| Incidental findings on brain magnetic resonance imaging: systematic review and meta-analysis Z Morris, WN Whiteley, WT Longstreth, F Weber, YC Lee, Y Tsushima, ... Bmj 339, 2009 | 840 | 2009 |
| Mutations in KCND3 cause spinocerebellar ataxia type 22 YC Lee, A Durr, K Majczenko, YH Huang, YC Liu, CC Lien, PC Tsai, ... Annals of neurology 72 (6), 859-869, 2012 | 180 | 2012 |
| Cutoff scores of the cognitive abilities screening instrument, Chinese version in screening of dementia KN Lin, PN Wang, CY Liu, WT Chen, YC Lee, HC Liu Dementia and geriatric cognitive disorders 14 (4), 176-182, 2002 | 165 | 2002 |
| Comparison of sensitivity of transcarpal median motor conduction velocity and conventional conduction techniques in electrodiagnosis of carpal tunnel syndrome MH Chang, LH Liu, YC Lee, SJ Wei, HL Chiang, PF Hsieh Clinical neurophysiology 117 (5), 984-991, 2006 | 130 | 2006 |
| A Recurrent loss‐of‐function alanyl‐tRNA synthetase (AARS ) mutation in patients with charcot‐marie‐tooth disease type 2N (CMT2N) HM McLaughlin, R Sakaguchi, W Giblin, ... Human mutation 33 (1), 244-253, 2012 | 125 | 2012 |
| ATXN2 trinucleotide repeat length correlates with risk of ALS W Sproviero, A Shatunov, D Stahl, M Shoai, W van Rheenen, AR Jones, ... Neurobiology of aging 51, 178. e1-178. e9, 2017 | 113 | 2017 |
| The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan KP Lin, BW Soong, CC Yang, LW Huang, MH Chang, IH Lee, A Antonellis, ... PLoS One 6 (12), e29393, 2011 | 112 | 2011 |
| The ‘hot cross bun’sign in the patients with spinocerebellar ataxia YC Lee, CS Liu, HM Wu, PS Wang, MH Chang, BW Soong European journal of neurology 16 (4), 513-516, 2009 | 106 | 2009 |
| Characterization of CADASIL among the Han Chinese in Taiwan: distinct genotypic and phenotypic profiles YC Liao, CT Hsiao, JL Fuh, CM Chern, WJ Lee, YC Guo, SJ Wang, IH Lee, ... PloS one 10 (8), e0136501, 2015 | 104 | 2015 |
| Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese YC Lee, CS Liu, MH Chang, KP Lin, JL Fuh, YC Lu, YF Liu, BW Soong Journal of neurology 256, 249-255, 2009 | 103 | 2009 |
| A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy PC Tsai, BW Soong, I Mademan, YH Huang, CR Liu, CT Hsiao, HT Wu, ... Brain 140 (5), 1252-1266, 2017 | 88 | 2017 |
| FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS CP Tsai, BW Soong, KP Lin, PH Tu, JL Lin, YC Lee Neurobiology of aging 32 (3), 553. e13-553. e21, 2011 | 80 | 2011 |
| Mutations in ATP1A1 cause dominant Charcot-Marie-Tooth type 2 P Lassuthova, AP Rebelo, G Ravenscroft, PJ Lamont, MR Davis, ... The American Journal of Human Genetics 102 (3), 505-514, 2018 | 77 | 2018 |
| Mutational analysis of MATR3 in Taiwanese patients with amyotrophic lateral sclerosis KP Lin, PC Tsai, YC Liao, WT Chen, CP Tsai, BW Soong, YC Lee Neurobiology of aging 36 (5), 2005. e1-2005. e4, 2015 | 71 | 2015 |
| A hexanucleotide repeat expansion in C9ORF72 causes familial and sporadic ALS in Taiwan CP Tsai, BW Soong, PH Tu, KP Lin, JL Fuh, PC Tsai, YC Lu, IH Lee, ... Neurobiology of aging 33 (9), 2232. e11-2232. e18, 2012 | 69 | 2012 |
| Cognitive reserve: a SPECT study of 132 Alzheimer’s disease patients with an education range of 0–19 years YC Liao, RS Liu, EL Teng, YC Lee, PN Wang, KN Lin, CP Chung, HC Liu Dementia and geriatric cognitive disorders 20 (1), 8-14, 2005 | 69 | 2005 |
| PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defects YT Liu, FS Nian, WJ Chou, CY Tai, SY Kwan, C Chen, PW Kuo, PH Lin, ... Oncotarget 7 (26), 39184, 2016 | 67 | 2016 |
| Comparison of cerebellar ataxias: A three‐year prospective longitudinal assessment Y Lee, Y Liao, P Wang, IH Lee, K Lin, B Soong Movement Disorders 26 (11), 2081-2087, 2011 | 65 | 2011 |
| Exome sequencing identifies GNB4 mutations as a cause of dominant intermediate Charcot-Marie-Tooth disease BW Soong, YH Huang, PC Tsai, CC Huang, HC Pan, YC Lu, HJ Chien, ... The American Journal of Human Genetics 92 (3), 422-430, 2013 | 64 | 2013 |
| Mutational analysis of TBK1 in Taiwanese patients with amyotrophic lateral sclerosis PC Tsai, YC Liu, KP Lin, YT Liu, YC Liao, CT Hsiao, BW Soong, PK Yip, ... Neurobiology of aging 40, 191. e11-191. e16, 2016 | 60 | 2016 |
