公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2014 | Lack of C9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders | CHIN-HSIEN LIN ; TA-FU CHEN ; MING-JANG CHIU ; Lin H.-I.; RUEY-MEEI WU | Frontiers in Neurology | 11 | 15 | |
2015 | Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population | Fan T.-S.; Lin H.-I.; CHIN-HSIEN LIN ; RUEY-MEEI WU | Neurobiology of Aging | 17 | 17 | |
2009 | Lack of evidence for association of a parkin promoter polymorphism with early-onset Parkinson's disease in a Chinese population | Taylor J.M.; RUEY-MEEI WU ; CHIN-HSIEN LIN ; Delatycki M.B.; Lockhart P.J. | Parkinsonism and Related Disorders | 2 | 2 | |
2004 | Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism | Lockhart P.J.; Bounds R.; Hulihan M.; Kachergus J.; Lincoln S.; CHIN-HSIEN LIN ; RUEY-MEEI WU ; Farrer M.J. | Movement Disorders | 29 | 15 | |
2007 | Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (Ethnic Chinese) cohort of familial and early-onset parkinsonism | CHIN-HSIEN LIN ; WUH-LIANG HWU ; Chiang S.-C.; CHUN-HWEI TAI ; RUEY-MEEI WU | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 8 | 7 | |
2021 | Lack of PTRHD1 mutation in patients with young-onset and familial Parkinson's disease in a Taiwanese population | Chen S.-J.; Ho C.-H.; Lin H.-Y.; CHIN-HSIEN LIN ; RUEY-MEEI WU | Neurobiology of Aging | 4 | 4 | |
2017 | Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort | Lin H.-H.; RUEY-MEEI WU ; Lin H.-I.; Chen M.-L.; CHUN-HWEI TAI ; CHIN-HSIEN LIN | Neurobiology of Aging | 9 | 8 | |
2017 | Lack of TMEM230 mutations in patients with familial and sporadic Parkinson's disease in a Taiwanese population | Fan T.-S.; CHIN-HSIEN LIN ; Lin H.-I.; Chen M.-L.; RUEY-MEEI WU | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 9 | 8 | |
2021 | Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation: A Novel DARS2 Mutation and Intra-Familial Heterogeneity | Li, Jeng-Lin; NI-CHUNG LEE ; Chen, Pin-Shiuan; Lee, Gin Hoong; RUEY-MEEI WU | Movement disorders clinical practice | 3 | 2 | |
2022 | Level I PD-MCI Using Global Cognitive Tests and the Risk for Parkinson's Disease Dementia | Boel, Judith A; de Bie, Rob M A; Schmand, Ben A; Dalrymple-Alford, John C; Marras, Connie; Adler, Charles H; Goldman, Jennifer G; Tröster, Alexander I; Burn, David J; Litvan, Irene; Geurtsen, Gert J; Bernard, Bryan; Stebbins, Glenn; Filoteo, J. Vincent; Weintraub, Daniel; Caviness, John N.; RUEY-MEEI WU ; Williams-Gray, Caroline H.; Breen, David P.; Barker, Roger A. | Movement disorders clinical practice | 8 | 4 | |
2022 | Long-term efficacy of bilateral subthalamic deep brain stimulation in the parkinsonism of SCA 3: A rare case report | MING-CHE KUO ; CHUN-HWEI TAI ; SHENG-HONG TSENG ; RUEY-MEEI WU | European journal of neurology | 6 | 6 | |
2022 | Long-Term Outcomes of Idiopathic and Acquired Dystonia After Pallidal Deep Brain Stimulation: A Case Series | CHUN-HWEI TAI ; SHENG-CHE CHOU ; CHIN-HSIEN LIN ; WANG-TSO LEE ; RUEY-MEEI WU ; SHENG-HONG TSENG | World neurosurgery | 0 | 0 | |
2016 | Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3β activity | CHIN-HSIEN LIN ; Lin H.-I.; Chen M.-L.; Lai T.-T.; Cao L.-P.; Farrer M.J.; RUEY-MEEI WU ; Chien C.-T. | Human Molecular Genetics | 43 | 37 | |
2018 | LRRK 2 gene mutations in the pathophysiology of the ROCO domain and therapeutic targets for Parkinson's disease: A review Julie Y.H. Chan | Chen M.-L; RUEY-MEEI WU | Journal of Biomedical Science | 27 | 25 | |
2015 | Lrrk regulates the dynamic profile of dendritic Golgi outposts through the golgin Lava lamp | CHIN-HSIEN LIN ; Li H.; Lee Y.-N.; Cheng Y.-J.; RUEY-MEEI WU ; Chien C.-T. | Journal of Cell Biology | 41 | 37 | |
2010 | LRRK2 G2019S mutation induces dendrite degeneration through mislocalization and phosphorylation of tau by recruiting autoactivated GSK3β | CHIN-HSIEN LIN ; Tsai P.-I.; RUEY-MEEI WU ; Chien C.-T. | Journal of Neuroscience | 140 | 135 | |
2007 | Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia | Farrer M.J.; Stone J.T.; CHIN-HSIEN LIN ; D?chsel J.C.; Hulihan M.M.; Haugarvoll K.; Ross O.A.; RUEY-MEEI WU | Parkinsonism and Related Disorders | 176 | 154 | |
2009 | LRRK2 G2385R modulates age at onset in Parkinson's disease: A multi-center pooled analysis | Tan E.K; Peng R; Wu Y.R; RUEY-MEEI WU ; Wu-Chou Y.H; Tan L.C; An X.K; Chen C.M; Fook-Chong S; Lu C.S. | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 28 | 26 | |
2008 | LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: Clinical, PET, and functional studies | CHIN-HSIEN LIN ; KAI-YUAN TZEN ; Yu C.-Y.; CHUN-HWEI TAI ; Farrer M.J.; RUEY-MEEI WU | Journal of Biomedical Science | 50 | 46 | |
2011 | LRRK2 Parkinson's disease: From animal models to cellular mechanisms | CHIN-HSIEN LIN ; Tsai P.-I.; RUEY-MEEI WU ; Chin C.-T. | Reviews in the Neurosciences | 10 | 11 | |