Publications
Showing 291 to 300 of 555 Publications
Title | Authors | Year | Journal |
---|---|---|---|
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. | 2018 | 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 |
Frailty Prevalence in the COMPASS-ND Study of Neurodegenerative Disorders | Burt JR*, Godin J*, Filion J**, Montero-Odasso M**, Rockwood K**, Andrew MK**, Camicioli R** | 2019 | Canadian Geriatrics Journal |
Showing 291 to 300 of 555 Publications