Christine Sato Tanz Centre for Research in Neurodegenerative Diseases University of Toronto Biography Publications Institution JoVE Articles Christine Sato has not added a biography. If you are Christine Sato and would like to personalize this page please email our Author Liaison for assistance. Publications Unaffected Mosaiccase: RNA Foci, Dipeptide Proteins, but Upregulated C9orf72 Expression Neurology. Jan, 2018 | Pubmed ID: 29282338 DNA Methylation Age-acceleration is Associated with Disease Duration and Age at Onset in C9orf72 Patients Acta Neuropathologica. Aug, 2017 | Pubmed ID: 28439722 C9orf72 and ATXN2 Repeat Expansions Coexist in a Family with Ataxia, Dementia, and Parkinsonism Movement Disorders : Official Journal of the Movement Disorder Society. Jan, 2017 | Pubmed ID: 28124431 The ONDRISeq Panel: Custom-designed Next-generation Sequencing of Genes Related to Neurodegeneration NPJ Genomic Medicine. 2016 | Pubmed ID: 29263818 Drug Repositioning for Alzheimer's Disease Based on Systematic 'omics' Data Mining PloS One. 2016 | Pubmed ID: 28005991 Genetic and Epigenetic Study of ALS-discordant Identical Twins with Double Mutations in SOD1 and ARHGEF28 Journal of Neurology, Neurosurgery, and Psychiatry. 11, 2016 | Pubmed ID: 27154192 Mutation Analysis of the MS4A and TREM Gene Clusters In a case-control Alzheimer's Disease Data Set Neurobiology of Aging. 06, 2016 | Pubmed ID: 27084067 Novel GRN Mutations in Patients with Corticobasal Syndrome Scientific Reports. Mar, 2016 | Pubmed ID: 26961809 Mutation Analysis of CHCHD2 in Canadian Patients with Familial Parkinson's Disease Neurobiology of Aging. Feb, 2016 | Pubmed ID: 26639156 Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals JAMA Neurology. Nov, 2015 | Pubmed ID: 26366463 Mutation Analysis of C9orf72 in Patients with Corticobasal Syndrome Neurobiology of Aging. Oct, 2015 | Pubmed ID: 26166205 Rare Coding Mutations Identified by Sequencing of Alzheimer Disease Genome-wide Association Studies Loci Annals of Neurology. Sep, 2015 | Pubmed ID: 26101835 Jump from Pre-mutation to Pathologic Expansion in C9orf72 American Journal of Human Genetics. Jun, 2015 | Pubmed ID: 26004200 Mutation Analysis of CHCHD10 in Different Neurodegenerative Diseases Brain : a Journal of Neurology. Sep, 2015 | Pubmed ID: 25833818 The C9orf72 Repeat Expansion Itself is Methylated in ALS and FTLD Patients Acta Neuropathologica. May, 2015 | Pubmed ID: 25716178 Mutation Analysis of Patients with Neurodegenerative Disorders Using NeuroX Array Neurobiology of Aging. Jan, 2015 | Pubmed ID: 25174650 Identical Twins with the C9orf72 Repeat Expansion Are Discordant for ALS Neurology. Oct, 2014 | Pubmed ID: 25209579 Hypermethylation of the CpG-island Near the C9orf72 G₄C₂-repeat Expansion in FTLD Patients Human Molecular Genetics. Nov, 2014 | Pubmed ID: 24908669 Evidence of Recessive Alzheimer Disease Loci in a Caribbean Hispanic Data Set: Genome-wide Survey of Runs of Homozygosity JAMA Neurology. Oct, 2013 | Pubmed ID: 23978990 Hypermethylation of the CpG Island Near the G4C2 Repeat in ALS with a C9orf72 Expansion American Journal of Human Genetics. Jun, 2013 | Pubmed ID: 23731538 Segmental Duplications in Genome-wide Significant Loci and Housekeeping Genes; Warning for GAPDH and ACTB Neurobiology of Aging. Jun, 2013 | Pubmed ID: 23238109 C9orf72 在 4 调查神经退行性疾病。 Archives of Neurology. Sep, 2012 | Pubmed ID: 22964832 Genetic Association of CR1 with Alzheimer's Disease: a Tentative Disease Mechanism Neurobiology of Aging. Dec, 2012 | Pubmed ID: 22819390 Epidemiology and Genetics of Frontotemporal Dementia: a Door-to-door Survey in Southern Italy Neurobiology of Aging. Dec, 2012 | Pubmed ID: 22819134 LIV-1 ZIP Ectodomain Shedding in Prion-infected Mice Resembles Cellular Response to Transition Metal Starvation Journal of Molecular Biology. Sep, 2012 | Pubmed ID: 22687393 Genome-wide Survey of Large Rare Copy Number Variants in Alzheimer's Disease Among Caribbean Hispanics G3 (Bethesda, Md.). Jan, 2012 | Pubmed ID: 22384383 手摇和 IFT74 在萎缩侧索硬化症的遗传学研究。 Neurobiology of Aging. Aug, 2008 | Pubmed ID: 17383054 Association Studies Between the Plasmin Genes and Late-onset Alzheimer's Disease Neurobiology of Aging. Jul, 2007 | Pubmed ID: 16828203 Association Studies of Cholesterol Metabolism Genes (CH25H, ABCA1 and CH24H) in Alzheimer's Disease Neuroscience Letters. Jan, 2006 | Pubmed ID: 16157450 Analysis of the Glucocerebrosidase Gene in Parkinson's Disease Movement Disorders : Official Journal of the Movement Disorder Society. Mar, 2005 | Pubmed ID: 15517592 Analysis of the PINK1 Gene in a Large Cohort of Cases with Parkinson Disease Archives of Neurology. Dec, 2004 | Pubmed ID: 15596610 Genetic Association Study of PINK1 Coding Polymorphisms in Parkinson's Disease Neuroscience Letters. Dec, 2004 | Pubmed ID: 15542245 Clinical Findings in a Large Family with a Parkin Ex3delta40 Mutation Archives of Neurology. May, 2004 | Pubmed ID: 15148147 Brain Levels of CDK5 Activator P25 Are Not Increased in Alzheimer's or Other Neurodegenerative Diseases with Neurofibrillary Tangles Journal of Neurochemistry. Aug, 2003 | Pubmed ID: 12859671 有针对性的下一代测序和生物信息学管道评价宪政疾病的遗传决定因素 Allison A. Dilliott1,2, Sali M.K. Farhan3, Mahdi Ghani4, Christine Sato4, Eric Liang5, Ming Zhang4, Adam D. McIntyre1, Henian Cao1, Lemuel Racacho6,7, John F. Robinson1, Michael J. Strong1,8, Mario Masellis9,10, Dennis E. Bulman6,7, Ekaterina Rogaeva4, Anthony Lang10,11, Carmela Tartaglia4,10, Elizabeth Finger12,13, Lorne Zinman9, John Turnbull14, Morris Freedman10,15, Rick Swartz9, Sandra E. Black9,16, Robert A. Hegele1,2 1Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, 2Department of Biochemistry, Schulich School of Medicine and Dentistry, Western University, 3Analytic and Translational Genetics Unit, Center for Genomic Medicine, Harvard Medical School, Massachusetts General Hospital, Stanley Centre for Psychiatric Research, Broad Institute of MIT and Harvard, 4Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 5School of Medicine, Faculty of Health Sciences, Queen's University, 6Faculty of Medicine, Department of Biochemistry, Microbiology and Immunology, University of Ottawa, 7CHEO Research Institute, Faculty of Medicine, University of Ottawa, 8Department of Clinical Neurological Sciences, Western University, 9Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, 10Division of Neurology, Department of Medicine, University of Toronto, 11Morton and Gloria Shulman Movement Disorders Centre, Toronto Western Hospital, 12Department of Clinical Neurological Sciences, Schulich School of Medicine and Dentistry, Western University, 13Parkwood Institute, St. Joseph's Health Care, 14Department of Medicine, Division of Neurology, McMaster University, 15Division of Neurology, Department of Medicine, Baycrest Health Sciences, 16Canadian Partnership for Stroke Recovery Sunnybrook Site, Sunnybrook Health Science Centre, University of Toronto JoVE 57266 Genética
有针对性的下一代测序和生物信息学管道评价宪政疾病的遗传决定因素 Allison A. Dilliott1,2, Sali M.K. Farhan3, Mahdi Ghani4, Christine Sato4, Eric Liang5, Ming Zhang4, Adam D. McIntyre1, Henian Cao1, Lemuel Racacho6,7, John F. Robinson1, Michael J. Strong1,8, Mario Masellis9,10, Dennis E. Bulman6,7, Ekaterina Rogaeva4, Anthony Lang10,11, Carmela Tartaglia4,10, Elizabeth Finger12,13, Lorne Zinman9, John Turnbull14, Morris Freedman10,15, Rick Swartz9, Sandra E. Black9,16, Robert A. Hegele1,2 1Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, 2Department of Biochemistry, Schulich School of Medicine and Dentistry, Western University, 3Analytic and Translational Genetics Unit, Center for Genomic Medicine, Harvard Medical School, Massachusetts General Hospital, Stanley Centre for Psychiatric Research, Broad Institute of MIT and Harvard, 4Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 5School of Medicine, Faculty of Health Sciences, Queen's University, 6Faculty of Medicine, Department of Biochemistry, Microbiology and Immunology, University of Ottawa, 7CHEO Research Institute, Faculty of Medicine, University of Ottawa, 8Department of Clinical Neurological Sciences, Western University, 9Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, 10Division of Neurology, Department of Medicine, University of Toronto, 11Morton and Gloria Shulman Movement Disorders Centre, Toronto Western Hospital, 12Department of Clinical Neurological Sciences, Schulich School of Medicine and Dentistry, Western University, 13Parkwood Institute, St. Joseph's Health Care, 14Department of Medicine, Division of Neurology, McMaster University, 15Division of Neurology, Department of Medicine, Baycrest Health Sciences, 16Canadian Partnership for Stroke Recovery Sunnybrook Site, Sunnybrook Health Science Centre, University of Toronto JoVE 57266 Genética