公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
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 | |
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 | 26 | 26 | |
2014 | DNAJC13 mutations in Parkinson disease | Vilari?o-G?ell C; Rajput A; Milnerwood A.J; Shah B; Szu-Tu C; Trinh J; Yu I; Encarnacion M; Munsie L.N; Tapia L; Gustavsson E.K; Chou P; Tatarnikov I; Evans D.M; Pishotta F.T; Volta M; Beccano-Kelly D; Thompson C; Lin M.K; Sherman H.E; Han H.J; Guenther B.L; Wasserman W.W; Bernard V; Ross C.J; Appel-Cresswell S; Stoessl A.J; Robinson C.A; Dickson D.W; Ross O.A; Wszolek Z.K; Aasly J.O; RUEY-MEEI WU ; Hentati F; Gibson R.A; McPherson P.S; Girard M; Rajput M; Rajput A.H; Farrer M.J. | Human molecular genetics | 229 | 210 | |
2011 | Erratum: VPS35 mutations in Parkinson disease (American Journal of Human Genetics (2011) 89 (162-167)) | Vilari?o-G?ell C; Wider C; Ross O.A; Dachsel J.C; Kachergus J.M; Lincoln S.J; Soto-Ortolaza A.I; Cobb S.A; Wilhoite G.J; Bacon J.A; Behrouz B; Melrose H.L; Hentati E; Puschmann A; Evans D.M; Conibear E; Wasserman W.W; Aasly J.O; Burkhard P.R; Djaldetti R; Ghika J; Hentati F; Krygowska-Wajs A; Lynch T; Melamed E; Rajput A; Rajput A.H; Solida A; RUEY-MEEI WU ; Uitti R.J; Wszolek Z.K; Vingerhoets F; Farrer M.J. | American Journal of Human Genetics | 2 | 2 | |
2009 | GCH1 in early-onset Parkinson's disease | Cobb S.A; Wider C; Ross O.A; Mata I.F; Adler C.H; Rajput A; Rajput A.H; RUEY-MEEI WU ; Hauser R; Josephs K.A; Carr J; Gwinn K; Heckman M.G; Aasly J.O; Lynch T; Uitti R.J; Wszolek Z.K; Kapatos G; Farrer M.J. | Movement Disorders | 17 | 15 | |
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 | |
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 | 31 | 27 | |
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 | |
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 | |
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 | |
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 | |
2005 | Lrrk2 pathogenic substitutions in Parkinson's disease | Mata I.F; Kachergus J.M; Taylor J.P; Lincoln S; Aasly J; Lynch T; Hulihan M.M; Cobb S.A; RUEY-MEEI WU ; Lu C.-S; Lahoz C; Wszolek Z.K; Farrer M.J. | Neurogenetics | 206 | 194 | |
2020 | Parkinson disease risk variants in East Asian populations | RUEY-MEEI WU ; Farrer M.J. | Nature Reviews Neurology | 4 | 3 | |
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 | |
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 | |
2021 | Reply: UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population | CHIN-HSIEN LIN ; Farrer M.J.; RUEY-MEEI WU | Brain : a journal of neurology | 0 | 1 | |
2013 | STX6 rs1411478 is not associated with increased risk of Parkinson's disease | Trinh J; Vilari?o-G?ell C; Donald A; Shah B; Yu I; Szu-Tu C; Aasly J.O; RUEY-MEEI WU ; Hentati F; Rajput A.H; Rajput A; Farrer M.J. | Parkinsonism and Related Disorders | 15 | 15 | |
2011 | VPS35 mutations in parkinson disease | Vilari?o-G?ell C; Wider C; Ross O.A; Dachsel J.C; Kachergus J.M; Lincoln S.J; Soto-Ortolaza A.I; Cobb S.A; Wilhoite G.J; Bacon J.A; Bahareh Behrouz, Melrose H.L; Hentati E; Puschmann A; Evans D.M; Conibear E; Wasserman W.W; Aasly J.O; Burkhard P.R; Djaldetti R; Ghika J; Hentati F; Krygowska-Wajs A; Lynch T; Melamed E; Rajput A; Rajput A.H; Solida A; RUEY-MEEI WU ; Uitti R.J; Wszolek Z.K; Vingerhoets F; Farrer M.J. | American Journal of Human Genetics | 665 | 617 |