Ting JT, Feng G. Unfolding neurodevelopmental disorders: found in translation. Nat Med. 2011;17(11):1352-3. doi:10.1038/nm.2553.

Leonenko G, Richards AL, Walters JT, et al. Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia. Am J Med Genet B Neuropsychiatr Genet. 2017;174(7):724-731. doi:10.1002/ajmg.b.32560.

Genereux DP, Laird CD. At what rate do new premutation alleles arise at the fragile X locus?. Hum Genet. 2013;132(6):715-7. doi:10.1007/s00439-013-1291-6.

Jones KJ, Templet S, Zemoura K, et al. Rapid, experience-dependent translation of neurogranin enables memory encoding. Proc Natl Acad Sci U S A. 2018;115(25):E5805-E5814. doi:10.1073/pnas.1716750115.

Purcell SM, Moran JL, Fromer M, et al. A polygenic burden of rare disruptive mutations in schizophrenia. Nature. 2014;506(7487):185-90. doi:10.1038/nature12975.

Fromer M, Pocklington AJ, Kavanagh DH, et al. De novo mutations in schizophrenia implicate synaptic networks. Nature. 2014;506(7487):179-84. doi:10.1038/nature12929.

Wright J. Genetics: Unravelling complexity. Nature. 2014;508(7494):S6-7. doi:10.1038/508S6a.