Publications

Résultats 431 à 440 sur 563 Publications
Titre Auteurs
Chercheurs du CCNV* / Stagiaires du CCNV**
Année Revue
TOX3 variants are involved in restless legs syndrome and Parkinson’s Disease with opposite effects Mohtashami, S., He, Q., Ruskey, J.A., Zhou, S., Dion, P.A., Allen, R.P., Earley, C.J., Fon, E.A., Xiong, L., Dupre, N., Dauvillers, Y., Rouleau, G.A., & Gan-Or, Z. 2018 Journal of Molecular Neuroscience
Metabolomics analyses of saliva detect novel biomarkers of Alzheimer’s disease Huan, T., Tran, T., Zheng, J., Sapkota, S., Camicioli, R., Dixon, R.A., & Li, L. 2018 Journal of Alzheimer's Disease
Emotion and motivation in cognitive assistive technologies for dementia Robillard, J.M. & Hoey, J. 2018 Computer
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
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 Journal of Magnetic Resonance Imaging
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
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
Résultats 431 à 440 sur 563 Publications
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