| Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1 Z Cen, Z Jiang, Y Chen, X Zheng, F Xie, X Yang, X Lu, Z Ouyang, H Wu, ... Brain 141 (8), 2280-2288, 2018 | 87 | 2018 |
| Altered brain network centrality in depressed Parkinson's disease patients Y Lou, P Huang, D Li, Z Cen, B Wang, J Gao, M Xuan, H Yu, M Zhang, ... Movement Disorders 30 (13), 1777-1784, 2015 | 85 | 2015 |
| Biallelic loss-of-function mutations in JAM2 cause primary familial brain calcification Z Cen, Y Chen, S Chen, H Wang, D Yang, H Zhang, H Wu, L Wang, ... Brain 143 (2), 491-502, 2020 | 66 | 2020 |
| Abnormal baseline brain activity in Parkinson's disease with and without REM sleep behavior disorder: A resting‐state functional MRI study D Li, P Huang, Y Zang, Y Lou, Z Cen, Q Gu, M Xuan, F Xie, Z Ouyang, ... Journal of Magnetic Resonance Imaging 46 (3), 697-703, 2017 | 43 | 2017 |
| Fine mapping and whole‐exome sequencing of a familial cortical myoclonic tremor with epilepsy family Z Cen, F Xie, D Lou, X Lu, Z Ouyang, L Liu, J Cao, D Li, H Yin, Z Wang, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168 …, 2015 | 31 | 2015 |
| Homozygous p. D331Y mutation in PLA2G6 in two patients with pure autosomal-recessive early-onset parkinsonism: further evidence of a fourth phenotype of PLA2G6-associated … F Xie, Z Cen, Z Ouyang, S Wu, J Xiao, W Luo Parkinsonism & related disorders 21 (4), 420-422, 2015 | 30 | 2015 |
| LRP10 in autosomal‐dominant Parkinson's disease Y Chen, Z Cen, X Zheng, Q Pan, X Chen, L Zhu, S Chen, H Wu, F Xie, ... Movement Disorders 34 (6), 912-916, 2019 | 26 | 2019 |
| Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy Z Cen, C Huang, H Yin, X Ding, F Xie, X Lu, Z Ouyang, Y Lou, X Qiu, ... Movement Disorders 31 (11), 1704-1710, 2016 | 26 | 2016 |
| Evaluation of MYORG mutations as a novel cause of primary familial brain calcification Y Chen, F Fu, S Chen, Z Cen, H Tang, J Huang, F Xie, X Zheng, D Yang, ... Movement Disorders 34 (2), 291-297, 2019 | 25 | 2019 |
| Dramatic response to pyridoxine in a girl with absence epilepsy with ataxia caused by a de novo CACNA1A mutation X Du, Y Chen, Y Zhao, W Luo, Z Cen, W Hao Seizure-European Journal of Epilepsy 45, 189-191, 2017 | 25 | 2017 |
| Altered cerebello‐motor network in familial cortical myoclonic tremor with epilepsy type 1 B Wang, J Wang, Z Cen, W Wei, F Xie, Y Chen, H Sun, Y Hu, D Yang, ... Movement Disorders 35 (6), 1012-1020, 2020 | 24 | 2020 |
| Intronic (TTTGA)n insertion in SAMD12 also causes familial cortical myoclonic tremor with epilepsy Z Cen, Y Chen, D Yang, Q Zhu, S Chen, X Chen, B Wang, F Xie, ... Movement Disorders 34 (10), 1571-1576, 2019 | 24 | 2019 |
| A clinical study of the coronal plane deformity in Parkinson disease X Ye, D Lou, X Ding, C Xie, J Gao, Y Lou, Z Cen, Y Xiao, Q Miao, F Xie, ... European Spine Journal 26, 1862-1870, 2017 | 24 | 2017 |
| Genetic analysis of SPG4 and SPG3A genes in a cohort of Chinese patients with hereditary spastic paraplegia X Lu, Z Cen, F Xie, Z Ouyang, B Zhang, G Zhao, W Luo Journal of the Neurological Sciences 347 (1-2), 368-371, 2014 | 24 | 2014 |
| Alteration of brain functional connectivity in Parkinson’s disease patients with dysphagia J Gao, X Guan, Z Cen, Y Chen, X Ding, Y Lou, S Wu, B Wang, Z Ouyang, ... Dysphagia 34, 600-607, 2019 | 23 | 2019 |
| Neuronal intranuclear inclusion disease tremor‐dominant subtype: A mimicker of essential tremor D Yang, Z Cen, L Wang, X Chen, P Liu, H Wang, Z Ouyang, Y Chen, ... European Journal of Neurology 29 (2), 450-458, 2022 | 21 | 2022 |
| L-3-n-butylphthalide protects HSPB8 K141N mutation-induced oxidative stress by modulating the mitochondrial apoptotic and Nrf2 pathways XD Yang, ZD Cen, HP Cheng, K Shi, J Bai, F Xie, HW Wu, BB Li, W Luo Frontiers in Neuroscience 11, 402, 2017 | 20 | 2017 |
| Two cases of dural arteriovenous fistula presenting with parkinsonism and progressive cognitive dysfunction Y Luo, J Qi, Z Cen, H Hu, B Jiang, W Luo Journal of the Neurological Sciences 343 (1-2), 211-214, 2014 | 20 | 2014 |
| Loss of function of CMPK2 causes mitochondria deficiency and brain calcification M Zhao, HZ Su, YH Zeng, Y Sun, XX Guo, YL Li, C Wang, ZY Zhao, ... Cell Discovery 8 (1), 128, 2022 | 18 | 2022 |
| Underestimated disease prevalence and severe phenotypes in patients with biallelic variants: a cohort study of primary familial brain calcification from China SI Chen, Z Cen, F Fu, Y Chen, X Chen, D Yang, H Wang, H Wu, X Zheng, ... Parkinsonism & Related Disorders 64, 211-219, 2019 | 17 | 2019 |
