Human Genome Epidemiology Literature Finder
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Records 1 - 29 (of 29 Records) |
| Query Trace: Autoimmune Diseases and PSS[original query] |
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| Autoantibodies detectable in the sera of silicosis patients. The relationship between the anti-topoisomerase I antibody response and HLA-DQB1*0402 allele in Japanese silicosis patients. The Science of the total environment 2001 Apr 270 (1-3): 141-8. Ueki A, Isozaki Y, Tomokuni A, Tanaka S, Otsuki T, Kishimoto T, Kusaka M, Aikoh T, Sakaguchi H, Hydoh |
| PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases. Genes and immunity 2005 Oct 6 (7): 628-31. Gomez L M, Anaya J-M, Gonzalez C I, Pineda-Tamayo R, Otero W, Arango A, Martín |
| No evidence for association between 1858 C/T single-nucleotide polymorphism of PTPN22 gene and primary Sjögren's syndrome. Genes and immunity 2005 Aug 6 (5): 457-8. Ittah M, Gottenberg J-E, Proust A, Hachulla E, Puechal X, Loiseau P, Mariette X, Miceli-Richard |
| No evidence for an association between the -871 T/C promoter polymorphism in the B-cell-activating factor gene and primary Sjögren's syndrome. Arthritis research & therapy 2006 8 (1): R30. Gottenberg Jacques-Eric, Sellam Jérémie, Ittah Marc, Lavie Frédéric, Proust Alexis, Zouali Habib, Sordet Christelle, Sibilia Jean, Kimberly Robert P, Mariette Xavier, Miceli-Richard Corin |
| CTLA-4 +49A/G and CT60 gene polymorphisms in primary Sjögren syndrome. Arthritis research & therapy 2007 9 (2): R24. Gottenberg Jacques-Eric, Loiseau Pascale, Azarian Mariam, Chen Chun, Cagnard Nicolas, Hachulla Eric, Puechal Xavier, Sibilia Jean, Charron Dominique, Mariette Xavier, Miceli-Richard Corin |
| TIRAP (MAL) S180L polymorphism is a common protective factor against developing tuberculosis and systemic lupus erythematosus. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2008 Sep 8 (5): 541-4. Castiblanco John, Varela Diana-Cristina, Castaño-Rodríguez Natalia, Rojas-Villarraga Adriana, Hincapié María-Eugenia, Anaya Juan-Manu |
| Non-synonymous variant (Gly307Ser) in CD226 is associated with susceptibility to multiple autoimmune diseases. Rheumatology (Oxford, England) 2010 Jul 49 (7): 1239-44. Maiti Amit K, Kim-Howard Xana, Viswanathan Parvathi, Guillén Laura, Qian Xiaoxia, Rojas-Villarraga Adriana, Sun Celi, Cañas Carlos, Tobón Gabriel J, Matsuda Koichi, Shen Nan, Cherñavsky Alejandra C, Anaya Juan-Manuel, Nath Swapan |
| HLA and Sjögren's syndrome susceptibility. A meta-analysis of worldwide studies. Autoimmunity reviews 2012 Feb 11 (4): 281-7. Cruz-Tapias Paola, Rojas-Villarraga Adriana, Maier-Moore Shannon, Anaya Juan-Manu |
| Low copy number of the Fc-? receptor 3B gene FCGR3B is a risk factor for primary Sjogren's syndrome. The Journal of rheumatology 2012 Sep . Nossent JC, Rischmueller M, Lester S |
| Association of STAT4 rs7574865 polymorphism with autoimmune diseases: a meta-analysis. Molecular biology reports 2012 Sep 39 (9): 8873-82. Liang Ya-Ling, Wu Hua, Shen Xi, Li Pei-Qiang, Yang Xiao-Qing, Liang Li, Tian Wei-Hua, Zhang Li-Feng, Xie Xiao-Do |
| CD226 Gly307Ser association with multiple autoimmune diseases: a meta-analysis. Human immunology 2012 Oct . Qiu ZX, Zhang K, Qiu XS, Zhou M, Li WM |
| Polymorphisms in the FAM167A-BLK, but not BANK1, are associated with primary Sjögren's syndrome in a Han Chinese population. Clinical and experimental rheumatology 0 31 (5): 704-10. Sun Fei, Xu Juanjuan, Wu Ziyan, Li Ping, Chen Hua, Su Jinmei, You Xin, Li Mengtao, Zhao Yan, Tian Xinping, Li Yongzhe, Zhang Fengch |
| Association studies of TNFSF4, TNFAIP3 and FAM167A-BLK polymorphisms with primary Sjogren's syndrome in Han Chinese. Journal of human genetics 2013 Jul 58 (7): 475-9. Sun Fei, Li Ping, Chen Hua, Wu Ziyan, Xu Juanjuan, Shen Min, Leng Xiaomei, Shi Qun, Zhang Wen, Tian Xinping, Li Yongzhe, Zhang Fengch |
| Germline and somatic genetic variations of TNFAIP3 in lymphoma complicating primary Sjogren's syndrome. Blood 2013 Dec 122 (25): 4068-76. Nocturne Gaetane, Boudaoud Saida, Miceli-Richard Corinne, Viengchareun Say, Lazure Thierry, Nititham Joanne, Taylor Kimberly E, Ma Averil, Busato Florence, Melki Judith, Lessard Christopher J, Sivils Kathy L, Dubost Jean-Jacques, Hachulla Eric, Gottenberg Jacques Eric, Lombès Marc, Tost Jorg, Criswell Lindsey A, Mariette Xavi |
| Impact of the leucocyte immunoglobulin-like receptor A3 (LILRA3) on susceptibility and subphenotypes of systemic lupus erythematosus and Sjögren's syndrome. Annals of the rheumatic diseases 2014 Jun . Du Yan, Su Yin, He Jing, Yang Yue, Shi Yamei, Cui Yong, Luo Cainan, Wu Xinyu, Liu Xu, Hu Fanlei, Ma Xiaoxu, Zheng Li, Zhang Jing, Zuo Xianbo, Sheng Yujun, Wu Lijun, Zhang Xuejun, Guo Jianping, Li Zhang |
| Lack of association of vitamin D receptor gene polymorphisms/haplotypes in Sjögren's syndrome. Clinical rheumatology 2015 Feb 34 (2): 247-53. Zilahi Erika, Chen Ji-Qing, Papp Gábor, Szántó Antónia, Zeher Marg |
| Association between FCGR3B copy number variations and susceptibility to autoimmune diseases: a meta-analysis. Inflammation research : official journal of the European Histamine Research Society ... [et al.] 2015 Sep . Lee Young Ho, Bae Sang-Cheol, Seo Young Ho, Kim Jae-Hoon, Choi Sung Jae, Ji Jong Dae, Song Gwan G |
| Analysis of IL10 haplotypes in primary Sjögren's syndrome patients from Western Mexico: Relationship with mRNA expression, IL-10 soluble levels, and autoantibodies. Human immunology 2015 Jul 76 (7): 473-9. Vázquez-Villamar M, Palafox-Sánchez C A, Muñoz-Valle J F, Valle Y, Orozco-Barocio G, Hernández-Bello J, Oregon-Romero |
| Association of FAM167A-BLK rs2736340 Polymorphism with Susceptibility to Autoimmune Diseases: A Meta-Analysis. Immunological investigations 2016 May 45 (4): 336-48. Zhou Yingbo, Li Xiangpei, Wang Guosheng, Li Xiaom |
| No association of single nucleotide polymorphisms within H19 and HOX transcript antisense RNA (HOTAIR) with genetic susceptibility to systemic lupus erythematosus, rheumatoid arthritis, and primary Sjögren's syndrome in a Chinese Han population. Clinical rheumatology 2017 Sep . Huang An-Fang, Su Lin-Chong, Jia Hong, Liu Yi, Xu Wang-Do |
| Common variants near IKZF1 are associated with primary Sjögren's syndrome in Han Chinese. PloS one 2017 12 (5): e0177320. Qu Susu, Du Yang, Chang Suhua, Guo Liyuan, Fang Kechi, Li Yongzhe, Zhang Fengchun, Zhang Kunlin, Wang Ji |
| TNFAIP3 Gene Polymorphisms in Three Common Autoimmune Diseases: Systemic Lupus Erythematosus, Rheumatoid Arthritis, and Primary Sjogren Syndrome-Association with Disease Susceptibility and Clinical Phenotypes in Italian Patients. Journal of immunology research 2019 9 2019 6728694. Ciccacci C, Latini A, Perricone C, Conigliaro P, Colafrancesco S, Ceccarelli F, Priori R, Conti F, Perricone R, Novelli G, Borgiani |
| Association between TL1A gene polymorphisms and systemic lupus erythematosus in a Chinese Han population. Journal of cellular physiology 2019 May . Xu Wang-Dong, Fu Lu, Liu Xiao-Yan, Wang Jia-Min, Yuan Zhi-Chao, Su Lin-Chong, Huang An-Fa |
| Associations between TNFSF4 gene polymorphisms (rs2205960 G > A, rs704840 T > G and rs844648 G > A) and susceptibility to autoimmune diseases in Asians: a meta-analysis. Immunological investigations 2020 Mar 1-17. Yang Yangyang, Li Xiahui, Li Bowen, Mu Liying, Wang Jin, Cheng Yunmeng, Gu Yao, Wu Huiji |
| TNFSF4 is a risk factor for rheumatoid arthritis but not for primary Sjögren's syndrome in the Mexican population. Immunobiology 2022 Jul 227 (4): 152244. Ramírez-Bello Julian, Jiménez-Morales Silvia, Barbosa-Cobos Rosa Elda, Sánchez-Zauco Norma, Hernández-Molina Gabriela, Luria-Pérez Rosendo, Fragoso José M, Cabello-Gutiérrez Carlos, Montúfar-Robles Ise |
| Analysis of TNFSF13B polymorphisms and BAFF expression in rheumatoid arthritis and primary Sjögren's syndrome patients. Molecular genetics & genomic medicine 2022 4 10 (6): e1950. Santillán-López Enrique, Muñoz-Valle José Francisco, Oregon-Romero Edith, Espinoza-García Noemí, Treviño-Talavera Beatriz Alejandra, Salazar-Camarena Diana Celeste, Marín-Rosales Miguel, Cruz Alvaro, Alvarez-Gómez Jhonatan Antonio, Sagrero-Fabela Nefertari, Cerpa-Cruz Sergio, Palafox-Sánchez Claudia Azuce |
| 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 |
| Characterization of primary Sjögren's syndrome in the Taiwan Han population through a genome-wide association study and polygenic risk score analysis. Clinical immunology (Orlando, Fla.) 2024 10 269 110381. Ting-Yuan Liu, Min-Rou Lin, Hsing-Fang Lu, Yu-Chia Chen, Hui-Ju Lin, Wan-Hsuan Chou, Chun-Yu Wei, Poppy Diah Palupi, Chi-Chou Liao, Yen-Ting Chang, Wei-Chiao Chang, Fuu-Jen Ts |
| [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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