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UCHL1 is a Parkinson's disease susceptibility gene
UCHL1 is a Parkinson's disease susceptibility gene
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UCHL1 is a Parkinson's disease susceptibility gene

Maraganore, Demetrius M. ; Lesnick, Timothy G. ; Elbaz, Alexis ; Chartier-Harlin, Marie-Christine ; Gasser, Thomas ; Krüger, Rejko ; Hattori, Nobutaka ; Mellick, George D. ; Quattrone, Aldo ; Satoh, Jun-Ichi ; Toda, Taksushi ; Wang, Jian ; Ioannidis, John P.A. ; de Andrade, Mariza ; Rocca, Walter A.

Annals of neurology, 2004-04, Vol.55 (4), p.512-521 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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2
Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families
Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families
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Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families

Winkelmann, Juliane ; Muller-Myhsok, Bertram ; Wittchen, Hans-Ulrich ; Hock, Bettina ; Prager, Muriel ; Pfister, Hildegard ; Strohle, Andreas ; Eisensehr, Ilonka ; Dichgans, Martin ; Gasser, Thomas ; Trenkwalder, Claudia

Annals of neurology, 2002-09, Vol.52 (3), p.297-302 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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3
Polygenic risk of Parkinson disease is correlated with disease age at onset
Polygenic risk of Parkinson disease is correlated with disease age at onset
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Polygenic risk of Parkinson disease is correlated with disease age at onset

Escott-Price, Valentina ; Nalls, Mike A. ; Morris, Huw R. ; Lubbe, Steven ; Brice, Alexis ; Gasser, Thomas ; Heutink, Peter ; Wood, Nicholas W. ; Hardy, John ; Singleton, Andrew B. ; Williams, Nigel M.

Annals of neurology, 2015-04, Vol.77 (4), p.582-591 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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4
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
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Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis

van Es, Michael A. ; Schelhaas, Helenius J. ; van Vught, Paul W. J. ; Ticozzi, Nicola ; Andersen, Peter M. ; Groen, Ewout J. N. ; Schulte, Claudia ; Blauw, Hylke M. ; Koppers, Max ; Diekstra, Frank P. ; Fumoto, Katsumi ; LeClerc, Ashley Lyn ; Keagle, Pamela ; Bloem, Bastiaan R. ; Scheffer, Hans ; van Nuenen, Bart F. L. ; van Blitterswijk, Marka ; van Rheenen, Wouter ; Wills, Anne-Marie ; Lowe, Patrick P. ; Hu, Guo-fu ; Yu, Wenhao ; Kishikawa, Hiroko ; Wu, David ; Folkerth, Rebecca D. ; Mariani, Claudio ; Goldwurm, Stefano ; Pezzoli, Gianni ; Van Damme, Philip ; Lemmens, Robin ; Dahlberg, Caroline ; Birve, Anna ; Fernández-Santiago, Rubén ; Waibel, Stefan ; Klein, Christine ; Weber, Markus ; van der Kooi, Anneke J. ; de Visser, Marianne ; Verbaan, Dagmar ; van Hilten, Jacobus J. ; Heutink, Peter ; Hennekam, Eric A. M. ; Cuppen, Edwin ; Berg, Daniela ; Brown Jr, Robert H. ; Silani, Vincenzo ; Gasser, Thomas ; Ludolph, Albert C. ; Robberecht, Wim ; Ophoff, Roel A. ; Veldink, Jan H. ; Pasterkamp, R. Jeroen ; de Bakker, Paul I. W. ; Landers, John E. ; van de Warrenburg, Bart P. ; van den Berg, Leonard H.

Annals of neurology, 2011-12, Vol.70 (6), p.964-973 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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5
SNCA variants are associated with increased risk for multiple system atrophy
SNCA variants are associated with increased risk for multiple system atrophy
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SNCA variants are associated with increased risk for multiple system atrophy

Scholz, Sonja W. ; Houlden, Henry ; Schulte, Claudia ; Sharma, Manu ; Li, Abi ; Berg, Daniela ; Melchers, Anna ; Paudel, Reema ; Gibbs, J. Raphael ; Simon-Sanchez, Javier ; Paisan-Ruiz, Coro ; Bras, Jose ; Ding, Jinhui ; Chen, Honglei ; Traynor, Bryan J. ; Arepalli, Sampath ; Zonozi, Ryan R. ; Revesz, Tamas ; Holton, Janice ; Wood, Nick ; Lees, Andrew ; Oertel, Wolfgang ; Wüllner, Ullrich ; Goldwurm, Stefano ; Pellecchia, Maria Teresa ; Illig, Thomas ; Riess, Olaf ; Fernandez, Hubert H. ; Rodriguez, Ramon L. ; Okun, Michael S. ; Poewe, Werner ; Wenning, Gregor K. ; Hardy, John A. ; Singleton, Andrew B. ; Gasser, Thomas

Annals of neurology, 2009-05, Vol.65 (5), p.610-614 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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6
Multiple regions of α-synuclein are associated with Parkinson's disease
Multiple regions of α-synuclein are associated with Parkinson's disease
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Multiple regions of α-synuclein are associated with Parkinson's disease

Mueller, Jakob C. ; Fuchs, Julia ; Hofer, Anne ; Zimprich, Alexander ; Lichtner, Peter ; Illig, Thomas ; Berg, Daniela ; Wüllner, Ullrich ; Meitinger, Thomas ; Gasser, Thomas

Annals of neurology, 2005-04, Vol.57 (4), p.535-541 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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7
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors
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Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors

Liu, Hui ; Dehestani, Mohammad ; Blauwendraat, Cornelis ; Makarious, Mary B. ; Leonard, Hampton ; Kim, Jonggeol J. ; Schulte, Claudia ; Noyce, Alastair ; Jacobs, Benjamin M. ; Foote, Isabelle ; Sharma, Manu ; Koks, Sulev ; Mellick, George D ; Pirker, Walter ; Zimprich, Alexander ; Lang, Anthony E ; Rogaeva, Ekaterina ; Taba, Pille ; Brice, Alexis ; Chartier‐Harlin, Marie‐Christine ; Corvol, Jean‐Christophe ; Domenighetti, Cloé ; Elbaz, Alexis ; Lesage, Suzanne ; Mutez, Eugenie ; Sugier, Pierre‐Emmanuel ; Sreelatha, Ashwin Ashok Kumar ; Grover, Sandeep ; Brockmann, Kathrin ; Deutschländer, Angela B ; Gasser, Thomas ; Krüger, Jens ; Lichtner, Peter ; Radivojkov‐Blagojevic, Milena ; Schulte, Claudia ; Sharma, Manu ; Dardiotis, Efthimos ; Hadjigeorgiou, Georges M ; Simitsi, Athina Maria ; Stefanis, Leonidas ; Annesi, Grazia ; Brighina, Laura ; Ferrarese, Carlo ; Petrucci, Simona ; Pezzoli, Gianni ; Quattrone, Andrea ; Straniero, Letizia ; Gagliardi, Monica ; Valente, Enza Maria ; Zecchinelli, Anna ; Hattori, Nobutaka ; Nakayama, Akiyoshi ; Matsuo, Hirotaka ; Nishioka, Kenya ; Bobbili, Dheeraj ; Kruger, Rejko ; Landoulsi, Zied ; May, Patrick ; Pavelka, Lukas ; Bloem, Bastiaan R ; Warrenburg, Bart PC ; Aasly, Jan ; Pihlstrøm, Lasse ; Toft, Mathias ; Ferreira, Joaquim J ; Guedes, Leonor Correia ; Bardien, Soraya ; Carr, Jonathan ; Chung, Sun Ju ; Kim, Yun Joong ; Diez‐Fairen, Monica ; Ezquerra, Mario ; Pastor, Pau ; Tolosa, Eduardo ; Belin, Andrea C ; Pedersen, Nancy L ; Puschmann, Andreas ; Ran, Caroline ; Rödström, Emil Y ; Wirdefeldt, Karin ; Clarke, Carl E ; Morrison, Karen E ; Tan, Manuela ; Edsall, Connor ; Farrer, Matt J ; Krainc, Dimitri ; Singleton, Andrew B ; Burbulla, Lena F ; Hernandez, Dena G ; Nalls, Mike ; Singleton, Andrew ; Gasser, Thomas ; Bandres‐Ciga, Sara

Annals of neurology, 2022-08, Vol.92 (2), p.270-278 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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8
Genomic investigation of α-synuclein multiplication and parkinsonism
Genomic investigation of α-synuclein multiplication and parkinsonism
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Genomic investigation of α-synuclein multiplication and parkinsonism

Ross, Owen A. ; Braithwaite, Adam T. ; Skipper, Lisa M. ; Kachergus, Jennifer ; Hulihan, Mary M. ; Middleton, Frank A. ; Nishioka, Kenya ; Fuchs, Julia ; Gasser, Thomas ; Maraganore, Demetrius M. ; Adler, Charles H. ; Larvor, Lydie ; Chartier-Harlin, Marie-Christine ; Nilsson, Christer ; Langston, J. William ; Gwinn, Katrina ; Hattori, Nobutaka ; Farrer, Matthew J.

Annals of neurology, 2008-06, Vol.63 (6), p.743-750 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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9
Independent and joint effects of the MAPT and SNCA genes in Parkinson disease
Independent and joint effects of the MAPT and SNCA genes in Parkinson disease
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Independent and joint effects of the MAPT and SNCA genes in Parkinson disease

Elbaz, Alexis ; Ross, Owen A. ; Ioannidis, John P. A. ; Soto-Ortolaza, Alexandra I. ; Moisan, Frédéric ; Aasly, Jan ; Annesi, Grazia ; Bozi, Maria ; Brighina, Laura ; Chartier-Harlin, Marie-Christine ; Destée, Alain ; Ferrarese, Carlo ; Ferraris, Alessandro ; Gibson, J. Mark ; Gispert, Suzana ; Hadjigeorgiou, Georgios M. ; Jasinska-Myga, Barbara ; Klein, Christine ; Krüger, Rejko ; Lambert, Jean-Charles ; Lohmann, Katja ; van de Loo, Simone ; Loriot, Marie-Anne ; Lynch, Timothy ; Mellick, George D. ; Mutez, Eugénie ; Nilsson, Christer ; Opala, Grzegorz ; Puschmann, Andreas ; Quattrone, Aldo ; Sharma, Manu ; Silburn, Peter A. ; Stefanis, Leonidas ; Uitti, Ryan J. ; Valente, Enza Maria ; Vilariño-Güell, Carles ; Wirdefeldt, Karin ; Wszolek, Zbigniew K. ; Xiromerisiou, Georgia ; Maraganore, Demetrius M. ; Farrer, Matthew J.

Annals of neurology, 2011-05, Vol.69 (5), p.778-792 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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10
Is the MC1R variant p.R160W associated with Parkinson's?
Is the MC1R variant p.R160W associated with Parkinson's?
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Is the MC1R variant p.R160W associated with Parkinson's?

Lubbe, Steven J. ; Escott-Price, Valentina ; Brice, Alexis ; Gasser, Thomas ; Hardy, John ; Heutink, Peter ; Sharma, Manu ; Wood, Nicholas W. ; Nalls, Mike ; Singleton, Andrew B. ; Williams, Nigel M. ; Morris, Huw R.

Annals of neurology, 2016-01, Vol.79 (1), p.159-161 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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