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.32688PubMedDOIGoogle Scholar
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/s41588-018-0255-0PubMedDOIGoogle Scholar
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.0202022PubMedDOIGoogle Scholar
Peça J, Ting J, Feng G. SnapShot: Autism and the synapse. Cell. 2011;147(3):706, 706.e1. doi:10.1016/j.cell.2011.10.015PubMedDOIGoogle Scholar
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/nature09965PubMedDOIGoogle Scholar
Salter MW, Stevens B. Microglia emerge as central players in brain disease. Nat Med. 2017;23(9):1018-1027. doi:10.1038/nm.4397PubMedDOIGoogle Scholar
Balasubramanian S, Fu Y, Pawashe M, et al. Using ALoFT to determine the impact of putative loss-of-function variants in protein-coding genes. Nat Commun. 2017;8(1):382. doi:10.1038/s41467-017-00443-5PubMedDOIGoogle Scholar
Escamilla CO, Filonova I, Walker AK, et al. Kctd13 deletion reduces synaptic transmission via increased RhoA. Nature. 2017;551(7679):227-231. doi:10.1038/nature24470PubMedDOIGoogle Scholar
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/s00439-019-02096-4PubMedDOIGoogle Scholar
Guissart C, Latypova X, Rollier P, et al. Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia. Am J Hum Genet. 2018;102(5):744-759. doi:10.1016/j.ajhg.2018.02.021PubMedDOIGoogle Scholar