Publications
Showing 81 to 90 of 560 Publications
Title | Authors | Year | Journal |
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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 |
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 |
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 |
Neuropsychiatric symptoms predict hypometabolism in preclinical Alzheimer disease. | Ng KP, Pascoal TA, Mathotaarachchi S, Chung CO, Benedet AL, Shin M, Kang MS, Li X, Ba M, Kandiah N, Rosa-Neto P, Gauthier S | Neurology | |
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 |
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 |
Odor identification as a biomarker of preclinical AD in older adults at risk | Lafaille-Magnan, M. E., Poirier, J., Etienne, P., Tremblay-Mercier, J., Frenette, J., Rosa-Neto, P., & Breitner, J. C. S. for the Prevent-AD Research Group | 2017 | 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 |
Showing 81 to 90 of 560 Publications