De novo mutations revealed by whole-exome sequencing are strongly associated with autism
Nature2012Vol. 485(7397), pp. 237–241
Citations Over TimeTop 1% of 2012 papers
Stephan Sanders, Michael T. Murtha, Abha R. Gupta, John D. Murdoch, Melanie J. Raubeson, A. Jeremy Willsey, A. Gulhan Ercan‐Sencicek, Nicholas M. DiLullo, Neelroop Parikshak, Jason L. Stein, Michael F. Walker, G Ober, Nicole A. Teran, Youeun Song, Paul El-Fishawy, Ryan Murtha, Murim Choi, John D. Overton, Robert Bjornson, Nicholas Carriero, Kyle A. Meyer, Kaya Bilgüvar, Shrikant Mane, Nenad Šestan, Richard P. Lifton, Murat Günel, Kathryn Roeder, Daniel H. Geschwind, Bernie Devlin, Matthew W. State
Related Papers
- → Whole exome sequencing of families with 1q21.1 microdeletion or microduplication(2017)45 cited
- → Rare copy number variants are common in young children with autism spectrum disorder(2015)23 cited
- → A novel nonsense mutation of ZEB2 gene in a Chinese patient with Mowat‐Wilson syndrome(2020)4 cited
- → Molecular Pathways within Autism Spectrum Disorder Endophenotypes(2021)5 cited
- Whole Exome Sequencing Analysis of Individuals with Autism Spectrum Disorder(2016)