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Roy Alcalay
Roy Alcalay
Chief, Division of Movement Disorders, Tel Aviv Soursky Medical Center; Associate Professor of
Verified email at columbia.edu
Title
Cited by
Cited by
Year
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
15292019
T cells from patients with Parkinson’s disease recognize α-synuclein peptides
D Sulzer, RN Alcalay, F Garretti, L Cote, E Kanter, J Agin-Liebes, C Liong, ...
Nature 546 (7660), 656-661, 2017
7272017
Glucocerebrosidase activity in Parkinson’s disease with and without GBA mutations
RN Alcalay, OA Levy, CH Waters, S Fahn, B Ford, SH Kuo, P Mazzoni, ...
Brain 138 (9), 2648-2658, 2015
3942015
The neuropathology of genetic Parkinson's disease
M Poulopoulos, OA Levy, RN Alcalay
Movement Disorders 27 (7), 831-842, 2012
3322012
Clinical correlations with Lewy body pathology in LRRK2-related Parkinson disease
LV Kalia, AE Lang, LN Hazrati, S Fujioka, ZK Wszolek, DW Dickson, ...
JAMA neurology 72 (1), 100-105, 2015
3232015
Cognitive performance of GBA mutation carriers with early-onset PD: The CORE-PD study
RN Alcalay, E Caccappolo, H Mejia-Santana, MX Tang, L Rosado, ...
Neurology 78 (18), 1434-1440, 2012
2942012
Neuropathology of genetic synucleinopathies with parkinsonism: review of the literature
SA Schneider, RN Alcalay
Movement Disorders 32 (11), 1504-1523, 2017
2802017
Impact of the COVID‐19 pandemic on Parkinson's disease and movement disorders
SM Papa, P Brundin, VSC Fung, UJ Kang, DJ Burn, C Colosimo, ...
Movement disorders clinical practice 7 (4), 357, 2020
2612020
The association between Mediterranean diet adherence and Parkinson's disease
RN Alcalay, Y Gu, H Mejia‐Santana, L Cote, KS Marder, N Scarmeas
Movement Disorders 27 (6), 771-774, 2012
2492012
Comparison of Parkinson risk in Ashkenazi Jewish patients with Gaucher disease and GBA heterozygotes
RN Alcalay, T Dinur, T Quinn, K Sakanaka, O Levy, C Waters, S Fahn, ...
JAMA neurology 71 (6), 752-757, 2014
2132014
Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study
RN Alcalay, E Caccappolo, H Mejia-Santana, MX Tang, L Rosado, ...
Archives of neurology 67 (9), 1116-1122, 2010
1832010
Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia
C Blauwendraat, X Reed, L Krohn, K Heilbron, S Bandres-Ciga, M Tan, ...
Brain 143 (1), 234-248, 2020
1782020
Assessment of heterogeneity among participants in the Parkinson's Progression Markers Initiative cohort using α-synuclein seed amplification: a cross-sectional study
A Siderowf, L Concha-Marambio, DE Lafontant, CM Farris, Y Ma, ...
The Lancet Neurology 22 (5), 407-417, 2023
1672023
Arm swing as a potential new prodromal marker of Parkinson's disease
A Mirelman, H Bernad‐Elazari, A Thaler, E Giladi‐Yacobi, T Gurevich, ...
Movement Disorders 31 (10), 1527-1534, 2016
1662016
Ser (P)‐1292 LRRK2 in urinary exosomes is elevated in idiopathic Parkinson's disease
KB Fraser, AB Rawlins, RG Clark, RN Alcalay, DG Standaert, N Liu, ...
Movement Disorders 31 (10), 1543-1550, 2016
1632016
Age-specific penetrance of LRRK2 G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium
K Marder, Y Wang, RN Alcalay, H Mejia-Santana, MX Tang, A Lee, ...
Neurology 85 (1), 89-95, 2015
1592015
Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry
AJ Lee, Y Wang, RN Alcalay, H Mejia‐Santana, R Saunders‐Pullman, ...
Movement Disorders 32 (10), 1432-1438, 2017
1552017
Genetic forms of Parkinson's disease
CY Kim, RN Alcalay
Seminars in neurology 37 (02), 135-146, 2017
1502017
Prediction of cognition in Parkinson's disease with a clinical–genetic score: a longitudinal analysis of nine cohorts
G Liu, JJ Locascio, JC Corvol, B Boot, Z Liao, K Page, D Franco, K Burke, ...
The Lancet Neurology 16 (8), 620-629, 2017
1472017
GBA mutations are associated with rapid eye movement sleep behavior disorder
Z Gan‐Or, A Mirelman, RB Postuma, I Arnulf, A Bar‐Shira, Y Dauvilliers, ...
Annals of clinical and translational neurology 2 (9), 941-945, 2015
1422015
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