Human Genome Epidemiology Literature Finder
Records 1 - 29 (of 29 Records) |
Query Trace: CHCHD2[original query] |
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Mutation analysis of CHCHD2 gene in Chinese familial Parkinson's disease. Neurobiology of aging 2015 Aug . Liu Zhenhua, Guo Jifeng, Li Kai, Qin Lixia, Kang Jifeng, Shu Li, Zhang Yuan, Wei Yang, Yang Nannan, Luo Yang, Sun Qiying, Xu Qian, Yan Xinxiang, Tang Beis |
Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease. Neurobiology of aging 2015 Nov . Zhang Ming, Xi Zhengrui, Fang Shilun, Ghani Mahdi, Sato Christine, Moreno Danielle, Liang Yan, Lang Anthony E, Rogaeva Ekateri |
CHCHD2 gene mutations in familial and sporadic Parkinson's disease. Neurobiology of aging 2015 Nov . Shi Chang-He, Mao Cheng-Yuan, Zhang Shu-Yu, Yang Jing, Song Bo, Wu Ping, Zuo Chuan-Tao, Liu Yu-Tao, Ji Yan, Yang Zhi-Hua, Wu Jun, Zhuang Zheng-Ping, Xu Yu-Mi |
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders. Neurology 2015 Nov . Ogaki Kotaro, Koga Shunsuke, Heckman Michael G, Fiesel Fabienne C, Ando Maya, Labbé Catherine, Lorenzo-Betancor Oswaldo, Moussaud-Lamodière Elisabeth L, Soto-Ortolaza Alexandra I, Walton Ronald L, Strongosky Audrey J, Uitti Ryan J, McCarthy Allan, Lynch Timothy, Siuda Joanna, Opala Grzegorz, Rudzinska Monika, Krygowska-Wajs Anna, Barcikowska Maria, Czyzewski Krzysztof, Puschmann Andreas, Nishioka Kenya, Funayama Manabu, Hattori Nobutaka, Parisi Joseph E, Petersen Ronald C, Graff-Radford Neill R, Boeve Bradley F, Springer Wolfdieter, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen |
Genetic analysis of CHCHD2 gene in Chinese Parkinson's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2016 Sep . Li Nan-Nan, Wang Ling, Tan Eng-King, Cheng Lan, Sun Xiao-Yi, Lu Zhong-Jiao, Li Jun-Ying, Zhang Jin-Hong, Peng Ro |
Mutational analysis of CHCHD2 in Chinese patients with multiple system atrophy and amyotrophic lateral sclerosis. Journal of the neurological sciences 2016 Sep 368 389-91. Yang Xinglong, An Ran, Zhao Quanzhen, Zheng Jinhua, Tian Sijia, Chen Yalan, Xu Yanmi |
Mutational scanning of the CHCHD2 gene in Han Chinese patients with Parkinson's disease and meta-analysis of the literature. Parkinsonism & related disorders 2016 May . Yang Xinglong, Zhao Quanzhen, An Ran, Zheng JinHua, Tian Sijia, Chen Yalan, Xu Yanmi |
Genetic analysis of the CHCHD2 gene in a cohort of Chinese patients with Parkinson disease. Neuroscience letters 2016 Jun . Wu Hongwei, Lu Xingjiao, Xie Fei, Cen Zhidong, Zheng Xiaosheng, Luo W |
Exonic rearrangements in the known Parkinson's disease-causing genes are a rare cause of the disease in South African patients. Neuroscience letters 2016 Mar 619 168-171. van der Merwe Celia, Carr Jonathan, Glanzmann Brigitte, Bardien Sora |
Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria. Neurobiology of aging 2016 Oct . Gagliardi Monica, Iannello Grazia, Colica Carmela, Annesi Grazia, Quattrone Al |
Genetic analysis of CHCHD2 in a southern Spanish population. Neurobiology of aging 2016 Oct . Tejera-Parrado Cristina, Jesús Silvia, Huertas-Fernández Ismael, Bernal-Bernal Inmaculada, Bonilla-Toribio Marta, Córdoba-Tevar Isabel, Abreu-Rodríguez Irene, Carrillo Fátima, Bernal-Escudero Maravilla, Vargas-González Laura, Carballo Manuel, Gómez-Garre Pilar, Mir Pab |
Genetic analysis of the CHCHD2 gene in Chinese patients with familial essential tremor. Neuroscience letters 2016 Oct . Wu Hongwei, Lu Xingjiao, Cen Zhidong, Xie Fei, Zheng Xiaosheng, Chen You, Luo W |
Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population. Neurobiology of aging 2015 Dec . Fan Tian-Sin, Lin Hang-I, Lin Chin-Hsien, Wu Ruey-Me |
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 |
Identification of CHCHD2 mutations in patients with Alzheimer's disease, amyotrophic lateral sclerosis and frontotemporal dementia in China. Molecular medicine reports 2018 May . Liu Xixi, Jiao Bin, Zhang Weiwei, Xiao Tingting, Hou Lihua, Pan Chuzheng, Tang Beisha, Shen |
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 |
CHCHD2 mutational screening in Brazilian patients with familial Parkinson's disease. Neurobiology of aging 2019 02 74 236.e7-236.e8. Voigt Danielle D, Nascimento Caroline M, de Souza Ritiele B, Cabello Acero Pedro H, Campos Júnior Mário, da Silva Camilla P, Pereira João S, Rosso Ana Lucia, Araujo Leite Marco A, Vasconcellos Luiz Felipe R, Della Coletta Marcus V, da Silva Delson J, Nicaretta Denise H, Gonçalves Andressa P, Dos Santos Jussara M, Calassara Veluma, Santos-Rebouças Cíntia B, Pimentel Márcia M |
Mutation Screening of the CHCHD2 Gene for Alzheimer's Disease and Frontotemporal Dementia in Chinese Mainland Population. Journal of Alzheimer's disease : JAD 2018 61 (4): 1283-1288. Che Xiang-Qian, Zhao Qian-Hua, Huang Yue, Li Xia, Ren Ru-Jing, Chen Sheng-Di, Guo Qi-Hao, Wang Ga |
Associations with metabolites in Chinese suggest new metabolic roles in Alzheimer's and Parkinson's diseases.
Human molecular genetics 2020 Jan 29 (2): 189-201. Chai Jin-Fang, Raichur Suryaprakash, Khor Ing Wei, Torta Federico, Chew Wee Siong, Herr Deron Raymond, Ching Jianhong, Kovalik Jean-Paul, Khoo Chin Meng, Wenk Markus R, Tai E Shyong, Sim Xueli |
Systematically analyzing rare variants of autosomal-dominant genes for sporadic Parkinson's disease in a Chinese cohort. Neurobiology of aging 2019 1 76 215.e1-215.e7. Yang Nannan, Zhao Yuwen, Liu Zhenhua, Zhang Rui, He Yan, Zhou Yangjie, Xu Qian, Sun Qiying, Yan Xinxiang, Guo Jifeng, Tang Beis |
Analysis of rare variants of autosomal-dominant genes in a Chinese population with sporadic Parkinson's disease. Molecular genetics & genomic medicine 2020 Aug e1449. Zheng Ran, Jin Chong-Yao, Chen Ying, Ruan Yang, Gao Ting, Lin Zhi-Hao, Dong Jia-Xian, Yan Ya-Ping, Tian Jun, Pu Jia-Li, Zhang Bao-Ro |
Novel and reported variants in Parkinson's disease genes confer high disease burden among Indians. Parkinsonism & related disorders 2020 7 78 46-52. Kumar Sumeet, Yadav Navneesh, Pandey Sanjay, Muthane Uday B, Govindappa Shyla T, Abbas Masoom M, Behari Madhuri, Thelma B |
Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies. Acta neuropathologica communications 2020 Jan 8 (1): 5. Orme Tatiana, Hernandez Dena, Ross Owen A, Kun-Rodrigues Celia, Darwent Lee, Shepherd Claire E, Parkkinen Laura, Ansorge Olaf, Clark Lorraine, Honig Lawrence S, Marder Karen, Lemstra Afina, Rogaeva Ekaterina, St George-Hyslop Peter, Londos Elisabet, Zetterberg Henrik, Morgan Kevin, Troakes Claire, Al-Sarraj Safa, Lashley Tammaryn, Holton Janice, Compta Yaroslau, Van Deerlin Vivianna, Trojanowski John Q, Serrano Geidy E, Beach Thomas G, Lesage Suzanne, Galasko Douglas, Masliah Eliezer, Santana Isabel, Pastor Pau, Tienari Pentti J, Myllykangas Liisa, Oinas Minna, Revesz Tamas, Lees Andrew, Boeve Brad F, Petersen Ronald C, Ferman Tanis J, Escott-Price Valentina, Graff-Radford Neill, Cairns Nigel J, Morris John C, Pickering-Brown Stuart, Mann David, Halliday Glenda, Stone David J, Dickson Dennis W, Hardy John, Singleton Andrew, Guerreiro Rita, Bras Jo |
Somatic Functional Deletions of Upstream Open Reading Frame-Associated Initiation and Termination Codons in Human Cancer. Biomedicines 2021 6 9 (6): . Jürgens Lara, Manske Felix, Hubert Elvira, Kischka Tabea, Flötotto Lea, Klaas Oliver, Shabardina Victoria, Schliemann Christoph, Makalowski Wojciech, Wethmar Kla |
Frequency of Parkinson's Disease Genes and Role of PARK2 in Amyotrophic Lateral Sclerosis: An NGS Study. Genes 2022 Jul 13 (8): . Vacchiano Veria, Bartoletti-Stella Anna, Rizzo Giovanni, Avoni Patrizia, Parchi Piero, Salvi Fabrizio, Liguori Rocco, Capellari Sabi |
The mutation spectrum of Parkinson-disease-related genes in early-onset Parkinson's disease in ethnic Chinese. European journal of neurology 2022 Jul . Chen Yong-Ping, Yu Shi-Hui, Zhang Guo-Hui, Hou Yan-Bing, Gu Xiao-Jing, Ou Ru-Wei, Shen Ying, Song Wei, Chen Xue-Ping, Zhao Bi, Cao Bei, Zhang Ling-Yu, Sun Ming-Ming, Liu Fei-Fei, Wei Qian-Qian, Liu Kun-Cheng, Lin Jun-Yu, Yang Tian-Mi, Yang Jing, Wu Ying, Jiang Zheng, Liu Jiao, Cheng Yang-Fan, Xiao Yi, Su Wei-Ming, Feng Fei, Cai Ying-Ying, Li Shi-Rong, Hu Tao, Yuan Xiao-Qin, Zhou Qing-Qing, Shao Na, Ma Sha, Shang Hui-Fa |
Genetic Analysis of Patients With Early-Onset Parkinson's Disease in Eastern China. Frontiers in aging neuroscience 2022 14 849462. Hua Ping, Zhao Yuwen, Zeng Qian, Li Lanting, Ren Jingru, Guo Jifeng, Tang Beisha, Liu Weig |
The genetic spectrum of a cohort of patients clinically diagnosed as Parkinson's disease in mainland China. NPJ Parkinson's disease 2023 5 9 (1): 76. Yi-Min Sun, Xin-Yue Zhou, Xiao-Niu Liang, Jin-Ran Lin, Yi-Dan Xu, Chen Chen, Si-Di Wei, Qi-Si Chen, Feng-Tao Liu, Jue Zhao, Yi-Lin Tang, Bo Shen, Lin-Hua Gan, Boxun Lu, Zheng-Tong Ding, Yu An, Jian-Jun Wu, Jian Wa |
Genetic screening of Filipinos suspected with familial Parkinson's disease: A pilot study. Parkinsonism & related disorders 2023 2 108 105319. Caritativo Erin Camille A, Yu Jeryl Ritzi T, Bautista Juan Miguel P, Nishioka Kenya, Jamora Roland Dominic G, Yalung Patrick M, Ng Arlene R, Hattori Nobuta |
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- Page last updated:Apr 22, 2024
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