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Eric Yu
Eric Yu
在 mail.mcgill.ca 的电子邮件经过验证
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Fine mapping of the HLA locus in Parkinson’s disease in Europeans
E Yu, A Ambati, MS Andersen, L Krohn, MA Estiar, P Saini, K Senkevich, ...
npj Parkinson's Disease 7 (1), 84, 2021
442021
Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease
E Yu, U Rudakou, L Krohn, K Mufti, JA Ruskey, F Asayesh, MA Estiar, ...
Movement Disorders 36 (1), 178-187, 2021
402021
Targeted sequencing of Parkinson’s disease loci genes highlights SYT11, FGF20 and other associations
U Rudakou, E Yu, L Krohn, JA Ruskey, F Asayesh, Y Dauvilliers, ...
Brain 144 (2), 462-472, 2021
372021
Common X‐chromosome variants are associated with Parkinson disease risk
Y Le Guen, V Napolioni, ME Belloy, E Yu, L Krohn, JA Ruskey, Z Gan‐Or, ...
Annals of neurology 90 (1), 22-34, 2021
352021
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
L Krohn, K Heilbron, C Blauwendraat, RH Reynolds, E Yu, K Senkevich, ...
Nature communications 13 (1), 7496, 2022
312022
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease
P Saini, U Rudakou, E Yu, JA Ruskey, F Asayesh, SB Laurent, ...
Neurobiology of aging 100, 119. e7-119. e13, 2021
282021
Comprehensive analysis of familial parkinsonism genes in rapid‐eye‐movement sleep behavior disorder
K Mufti, U Rudakou, E Yu, L Krohn, JA Ruskey, F Asayesh, SB Laurent, ...
Movement Disorders 36 (1), 235-240, 2021
18*2021
LRRK2 p. M1646T is associated with glucocerebrosidase activity and with Parkinson's disease
YL Sosero, E Yu, L Krohn, U Rudakou, K Mufti, JA Ruskey, F Asayesh, ...
Neurobiology of aging 103, 142. e1-142. e5, 2021
162021
GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson’s disease
Brain, 2022
14*2022
Variants in the Niemann–Pick type C gene NPC1 are not associated with Parkinson's disease
BOA Bencheikh, K Senkevich, U Rudakou, E Yu, K Mufti, JA Ruskey, ...
Neurobiology of aging 93, 143. e1-143. e4, 2020
142020
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
132021
Novel Associations of BST1 and LAMP3 With REM Sleep Behavior Disorder
K Mufti, E Yu, U Rudakou, L Krohn, JA Ruskey, F Asayesh, SB Laurent, ...
Neurology 96 (10), e1402-e1412, 2021
132021
Axial impairment following deep brain stimulation in Parkinson’s disease: A surgicogenomic approach
NP Visanji, M Ghani, E Yu, EG Kakhki, C Sato, D Moreno, T Naranian, ...
Journal of Parkinson's Disease 12 (1), 117-128, 2022
102022
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
92022
Multiancestry analysis of the HLA locus in Alzheimer’s and Parkinson’s diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes
Y Le Guen, G Luo, A Ambati, V Damotte, I Jansen, E Yu, A Nicolas, ...
Proceedings of the National Academy of Sciences 120 (36), e2302720120, 2023
82023
Potential protective link between type I diabetes and Parkinson's disease risk and progression
K Senkevich, P Alipour, E Chernyavskaya, E Yu, AJ Noyce, Z Gan‐Or
Movement Disorders 38 (7), 1350-1355, 2023
72023
Association of Rare Variants in ARSA with Parkinson's Disease
K Senkevich, M Beletskaia, A Dworkind, E Yu, J Ahmad, JA Ruskey, ...
Movement Disorders 38 (10), 1806-1812, 2023
62023
Neuroanatomical correlates of genetic risk for obesity in children
F Morys, E Yu, M Shishikura, C Paquola, U Vainik, G Nave, P Koellinger, ...
Translational Psychiatry 13 (1), 1, 2023
62023
Neuroanatomical correlates of polygenic risk for Parkinson’s Disease
N Abbasi, C Tremblay, R Rajimehr, E Yu, RD Markello, G Shafiei, ...
medRxiv, 2022.01. 17.22269262, 2022
62022
Rare PSAP variants and possible interaction with GBA in REM sleep behavior disorder
YL Sosero, E Yu, MA Estiar, L Krohn, K Mufti, U Rudakou, JA Ruskey, ...
Journal of Parkinson's disease 12 (1), 333-340, 2022
62022
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