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J. Raphael Gibbs

Brain : a journal of neurology
8
Role
Title
Level Year L/R
🐜 Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
137 auth. L. Robak, I. Jansen, J. V. van Rooij, A. Uitterlinden, R. Kraaij, J. Jankovic, P. Heutink, J. Shulman, M. Nalls, Vincent Plagnol, Dena G. Hernandez, M. Sharma, U. Sheerin, M. Saad, J. Simón-Sánchez, ... C. Schulte, S. Lesage, S. Sveinbjörnsdóttir, S. Arepalli, Roger A Barker, Yoav Ben-, H. Berendse, Daniela Berg, K. Bhatia, R. D. de Bie, Alessandro Biffi, B. Bloem, Z. Bochdanovits, Michael Bonin, J. Bras, K. Brockmann, J. Brooks, David J. Burn, E. Majounie, G. Charlesworth, C. Lungu, Honglei Chen, P. Chinnery, Sean B. Chong, Carl E. Clarke, M. Cookson, J. Mark Cooper, J. Corvol, Carl Counsell, P. Damier, J. Dartigues, P. Deloukas, Günther Deuschl, David Dexter, K. van Dijk, Allissa Dillman, F. Durif, A. Dürr, S. Edkins, J. Evans, T. Foltynie, Jing Dong, M. Gardner, J. Raphael Gibbs, Alison M. Goate, Emma V. Gray, Rita Guerreiro, C. Harris, J. J. van Hilten, A. Hofman, A. Hollenbeck, J. Holton, Michele T M Hu, Xuemei Huang, I. Wurster, W. Mätzler, G. Hudson, Sarah E. Hunt, J. Huttenlocher, T. Illig, Pálmi V. Jónsson, J. Lambert, C. Langford, A. Lees, P. Lichtner, P. Limousin, G. Lopez, D. Lorenz, A. McNeill, C. Moorby, Matthew Moore, Huw R Morris, K. Morrison, V. Escott-Price, E. Mudanohwo, S. O'sullivan, J. Pearson, J. Perlmutter, H. Petursson, Pierre Pollak, Bart Post, Simon C. Potter, Bernard Ravina, T. Révész, Olaf Riess, F. Rivadeneira, P. Rizzu, M. Ryten, S. Sawcer, A. Schapira, Hans Scheffer, K. Shaw, Ira Shoulson, Joshua M. Shulman, E. Sidransky, Colin Smith, C. Spencer, H. Stefánsson, F. Bettella, J. Stockton, A. Strange, Kevin Talbot, C. Tanner, Avazeh Tashakkori-Ghanbaria, François Tison, D. Trabzuni, B. Traynor, D. Velseboer, M. Vidailhet, R. Walker, Bart P C van de Warrenburg, M. Wickremaratchi, N. Williams, C. Williams-Gray, S. Winder-Rhodes, K. Stefansson, Miguel Ángel Martínez, N. Wood, John A Hardy, A. Brice, Thomas Gasser, Andrew B. Singleton
8 2017
8
🐜
🐜 Parkinson’s disease genetics: identifying novel risk loci, providing causal insights and improving estimates of heritable risk
48 auth. M. Nalls, C. Blauwendraat, C. Vallerga, K. Heilbron, S. Bandres-Ciga, Diana Chang, M. Tan, D. Kia, A. Noyce, Angli Xue, J. Bras, Emily Young, R. von Coelln, J. Simón-Sánchez, C. Schulte, ... M. Sharma, L. Krohn, L. Pihlstrøm, A. Siitonen, H. Iwaki, H. Leonard, F. Faghri, J. Raphael Gibbs, D. Hernandez, Sonja W. Scholz, J. Botía, Miguel Ángel Martínez, J. Corvol, S. Lesage, J. Jankovic, L. Shulman, P. Tienari, K. Majamaa, M. Toft, A. Brice, Jian Yang, Z. Gan-Or, T. Gasser, P. Heutink, J. Shulman, N. Wood, D. Hinds, J. Hardy, H. Morris, J. Gratten, P. Visscher, R. Graham, A. Singleton
6 2018
6
🐜
🐜 A comprehensive assessment of benign genetic variability for neurodegenerative disorders
19 auth. R. Guerreiro, C. Sassi, J. Raphael Gibbs, Connor Edsall, D. Hernandez, K. Brown, Michelle K. Lupton, Laura Parkinnen, O. Ansorge, A. Hodges, ... M. Ryten, P. Tienari, Vivanna M Van Deerlin, J. Trojanowski, K. Morgan, J. Powell, A. Singleton, J. Hardy, J. Bras
4 2018
4
🐜