Mahdi Ghani

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
Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics. G3 (Bethesda, Md.)\| PubMed ID: 22384383	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
Role of p73 in Alzheimer disease: lack of association in mouse models or in human cohorts. Molecular neurodegeneration\| PubMed ID: 23414597	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
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
Coding mutations in SORL1 and Alzheimer disease. Annals of neurology\| PubMed ID: 25382023	2015
Inbreeding among Caribbean Hispanics from the Dominican Republic and its effects on risk of Alzheimer disease. Genetics in medicine : official journal of the American College of Medical Genetics\| PubMed ID: 25394174	2015
Mutation analysis of CHCHD10 in different neurodegenerative diseases. Brain : a journal of neurology\| PubMed ID: 25833818	2015
Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci. Annals of neurology\| PubMed ID: 26101835	2015
Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals. JAMA neurology\| PubMed ID: 26366463	2015
MTHFSD and DDX58 are novel RNA-binding proteins abnormally regulated in amyotrophic lateral sclerosis. Brain : a journal of neurology\| PubMed ID: 26525917	2016
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
Genetic Variations in ABCA7 Can Increase Secreted Levels of Amyloid-β40 and Amyloid-β42 Peptides and ABCA7 Transcription in Cell Culture Models. Journal of Alzheimer's disease : JAD\| PubMed ID: 27314524	2016
Characterizing familial corticobasal syndrome due to Alzheimer's disease pathology and PSEN1 mutations. Alzheimer's & dementia : the journal of the Alzheimer's Association\| PubMed ID: 27743520	2017
The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration. NPJ genomic medicine\| PubMed ID: 29263818	2016
An APOE-independent cis-eSNP on chromosome 19q13.32 influences tau levels and late-onset Alzheimer's disease risk. Neurobiology of aging\| PubMed ID: 29395286	2018