1.Sun YM, Dong Y, Wang J, Lu JH, Chen Y, Wu JJ. A novel mutation of VAPB in one Chinese familial amyotrophic lateral sclerosis pedigree and its clinical characteristics. J Neurol. 2017; 264(12):2387-2393.
2.Chen K, Yang YJ, Liu FT, Li DK, Bu LL, Yang K, Wang Y, Shen B, Guan RY, Song J, Wang J, Wu JJ. Evaluation of PDQ-8 and its relationship with PDQ-39 in China: a three-year longitudinal study. Health Qual Life Outcomes. 2017 Aug 24;15(1):170.
3.Wang YX, Zhao J, Li DK, Peng F, Wang Y, Yang K, Liu ZY, Liu FT, Wu JJ, Wang J. Associations between cognitiveimpairment and motor dysfunction in Parkinson“s disease. Brain Behav. 2017;7(6):e00719.
4.Wang Y, Wu JJ, Liu FT, Chen K, Chen C, Luo SS, Wang YX, Li DK, Guan RY, Yang YJ, An Y, Wang J, Sun YM. Olfaction in Parkin carriers in Chinese patients with Parkinson disease. Brain Behav. 2017;7(5):e00680.
5.Peng F, Sun YM, Chen C, Luo SS, Li DK, Wang YX, Yang K, Liu FT, Zuo CT, Ding ZT, An Y, Wu JJ, Wang J, The heterozygous R1441C mutation of leucine-rich repeat kinase 2 gene in a Chinese patient with Parkinson disease: A five-year follow-up and literatures review, J Neurol Sci, 2017; 373: 23-26.
6.Xiong WX, Sun YM, Guan RY, Luo SS, Chen C, An Y, Wang J, Wu JJ. The heterozygous A53T mutation in the alphasynuclein gene in a Chinese Han patient with Parkinson disease: case report and literature review. J Neurol. 2016;263(10):1984-1992.
7.陈嬿,董漪,卢家红,刘丰韬,蒋雨平,邬剑军.中国华东地区家族性肌萎缩侧索硬化症患者SOD1基因突变检测及临床特点分析.中国临床神经科学. 2016, 24(2): 146-152.
8.Liu SY, Wu JJ, Zhao J, Huang SF, Wang YX, Ge JJ, Wu P, Zuo CT, Ding ZT, Wang J. Onset-related subtypes of Parkinson“s disease differ in the patterns of striatal dopaminergic dysfunction: A positron emission tomography study. Parkinsonism Relat Disord. 2015, 21(12):1448-1453
9.Liu FT, Chen Y, Yang YJ, Yang L, Yu M, Zhao J, Wu JJ, Huang F, Liu W, Ding ZT, Wang J. Involvement of mortalin/GRP75/mthsp70 in the mitochondrial impairments induced by A53T mutantα-synuclein. Brain Res. 2015, 1604: 52-61
10.Dong Y, Wu JJ, Wu ZY. Identification of 46 CAG repeats within PPP2R2B as probably the shortest pathogenic allele for SCA12. Parkinsonism Relat Disord. 2015, 21(4):398-401