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Matthew J. Gazzellone

Observed names: Gazzellone, Matthew, M J Gazzellone, M. J. Gazzellone, M.J. Gazzellone, Matthew Gazzellone, Matthew J Gazzellone
Observed institutions: University Health Network, Centre for Addiction and Mental Health, University of Toronto, Queen's University, Hospital for Sick Children, McKenzie Health, Centre for Applied Genomics, Campbell Family Mental Health Research Institute
OpenAlex ID: A5044967187
Whole-genome sequencing of quartet families with autism spectrum disorder
2015 · Ryan K C Yuen, Bhooma Thiruvahindrapuram, et al. · Nature Medicine · 512
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder
2015 · Kristiina Tammimies, Christian R. Marshall, et al. · JAMA · 418
Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD
2011 · Anath C. Lionel, Jennifer Crosbie, et al. · Science Translational Medicine · 371
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
2013 · A. C. Lionel, K. Tammimies, et al. · Human Molecular Genetics · 163
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Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures
2013 · Anath C. Lionel, Andrea K. Vaags, et al. · Human Molecular Genetics · 162
Clinically relevant copy number variations detected in cerebral palsy
2015 · Maryam Oskoui, Matthew J. Gazzellone, et al. · Nature Communications · 152
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De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy
2017 · Mehdi Zarrei, Darcy L. Fehlings, et al. · Genetics in Medicine · 99
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Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression
2016 · Chelsea Lowther, Marsha Speevak, et al. · Genetics in Medicine · 97
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Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome
2017 · Anne S. Bassett, Chelsea Lowther, et al. · American Journal of Psychiatry · 96
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A high-resolution copy-number variation resource for clinical and population genetics
2014 · Mohammed Uddin, Bhooma Thiruvahindrapuram, et al. · Genetics in Medicine · 80
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Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation
2016 · Matthew J. Gazzellone, Mehdi Zarrei, et al. · Journal of Neurodevelopmental Disorders · 78
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CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
2016 · O Mercati, G Huguet, et al. · Molecular Psychiatry · 78
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Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditions
2016 · Maria Tropeano, Deirdre Howley, et al. · Journal of Medical Genetics · 67
Copy number variation in Han Chinese individuals with autism spectrum disorder
2014 · Matthew J Gazzellone, Xue Zhou, et al. · Journal of Neurodevelopmental Disorders · 59
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Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome
2015 · Daniele Merico, Mehdi Zarrei, et al. · G3 Genes Genomes Genetics · 50
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Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay
2016 · Mohammed Uddin, Giovanna Pellecchia, et al. · Scientific Reports · 44
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Adult neuropsychiatric expression and familial segregation of 2q13 duplications
2014 · Gregory Costain, Anath C. Lionel, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 29
Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity
2018 · Thanuja Selvanayagam, Susan Walker, et al. · European Journal of Human Genetics · 27
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Atypical antipsychotics, dystonia, and psychotic depression: old solutions for new problems
2022 · Matthew J. Gazzellone, Dijana Oliver, et al. · Journal of Psychiatry and Neuroscience · 1
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1352 Treatment Considerations in Co-Morbid Schizophrenia and Narcolepsy: A Case Report
2026 · Mai Malkin, Weam Sieffien, et al. · SLEEP
Treatment Considerations in Co-morbid Schizophrenia and Narcolepsy: A Case Report
2026 · M.S. Mak, M.J. Gazzellone, et al. · Sleep Medicine
Additional file 2: of Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation
2016 · Gazzellone, Matthew, Zarrei, Mehdi, et al. · Figshare
Additional file 4: of Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation
2016 · Gazzellone, Matthew, Zarrei, Mehdi, et al. · Figshare
Additional file 3: of Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation
2016 · Gazzellone, Matthew, Zarrei, Mehdi, et al. · Figshare
Additional file 1: of Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation
2016 · Gazzellone, Matthew, Zarrei, Mehdi, et al. · Figshare
Works count: 28
Citation count: 2,582
H-index: 18
I10-index: 18
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