Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Amyotrophic Lateral Sclerosis and CHCHD10[original query] |
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| The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patients. Neurobiology of aging 2015 Oct 36 (10): 2908.e17-8. Wong Chun Hao, Topp Simon, Gkazi Athina Soragia, Troakes Claire, Miller Jack W, de Majo Martina, Kirby Janine, Shaw Pamela J, Morrison Karen E, de Belleroche Jacqueline, Vance Caroline A, Al-Chalabi Ammar, Al-Sarraj Safa, Shaw Christopher E, Smith Bradley |
| CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients. Neurobiology of aging 2015 Apr 36 (4): 1767.e3-6. Chiò Adriano, Mora Gabriele, Sabatelli Mario, Caponnetto Claudia, Traynor Bryan J, Johnson Janel O, Nalls Mike A, Calvo Andrea, Moglia Cristina, Borghero Giuseppe, Monsurrò Maria Rosaria, La Bella Vincenzo, Volanti Paolo, Simone Isabella, Salvi Fabrizio, Logullo Francesco O, Nilo Riva, Battistini Stefania, Mandrioli Jessica, Tanel Raffaella, Murru Maria Rita, Mandich Paola, Zollino Marcella, Conforti Francesca L, , Brunetti Maura, Barberis Marco, Restagno Gabriella, Penco Silvana, Lunetta Christi |
| Identification of CHCHD10 Mutation in Chinese Patients with Alzheimer Disease. Molecular neurobiology 2016 Aug . Xiao Tingting, Jiao Bin, Zhang Weiwei, Pan Chuzheng, Wei Jingya, Liu Xiaoyan, Zhou Yafang, Zhou Lin, Tang Beisha, Shen |
| Mutation Screening of the CHCHD10 Gene in Chinese Patients with Amyotrophic Lateral Sclerosis. Molecular neurobiology 2016 Apr . Zhou QingQing, Chen YongPing, Wei QianQian, Cao Bei, Wu Ying, Zhao Bi, Ou RuWei, Yang Jing, Chen XuePing, Hadano Shinji, Shang Hui-Fa |
| CHCHD10 is not a frequent causative gene in Chinese ALS patients. Amyotrophic lateral sclerosis & frontotemporal degeneration 0 17 (5-6): 458-60. Li Xiao Ling, Shu Shi, Li Xiao Guang, Liu Qing, Liu Fang, Cui Bo, Liu Ming Sheng, Peng Bin, Cui Li Ying, Zhang X |
| Mutational analysis of TBK1 in Taiwanese patients with amyotrophic lateral sclerosis. Neurobiology of aging 2016 Apr 40 191.e11-191.e16. Tsai Pei-Chien, Liu Yi-Chien, Lin Kon-Ping, Liu Yo-Tsen, Liao Yi-Chu, Hsiao Cheng-Tsung, Soong Bing-Wen, Yip Ping-Keung, Lee Yi-Chu |
| CHCHD10 mutations in patients with amyotrophic lateral sclerosis in Mainland China. Neurobiology of aging 2017 Feb . Shen Shen, He Ji, Tang Lu, Zhang Nan, Fan Dongshe |
| Investigating CCNF mutations in a Taiwanese cohort with amyotrophic lateral sclerosis. Neurobiology of aging 2017 Oct . Tsai Pei-Chien, Liao Yi-Chu, Chen Po-Lin, Guo Yuh-Cherng, Chen Ying-Hao, Jih Kang-Yang, Lin Kon-Ping, Soong Bing-Wen, Tsai Ching-Paio, Lee Yi-Chu |
| Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients. Neurobiology of aging 2017 03 51 177.e9-177.e16. Perrone Federica, Nguyen Hung Phuoc, Van Mossevelde Sara, Moisse Matthieu, Sieben Anne, Santens Patrick, De Bleecker Jan, Vandenbulcke Mathieu, Engelborghs Sebastiaan, Baets Jonathan, Cras Patrick, Vandenberghe Rik, De Jonghe Peter, De Deyn Peter P, Martin Jean-Jacques, Van Damme Philip, Van Broeckhoven Christine, van der Zee Julie, |
| CHCHD10 variants in amyotrophic lateral sclerosis: Where is the evidence? Annals of neurology 2018 Jul . Authors are not available |
| ALS Genes in the Genomic Era and their Implications for FTD. Trends in genetics : TIG 2018 4 34 (6): 404-423. Nguyen Hung Phuoc, Van Broeckhoven Christine, van der Zee Jul |
| Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy. Neurobiology of aging 2018 3 66 181.e1-181.e2. Rubino Elisa, Zhang Ming, Mongini Tiziana, Boschi Silvia, Vercelli Liliana, Vacca Alessandro, Govone Flora, Gai Annalisa, Giordana Maria Teresa, Grinberg Mark, Rogaeva Ekaterina, Rainero Innocen |
| Comparison of the clinical and genetic features of amyotrophic lateral sclerosis across Cuban, Uruguayan and Irish clinic-based populations. Journal of neurology, neurosurgery, and psychiatry 2019 3 90 (6): 659-665. Ryan Marie, Zaldívar Vaillant Tatiana, McLaughlin Russell L, Doherty Mark A, Rooney James, Heverin Mark, Gutierrez Joel, Lara-Fernández Gloria Esther, Pita Rodríguez Mariana, Hackembruch Jochen, Perna Abayubá, Vazquez Maria Cristina, Musio Marco, Ketzoian Carlos N, Logroscino Giancarlo, Hardiman Or |
| Meta-analysis of the association between CHCHD10 Pro34Ser variant and the risk of amyotrophic lateral sclerosis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2020 Jul . Yang Baiyuan, Yang Chenghui, Ren Junwei, Zhong Chengqing, Liu Keting, Zhao Liusha, Li Li, Wang Han, Zhu Mingling, Lin Zhenfa |
| Genetics of frontotemporal dementia in China. Amyotrophic lateral sclerosis & frontotemporal degeneration 2021 2 22 (5-6): 321-335. Jiang Yaling, Jiao Bin, Xiao Xuewen, Shen |
| Increased copy-number variant load of associated risk genes in sporadic cases of amyotrophic lateral sclerosis. Cellular and molecular life sciences : CMLS 2024 7 81 (1): 316. Maria Guarnaccia, Giovanna Morello, Valentina La Cognata, Vincenzo La Bella, Francesca Luisa Conforti, Sebastiano Cavalla |
- Page last reviewed:Feb 1, 2024
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