Michael F. Walker

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

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

Donna M. Werling, Harrison Brand, Joon‐Yong An et al. · Nature Genetics · 2018 · 335 citations · Full text

Genome-wide Association Study, Syndromic Autism, Genetics +8

Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons

Karina Griesi‐Oliveira, Allan Acab, Arpana Gupta et al. · Molecular Psychiatry · 2014 · 246 citations · Full text

Neurodevelopmental Disorders, Human Neurons, Molecular Neuroscience +12