List of works by Matthew J Gazzellone

Clinically relevant copy number variations detected in cerebral palsy

scientific article

Copy number variation in Han Chinese individuals with autism spectrum disorder

scientific article

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

scientific article

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

scientific article published on 30 December 2013

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

scientific article published on July 2016

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

scientific article published on September 2015

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

scientific article published on 28 July 2017

Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.

scientific article

Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures

scientific article published on 7 February 2013

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

scientific article published on 18 October 2016

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

scientific article

Whole-genome sequencing of quartet families with autism spectrum disorder

scientific article published on 26 January 2015

Paulina is supported by:

About Paulina

Help