| 臺大學術典藏 |
2020-02-25T08:01:45Z |
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;Lin C.-H;Ruey-Meei Wu;Farrer M.J.; Lockhart P.J; Bounds R; Hulihan M; Kachergus J; Lincoln S; Lin C.-H; RUEY-MEEI WU; Farrer M.J. |
| 臺大學術典藏 |
2020-02-25T08:01:44Z |
Lrrk2 pathogenic substitutions in Parkinson's disease
|
Cobb S.A; RUEY-MEEI WU; Lu C.-S; Lahoz C; Wszolek Z.K; Farrer M.J.; Hulihan M.M; 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.; Mata I.F; Kachergus J.M; Taylor J.P; Lincoln S; Aasly J; Lynch T |
| 臺大學術典藏 |
2020-02-25T08:01:44Z |
Lrrk2 pathogenic substitutions in Parkinson's disease
|
Cobb S.A; RUEY-MEEI WU; Lu C.-S; Lahoz C; Wszolek Z.K; Farrer M.J.; Hulihan M.M; 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.; Mata I.F; Kachergus J.M; Taylor J.P; Lincoln S; Aasly J; Lynch T |
| 臺大學術典藏 |
2020-02-25T08:01:43Z |
Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia
|
Farrer M.J; Stone J.T; Lin C.-H; D?chsel J.C; Hulihan M.M; Haugarvoll K; Ross O.A; RUEY-MEEI WU |
| 臺大學術典藏 |
2020-02-25T08:01:42Z |
LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: Clinical, PET, and functional studies
|
Lin C.-H; Tzen K.-Y; Yu C.-Y; Tai C.-H; Farrer M.J; RUEY-MEEI WU |
| 臺大學術典藏 |
2020-02-25T08:01:42Z |
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
|
Ross O.A;Wu Y.-R;Lee M.-C;Funayama M;Chen M.-L;Soto A.I;Mata I.F;Lee-Chen G.-J;Chiung M.C;Tang M;Zhao Y;Hattori N;Farrer M.J;Tan E.-K;Ruey-Meei Wu; Ross O.A; Wu Y.-R; Lee M.-C; Funayama M; Chen M.-L; Soto A.I; Mata I.F; Lee-Chen G.-J; Chiung M.C; Tang M; Zhao Y; Hattori N; Farrer M.J; Tan E.-K; RUEY-MEEI WU |
| 臺大學術典藏 |
2020-02-25T08:01:42Z |
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
|
Ross O.A;Wu Y.-R;Lee M.-C;Funayama M;Chen M.-L;Soto A.I;Mata I.F;Lee-Chen G.-J;Chiung M.C;Tang M;Zhao Y;Hattori N;Farrer M.J;Tan E.-K;Ruey-Meei Wu; Ross O.A; Wu Y.-R; Lee M.-C; Funayama M; Chen M.-L; Soto A.I; Mata I.F; Lee-Chen G.-J; Chiung M.C; Tang M; Zhao Y; Hattori N; Farrer M.J; Tan E.-K; RUEY-MEEI WU |
| 臺大學術典藏 |
2020-02-25T08:01:40Z |
Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism
|
Lee M.-J; Mata I.F; Lin C.-H; Tzen K.-Y; Lincoln S.J; Bounds R; Lockhart P.J; Hulihan M.M; Farrer M.J; RUEY-MEEI WU |
| 臺大學術典藏 |
2020-02-25T08:01:39Z |
Analysis of PArkin Co-Regulated Gene in a Taiwanese-Ethnic Chinese cohort with early-onset Parkinson's disease
|
Taylor J.M; RUEY-MEEI WU; Farrer M.J; Delatycki M.B; Lockhart P.J. |
| 臺大學術典藏 |
2020-02-25T08:01:35Z |
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. |
| 臺大學術典藏 |
2020-02-25T08:01:34Z |
Association of pyridoxal kinase and parkinson disease
|
Vilari?O-G?Ell C;Wider C;Aasly J.O;White L.R;Rajput A;Rajput A.H;Lynch T;Krygowska-Wajs A;Jasinska-Myga B;Opala G;Barcikowska M;Czyzewski K;Ruey-Meei Wu;Uitti R.J;Wszolek Z.K;Farrer M.J;Ross O.A.; Vilari?o-G?ell C; Wider C; Aasly J.O; White L.R; Rajput A; Rajput A.H; Lynch T; Krygowska-Wajs A; Jasinska-Myga B; Opala G; Barcikowska M; Czyzewski K; RUEY-MEEI WU; Uitti R.J; Wszolek Z.K; Farrer M.J; Ross O.A. |
| 臺大學術典藏 |
2020-02-25T08:01:34Z |
Association of pyridoxal kinase and parkinson disease
|
Vilari?O-G?Ell C;Wider C;Aasly J.O;White L.R;Rajput A;Rajput A.H;Lynch T;Krygowska-Wajs A;Jasinska-Myga B;Opala G;Barcikowska M;Czyzewski K;Ruey-Meei Wu;Uitti R.J;Wszolek Z.K;Farrer M.J;Ross O.A.; Vilari?o-G?ell C; Wider C; Aasly J.O; White L.R; Rajput A; Rajput A.H; Lynch T; Krygowska-Wajs A; Jasinska-Myga B; Opala G; Barcikowska M; Czyzewski K; RUEY-MEEI WU; Uitti R.J; Wszolek Z.K; Farrer M.J; Ross O.A. |
| 臺大學術典藏 |
2020-02-25T08:01:33Z |
An independent replication of park16 in asian samples
|
Vilari?O-G?Ell C;Ross O.A;Aasly J.O;White L.R;Rajput A;Rajput A.H;Lynch T;Krygowska-Wajs A;Jasinska-Myga B;Opala G;Barcikowska M;Lee M.-C;Hentati F;Uitti R.J;Wszolek Z.K;Farrer M.J;Ruey-Meei Wu; Vilari?o-G?ell C; Ross O.A; Aasly J.O; White L.R; Rajput A; Rajput A.H; Lynch T; Krygowska-Wajs A; Jasinska-Myga B; Opala G; Barcikowska M; Lee M.-C; Hentati F; Uitti R.J; Wszolek Z.K; Farrer M.J; RUEY-MEEI WU |
| 臺大學術典藏 |
2020-02-25T08:01:33Z |
An independent replication of park16 in asian samples
|
Vilari?O-G?Ell C;Ross O.A;Aasly J.O;White L.R;Rajput A;Rajput A.H;Lynch T;Krygowska-Wajs A;Jasinska-Myga B;Opala G;Barcikowska M;Lee M.-C;Hentati F;Uitti R.J;Wszolek Z.K;Farrer M.J;Ruey-Meei Wu; Vilari?o-G?ell C; Ross O.A; Aasly J.O; White L.R; Rajput A; Rajput A.H; Lynch T; Krygowska-Wajs A; Jasinska-Myga B; Opala G; Barcikowska M; Lee M.-C; Hentati F; Uitti R.J; Wszolek Z.K; Farrer M.J; RUEY-MEEI WU |
| 臺大學術典藏 |
2020-02-25T08:01:32Z |
Death-associated protein kinase 1 variation and Parkinson's disease
|
Wider C; Vilari?o-G?ell C; Aasly J.O; Rajput A; Rajput A.H; Lynch T; Craig D; Krygowska-Wajs A; Jasinska-Myga B; Opala G; Barcikowska M; Czyzewski K; RUEY-MEEI WU; Heckman M.G; Uitti R.J; Wszolek Z.K; Farrer M.J; Ross O.A.; Dachsel J.C |
| 臺大學術典藏 |
2020-02-25T08:01:32Z |
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; Lin C.-H; 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. |
| 臺大學術典藏 |
2020-02-25T08:01:31Z |
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.; 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. |
| 臺大學術典藏 |
2020-02-25T08:01:31Z |
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.; 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. |
| 臺大學術典藏 |
2020-02-25T08:01:30Z |
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. |
| 臺大學術典藏 |
2020-02-25T08:01:27Z |
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. |
| 臺大學術典藏 |
2020-02-25T08:01:26Z |
Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium
|
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; Vilari?o-G?ell C; White L.R; Wirdefeldt K; Wszolek Z.K; RUEY-MEEI WU; Hentati F; Farrer M.J; Ross O.A.; Nilsson C; Mutez E; Mellick G.D; 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; Lin C.-H; Lynch T; Maraganore D.M |
| 臺大學術典藏 |
2020-02-25T08:01:25Z |
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; Lin C.-H; 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. |
| 臺大學術典藏 |
2020-02-25T08:01:24Z |
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. |
| 臺大學術典藏 |
2020-02-25T08:01:20Z |
DCTN1 p.K56R in progressive supranuclear palsy
|
Gustavsson E.K;Trinh J;Guella I;Szu-Tu C;Khinda J;Lin C.-H;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.; Gustavsson E.K; Trinh J; Guella I; Szu-Tu C; Khinda J; Lin C.-H; 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. |
| 臺大學術典藏 |
2020-02-25T08:01:20Z |
DCTN1 p.K56R in progressive supranuclear palsy
|
Gustavsson E.K;Trinh J;Guella I;Szu-Tu C;Khinda J;Lin C.-H;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.; Gustavsson E.K; Trinh J; Guella I; Szu-Tu C; Khinda J; Lin C.-H; 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. |
