Publications
Showing 151 to 160 of 560 Publications
| Title | Authors | Year | Journal |
|---|---|---|---|
| Biomarker modeling of Alzheimer’s disease using PET-based Braak staging | Therriault, J.**, Pascoal, T. A**., Lussier, F. Z., Tissot, C., Chamoun, M., Bezgin, G., Servaes S., Benedet A.L., Ashton N.J., Karikari T.K., Lantero-Rodriguez J., Kunach P., Wang Y-T., Fernandez-Arias J., Massarweh G., Vitali P., Soucy J-P., Saha-Chaudhuri P., Blennow, K., Zetterberg H., Gauthie S.*, & Rosa-Neto, P.* | 2022 | Nature Aging |
| The degree of frailty as a translational measure of health in aging | Howlett SE, Rutenberg AD, Rockwood K* | 2021 | Nature Aging |
| A two-step workflow based on plasma p-tau217 to screen for amyloid β positivity with further confirmatory testing only in uncertain cases | Brum, W. S., Cullen, N. C., Janelidze, S., Ashton, N. J., Zimmer, E. R., Therriault, J.**, Benedet, A. L., Rahmouni, N.**, Tissot, C.**, Stevenson, J., Servaes, S., Triana-Baltzer, G., Kolb, H. C., Palmqvist, S., Stomrud, E., Rosa-Neto, P.*, Blennow, K., & Hansson, O | 2023 | Nature aging |
| SMPD1 mutations, activity, and alpha-synuclein accumulation in Parkinson’s disease. | Alcalay, R.N., Mallett, V., Vanderperre, B., Tavassoly, O., Dauvilliers, Y., Wu, R.Y.J., Ruskey, J.A., Leblond, C.S., Ambalavanan, A., Laurent, S.B., Spiegelman, D., Dionne-Laporte, A., Liong, C., Levy, O.A., Fahn, S., Waters, C., Kuo, S.H., Chung, W.K., Ford, B., Marder, K.S., Kang, U.J., Hassin-Baer, S., Greenbaum, L., Trempe, J.F., Wolf, P., Oliva, P., Zhang, X.K., Clark, L.N., Langlois, M., Dion, P.A., Fon, E.A.**, Dupre, N.**, Rouleau, G.A.**, Gan-Or, Z**. | 2019 | Movement Disorders. |
| Analysis of Heterozygous PRKN Variants and Copy-Number Variations in Parkinson’s Disease | Yu E, Rudakou U, Krohn L, Mufti K, Ruskey JA, Asayesh F, Estiar MA, Spiegelman D, Surface M, Fahn S, Waters CH, Greenbaum L, Espay AJ, Dauvilliers Y, Dupré N, Rouleau GA*, Hassin-Baer S, Fon EA*, Alcalay RN, Gan-Or Z* | 2020 | Movement Disorders |
| C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonism. | Zhang M, Xi Z, Misquitta K, Sato C, Moreno D, Liang Y, Slow E, Rogaeva E, Tartaglia MC | Movement Disorders | |
| Profiling novel metabolic biomarkers for Parkinson’s disease using in‐depth metabolomic analysis | Han, W., Sapkota, S., Camicioli, R., Dixon, R. A., & Li, L. | 2017 | Movement Disorders |
| 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 |
| C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonism. | Zhang, M.**, Xi, Z., Misquitta, K., Sato, C., Moreno, D., Liang, Y., Slow, E., Rogaeva, E., & Tartaglia, M. C. | 2017 | Movement Disorders |
| Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder | Mufti K, Yu E, Ruskey JA, Laurent SB, Arnault I, Hu MTM, Montplaisir JY, Gagnon JF, Desautels A, Gigli GL, Janes F, Stefani A, Sonka K, Oertel W, Plazzi G, Figorilli M, Puligheddu M, Trenkwalder C, Sixel-Doring F, Cochen De Cock V, Monaca CC, Heidbreder A, Djikstra F, Abril B, Postuma RB*, Rouleau GA*, Gan-Or Z* | 2020 | Movement Disorders |
Showing 151 to 160 of 560 Publications