Publications
Résultats 291 à 300 sur 558 Publications
| Titre | Auteurs | Année | Revue |
|---|---|---|---|
| Gender specific factors contributing to cognitive resilience in APOE ɛ4 positive older adults in a population-based sample | Zheng, L., Eramudugolla, R., Cherbuin, N., Drouin, S. M.**, Dixon, R. A.*, & Anstey, K. J. | 2023 | Scientific Reports |
| Gender and pathology-specific effect of apolipoprotein E genotype on psychosis in Alzheimer’s Disease | Kim, J., Fischer, C. E., Schweizer, T. A., & Munoz, D. G. | 2017 | Current Alzheimer Research |
| GBA variation and susceptibility to multiple system atrophy | Wernick AI, Walton RL, Koga S, Soto-Beasley AI, Heckman MG, Gan-Or Z*, Ren Y, Rademakers R*, Uitti RJ, Wszolek ZK, Cheshire WP, Dickson DW, Ross OA | 2020 | Parkinsonism and Related Disorders |
| GBA variants in REM sleep behavior disorder: a multicenter study | Krohn L, Ruskey JA, Rudakou U, Leveille E, Asayesh F, Hu MTM, Arnulf I, Dauvilliers Y, Högl B, Stefani A, Monaca CC, Beatriz A, Plazzi G, Antelmi E, Ferini-Strambi L, Heidbreder A, Boeve BF, Espay AJ, Cochen De Cock V, Mollenhauer B, Sixel-Döring F, Trenkwalder C, Sonka K, Kemlink D, Figorilli M, Puligheddu M, Dijkstra F, Viaene M, Oertel W, Toffoli M, Gigli GL, Valente M, Gagnon JF*, Desautels A*, Montplaisir JY, Postuma RB*, Rouleau GA* and Gan-Or Z* | 2020 | Neurology |
| Gait Variability Across Neurodegenerative and Cognitive Disorders: Results from the Canadian Consortium of Neurodegeneration in Aging (CCNA) and The Gait & Brain Study | Pieruccini-Faria F**, Black SE*, Masellis M*, Smith EE*, Almeida QJ*, Li KZH*, Bherer L*, Camicioli R*, Montero-Odasso M* | 2021 | Alzheimer's & Dementia |
| Gait Disorders in Alzheimer’s Disease and Other Dementias: There is Something in the Way You Walk | Montero-Odasso M*, Perry G | 2019 | Journal of Alzheimer's Disease |
| FUS Phase Separation Is Modulated by a Molecular Chaperone and Methylation of Arginine Cation-π Interactions | Qamar S., Wang G., Randle S.J., Ruggeri F.S., Varela J.A., Lin J.Q., Phillips E.C., Miyashita A., Williams D., Strohl F., Meadows W., Ferry R., Dardov V.J., Tartaglia G.G., Farrer L.A., Kaminski Schierle G.S., Kaminski C.F., Holt C.E., Fraser P.E., Schmitt-Ulms G., Klenerman D., Knowles T., Vendruscolo M., St George-Hyslop P. | Cell | |
| Full sequencing and haplotype analysis of MAPT in Parkinson’s disease and rapid eye movement sleep behavior disorder | Li, J., Ruskey, J.A., Arnulf, I., Dauvilliers, Y., Hu, M.T.M., Hogl, B., Leblond, C.S., Zhou, S., Ambalavanan, A., Ross, J.P., Bourassa, C.V., Spiegelman, D., Laurent, S.B., Stefani, A., Charley Monaca, C., Cochen De Cock, V., Boivin, M., Ferini-Strambi, L., Plazzi, G., Antelmi, E., Young, P., Heidbreder, A., Labbe, C., Ferman, T.J., Dion, P.A., Fan, D., Desautels, A., Gagnon, J.F., Dupre, N., Fon, E.A., Montplaisir, J.Y., Boeve, B.F., Postuma, R.B., Rouleau, G.A., Ross, O.A., & Gan-Or, Z. | 2018 | Movement Disorders |
| Frequency of loss of function variants in LRRK2 in Parkinson Disease | Blauwendraat, C., Reed, X., Kia, D.A., Gan-Or, Z., Lesage, S., Pihlstrom, L., Guerreiro, R., Gibbs, J.R., Sabir M., Ahmed, S., Ding, J., Alcalay, R.N., Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease. Hassin-Baer, S., Pittma,n A.M., Brooks, J., Edsall, C., Hernandez, D.G., Chung, S.J., Goldwurm, S., Toft, M., Schulte, C., Bras, J., Wood, N.W., Brice, A., Morris, H.R., Scholz, S.W., Nalls, M.A., Singleton, A.B., Cookson, M.R., for the COURAGE-PD Consortium, the French Parkinson's Disease Consortium, & the International Parkinson's Disease Genomics Consortium. | 2018 | JAMA Neurology |
| Frailty, lifestyle, genetics and dementia risk | Ward, D. D., Ranson, J. M., Wallace, L.**, Llewellyn, D. J., & Rockwood, K.* | 2021 | Journal of Neurology, Neurosurgery, and Psychiatry |
Résultats 291 à 300 sur 558 Publications