Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Disease and CHCHD10[original query] |
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| Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66Val. Acta neurologica Scandinavica 2015 Jul . Pasanen P, Myllykangas L, Pöyhönen M, Kiuru-Enari S, Tienari P J, Laaksovirta H, Toppila J, Ylikallio E, Tyynismaa H, Auranen |
| 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 |
| The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Jul . Blauwendraat Cornelis, Wilke Carlo, Simón-Sánchez Javier, Jansen Iris E, Reifschneider Anika, Capell Anja, Haass Christian, Castillo-Lizardo Melissa, Biskup Saskia, Maetzler Walter, Rizzu Patrizia, Heutink Peter, Synofzik Matth |
| 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 |
| Genetic risk factors in Finnish patients with Parkinson's disease. Parkinsonism & related disorders 2017 Sep . Ylönen Susanna, Siitonen Ari, Nalls Michael A, Ylikotila Pauli, Autere Jaana, Eerola-Rautio Johanna, Gibbs Raphael, Hiltunen Mikko, Tienari Pentti J, Soininen Hilkka, Singleton Andrew B, Majamaa Ka |
| Genetic analysis of CHCHD2 and CHCHD10 in Italian patients with Parkinson's disease. Neurobiology of aging 2017 Jan . Rubino Elisa, Brusa Livia, Zhang Ming, Boschi Silvia, Govone Flora, Vacca Alessandro, Gai Annalisa, Pinessi Lorenzo, Lopiano Leonardo, Rogaeva Ekaterina, Rainero Innocen |
| 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 |
| 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 |
| The role of genetics in neurodegenerative dementia: a large cohort study in South China. NPJ genomic medicine 2021 8 6 (1): 69. Jiao Bin, Liu Hui, Guo Lina, Xiao Xuewen, Liao Xinxin, Zhou Yafang, Weng Ling, Zhou Lu, Wang Xin, Jiang Yaling, Yang Qijie, Zhu Yuan, Zhou Lin, Zhang Weiwei, Wang Junling, Yan Xinxiang, Li Jinchen, Tang Beisha, Shen |
| 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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