第 1 到 64 筆結果,共 64 筆。
公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 | |
---|---|---|---|---|---|---|---|
1 | 2020 | Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy | CHIN-HSIEN LIN ; Tsai, Pei-I; Lin, Han-Yi; Hattori, Nobutaka; Funayama, Manabu; Jeon, Beomseok; Sato, Kota; Abe, Koji; Mukai, Yohei; Takahashi, Yuji; Li, Yuanzhe; Nishioka, Kenya; Yoshino, Hiroyo; Daida, Kensuke; Chen, Meng-Ling; Cheng, Jay; Huang, Cheng-Yen; SHIOU-RU TZENG ; Wu, Yen-Sheng; Lai, Hsing-Jung; Tsai, Hsin-Hsi; RUOH-FANG YEN ; NI-CHUNG LEE ; Lo, Wen-Chun; Hung, Yu-Chien; CHIH-CHIANG CHAN ; Ke, Yi-Ci; CHI-CHAO CHAO ; SUNG-TSANG HSIEH ; Farrer, Matthew; RUEY-MEEI WU | Brain : a journal of neurology | 29 | 32 | |
2 | 2019 | Genetic analysis of PODXL gene in patients with familial and young-onset Parkinson's disease in a Taiwanese population | Chen S.-J.; RUEY-MEEI WU ; Ho C.-H.; Cheng J.; Lin H.-Y.; CHIN-HSIEN LIN | Neurobiology of Aging | 1 | 1 | |
3 | 2019 | Using global team science to identify genetic parkinson's disease worldwide | Vollstedt E.-J.; Kasten M.; Klein C.; Aasly J.; Adler C.; Ahmad-Annuar A.; Albanese A.; Alcalay R.N.; Al-Mubarak B.; Alvarez V.; Andree-Mu?oz B.; Annesi G.; Appel-Cresswell S.; Arkadir D.; Armasu S.; Barber T.R.; Bardien S.; Barkhuizen M.; Barrett M.J.; Ba?ak A.N.; Beach T.; Benitez B.A.; Berg D.; Bhatia K.; Binkofski F.; Blauwendraat C.; Bonifati V.; Borges V.; Bozi M.; Brice A.; Brighina L.; Brockmann K.; Br?cke T.; Br?ggemann N.; Camacho M.; Cardoso F.; Belin A.C.; Carr J.; Chan P.; Chang-Castello J.; Chase B.; Chen-Plotkin A.; Ju Chung S.; Cilia R.; Clarimon J.; Clark L.; Cornejo-Olivas M.; Corvol J.-C.; Cosentino C.; Cras P.; Crosiers D.; Dam?sio J.; Das P.; de Carvalho Aguiar P.; De Michele G.; De Rosa A.; Dieguez E.; Dorszewska J.; Erer S.; Ertan S.; Farrer M.; Fedotova E.; Ferese R.; Ferrarese C.; Ferraz H.; Fiala O.; Foroud T.; Friedman A.; Frigerio R.; Funayama M.; Gambardella S.; Garraux G.; Gatto E.M.; Gen? G.; Giladi N.; Goldwurm S.; Gomez-Esteban J.C.; G?mez-Garre P.; Gorostidi A.; Grosset D.; Hanagasi H.; Hardy J.; Hassan A.; Hattori N.; Hauser R.A.; Hedera P.; Hentati F.; Hertz J.M.; Holton J.L.; Houlden H.; Hutz M.H.; Ikeuchi T.; Illarioshkin S.; Inca-Martinez M.; Infante J.; Jankovic J.; Jeon B.S.; Jes?s S.; Jimenez-Del-Rio M.; Kaasinen V.; Kasten M.; Kataoka H.; Kawakami H.; Kim Y.J.; Klein C.; Kliv?nyi P.; Koks S.; K?nig I.R.; Kosti? V.; Koziorowski D.; Kr?ger R.; Krygowska-Wajs A.; Kulisevsky J.; Lai D.; Lang A.; LeDoux M.; Lesage S.; Lim S.-Y.; CHIN-HSIEN LIN ; Lohmann K.; Lopera F.; Lopez G.; Lu C.-S.; Lynch T.; Machaczka M.; Madoev H.; Magalh?es M.; Majamaa K.; Maraganore D.; Marder K.; Markopoulou K.; Martikainen M.H.; Mata I.; Mazzetti P.; Mellick G.; Men?ndez-Gonz?lez M.; Micheli F.; Mirelman A.; Mir P.; Morino H.; Morris H.; Munhoz R.P.; Naito A.; Olszewska D.A.; Ozelius L.J.; Padmanabhan S.; Pais?n-Ruiz C.; Payami H.; Peluso S.; Petkovic S.; Petrucci S.; Pezzoli G.; Pimentel M.; Pirker W.; Pramstaller P.P.; Pulkes T.; Puschmann A.; Quattrone A.; Raggio V.; Ransmayr G.; Rieder C.; Riess O.; Rodriguez-Porcel F.; Rogaeva E.; Ross O.A.; Ruiz-Martinez J.; Sammler E.; San Luciano M.; Satake W.; Saunders-Pullman R.; Sazci A.; Scherzer C.; Schrag A.; Schumacher-Schuh A.; Sharma M.; Sidransky E.; Singleton A.B.; Petersen M.S.; Smolders S.; Spitz M.; Stefanis L.; Struhal W.; Sue C.M.; Swan M.; Swanberg M.; Taba P.; Taipa R.; Tan M.; Tan A.H.; Tan E.-K.; Tang B.; Tayebi N.; Thaler A.; Thomas A.; Toda T.; Toft M.; Torres L.; Tumas V.; Valente E.M.; Van Broeckhoven C.; Vecsei L.; Velez-Pardo C.; Vidailhet M.; Vollstedt E.-J.; Warner T.T.; Williams-Gray C.H.; Winkelmann J.; Woitalla D.; Wood N.W.; Wszolek Z.K.; RUEY-MEEI WU ; Wu Y.-R.; Xie T.; Yoshino H.; Zhang B.; Zimprich A.; MJFF Global Genetic Parkinson's Disease Study Group | Annals of Neurology | 22 | 24 | |
4 | 2019 | A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing | CHIN-HSIEN LIN ; PEI-LUNG CHEN ; CHUN-HWEI TAI ; Lin H.-I.; Chen C.-S.; Chen M.-L.; RUEY-MEEI WU | Movement Disorders | 65 | 58 | |
5 | 2018 | PINK1 Phosphorylates MIC60/Mitofilin to Control Structural Plasticity of Mitochondrial Crista Junctions | Tsai P.-I.; CHIN-HSIEN LIN ; Hsieh C.-H.; Papakyrikos A.M.; Kim M.J.; Napolioni V.; Schoor C.; Couthouis J.; RUEY-MEEI WU ; Wszolek Z.K.; Winter D.; Greicius M.D.; Ross O.A.; Wang X. | Molecular Cell | 84 | 73 | |
6 | 2018 | PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population | Fan T.-S.; RUEY-MEEI WU ; Lin H.-I.; Cheng C.; CHIN-HSIEN LIN | Neurobiology of Aging | 1 | 1 | |
7 | 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 | |
8 | 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 | |
9 | 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 | |
10 | 2016 | National Trends of Antiparkinsonism Treatment in Taiwan: 2004-2011 | Liu W.-M.; RUEY-MEEI WU ; CHIA-HSUIN CHANG ; JOU-WEI LIN ; Liu Y.-C.; CHIN-HSIEN LIN | Parkinson's Disease | 11 | 10 | |
11 | 2016 | Pathophysiology of small-fiber sensory system in Parkinson's disease: Skin innervation and contact heat evoked potential | CHIN-HSIEN LIN ; CHI-CHAO CHAO ; Wu S.-W.; PAUL-CHEN HSIEH ; Feng F.-P.; Lin Y.-H.; Chen Y.-M.; RUEY-MEEI WU ; SUNG-TSANG HSIEH | Medicine (United States) | 23 | 16 | |
12 | 2016 | Time trends in the prevalence and incidence of Parkinson's disease in Taiwan: A nationwide, population-based study | Liu W.-M.; RUEY-MEEI WU ; JOU-WEI LIN ; Liu Y.-C.; CHIA-HSUIN CHANG ; CHIN-HSIEN LIN | Journal of the Formosan Medical Association | 52 | 48 | |
13 | 2016 | DCTN1 p.K56R in progressive supranuclear palsy | Gustavsson E.K.; Trinh J.; Guella I.; Szu-Tu C.; Khinda J.; CHIN-HSIEN LIN ; RUEY-MEEI WU ; Stoessl J.; Appel-Cresswell S.; McKeown M.; Rajput A.; Rajput A.H.; Petersen M.S.; Jeon B.S.; Aasly J.O.; Farrer M.J. | Parkinsonism and Related Disorders | 27 | 26 | |
14 | 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 | |
15 | 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 | |
16 | 2015 | COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese | CHIN-HSIEN LIN ; Tan E.-K.; Yang C.-C.; Yi Z.; RUEY-MEEI WU | Movement Disorders | 33 | 31 | |
17 | 2015 | The impact of nonmotor symptoms on quality of life in patients with parkinson's disease in Taiwan | Liu W.-M.; Lin R.-J.; Yu R.-L.; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; RUEY-MEEI WU | Neuropsychiatric Disease and Treatment | 31 | 26 | |
18 | 2015 | Biomarkers of cognitive decline in Parkinson's disease | CHIN-HSIEN LIN ; RUEY-MEEI WU | Parkinsonism and Related Disorders | 77 | 72 | |
19 | 2015 | COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population | CHIN-HSIEN LIN ; Lin H.-I.; Chen M.-L.; RUEY-MEEI WU | Neurobiology of Aging | 4 | 3 | |
20 | 2015 | Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population | KAI-HSIANG CHEN ; RUEY-MEEI WU ; Lin H.-I.; CHUN-HWEI TAI ; CHIN-HSIEN LIN | Neurobiology of Aging | 14 | 12 | |
21 | 2014 | HIV-associated parkinsonism reversed with antiretroviral therapy | Cheng Y.-W; CHIN-HSIEN LIN ; RUEY-MEEI WU | Neurology Asia | 2 | ||
22 | 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 | |
23 | 2014 | Association of candidate genetic variants with restless legs syndrome in end stage renal disease: A multicenter case-control study in Taiwan | CHIN-HSIEN LIN ; Chen M.-L.; VIN-CENT WU ; WEN-YI LI ; Sy H.-N.; Wu S.-L.; Chang C.-C.; Chiu P.-F.; HORNG-HUEI LIOU ; Lin C.-Y.; Chang H.-W.; Lin S.-Y.; KWAN-DUN WU ; YUNG-MING CHEN ; RUEY-MEEI WU | European Journal of Neurology | 21 | 19 | |
24 | 2014 | The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants | Heckman M.G.; Elbaz A.; Soto-Ortolaza A.I.; Serie D.J.; Aasly J.O.; Annesi G.; Auburger G.; Bacon J.A.; Boczarska-Jedynak M.; Bozi M.; Brighina L.; Chartier-Harlin M.-C.; Dardiotis E.; Dest?e A.; Ferrarese C.; Ferraris A.; Fiske B.; Gispert S.; Hadjigeorgiou G.M.; Hattori N.; Ioannidis J.P.A.; Jasinska-Myga B.; Jeon B.S.; Kim Y.J.; Klein C.; Kruger R.; Kyratzi E.; CHIN-HSIEN LIN ; Lohmann K.; Loriot M.-A.; Lynch T.; Mellick G.D.; Mutez E.; Opala G.; Park S.S.; Petrucci S.; Quattrone A.; Sharma M.; Silburn P.A.; Sohn Y.H.; Stefanis L.; Tadic V.; Tomiyama H.; Uitti R.J.; Valente E.M.; Vassilatis D.K.; Vilari?o-G?ell C.; White L.R.; Wirdefeldt K.; Wszolek Z.K.; RUEY-MEEI WU ; Xiromerisiou G.; Maraganore D.M.; Farrer M.J.; Ross O.A. | Neurobiology of Aging | 30 | 13 | |
25 | 2014 | Antihypertensive agents and risk of Parkinson's disease: A nationwide cohort study | Lee Y.-C.; CHIN-HSIEN LIN ; RUEY-MEEI WU ; JOU-WEI LIN ; CHIA-HSUIN CHANG ; Lai M.-S. | PLoS ONE | 80 | 46 | |
26 | 2014 | Mutational analysis of Angiogenin gene in Parkinson's disease | Chen M.-L.; RUEY-MEEI WU ; CHUN-HWEI TAI ; CHIN-HSIEN LIN | PLoS ONE | 5 | 5 | |
27 | 2014 | Risk of Parkinson's disease following severe constipation: A nationwide population-based cohort study | CHIN-HSIEN LIN ; JOU-WEI LIN ; Liu Y.-C.; CHIA-HSUIN CHANG ; RUEY-MEEI WU | Parkinsonism and Related Disorders | 90 | 80 | |
28 | 2014 | The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease. | RUEY-MEEI WU ; CHIN-HSIEN LIN ; Lin H.I. | Neurology | 13 | 12 | |
29 | 2014 | BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese population | Chen M.-L.; CHIN-HSIEN LIN ; MING-JEN LEE ; RUEY-MEEI WU | Parkinsonism and Related Disorders | 27 | 20 | |
30 | 2014 | Vitamin D receptor genetic variants and Parkinson's disease in a Taiwanese population | CHIN-HSIEN LIN ; KAI-HSIANG CHEN ; Chen M.-L.; Lin H.-I.; RUEY-MEEI WU | Neurobiology of Aging | 30 | 25 | |
31 | 2013 | Mutational analysis of FBXO7 gene in Parkinson's disease in a Taiwanese population | CHIN-HSIEN LIN ; Chen M.-L.; Lai T.-T.; CHUN-HWEI TAI ; RUEY-MEEI WU | Neurobiology of Aging | 18 | 14 | |
32 | 2013 | Mystery Case: Hemiballism in a patient with parietal lobe infarction | MENG-CHEN WU ; RUOH-FANG YEN ; CHIN-HSIEN LIN ; RUEY-MEEI WU ; Nita D.A. | Neurology | 3 | 2 | |
33 | 2013 | Discontinuation of statin therapy associates with Parkinson disease: A population-based study | Yen-Chieh Lee; CHIN-HSIEN LIN ; RUEY-MEEI WU ; Min-Shung Lin; JOU-WEI LIN ; CHIA-HSUIN CHANG ; Mei-Shu Lai | Neurology | 110 | 101 | |
34 | 2013 | Predictors of road crossing safety in pedestrians with Parkinson's disease | CHIN-HSIEN LIN ; Ou Y.-K.; RUEY-MEEI WU ; Liu Y.-C. | Accident Analysis and Prevention | 11 | 11 | |
35 | 2013 | Restless legs syndrome in end-stage renal disease: A multicenter study in Taiwan | CHIN-HSIEN LIN ; VIN-CENT WU ; WEN-YI LI ; Sy H.-N.; Wu S.-L.; Chang C.-C.; Chiu P.-F.; Lion H.-H.; Lin C.-Y.; Chang H.-W.; Lin S.-Y.; YUNG-MING CHEN ; KWAN-DUN WU ; RUEY-MEEI WU | European Journal of Neurology | 53 | 47 | |
36 | 2013 | Preceding pain symptoms and Parkinson's disease: A nationwide population-based cohort study | CHIN-HSIEN LIN ; RUEY-MEEI WU ; Chang H.-Y.; Chiang Y.-T.; HSIEN-HO LIN | European Journal of Neurology | 54 | 46 | |
37 | 2013 | Reaffirmation of GAK, but not HLA-DRA, as a Parkinson's disease susceptibility gene in a Taiwanese population | CHIN-HSIEN LIN ; Chen M.-L.; Tai Y.-C.; Yu C.-Y.; RUEY-MEEI WU | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 15 | 12 | |
38 | 2013 | RIT2 variant is not associated with Parkinson's disease in a Taiwanese population | CHIN-HSIEN LIN ; Chen M.-L.; Yu C.-Y.; RUEY-MEEI WU | Neurobiology of Aging | 10 | 1 | |
39 | 2013 | Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium | Heckman M.G.; Soto-Ortolaza A.I.; Aasly J.O.; Abahuni N.; Annesi G.; Bacon J.A.; Bardien S.; Bozi M.; Brice A.; Brighina L.; Carr J.; Chartier-Harlin M.-C.; Dardiotis E.; Dickson D.W.; Diehl N.N.; Elbaz A.; Ferrarese C.; Fiske B.; Gibson J.M.; Gibson R.; Hadjigeorgiou G.M.; Hattori N.; Ioannidis J.P.A.; Boczarska-Jedynak M.; Jasinska-Myga B.; Jeon B.S.; Kim Y.J.; Klein C.; Kruger R.; Kyratzi E.; Lesage S.; CHIN-HSIEN LIN ; Lynch T.; Maraganore D.M.; Mellick G.D.; Mutez E.; Nilsson C.; Opala G.; Park S.S.; Petrucci S.; Puschmann A.; Quattrone A.; Sharma M.; Silburn P.A.; Sohn Y.H.; Stefanis L.; Tadic V.; Theuns J.; Tomiyama H.; Uitti R.J.; Valente E.M.; Van Broeckhoven C.; Van De Loo S.; Vassilatis D.K.; Vilariño-Güell C.; White L.R.; Wirdefeldt K.; Wszolek Z.K.; RUEY-MEEI WU ; Hentati F.; Farrer M.J.; Ross O.A. | Movement Disorders | 27 | 26 | |
40 | 2012 | Unusual association of diseases/symptoms: Psychotic-affective symptoms and multiple system atrophy expand phenotypes of spinocerebellar ataxia type 2 | KAI-HSIANG CHEN ; CHIN-HSIEN LIN ; RUEY-MEEI WU | BMJ Case Reports | 7 | 0 | |
41 | 2012 | Early-onset autosomal-recessive parkinsonian-pyramidal syndrome | Lai H.-J; CHIN-HSIEN LIN ; RUEY-MEEI WU | Acta Neurologica Taiwanica | 9 | 0 | |
42 | 2012 | Neuropsychological profile in patients with early stage of Parkinson's disease in Taiwan | Yu R.-L.; RUEY-MEEI WU ; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; Cheng T.-W.; Hua M.-S. | Parkinsonism and Related Disorders | 41 | 35 | |
43 | 2012 | Advanced Theory of Mind in patients at early stage of Parkinson's disease | Yu R.-L.; RUEY-MEEI WU ; MING-JANG CHIU ; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; Hua M.-S. | Parkinsonism and Related Disorders | 43 | 40 | |
44 | 2011 | Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria | CHIN-HSIEN LIN ; Chen M.-L.; Chen G.S.; CHUN-HWEI TAI ; RUEY-MEEI WU | Human Genetics | 48 | 26 | |
45 | 2011 | Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: A case-control study | Ross O.A.; Soto-Ortolaza A.I.; Heckman M.G.; Aasly J.O.; Abahuni N.; Annesi G.; Bacon J.A.; Bardien S.; Bozi M.; Brice A.; Brighina L.; Van Broeckhoven C.; Carr J.; Chartier-Harlin M.-C.; Dardiotis E.; Dickson D.W.; Diehl N.N.; Elbaz A.; Ferrarese C.; Ferraris A.; Fiske B.; Gibson J.M.; Gibson R.; Hadjigeorgiou G.M.; Hattori N.; Ioannidis J.P.A.; Jasinska-Myga B.; Jeon B.S.; Kim Y.J.; Klein C.; Kruger R.; Kyratzi E.; Lesage S.; CHIN-HSIEN LIN ; Lynch T.; Maraganore D.M.; Mellick G.D.; Mutez E.; Nilsson C.; Opala G.; Park S.S.; Puschmann A.; Quattrone A.; Sharma M.; Silburn P.A.; Sohn Y.H.; Stefanis L.; Tadic V.; Theuns J.; Tomiyama H.; Uitti R.J.; Valente E.M.; van de Loo S.; Vassilatis D.K.; Vilari?o-G?ell C.; White L.R.; Wirdefeldt K.; Wszolek Z.K.; RUEY-MEEI WU ; Farrer M.J. | The Lancet Neurology | 258 | 241 | |
46 | 2011 | Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease | CHIN-HSIEN LIN ; RUEY-MEEI WU ; CHUN-HWEI TAI ; Chen M.-L.; Hu F.-C. | Parkinsonism and Related Disorders | 31 | 28 | |
47 | 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 | |
48 | 2011 | Minimal detectable change of the timed "up & go" test and the dynamic gait index in people with parkinson disease | SHEAU-LING HUANG ; CHING-LIN HSIEH ; RUEY-MEEI WU ; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; Lu W.-S. | Physical Therapy | 258 | 233 | |
49 | 2010 | Deep brain stimulation therapy for Parkinson's disease using frameless stereotaxy: Comparison with frame-based surgery | CHUN-HWEI TAI ; RUEY-MEEI WU ; CHIN-HSIEN LIN ; MING-KAI PAN ; YA-FANG CHEN ; HON-MAN LIU ; Lu H.-H.; Tsai C.-W.; SHENG-HONG TSENG | European Journal of Neurology | 29 | 23 | |
50 | 2010 | A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndrome | Chan H.-F.; Chen M.-L.; JEN-JEN SU ; Ko L.-C.; CHIN-HSIEN LIN ; RUEY-MEEI WU | Journal of Human Genetics | 26 | 24 | |
51 | 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 | |
52 | 2010 | Multiple LRRK2 variants modulate risk of Parkinson disease: A Chinese multicenter study | Tan E.-K.; Peng R.; Teo Y.-Y.; Tan L.C.; Angeles D.; Ho P.; Chen M.-L.; CHIN-HSIEN LIN ; Mao X.-Y.; Chang X.-L.; Prakash K.M.; Liu J.-J.; Au W.-L.; Le W.-D.; Jankovic J.; Burgunder J.-M.; Zhao Y.; RUEY-MEEI WU | Human Mutation | 106 | 103 | |
53 | 2010 | Feeling-of-knowing in episodic memory in patients with Parkinson's disease with various motor symptoms | Yu R.-L.; RUEY-MEEI WU ; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; Hua M.-S. | Movement Disorders | 18 | 17 | |
54 | 2009 | Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism | Ross O.A.; Spanaki C.; Griffith A.; CHIN-HSIEN LIN ; Kachergus J.; Haugarvoll K.; Latsoudis H.; Plaitakis A.; Ferreira J.J.; Sampaio C.; Bonifati V.; RUEY-MEEI WU ; Zabetian C.P.; Farrer M.J. | Parkinsonism and Related Disorders | 32 | 27 | |
55 | 2009 | Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism | MING-JEN LEE ; Mata I.F.; CHIN-HSIEN LIN ; KAI-YUAN TZEN ; Lincoln S.J.; Bounds R.; Lockhart P.J.; Hulihan M.M.; Farrer M.J.; RUEY-MEEI WU | Movement Disorders | 29 | 23 | |
56 | 2009 | Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation | CHUN-HWEI TAI ; RUOH-FANG YEN ; CHIN-HSIEN LIN ; Yen K.-Y.; Yip P.-K.; RUEY-MEEI WU ; MING-JEN LEE | Parkinsonism and Related Disorders | 3 | 2 | |
57 | 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 | |
58 | 2008 | Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore | CHIN-HSIEN LIN ; Tan E.K.; Chen M.L.; Tan L.C.; Lim H.Q.; Chen G.S.; RUEY-MEEI WU | Neurology | 83 | 78 | |
59 | 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 | |
60 | 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 | |
61 | 2007 | Acute disseminated encephalomyelitis: A follow-up study in Taiwan | CHIN-HSIEN LIN ; JIANN-SHING JENG ; SUNG-TSANG HSIEH ; Yip P.-K.; RUEY-MEEI WU | Journal of Neurology, Neurosurgery and Psychiatry | 58 | 45 | |
62 | 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 | |
63 | 2005 | Parkin mutations and early-onset parkinsonism in a Taiwanese cohort | RUEY-MEEI WU ; Bounds R.; Lincoln S.; Hulihan M.; CHIN-HSIEN LIN ; WUH-LIANG HWU ; Chen J.; Gwinn-Hardy K.; Farrer M. | Archives of Neurology | 66 | 58 | |
64 | 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 |