Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 166 Records) |
| Query Trace: Autoimmune Diseases and PTPN22[original query] |
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| PTPN22 1858 C/T Exon Polymorphism is not Associated with Graves' Disease in Kashmiri population. Indian journal of endocrinology and metabolism 0 22 (4): 457-460. Shehjar Faheem, Dil-Afroze , Misgar Riaz A, Malik Sajad A, Laway Bashir |
| Role of C1858T Polymorphism of Lymphoid Tyrosine Phosphatase in Egyptian Children and Adolescents with Type 1 Diabetes. Current diabetes reviews 2018 Jul . El Fotoh Wafaa Moustafa M Abo, El Razek Midan Dina Abd, El Shalakany Abeer Ham |
| The PTPN22 C1858T (R620W) functional polymorphism in inflammatory bowel disease. BMC research notes 2018 Nov 11 (1): 783. Zaid Younes, Senhaji Nezha, Bakhtaoui Fatima Zahra, Serrano Aurora, Serbati Nadia, Karkouri Mehdi, Badre Wafaa, Oudghiri Mounia, Martin Javier, Nadifi Sella |
| White blood cell mitochondrial DNA copy number is decreased in rheumatoid arthritis and linked with risk factors. A twin study. Journal of autoimmunity 2019 Jan 96 142-146. Svendsen Anders J, Tan Qihua, Jakobsen Marianne A, Thyagarajan Bharat, Nygaard Marianne, Christiansen Lene, Mengel-From Jon |
| Genetic Alleles Associated with SLE Susceptibility and Clinical Manifestations in Hispanic Patients from the Dominican Republic. Current molecular medicine 2019 Apr . Liu Zheng, Yu Yangsheng, Yue Yinshi, Hearth-Holmes Michelene, Lopez Persio David, Tineo Carmen, Paulino Glenny, Fu Wei-Neng, Loyo Esthela, Su Kaiho |
| Dual Role of PTPN22 but Not NLRP3 Inflammasome Polymorphisms in Type 1 Diabetes and Celiac Disease in Children. Frontiers in pediatrics 2019 7 63. Smigoc Schweiger Darja, Goricar Katja, Hovnik Tinka, Mendez Andrijana, Bratina Natasa, Brecelj Jernej, Vidan-Jeras Blanka, Battelino Tadej, Dolzan Vi |
| Association of PTPN22 1858C/T Polymorphism with Autoimmune Diseases: A Systematic Review and Bayesian Approach. Journal of clinical medicine 2019 Mar 8 (3): . Tizaoui Kalthoum, Kim Seon Hui, Jeong Gwang Hun, Kronbichler Andreas, Lee Kwang Seob, Lee Keum Hwa, Shin Jae |
| The Autoimmune-Associated Single Nucleotide Polymorphism Within PTPN22 Correlates With Clinical Outcome After Lung Transplantation. Frontiers in immunology 2018 9 3105. Budding Kevin, van Setten Jessica, van de Graaf Eduard A, van Rossum Oliver A, Kardol-Hoefnagel Tineke, Kwakkel-van Erp Johanna M, Oudijk Erik-Jan D, Hack C Erik, Otten Henderikus |
| Type 1 diabetes linked PTPN22 gene polymorphism is associated with the frequency of circulating regulatory T cells. European journal of immunology 2019 Dec . Milla Valta, Mahfuz Gazali Ahmad, Tyyne Viisanen, Emmi-Leena Ihantola, Ilse Ekman, Jorma Toppari, Mikael Knip, Riitta Veijola, Jorma Ilonen, Johanna Lempainen, Tuure Kinnun |
| Transethnic associations among immune-mediated diseases and single-nucleotide polymorphisms of the aryl hydrocarbon response gene ARNT and the PTPN22 immune regulatory gene. Journal of autoimmunity 2019 Nov 102363. Schurman Shepherd H, O'Hanlon Terrance P, McGrath John A, Gruzdev Artiom, Bektas Arsun, Xu Hong, Garantziotis Stavros, Zeldin Darryl C, Miller Frederick |
| Efficient CRISPR/Cas9 Disruption of Autoimmune-Associated Genes Reveals Key Signaling Programs in Primary Human T Cells. Journal of immunology (Baltimore, Md. : 1950) 2019 Nov . Anderson Warren, Thorpe Jerill, Long S Alice, Rawlings David |
| PTPN22 1858 C/T polymorphism is associated with alteration of cytokine profiles as a potential pathogenic mechanism in rheumatoid arthritis. Immunology letters 2019 Oct . Ghorban Khodayar, Ezzeddini Rana, Eslami Majid, Yousefi Bahman, Sadighi Moghaddam Bizhan, Tahoori Mohammad-Taher, Dadmanesh Maryam, Salek Farrokhi Am |
| Analysis of the rs2476601 polymorphism of PTPN22 in Mexican mestizo patients with leprosy. Biomedical reports 2019 1 10 (2): 127-132. Escamilla-Tilch Mónica, Pérez-Suárez Thalía Gabriela, Torres-Carrillo Nora Magdalena, Rodríguez-Guillén Rosario, Arenas-Guzmán Roberto, Torres-Hernández Marcela, Fafutis-Morris Mary, Estrada-Parra Sergio, Estrada-Garía Iris, García-Lechuga Maricela, Granados Julio, Ramos-Payan Rosal |
| A Missense Variant in PTPN22 is a Risk Factor for Drug-induced Liver Injury. Gastroenterology 2019 Jan . Cirulli Elizabeth T, Nicoletti Paola, Abramson Karen, Andrade Raul J, Bjornsson Einar S, Chalasani Naga, Fontana Robert J, Hallberg Pär, Li Yi Ju, Lucena M Isabel, Long Nanye, Molokhia Mariam, Nelson Matthew R, Odin Joseph A, Pirmohamed Munir, Rafnar Thorunn, Serrano Jose, Stefánsson Kári, Stolz Andrew, Daly Ann K, Aithal Guruprasad P, Watkins Paul B, , |
| Single Nucleotide Polymorphisms of PTPN22 Gene in Iranian Patients with Ulcerative Colitis. Fetal and pediatric pathology 2019 Jan 1-6. Sadr Maryam, Moazzami Bobak, Soleimanifar Narjes, Elhamian Nazanin, Rezaei Arezoo, Ebrahimi Daryani Nasser, Rezaei Ni |
| Autoimmunity-Related Risk Variants in PTPN22 and CTLA4 Are Associated With ME/CFS With Infectious Onset. Frontiers in immunology 2020 11 578. Steiner Sophie, Becker Sonya C, Hartwig Jelka, Sotzny Franziska, Lorenz Sebastian, Bauer Sandra, Löbel Madlen, Stittrich Anna B, Grabowski Patricia, Scheibenbogen Carm |
| Association of Functional Polymorphism in Protein Tyrosine Phosphatase Nonreceptor 22 (PTPN22) Gene with Vitiligo. Biomarker insights 2020 15 1177271920903038. Huraib Ghaleb Bin, Al Harthi Fahad, Arfin Misbahul, Aljamal Abdulrahman, Alrawi Abdulqader Saeed, Al-Asmari Abdulrahm |
| PTPN22 gene polymorphism as a genetic risk factor for primary immune thrombocytopenia in Egyptian children. Expert review of hematology 2020 Oct . Hesham Mervat, Hassan Tamer, Fawzy Amal, Mohamed Noura, Alhejny Ebtihaj, Fathy Manar, El Gebaly Sherief, Zakaria Mar |
| Overexpression of the PTPN22 Autoimmune Risk Variant LYP-620W Fails to Restrain Human CD4 T Cell Activation. Journal of immunology (Baltimore, Md. : 1950) 2021 7 207 (3): 849-859. Perry Daniel J, Peters Leeana D, Lakshmi Priya Saikumar, Zhang Lin, Han Zhao, Wasserfall Clive H, Mathews Clayton E, Atkinson Mark A, Brusko Todd |
| Type 1 Diabetes and Autoimmune Thyroid Disease-The Genetic Link. Frontiers in endocrinology 2021 3 12 618213. Frommer Lara, Kahaly George |
| Association of PTPN22 single nucleotide polymorphisms with chronic spontaneous urticaria. Allergologia et immunopathologia 2021 2 49 (2): 40-45. Sadr Maryam, Khalili Neda, Mohebbi Bahareh, Mosharmovahed Banafsheh, Afradi Parivash, Rezaei Ni |
GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility.
Nature communications 2021 02 12 (1): 959. Eriksson Daniel, Røyrvik Ellen Christine, Aranda-Guillén Maribel, Berger Amund Holte, Landegren Nils, Artaza Haydee, Hallgren Åsa, Grytaas Marianne Aardal, Ström Sara, Bratland Eirik, Botusan Ileana Ruxandra, Oftedal Bergithe Eikeland, Breivik Lars, Vaudel Marc, Helgeland Øyvind, Falorni Alberto, Jørgensen Anders Palmstrøm, Hulting Anna-Lena, Svartberg Johan, Ekwall Olov, Fougner Kristian Johan, Wahlberg Jeanette, Nedrebø Bjørn Gunnar, Dahlqvist Per, , , Knappskog Per Morten, Wolff Anette Susanne Bøe, Bensing Sophie, Johansson Stefan, Kämpe Olle, Husebye Eystein Sver |
| 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 |
| Association of distance to swine concentrated animal feeding operations with immune-mediated diseases: An exploratory gene-environment study. Environment international 2022 12 171 107687. Ayala-Ramirez Montserrat, MacNell Nathaniel, McNamee Lucy E, McGrath John A, Akhtari Farida S, Curry Matthew D, Dunnon Askia K, Fessler Michael B, Garantziotis Stavros, Parks Christine G, Fargo David C, Schmitt Charles P, Motsinger-Reif Alison A, Hall Janet E, Miller Frederick W, Schurman Shepherd |
| 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 |
| 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 |
| SNP in PTPN22, PADI4, and STAT4 but Not TRAF1 and CD40 Increase the Risk of Rheumatoid Arthritis in Polish Population. International journal of molecular sciences 2023 4 24 (8): . Tomasz Budlewski, Joanna Sarnik, Grzegorz Galita, Grzegorz Dragan, Olga Brzezi?ska, Marta Pop?awska, Tomasz Pop?awski, Joanna Makows |
| 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 |
| [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 |
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