseases 2022 May . Sakyi Samuel Asamoah, Boateng Andy Opoku, Fondjo Linda Ahenkorah, Mensah Kwame Yeboah, Opoku Stephen, Senu Ebenezer, Buckman Tonnies Abeku, Sampson Joseph Ent |
| Associations between deduced first islet specific autoantibody with sex, age at diagnosis and genetic risk factors in young children with type 1 diabetes. Pediatric diabetes 2022 4 23 (6): 693-702. Ilonen Jorma, Laine Antti-Pekka, Kiviniemi Minna, Härkönen Taina, Lempainen Johanna, Knip Mikael, |
| Meta-Analysis of the Genetic Association between PTPN22 and CTLA-4 Variants and Risk of Uveitis. Ophthalmic research 2022 Feb . Zhang Jun, Zhou Peng, Hu Shuqiong, Qi Ji |
| The Association Between the PTPN22 C1858T Variant and Vasculitis: A Meta-analysis Update with Trial Sequential Analysis. Genetic testing and molecular biomarkers 2022 10 26 (10): 492-500. Lee Young Ho, Song Gwan G |
| Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study.
Proceedings of the National Academy of Sciences of the United States of America 2022 02 119 (5): . Chia Ruth, Saez-Atienzar Sara, Murphy Natalie, Chiò Adriano, Blauwendraat Cornelis, , Roda Ricardo H, Tienari Pentti J, Kaminski Henry J, Ricciardi Roberta, Guida Melania, De Rosa Anna, Petrucci Loredana, Evoli Amelia, Provenzano Carlo, Drachman Daniel B, Traynor Bryan |
| Inflammatory Bowel Disease Risk Variants Are Associated with an Increased Risk of Skin Cancer. Inflammatory bowel diseases 2022 1 28 (11): 1667-1676. Cushing Kelly C, Du Xiaomeng, Chen Yanhua, Stetson L C, Kuppa Annapurna, Chen Vincent L, Kahlenberg J Michelle, Gudjonsson Johann E, Vanderwerff Brett, Higgins Peter D R, Speliotes Elizabeth |
| Meta-analysis confirmed genetic susceptibility conferred by multiple risk variants from CTLA4 and SERPINA1 in granulomatosis with polyangiitis. International journal of rheumatic diseases 2022 Jun . Banerjee Pratibha, Kumar Uma, Khetarpal Preeti, Senapati Sabyasac |
| Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata. Biomolecules 2023 9 13 (9): . Monica M Van Acker, Rebekah R Schwartz, Kelly Andrews, Kristina Seiffert-Sinha, Animesh A Sin |
| Multiple autoimmune syndrome: Clinical, immunological and genotypic characterization. European journal of internal medicine 2023 6 . Mariana Fidalgo, Raquel Faria, Cláudia Carvalho, Graziela Carvalheiras, Denisa Mendonça, Fátima Farinha, Berta Martins da Silva, Carlos Vasconcel |
| Evaluation of polymorphisms and expression of PTPN22, NLRP1 and TYR genes in vitiligo patients. Postepy dermatologii i alergologii 2023 6 40 (2): 225-233. Kaja M?ci?ska-Jundzi??, Tadeusz Tadrowski, Arkadiusz Jundzi??, Henryk Witmanowski, Rafa? Czajkow |
| UBASH3A Interacts with PTPN22 to Regulate IL2 Expression and Risk for Type 1 Diabetes. International journal of molecular sciences 2023 5 24 (10): . Jeremy R B Newman, Patrick Concannon, Yan |
| Genetic variants and risk for the endocrine autoimmunity in relatives of patients with Addison's disease. Endocrine connections 2023 4 . Fichna Marta, Malecki Piotr P, ?urawek Magdalena, Furman Katarzyna, Gebarski Boleslaw, Fichna Piotr, Ruchala Mar |
| The association between PTPN22 C1858T gene polymorphism and type 1 diabetes mellitus: an Indonesian study. Annals of medicine 2023 3 55 (1): 1211-1215. Rochmah Nur, Arief Fatimah, Faizi Muhammad, Basuki Sukmawa |
| Analysis of PTPN22 -1123 G>C, +788 G>A and +1858 C>T Polymorphisms in Patients with Primary Sjögren's Syndrome. Diagnostics (Basel, Switzerland) 2023 3 13 (5): . Menchaca-Tapia Paula Annahi, Marín-Rosales Miguel, Salazar-Camarena Diana Celeste, Cruz Alvaro, Oregon-Romero Edith, Tapia-Llanos Raziel, Muñoz-Valle José Francisco, Palafox-Sánchez Claudia Azuce |
| HLA and Non-HLA gene polymorphisms in autoimmune hepatitis patients of North Indian adults. Frontiers in immunology 2023 2 13 984083. Ahuja Nishtha, Singh Jagdeep, Minz Ranjana Walker, Anand Shashi, Das Ashim, Taneja Sun |
| Analysis of IL-1?, TGF-?, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis. Molecular biology reports 2023 12 51 (1): 15. Raziye Burcu Ta?k?n, ?lyas Ayd?n, Gülçin Aytaç, Süleyman Imamoglu, Secil Conkar Tunçay, ?pek Kaplan Bulut, Neslihan Edeer Karaca, Güzide Aksu, Afig Berdeli, Necil Kütükçül |
| CTLA4, SH2B3 and CLEC16A diversely affect the progression of early islet autoimmunity in relatives of type 1 diabetes patients. Clinical and experimental immunology 2023 1 . Vandewalle Julie, Desouter Aster K, Van der Auwera Bart J, Tenoutasse Sylvie, Gillard Pieter, De Block Christophe, Keymeulen Bart, Gorus Frans K, Van de Casteele Mark, |
| Genetic Analysis of PTPN22 C1858T and GAD65 Antibodies in Iranian Children and Adolescents with Type 1 Diabetes. Iranian biomedical journal 2024 12 28 (7): 39. Pourya Fathollahzadeh, Farshad Foroughi, Shamim Nonejad, Fatemeh Saffari, Amir Javadi, Sanaz Keshavarz Shahb |
| [Predictive significance of genetic analysis of the development of dry eye disease of different origin]. Vestnik oftalmologii 2024 1 139 (6): 13-18. T N Safonova, G V Zaitseva, V I Loginov, A M Burdenn |
| Whole-Exome Sequencing: Discovering Genetic Causes of Granulomatous Mastitis. International journal of molecular sciences 2025 1 26 (1): . Beyza Ozcinar, Zeynep Ocak, Deryanaz Billur, Baris Ertugrul, Ozlem Timirci-Kahram |
- Page last reviewed:Feb 1, 2024
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