Matthew J. Gazzellone

Toronto, ON, Canada

Last Updated: 09/26/2026

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Found 18 publications

Atypical antipsychotics, dystonia, and psychotic depression: old solutions for new problems.

Atypical antipsychotics, dystonia, and psychotic depression: old solutions for new problems.

Journal: Journal of psychiatry & neuroscience : JPN

Published: May 04, 2022

Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity.

Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity.

Journal: European journal of human genetics : EJHG

Published: August 21, 2017

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.

Journal: The American journal of psychiatry

Published: July 29, 2017

De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy.

De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 23, 2016

Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.

Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.

Journal: Journal of neurodevelopmental disorders

Published: February 29, 2016

Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay.

Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay.

Journal: Scientific reports

Published: January 12, 2016

Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.

Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: January 05, 2016

Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditions.

Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditions.

Journal: Journal of medical genetics

Published: November 04, 2015

Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome.

Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome.

Journal: G3 (Bethesda, Md.)

Published: September 19, 2015

Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder.

Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder.

Journal: JAMA

Published: September 02, 2015

CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders.

CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders.

Journal: Molecular psychiatry

Published: August 18, 2015

Clinically relevant copy number variations detected in cerebral palsy.

Clinically relevant copy number variations detected in cerebral palsy.

Journal: Nature communications

Published: June 07, 2015

Showing 1-12 of 18

Last Updated: 09/26/2026