Christine Sato

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 41	2018

Other Publications

Article	Year
Brain levels of CDK5 activator p25 are not increased in Alzheimer's or other neurodegenerative diseases with neurofibrillary tangles. Journal of neurochemistry\| PubMed ID: 12859671	2003
Clinical findings in a large family with a parkin ex3delta40 mutation. Archives of neurology\| PubMed ID: 15148147	2004
Analysis of the glucocerebrosidase gene in Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society\| PubMed ID: 15517592	2005
Genetic association study of PINK1 coding polymorphisms in Parkinson's disease. Neuroscience letters\| PubMed ID: 15542245	2004
Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease. Archives of neurology\| PubMed ID: 15596610	2004
Association studies of cholesterol metabolism genes (CH25H, ABCA1 and CH24H) in Alzheimer's disease. Neuroscience letters\| PubMed ID: 16157450	2006
Association studies between the plasmin genes and late-onset Alzheimer's disease. Neurobiology of aging\| PubMed ID: 16828203	2007
Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis. Neurobiology of aging\| PubMed ID: 17383054	2008
Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics. G3 (Bethesda, Md.)\| PubMed ID: 22384383	2012
LIV-1 ZIP ectodomain shedding in prion-infected mice resembles cellular response to transition metal starvation. Journal of molecular biology\| PubMed ID: 22687393	2012
Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy. Neurobiology of aging\| PubMed ID: 22819134	2012
Genetic association of CR1 with Alzheimer's disease: a tentative disease mechanism. Neurobiology of aging\| PubMed ID: 22819390	2012
Investigation of C9orf72 in 4 Neurodegenerative Disorders. Archives of neurology\| PubMed ID: 22964832	2012
Segmental duplications in genome-wide significant loci and housekeeping genes; warning for GAPDH and ACTB. Neurobiology of aging\| PubMed ID: 23238109	2013
Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion. American journal of human genetics\| PubMed ID: 23731538	2013
Evidence of recessive Alzheimer disease loci in a Caribbean Hispanic data set: genome-wide survey of runs of homozygosity. JAMA neurology\| PubMed ID: 23978990	2013
Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patients. Human molecular genetics\| PubMed ID: 24908669	2014
Mutation analysis of patients with neurodegenerative disorders using NeuroX array. Neurobiology of aging\| PubMed ID: 25174650	2015
Identical twins with the C9orf72 repeat expansion are discordant for ALS. Neurology\| PubMed ID: 25209579	2014
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients. Acta neuropathologica\| PubMed ID: 25716178	2015
Mutation analysis of CHCHD10 in different neurodegenerative diseases. Brain : a journal of neurology\| PubMed ID: 25833818	2015
Jump from pre-mutation to pathologic expansion in C9orf72. American journal of human genetics\| PubMed ID: 26004200	2015
Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci. Annals of neurology\| PubMed ID: 26101835	2015
Mutation analysis of C9orf72 in patients with corticobasal syndrome. Neurobiology of aging\| PubMed ID: 26166205	2015
Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals. JAMA neurology\| PubMed ID: 26366463	2015
Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease. Neurobiology of aging\| PubMed ID: 26639156	2016
Novel GRN Mutations in Patients with Corticobasal Syndrome. Scientific reports\| PubMed ID: 26961809	2016
Mutation analysis of the MS4A and TREM gene clusters in a case-control Alzheimer's disease data set. Neurobiology of aging\| PubMed ID: 27084067	2016
Genetic and epigenetic study of ALS-discordant identical twins with double mutations in SOD1 and ARHGEF28. Journal of neurology, neurosurgery, and psychiatry\| PubMed ID: 27154192	2016
Drug Repositioning for Alzheimer's Disease Based on Systematic 'omics' Data Mining. PloS one\| PubMed ID: 28005991	2016
C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonism. Movement disorders : official journal of the Movement Disorder Society\| PubMed ID: 28124431	2017
DNA methylation age-acceleration is associated with disease duration and age at onset in C9orf72 patients. Acta neuropathologica\| PubMed ID: 28439722	2017
The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration. NPJ genomic medicine\| PubMed ID: 29263818	2016
Unaffected mosaiccase: RNA foci, dipeptide proteins, but upregulated C9orf72 expression. Neurology\| PubMed ID: 29282338	2018