Biblio
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Analysis of common and rare variants in late-onset Parkinson disease. Neurol Genet. 2020;6(1):385.
. Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype. Mol Genet Genomic Med. 2020;:e1052.
. Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies. Ann Neurol. 2020;.
. The Quebec Parkinson Network: A Researcher-Patient Matching Platform and Multimodal Biorepository. J Parkinsons Dis. 2020;10(1):301-313.
. Common and rare GCH1 variants are associated with Parkinson's disease. Neurobiol Aging. 2019;73:231.e1-231.e6.
. SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease. Mov Disord. 2019;34(4):526-535.
. Association study of essential tremor genetic loci in Parkinson's disease. Neurobiol Aging. 2018;66:178.e13-178.e15.
. Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder. Mov Disord. 2018;33(6):1016-1020.
. Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population. Sci Rep. 2018;8(1):4356.
. POLR3A variants in hereditary spastic paraplegia and ataxia. Brain. 2018;141(1):e1.
. Sequencing of the GBA coactivator, Saposin C, in Parkinson disease. Neurobiol Aging. 2018;.
. TOX3 Variants Are Involved in Restless Legs Syndrome and Parkinson's Disease with Opposite Effects. J Mol Neurosci. 2018;64(3):341-345.
. Clinical and genetic study of hereditary spastic paraplegia in Canada. Neurol Genet. 2017;3(1):e122.
. The dementia-associated APOE ε4 allele is not associated with rapid eye movement sleep behavior disorder. Neurobiol Aging. 2017;49:218.e13-218.e15.
. KCNA2 mutations are rare in hereditary spastic paraplegia. Ann Neurol. 2017;81(2):325-326.
. RIC3 variants are not associated with Parkinson's disease in French-Canadians and French. Neurobiol Aging. 2017;53:194.e9-194.e11.
. Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease. Neurobiol Aging. 2016;45:212.e13-212.e17.
. Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia. Am J Hum Genet. 2016;98(5):1038-1046.
. Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis. Neurobiol Aging. 2016;37:209.e17-209.e21.
. RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population. Am J Hum Genet. 2016;99(5):1072-1085.
. The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder. Neurobiol Aging. 2016;43:180.e7-180.e13.
. Genetic markers of Restless Legs Syndrome in Parkinson disease. Parkinsonism Relat Disord. 2015;21(6):582-5.
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