Matthew J. Gazzellone

Whole-genome sequencing of quartet families with autism spectrum disorder

Ryan K. C. Yuen, Bhooma Thiruvahindrapuram, Daniele Merico et al. · Nature Medicine · 2015 · 540 citations

Sequencing, Syndromic Autism, Next-generation Sequencing +8

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

Kristiina Tammimies, Christian R. Marshall, Susan Walker et al. · JAMA · 2015 · 432 citations

Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD

Anath C. Lionel, Jennifer Crosbie, Nicole Barbosa et al. · Science Translational Medicine · 2011 · 385 citations

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

A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags et al. · Human Molecular Genetics · 2013 · 172 citations · Full text

Astn2/trim32 Locus, Brain Development, Autism Spectrum Disorders +19

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

Anath C. Lionel, Andrea K. Vaags, Daisuke Sato et al. · Human Molecular Genetics · 2013 · 151 citations · Full text