Khalil R, Kenny C, Hill S, et al. PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features. Am J Med Genet B Neuropsychiatr Genet. 2018;177(8):736-745. doi:10.1002/ajmg.b.32688
O’Connor LJ, Price AL. Distinguishing genetic correlation from causation across 52 diseases and complex traits. Nat Genet. 2018;50(12):1728-1734. doi:10.1038/s41588-018-0255-0
Jabbari K, Bobbili DR, Lal D, et al. Rare gene deletions in genetic generalized and Rolandic epilepsies. PLoS One. 2018;13(8):e0202022. doi:10.1371/journal.pone.0202022
Peça J, Feng G. Cellular and synaptic network defects in autism. Curr Opin Neurobiol. 2012;22(5):866-72. doi:10.1016/j.conb.2012.02.015
Gogolla N, Takesian AE, Feng G, Fagiolini M, Hensch TK. Sensory integration in mouse insular cortex reflects GABA circuit maturation. Neuron. 2014;83(4):894-905. doi:10.1016/j.neuron.2014.06.033
Peça J, Ting J, Feng G. SnapShot: Autism and the synapse. Cell. 2011;147(3):706, 706.e1. doi:10.1016/j.cell.2011.10.015
Peça J, Feliciano C, Ting JT, et al. Shank3 mutant mice display autistic-like behaviours and striatal dysfunction. Nature. 2011;472(7344):437-42. doi:10.1038/nature09965
Salter MW, Stevens B. Microglia emerge as central players in brain disease. Nat Med. 2017;23(9):1018-1027. doi:10.1038/nm.4397
Liu S, Rao S, Xu Y, et al. Identifying common genome-wide risk genes for major psychiatric traits. Hum Genet. 2020;139(2):185-198. doi:10.1007/s00439-019-02096-4
Tatavarty V, Pacheco AT, Kuhnle CG, et al. Autism-Associated Shank3 Is Essential for Homeostatic Compensation in Rodent V1. Neuron. 2020;106(5):769-777.e4. doi:10.1016/j.neuron.2020.02.033