Publications

Showing 471 to 480 of 554 Publications
Title Authors
CCNA Researchers* / CCNA Trainees**
Year Journal
CVLT-II short form forced choice recognition in a clinical dementia sample: Cautions for performance validity assessment
Grewal K.S.**, Trites M., Kirk A.*, MacDonald S.W.S., Morgan D.*, Gowda-Sookochoff R., O'Connell M.E.* 2022 Applied Neuropsychology: Adult
Common X-chromosome variants are associated with Parkinson’s disease risk
Le Guen Y, Napolioni V, Belloy Me, Yu E**, Krohn L**, Ruskey JA, Gan-Or Z*, Kennedy G, Eger SJ, Greicius MD 2021 Annals of Neurology
Faster Cortical Thinning and Surface Area Loss in Presymptomatic and Symptomatic C9orf72 Repeat Expansion Adult Carriers
Le Blanc G, Jetté Pomerleau V, McCarthy J, Borroni B, van Swieten J, Galimberti D, Sanchez-Valle R, LaForce R Jr*, Moreno F, Synofzik M, Graff C, Masellis M*, Tartaglia MC*, Rowe JB, Vandenberghe R, Finger E*, Tagliavini F, de Mendonça A, Santana I, Butler C, Gerhard A, Danek A, Levin J, Otto M, Frisoni G, Sorbi S, Rohrer JD, Ducharme S*; Genetic Frontotemporal Dementia Initiative (GENFI). 2020 Annals of Neurology
Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies
Krohn L, Wu RYJ, Heilbron K, Ruskey JA, Laurent SB, Blauwendraat C, Alam A, Arnulf I, Hu MTM, Dauvilliers Y, Högl B, Toft M, Bjørnarå KA, Stefani A, Holzknecht E, Monaca CC, Abril B, Plazzi G, Antelmi E, Ferini-Strambi L, Young P, Heidbreder A, 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**, Nalls MA, Singleton AB; 23andMe Research Team, Desautels A**, Montplaisir JY, Cannon P, Ross OA, Boeve BF, Dupré N, Fon EA**, Postuma RB**, Pihlstrøm L, Rouleau GA**, Gan-Or Z** 2020 Annals of Neurology
Interprofessional Primary Care and Acute Care Hospital Use by People With Dementia: A Population-Based Study
Sourial, N.*, Schuster, T.*, Bronskill, S.E.*, Godard-Sebillotte, C.*, Etches, J., & Vedel I.* 2022 Annals of Family Medicine
Genetic, structural and functional evidence link TMEM175 to synucleinopathies. Krohn L*, Ozturk TN, Vanderperre B*, Ouled Amar Bencheikh B, Ruskey JA, Laurent SB, Spiegelman D, Postuma RB**, Arnulf I, Hu MTM, Dauvilliers Y, Hogl B, Stefani A, Monaca CC, Plazzi G, Antelmi E, Ferini-Strambi L, Heidbreder A, Rudakou U, Cochen De Cock V, Young P, Wolf P, Oliva P, Zhang XK, Greenbaum L, Liong C, Gagnon JF**, Desautels A, Hassin-Baer S, Montplaisir JY**, Dupre N**, Rouleau GA**, Fon EA**, Trempe JF, Lamoureux G, Alcalay RN, Gan-Or Z**. 2019 Ann Neurol
Clinicopathologic correlations in a family with a TBK1 mutation presenting as primary progressive aphasia and primary lateral sclerosis
Hirsch-Reinshagen V, Alfaify OA, Hsiung GYR*,Pottier C, Baker M, Pekerson III RB, Rademakers R*, Briemberg H, Foti DJ, Mackenzie IR 2019 Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
TDP-43 pathology in primary lateral sclerosis
Mackenzie IRA*, Briemberg H 2020 Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Assessing cognitive functioning in ALS: A focus on frontal lobe processes Gillingham, S. M., Yunusova, Y., Ganda, A., Rogaeva, E., Black, S. E., Stuss, D. T., & Zinman, L. 2017 Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Neuropathology of primary lateral sclerosis
Mackenzie IRA* 2020 Amyotrophic lateral sclerosis & Frontotemporal degeneration
Showing 471 to 480 of 554 Publications
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