Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Disease and TREX1[original query] |
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| TREX1 mutations are not associated with sporadic inclusion body myositis. European journal of neurology : the official journal of the European Federation of Neurological Societies 2010 Aug 17 (8): 1108-9. Cox F M, Boon E M J, van der Lans C A C, Bakker E, Verschuuren J J G M, Badrising U |
| DNA mismatch repair gene polymorphisms affect survival in pancreatic cancer. The oncologist 2011 16 (1): 61-70. Dong Xiaoqun, Li Yanan, Hess Kenneth R, Abbruzzese James L, Li Dongh |
| A homozygous NOTCH3 mutation p.R544C and a heterozygous TREX1 variant p.C99MfsX3 in a family with hereditary small vessel disease of the brain. Journal of the Chinese Medical Association : JCMA 2013 Jun 76 (6): 319-24. Soong Bing-Wen, Liao Yi-Chu, Tu Pang-Hsien, Tsai Pei-Chien, Lee I-Hui, Chung Chih-Ping, Lee Yi-Chu |
| Genetic variation in Trex1 affects HIV-1 disease progression. AIDS (London, England) 2014 Nov 28 (17): 2517-21. Booiman Thijs, Setiawan Laurentia C, Kootstra Neeltje |
| COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls. Neurology 2017 Sep . Rannikmäe Kristiina, Sivakumaran Vhinoth, Millar Henry, Malik Rainer, Anderson Christopher D, Chong Mike, Dave Tushar, Falcone Guido J, Fernandez-Cadenas Israel, Jimenez-Conde Jordi, Lindgren Arne, Montaner Joan, O'Donnell Martin, Paré Guillaume, Radmanesh Farid, Rost Natalia S, Slowik Agnieszka, Söderholm Martin, Traylor Matthew, Pulit Sara L, Seshadri Sudha, Worrall Brad B, Woo Daniel, Markus Hugh S, Mitchell Braxton D, Dichgans Martin, Rosand Jonathan, Sudlow Cathie L M, |
| Rare variants of the 3'-5' DNA exonuclease TREX1 in early onset small vessel stroke. Wellcome open research 2017 2 106. McGlasson Sarah, Rannikmäe Kristiina, Bevan Steven, Logan Clare, Bicknell Louise S, Jury Alexa, , Jackson Andrew P, Markus Hugh S, Sudlow Cathie, Hunt David P |
| Genetic contributors and soluble mediators in prediction of autoimmune comorbidity. Journal of autoimmunity 2019 8 104 102317. Nezos Adrianos, Evangelopoulos Maria-Eleutheria, Mavragani Clio |
| Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects. Brain : a journal of neurology 2019 3 142 (4): 1009-1023. Mishra Aniket, Chauhan Ganesh, Violleau Marie-Helene, Vojinovic Dina, Jian Xueqiu, Bis Joshua C, Li Shuo, Saba Yasaman, Grenier-Boley Benjamin, Yang Qiong, Bartz Traci M, Hofer Edith, Soumaré Aïcha, Peng Fen, Duperron Marie-Gabrielle, Foglio Mario, Mosley Thomas H, Schmidt Reinhold, Psaty Bruce M, Launer Lenore J, Boerwinkle Eric, Zhu Yicheng, Mazoyer Bernard, Lathrop Mark, Bellenguez Celine, Van Duijn Cornelia M, Ikram M Arfan, Schmidt Helena, Longstreth W T, Fornage Myriam, Seshadri Sudha, Joutel Anne, Tzourio Christophe, Debette Stephan |
| TREX1 531C>T Polymorphism is Associated with High Proviral Load Levels in HTLV-1-Infected Persons. Viruses 2019 Dec 12 (1): . Silva Denis de Castro, Amoras Ednelza da Silva Graça, Moura Tuane Carolina Ferreira, Lopes Felipe Teixeira, Gomes Samara Tatielle Monteiro, Costa Carlos A da, Sousa Maísa Silva, Ishak Ricardo, Vallinoto Antonio Carlos Rosário, Queiroz Maria Alice Freit |
| How common are single gene mutations as a cause for lacunar stroke? A targeted gene panel study. Neurology 2019 11 93 (22): e2007-e2020. Tan Rhea Y Y, Traylor Matthew, Megy Karyn, Duarte Daniel, Deevi Sri V V, Shamardina Olga, Mapeta Rutendo P, , Ouwehand Willem H, Gräf Stefan, Downes Kate, Markus Hugh |
| Global Assessment of Mendelian Stroke Genetic Prevalence in 101 635 Individuals From 7 Ethnic Groups. Stroke 2020 Feb STROKEAHA119028840. Grami Nickrooz, Chong Michael, Lali Ricky, Mohammadi-Shemirani Pedrum, Henshall David E, Rannikmäe Kristiina, Paré Guillau |
| Cerebrovascular reactivity in retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations. Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2021 3 41 (4): 831-840. Hoogeveen Evelien S, Pelzer Nadine, Ghariq Eidrees, van Osch Matthias Jp, Dahan Albert, Terwindt Gisela M, Kruit Mark |
| Frequency and Phenotype Associations of Rare Variants in 5 Monogenic Cerebral Small Vessel Disease Genes in 200,000 UK Biobank Participants. Neurology. Genetics 2022 8 8 (5): e200015. Ferguson Amy Christina, Thrippleton Sophie, Henshall David, Whittaker Ed, Conway Bryan, MacLeod Malcolm, Malik Rainer, Rawlik Konrad, Tenesa Albert, Sudlow Cathie, Rannikmae Kristii |
| Genetic Study of Cerebral Small Vessel Disease in Chinese Han Population. Frontiers in neurology 2022 4 13 829438. Wang Yunchao, Shi Changhe, Li Yusheng, Yu Wenkai, Wei Sen, Fan Yu, Mao Chengyuan, Yang Zhihua, Yu Lulu, Zhao Zichen, Li Shanshan, Gao Yuan, Xu Yumi |
| Genetic analysis reveals novel variants for vascular cognitive impairment. Acta neurologica Scandinavica 2022 3 146 (1): 42-50. Mönkäre Saana, Kuuluvainen Liina, Schleutker Johanna, Bras Jose, Roine Susanna, Pöyhönen Minna, Guerreiro Rita, Myllykangas Lii |
| Contribution of genetic variants associated with primary immunodeficiencies to childhood-onset systemic lupus erythematous. The Journal of allergy and clinical immunology 2022 12 . Wu Chao-Yi, Fan Wen-Lang, Yang Huang-Yu, Chu Pi-Shuang, Liao Pei-Chun, Chen Li-Chen, Yao Tsung-Chieh, Yeh Kuo-Wei, Ou Liang-Shiou, Lin Syh-Jae, Lee Wen-I, Huang Jing-Lo |
| High frequency of HTRA1 AND ABCC6 mutations in Japanese patients with adult-onset cerebral small vessel disease. Journal of neurology, neurosurgery, and psychiatry 2022 10 94 (1): 74-81. Uemura Masahiro, Hatano Yuya, Nozaki Hiroaki, Ando Shoichiro, Kondo Hajime, Hanazono Akira, Iwanaga Akira, Murota Hiroyuki, Osakada Yosuke, Osaki Masato, Kanazawa Masato, Kanai Mitsuyasu, Shibata Yoko, Saika Reiko, Miyatake Tadashi, Aizawa Hitoshi, Ikeuchi Takeshi, Tomimoto Hidekazu, Mizuta Ikuko, Mizuno Toshiki, Ishihara Tomohiko, Onodera Osa |
| Association of TREX1 polymorphism with disease progression in human immunodeficiency virus type-1 (HIV-1) infected patients. Virus genes 2023 9 . Nastaran Tohidi, Seyed Ali Dehghan Manshadi, Mahboubeh Hajiabdolbag |
| TREX1 531C/T Polymorphism and Autoantibodies Associated with the Immune Status of HIV-1-Infected Individuals. International journal of molecular sciences 2023 6 24 (11): . Maria Alice Freitas Queiroz, Tuane Carolina Ferreira Moura, Carlos David Araújo Bichara, Lorena Leticia Peixoto de Lima, Allysson Quintino Tenório de Oliveira, Ranilda Gama de Souza, Samara Tatielle Monteiro Gomes, Ednelza da Silva Graça Amoras, Antonio Carlos Rosário Vallino |
| Clinical characteristics of early-onset paediatric systemic lupus erythematosus in a single centre in China. Rheumatology (Oxford, England) 2023 2 . Hou Yipei, Wang Li, Luo Chong, Tang Wenjing, Dai Rongxin, An Yunfei, Tang Xuem |
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