An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Werling et al. Nature Genetics (2018)
Opposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures
Ben-Shalom et al. Biological Psychiatry (2017)
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Sanders et al. Neuron (2015)
Synaptic, transcriptional and chromatin genes disrupted in autism
De Rubeis et al. Nature (2014)
The contribution of de novo coding mutations to autism spectrum disorder
Iossifov et al. Nature (2014)
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
Sanders et al. Nature (2012)
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Sanders et al. Neuron (2011)
For a full list, please go to Google Scholar or Pubmed.
