Showing 11 to 20 of 123 Publications
Title Authors
CCNA Trainees* CCNA Researchers**
Year Journal
Alzheimer’s biomarkers from multiple modalities selectively discriminate clinical status: Relative importance of salivary metabolomics panels, genetic, lifestyle, cognitive, functional health and demographic risk markers Sapkota, S.*, Huan, T., Tran T., Zheng, J., Camicioli, R.**, Li, L.** & Dixon, R.A. ** 2018 Frontiers in Aging Neuroscience
A network of genetic effects on non-demented cognitive aging: Alzheimer’s genetic risk (CLU + CR1+PICALM) intensifies cognitive Aging genetic risk (COMT + BDNF) selectively for APOE4 carriers Sapkota, S.*, & Dixon, R. A.** 2018 Journal of Alzheimer's Disease
The GBA p Trp378Gly mutation is a probable French-Canadian founder mutation causing Gaucher disease and synucleinopathies Ruskey, J.A., Zhou, S., Santiago, R., Franche, L.A., Alam, A., Ronciere, L., Spiegelman, D., Fon, E.A.**, Trempe, J.F., Kalia, L.V., Postuma, R.B.**, Dupre, N.**, Rivard, G.E., Assouline, S., Amato, D., & Gan-Or, Z.** 2018 Clinical Genetics
APP21 transgenic rats develop age-dependent cognitive impairment and microglia accumulation within white matter tracts Weishaupt, N.**, Liu, Q., Shin, S., Singh, R., Agca, Y., Agca, C., Hachinski, V.**, & Whitehead, S.N.** 2018 Journal of Neuroinflammation
The Canadian Dementia Imaging Protocol: Harmonizing national cohorts Duchesne, S.**, Chouinard, I.**, Potvin, O., Fonov, V.S., Khademi, A.**, Bartha, R.**, Bellec, P.**, Collins, D.L.**, Descoteaux, M.**, Hoge, R., McCreary, C.R., Ramirez, J., Scott, C.J.M., Smith, E.E., Strother, S.C., Black, S.E. 2018
In vivo quantification of neurofibrillary tangles with [(18)F]MK-6240 Pascoal, T. A.*, Shin, M.*, Kang, M. S., Chamoun, M., Chartrand, D., Mathotaarachchi, S.*, Bennacef, I., Therriault, J.**, Ng, K. P., Hopewell, R., Bouhachi, R., Hsiao, H. H., Benedet, A. L.*, Soucy, J. P.**, Massarweh, G., Gauthier, S.**, & Rosa-Neto, P.** 2018 Alzheimer's Research and Therapy
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
Consent recommendations for research and international data sharing involving persons with dementia 2018 Alzheimer's & Dementia
Patient engagement in research related to dementia: a scoping review Bethell, J.*, Commisso, E., Rostad, H.M., Puts, M., Babineau, J., Grinbergs-Saull, A., Wighton, M.B., Hammel, J., Doyle, E.**, Nadeau, S.** & McGilton K.S.** In press Dementia
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