Matthew W. State

The contribution of de novo coding mutations to autism spectrum disorder

Ivan Iossifov, Brian J. O’Roak, Stephan Sanders et al. · Nature · 2014 · 2.7K citations · Full text

Neurodevelopmental Disorders, Spectrum Disorder, Syndromic Autism +8

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

Stephan Sanders, Michael T. Murtha, Abha R. Gupta et al. · Nature · 2012 · 2.1K citations

Neurodevelopmental Disorders, Syndromic Autism, Whole-exome Sequencing +9

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

Stephan Sanders, Xin He, A. Jeremy Willsey et al. · Neuron · 2015 · 1.5K citations · Full text

Genome-wide Association Study, Syndromic Autism, Genetics +6

Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder

Michael J. Gandal, Pan Zhang, Evi Hadjimichael et al. · Science · 2018 · 1.3K citations · Full text

Psychiatric Disorders, Genetics, Genetic Epidemiology +22

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus et al. · Neuron · 2011 · 1.3K citations · Full text

Neurodevelopmental Disorders, Williams Syndrome Region, Syndromic Autism +10