Mario Masellis

Division of Neurology, University of Toronto

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 41	2018

Other Publications

Article	Year
Absence of linkage for schizophrenia on the short arm of chromosome 5 in multiplex Canadian families. American journal of medical genetics\| PubMed ID: 9342193	1997
Psychiatric pharmacogenetics: personalizing psychostimulant therapy in attention-deficit/hyperactivity disorder. Behavioural brain research\| PubMed ID: 11864722	2002
Combining bupropion SR with venlafaxine, paroxetine, or fluoxetine: a preliminary report on pharmacokinetic, therapeutic, and sexual dysfunction effects. The Journal of clinical psychiatry\| PubMed ID: 11926715	2002
Pharmacogenomics in schizophrenia: the quest for individualized therapy. Human molecular genetics\| PubMed ID: 12351588	2002
Quality of life in OCD: differential impact of obsessions, compulsions, and depression comorbidity. Canadian journal of psychiatry. Revue canadienne de psychiatrie\| PubMed ID: 12655903	2003
Polymorphisms in glutamate decarboxylase genes: analysis in schizophrenia. Psychiatric genetics\| PubMed ID: 15091314	2004
The dopamine-4 receptor gene associated with binge eating and weight gain in women with seasonal affective disorder: an evolutionary perspective. Biological psychiatry\| PubMed ID: 15522250	2004
A birth-season/DRD4 gene interaction predicts weight gain and obesity in women with seasonal affective disorder: A seasonal thrifty phenotype hypothesis. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology\| PubMed ID: 16760922	2006
Novel 5-HTTLPR allele associates with higher serotonin transporter binding in putamen: a [(11)C] DASB positron emission tomography study. Biological psychiatry\| PubMed ID: 17210141	2007
Cholinesterase inhibitors in Alzheimer's disease and Lewy body spectrum disorders: the emerging pharmacogenetic story. Human genomics\| PubMed ID: 20038497	2009
Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN). Journal of Alzheimer's disease : JAD\| PubMed ID: 20930269	2010
Open-label study of the short-term effects of memantine on FDG-PET in frontotemporal dementia. Neuropsychiatric disease and treatment\| PubMed ID: 21792308	2011
Forward Look: Tenth Anniversary of the Human Genome Sequence and 21 Century Postgenomics Global Health - A Close Up on Africa and Women's Health. Current pharmacogenomics and personalized medicine\| PubMed ID: 22279516	2011
Ethical and Policy Considerations in the Application of Pharmacogenomic Testing for Tardive Dyskinesia: Case Study of the Dopamine D3 Receptor. Current pharmacogenomics and personalized medicine\| PubMed ID: 22282718	2011
End of the Beginning and Public Health Pharmacogenomics: Knowledge in 'Mode 2' and P5 Medicine. Current pharmacogenomics and personalized medicine\| PubMed ID: 22545073	2012
Fluorodeoxyglucose positron emission tomography in semantic dementia after 6 months of memantine: an open-label pilot study. International journal of geriatric psychiatry\| PubMed ID: 22674572	2013
Modulation of the default-mode network between rest and task in Alzheimer's Disease. Cerebral cortex (New York, N.Y. : 1991)\| PubMed ID: 22693345	2013
Investigation of C9orf72 in 4 Neurodegenerative Disorders. Archives of neurology\| PubMed ID: 22964832	2012
Clinical, imaging, and pathological heterogeneity of the Alzheimer's disease syndrome. Alzheimer's research & therapy\| PubMed ID: 23302773	2013
Public Health Pharmacogenomics and the Design Principles for Global Public Goods - Moving Genomics to Responsible Innovation. Current pharmacogenomics and personalized medicine\| PubMed ID: 23531886	2013
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies. JAMA neurology\| PubMed ID: 23588557	2013
Developing physician consensus on the reporting of patients with mild cognitive impairment and mild dementia to transportation authorities in a region with mandatory reporting legislation. The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry\| PubMed ID: 24406250	2014
Early-onset dementias: diagnostic and etiological considerations. Alzheimer's research & therapy\| PubMed ID: 24565469	2013
Fluid biomarkers for diagnosing dementia: rationale and the Canadian Consensus on Diagnosis and Treatment of Dementia recommendations for Canadian physicians. Alzheimer's research & therapy\| PubMed ID: 24565514	2013
Taking the Kidney Personally: The Quest for Novel Antigens of Idiopathic Membranous Nephropathy through Proteomic Approaches -? Current pharmacogenomics and personalized medicine\| PubMed ID: 24795785	2013
Differentiating between visual hallucination-free dementia with Lewy bodies and corticobasal syndrome on the basis of neuropsychology and perfusion single-photon emission computed tomography... Alzheimer's research & therapy\| PubMed ID: 25484929	2014
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis. The Lancet. Neurology\| PubMed ID: 25662776	2015
White matter hyperintensity burden in elderly cohort studies: The Sunnybrook Dementia Study, Alzheimer's Disease Neuroimaging Initiative, and Three-City Study. Alzheimer's & dementia : the journal of the Alzheimer's Association\| PubMed ID: 26208292	2016
DRD2 and SLC6A3 moderate impact of maternal depressive symptoms on infant cortisol. Psychoneuroendocrinology\| PubMed ID: 26342565	2015
Physiological fluctuations in white matter are increased in Alzheimer's disease and correlate with neuroimaging and cognitive biomarkers. Neurobiology of aging\| PubMed ID: 26476600	2016
Attenuation of functional hyperemia to visual stimulation in mild Alzheimer's disease and its sensitivity to cholinesterase inhibition. Biochimica et biophysica acta\| PubMed ID: 26521151	2016
Orthostatic hypotension, cerebral hypoperfusion, and visuospatial deficits in Lewy body disorders. Parkinsonism & related disorders\| PubMed ID: 26639982	2016
Summary cortisol reactivity indicators: Interrelations and meaning. Neurobiology of stress\| PubMed ID: 26844238	2015
MATERNAL SELF-REPORTED DEPRESSIVE SYMPTOMS AND MATERNAL CORTISOL LEVELS INTERACT TO PREDICT INFANT CORTISOL LEVELS. Infant mental health journal\| PubMed ID: 26939829	2016
Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis. PloS one\| PubMed ID: 27100392	2016
Dopamine D2 receptor gene variants and response to rasagiline in early Parkinson's disease: a pharmacogenetic study. Brain : a journal of neurology\| PubMed ID: 27190009	2016
Neurogenic orthostatic hypotension and supine hypertension in Parkinson's disease and related synucleinopathies: prioritisation of treatment targets. The Lancet. Neurology\| PubMed ID: 27478953	2016
'Under pressure': is there a link between orthostatic hypotension and cognitive impairment in α-synucleinopathies? Journal of neurology, neurosurgery, and psychiatry\| PubMed ID: 27613160	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
Lack of Frank Agrammatism in the Nonfluent Agrammatic Variant of Primary Progressive Aphasia. Dementia and geriatric cognitive disorders extra\| PubMed ID: 27790240	2016
The spatial coefficient of variation in arterial spin labeling cerebral blood flow images. Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism\| PubMed ID: 28058975	2017
Small vessel disease is linked to disrupted structural network covariance in Alzheimer's disease. Alzheimer's & dementia : the journal of the Alzheimer's Association\| PubMed ID: 28137552	2017
Molecular imaging to track Parkinson's disease and atypical parkinsonisms: New imaging frontiers. Movement disorders : official journal of the Movement Disorder Society\| PubMed ID: 28150432	2017
Imaging biomarkers in Parkinson's disease and Parkinsonian syndromes: current and emerging concepts. Translational neurodegeneration\| PubMed ID: 28360997	2017
Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's disease. Brain : a journal of neurology\| PubMed ID: 28369257	2017
The role of high-field magnetic resonance imaging in parkinsonian disorders: Pushing the boundaries forward. Movement disorders : official journal of the Movement Disorder Society\| PubMed ID: 28370449	2017
Development of cognitive screening test for the severely hearing impaired: Hearing-impaired MoCA. The Laryngoscope\| PubMed ID: 28409842	2017
Collagenosis of the Deep Medullary Veins: An Underrecognized Pathologic Correlate of White Matter Hyperintensities and Periventricular Infarction? Journal of neuropathology and experimental neurology\| PubMed ID: 28431180	2017
Comparison of arterial spin labeling registration strategies in the multi-center GENetic frontotemporal dementia initiative (GENFI). Journal of magnetic resonance imaging : JMRI\| PubMed ID: 28480617	2018
White matter hyperintensities are seen only inmutation carriers in the GENFI cohort. NeuroImage. Clinical\| PubMed ID: 28529873	2017
Heritability of hippocampal subfield volumes using a twin and non-twin siblings design. Human brain mapping\| PubMed ID: 28561418	2017
Motor Phenotype in Neurodegenerative Disorders: Gait and Balance Platform Study Design Protocol for the Ontario Neurodegenerative Research Initiative (ONDRI). Journal of Alzheimer's disease : JAD\| PubMed ID: 28671116	2017
Enhancement of automated blood flow estimates (ENABLE) from arterial spin-labeled MRI. Journal of magnetic resonance imaging : JMRI\| PubMed ID: 28681479	2018
Peripheral lipid oxidative stress markers are related to vascular risk factors and subcortical small vessel disease. Neurobiology of aging\| PubMed ID: 28756941	2017
Dopamine receptor D2 (DRD2), dopamine transporter solute carrier family C6, member 4 (SLC6A3), and catechol-O-methyltransferase (COMT) genes as moderators of the relation between maternal hi... Development and psychopathology\| PubMed ID: 28803562	2017
Maternal DRD2, SLC6A3, and OXTR genotypes as potential moderators of the relation between maternal history of care and maternal cortisol secretion in the context of mother-infant separation. Biological psychology\| PubMed ID: 28890000	2017
Deconstructing normal pressure hydrocephalus: Ventriculomegaly as early sign of neurodegeneration. Annals of neurology\| PubMed ID: 28892572	2017
Sex differences in the prevalence of genetic mutations in FTD and ALS: A meta-analysis. Neurology\| PubMed ID: 28916533	2017
Unraveling PINK1 regulation: Ubiquitination of its mature form and insights for Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society\| PubMed ID: 28976028	2017
Disinhibition in Alzheimer's Disease is Associated with Reduced Right Frontal Pole Cortical Thickness. Journal of Alzheimer's disease : JAD\| PubMed ID: 28984590	2017
Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study. Neurobiology of aging\| PubMed ID: 29146050	2018
Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study. Neurobiology of aging\| PubMed ID: 29172163	2018
The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration. NPJ genomic medicine\| PubMed ID: 29263818	2016
Comment: Unraveling DNA sequence to identify cerebral indicators of dementia risk. Neurology\| PubMed ID: 29282334	2018
Downregulation of exosomal miR-204-5p and miR-632 as a biomarker for FTD: a GENFI study. Journal of neurology, neurosurgery, and psychiatry\| PubMed ID: 29434051	2018