GBA variants in REM sleep behavior disorder: A multicenter study L Krohn, JA Ruskey, U Rudakou, E Leveille, F Asayesh, MTM Hu, I Arnulf, ... Neurology 95 (8), e1008-e1016, 2020 | 65 | 2020 |
Tau and MAPT genetics in tauopathies and synucleinopathies E Leveille, OA Ross, Z Gan-Or Parkinsonism & related disorders 90, 142-154, 2021 | 48 | 2021 |
The Quebec Parkinson network: a researcher-patient matching platform and multimodal biorepository Z Gan-Or, T Rao, E Leveille, C Degroot, S Chouinard, F Cicchetti, ... Journal of Parkinson's disease 10 (1), 301-313, 2020 | 47 | 2020 |
Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype MA Estiar, E Leveille, D Spiegelman, N Dupre, JF Trempe, GA Rouleau, ... Molecular genetics & genomic medicine 8 (3), e1052, 2020 | 26 | 2020 |
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease EE Brown, C Blauwendraat, J Trinh, M Rizig, MA Nalls, E Leveille, ... Neurobiology of Aging 97, 148. e17-148. e24, 2021 | 24 | 2021 |
Use of mobile health technologies for postoperative care in paediatric surgery: a systematic review N Nguyen, E Leveille, E Guadagno, LM Kalisya, D Poenaru Journal of telemedicine and telecare 28 (5), 331-341, 2022 | 23 | 2022 |
SYK and ZAP70 kinases in autoimmunity and lymphoid malignancies E Leveille, LN Chan, AS Mirza, K Kume, M Müschen Cellular signalling 94, 110331, 2022 | 20 | 2022 |
Investigating the relationship between the SNCA gene and cognitive abilities in idiopathic Parkinson’s disease using machine learning M Ramezani, P Mouches, E Yoon, D Rajashekar, JA Ruskey, E Leveille, ... Scientific Reports 11 (1), 4917, 2021 | 19 | 2021 |
Genetic events inhibiting apoptosis in diffuse large B cell lymphoma E Leveille, NA Johnson Cancers 13 (9), 2167, 2021 | 17 | 2021 |
SPTAN1 variants as a potential cause for autosomal recessive hereditary spastic paraplegia E Leveille, MA Estiar, L Krohn, D Spiegelman, A Dionne-Laporte, N Dupré, ... Journal of Human Genetics 64 (11), 1145-1151, 2019 | 17 | 2019 |
Association between BDNF Val66Met polymorphism and mild behavioral impairment in patients with Parkinson's disease M Ramezani, JA Ruskey, K Martens, M Kibreab, Z Javer, I Kathol, ... Frontiers in Neurology 11, 587992, 2021 | 15 | 2021 |
Evidence for non‐Mendelian inheritance in spastic paraplegia 7 MA Estiar, E Yu, I Haj Salem, JP Ross, K Mufti, F Akçimen, E Leveille, ... Movement Disorders 36 (7), 1664-1675, 2021 | 13 | 2021 |
Sequencing of the GBA coactivator, Saposin C B Ouled Amar Bencheikh, E Leveille, JA Ruskey, D Spiegelman, C Liong, ... Parkinson disease. Neurobiol. Aging 72 (187), e1-187, 2018 | 13 | 2018 |
Association study of essential tremor genetic loci in Parkinson's disease JP Ross, S Mohtashami, E Leveille, AM Johnson, L Xiong, PA Dion, E Fon, ... Neurobiology of aging 66, 178. e13-178. e15, 2018 | 12 | 2018 |
Genetic, structural and clinical analysis of spastic paraplegia 4 P Varghaei, MA Estiar, S Ashtiani, S Veyron, K Mufti, E Leveille, E Yu, ... Parkinsonism & Related Disorders 98, 62-69, 2022 | 11 | 2022 |
Sequencing of the GBA coactivator, Saposin C, in Parkinson disease BOA Bencheikh, E Leveille, JA Ruskey, D Spiegelman, C Liong, EA Fon, ... Neurobiology of aging 72, 187. e1-187. e3, 2018 | 11 | 2018 |
Triple A syndrome presenting as complicated hereditary spastic paraplegia E Leveille, HD Gonorazky, MF Rioux, LN Hazrati, JA Ruskey, A Carnevale, ... Molecular Genetics & Genomic Medicine 6 (6), 1134-1139, 2018 | 11 | 2018 |
GCH1 mutations in hereditary spastic paraplegia P Varghaei, G Yoon, MA Estiar, S Veyron, E Leveille, N Dupre, JF Trempe, ... Clinical Genetics 100 (1), 51-58, 2021 | 8 | 2021 |
The neurophysiological brain-fingerprint of Parkinson’s disease J da Silva Castanheira, AI Wiesman, JY Hansen, B Misic, S Baillet, ... eBioMedicine 105, 105201, 2024 | 6 | 2024 |
Clinical characterization of traumatic acute interhemispheric subdural hematoma E Léveillé, S Schur, A AlAzri, C Couturier, M Maleki, J Marcoux Canadian Journal of Neurological Sciences 47 (4), 504-510, 2020 | 6 | 2020 |