Publications
Résultats 81 à 90 sur 555 Publications
| Titre | Auteurs | Année | Revue |
|---|---|---|---|
| Genome-wide analyses identify KIF5A as a novel ALS gene | Nicolas, A., Kenna, K. P., Renton, A. E., Ticozzi, N., Faghri, F., Chia, R., Dominov, J. A., Kenna, B. J., Nalls, M. A., Keagle, P., Rivera, A. M., van Rheenen, W., Murphy, N. A., van Vugt, J. J. F. A., Geiger, J. T., Van der Spek, R. A., Pliner, H. A., Shankaracharya, Smith, B. N., Marangi, G., Topp, S. D., Abramzon, Y., Gkazi, A. S., Eicher, J. D., Kenna, A., Mora, G., Calvo, A., Mazzini, L., Riva, N., Mandrioli, J., Caponnetto, C., Battistini, S., Volanti, P., La Bella, V., Conforti, F. L., Borghero, G., Messina, S., Simone, I. L., Trojsi, F., Salvi, F., Logullo, F. O., D’Alfonso, S., Corrado, L., Capasso, M., Ferrucci, L., Moreno, C. d. A. M., Kamalakaran, S., Goldstein, D. B., Gitler, A. D., Harris, T., Myers, R. M., Phatnani, H., Musunuri, R. L., Evani, U. S., Abhyankar, A., Zody, M. C., Kaye, J., Finkbeiner, S., Wyman, S. K., LeNail, A., Lima, L., Fraenkel, E., Svendsen, C. N., Thompson, L. M., Van Eyk, J. E., Berry, J. D., Miller, T. M., Kolb, S. J., Cudkowicz, M., Baxi, E., Benatar, M., Taylor, J. P., Rampersaud, E., Wu, G., Wuu, J., Lauria, G., Verde, F., Fogh, I., Tiloca, C., Comi, G. P., Sorarù, G., Cereda, C., Corcia, P., Laaksovirta, H., Myllykangas, L., Jansson, L., Valori, M., Ealing, J., Hamdalla, H., Rollinson, S., Pickering-Brown, S., Orrell, R. W., Sidle, K. C., Malaspina, A., Hardy, J., Singleton, A. B., Johnson, J. O., Arepalli, S., Sapp, P. C., McKenna-Yasek, D., Polak, M., Asress, S., Al-Sarraj, S., King, A., Troakes, C., Vance, C., de Belleroche, J., Baas, F., ten Asbroek, A. L. M. A., Muñoz-Blanco, J. L., Hernandez, D. G., Ding, J., Gibbs, J. R., Scholz, S. W., Floeter, M. K., Campbell, R. H., Landi, F., Bowser, R., Pulst, S. M., Ravits, J. M., MacGowan, D. J. L., Kirby, J., Pioro, E. P., Pamphlett, R., Broach, J., Gerhard, G., Dunckley, T. L., Brady, C. B., Kowall, N. W., Troncoso, J. C., Le Ber, I., Mouzat, K., Lumbroso, S., Heiman-Patterson, T. D., Kamel, F., Van Den Bosch, L., Baloh, R. H., Strom, T. M., Meitinger, T., Shatunov, A., Van Eijk, K. R., de Carvalho, M., Kooyman, M., Middelkoop, B., Moisse, M., McLaughlin, R. L., Van Es, M. A., Weber, M., Boylan, K. B., Van Blitterswijk, M., Rademakers, R., Morrison, K. E., Basak, A. N., Mora, J. S., Drory, V. E., Shaw, P. J., Turner, M. R., Talbot, K., Hardiman, O., Williams, K. L., Fifita, J. A., Nicholson, G. A., Blair, I. P., Rouleau, G. A., Esteban-Pérez, J., García-Redondo, A., Al-Chalabi, A., Rogaeva, E., Zinman, L., Ostrow, L. W., Maragakis, N. J., Rothstein, J. D., Simmons, Z., Cooper-Knock, J., Brice, A., Goutman, S. A., Feldman, E. L., Gibson, S. B., Taroni, F., Ratti, A., Gellera, C., Van Damme, P., Robberecht, W., Fratta, P., Sabatelli, M., Lunetta, C., Ludolph, A. C., Andersen, P. M., Weishaupt, J. H., Camu, W., Trojanowski, J. Q., Van Deerlin, V. M., Brown, R. H., van den Berg, L. H., Veldink, J. H., Harms, M. B., Glass, J. D., Stone, D. J., Tienari, P., Silani, V., Chiò, A., Shaw, C. E., Traynor, B. J., & Landers, J. E. | 2018 | Neuron |
| Late-onset vs nonmendelian early-onset Alzheimer disease: A distinction without a difference? | Reitz C, Rogaeva E*, Beecham GW | 2020 | Neurology Genetics |
| Neuropathologic description of CHCHD10 mutated amyotrophic lateral sclerosis | Keith JL**, Swinkin E, Gao A, Alminawi S, Zhang M, McGoldrick P, McKeever P, Robertson J, Rogaeva E**, Zinman L | 2020 | Neurology Genetics |
| Analysis of common and rare VPS13C variants in late-onset Parkinson disease | Rudakou U, Ruskey JA, Krohn L, Laurent SB, Spiegelman D, Greenbaum L, Yahalom G, Desautels A*, Montplaisir JY, Fahn S, Waters CH, Levy O, Kehoe CM, Narayan S, DauvilliersY, Dupré N, Hassin-Baer S, Alcalay RN, Rouleau GA*, Fon EA*, Gan-Or Z* | 2020 | Neurology Genetics |
| CYP2C19 variant mitigates Alzheimer disease pathophysiology in vivo and postmortem | Benedet, A.L., Yu, L., Labbe, A., Mathotaarachchi, S., Pascoal, T.A., Shin, M., Kang, M.S., Gauthier, S., Rouleau, G.A., Poirier, J., Bennett, D.A., Rosa-Neto, P., Alzheimer's Disease Neuroimaging Initiative. | 2018 | Neurology Genetics |
| Topographical distribution of amyloid-β, tau and atrophy in behavioral / dysexecutive AD patients | Therriault J, Pascoal TA, Savard M, Benedet AL, Chamoun M, Tissot C, Lussier F, Kang MS, Thomas E, Terada T, Rej S, Massarweh G, Nasreddine Z, Vitali P, Soucy JP, Saha-Chaudhuri P, Gauthier S*, Rosa-Neto P* | 2020 | Neurology |
| Neuropsychiatric symptoms predict hypometabolism in preclinical Alzheimer disease | Ng, K. P., Pascoal, T. A., Mathotaarachchi, S., Chung, C. O., Benedet, A. L., Shin, M., Kang, M. S., Li, X., Ba, M., Kandiah, N., Rosa-Neto, P., Gauthier, S., & Alzheimer's Disease Neuroimaging Initiative | 2017 | Neurology |
| Astrocyte Biomarkers in Alzheimer Disease: A Systematic Review and Meta-analysis | Bellaver B, Ferrari-Souza JP, Uglione da Ros L, Carter SF, Rodriguez-Vieitez E, Nordberg A, Pellerin L, Rosa-Neto P*, Leffa T, Zimmer ER | 2021 | Neurology |
| Cerebrovascular Reactivity Across the Entire Brain in Cerebral Amyloid Angiopathy | Beaudin, A. E.**, McCreary, C. R., Mazerolle, E. L., Gee, M., Sharma, B.**, Subotic, A., Zwiers, A. M., Cox, E., Nelles, K., Charlton, A., Frayne, R.*, Ismail, Z.*, Beaulieu, C.*, Jickling, G., Camicioli, R. M.*, Pike, G. B.*, & Smith, E.* | 2022 | Neurology |
| 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 |
Résultats 81 à 90 sur 555 Publications