Ziv Gan-Or
Ziv Gan-Or
Montreal Neurological Institute, McGill University
Verified email at - Homepage
Cited by
Cited by
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
E Sidransky, MA Nalls, JO Aasly, J Aharon-Peretz, G Annesi, ER Barbosa, ...
New England Journal of Medicine 361 (17), 1651-1661, 2009
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
Risk and predictors of dementia and parkinsonism in idiopathic REM sleep behaviour disorder: a multicentre study
RB Postuma, A Iranzo, M Hu, B Högl, BF Boeve, R Manni, WH Oertel, ...
Brain 142 (3), 744-759, 2019
Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset
Z Gan-Or, N Giladi, U Rozovski, C Shifrin, S Rosner, T Gurevich, ...
Neurology 70 (24), 2277-2283, 2008
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
Differential effects of severe vs mild GBA mutations on Parkinson disease
Z Gan-Or, I Amshalom, LL Kilarski, A Bar-Shira, M Gana-Weisz, ...
Neurology 84 (9), 880-887, 2015
Genetic perspective on the role of the autophagy-lysosome pathway in Parkinson disease
Z Gan-Or, PA Dion, GA Rouleau
Autophagy 11 (9), 1443-1457, 2015
Parkinson's disease age at onset genome‐wide association study: defining heritability, genetic loci, and α‐synuclein mechanisms
C Blauwendraat, K Heilbron, CL Vallerga, S Bandres‐Ciga, R Von Coelln, ...
Movement Disorders 34 (6), 866-875, 2019
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
B Schormair, C Zhao, S Bell, E Tilch, AV Salminen, B Pütz, Y Dauvilliers, ...
The Lancet Neurology 16 (11), 898-907, 2017
Revisiting protein aggregation as pathogenic in sporadic Parkinson and Alzheimer diseases
AJ Espay, JA Vizcarra, L Marsili, AE Lang, DK Simon, A Merola, ...
Neurology 92 (7), 329-337, 2019
The p. L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease
Z Gan-Or, LJ Ozelius, A Bar-Shira, R Saunders-Pullman, A Mirelman, ...
Neurology 80 (17), 1606-1610, 2013
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
Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations
RN Alcalay, A Mirelman, R Saunders‐Pullman, MX Tang, ...
Movement Disorders 28 (14), 1966-1971, 2013
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
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
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
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia
Z Gan-Or, N Bouslam, N Birouk, A Lissouba, DB Chambers, J Vérièpe, ...
The American Journal of Human Genetics 98 (5), 1038-1046, 2016
Clinical and genetic study of hereditary spastic paraplegia in Canada
N Chrestian, N Dupré, Z Gan-Or, A Szuto, S Chen, A Venkitachalam, ...
Neurology Genetics 3 (1), 2017
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
R Chia, MS Sabir, S Bandres-Ciga, S Saez-Atienzar, RH Reynolds, ...
Nature genetics 53 (3), 294-303, 2021
GBA p. T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis
V Mallett, JP Ross, RN Alcalay, A Ambalavanan, E Sidransky, PA Dion, ...
Neurology Genetics 2 (5), 2016
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