Kajitani GS, Xavier G, Villena-Rueda BE, Karia BTR, Santoro ML. Extracellular vesicles in neurodegenerative, mental, and other neurological disorders: Perspectives into mechanisms, biomarker potential, and therapeutic implications. Current topics in membranes. 2024;94:299-336. doi:10.1016/bs.ctm.2024.06.002.

Kim S-W, Lee H, Song DY, et al. Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism. Genome medicine. 2024;16(1):114. doi:10.1186/s13073-024-01385-6.

DeSpenza T, Singh A, Allington G, et al. Pathogenic variants in autism gene cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics. Proceedings of the National Academy of Sciences of the United States of America. 2024;121(27):e2314702121. doi:10.1073/pnas.2314702121.

Zhang J, Weissenkampen D, Kember RL, et al. Phenotypic and ancestry-related assortative mating in autism. Molecular autism. 2024;15(1):27. doi:10.1186/s13229-024-00605-5.

McClellan JM, Zoghbi AW, Buxbaum JD, et al. An evolutionary perspective on complex neuropsychiatric disease. Neuron. 2024;112(1):7-24. doi:10.1016/j.neuron.2023.10.037.

Shi X, Lu C, Corman A, et al. Heterozygous deletion of the autism-associated gene CHD8 impairs synaptic function through widespread changes in gene expression and chromatin compaction. American journal of human genetics. 2023;110(10):1750-1768. doi:10.1016/j.ajhg.2023.09.004.

Stefanski A, Pérez-Palma E, Brünger T, et al. SLC6A1 variant pathogenicity, molecular function, and phenotype: a genetic and clinical analysis. Brain : a journal of neurology. 2023. doi:10.1093/brain/awad292.

Kipkemoi P, Kim HA, Christ B, et al. Phenotype and genetic analysis of data collected within the first year of NeuroDev. Neuron. 2023. doi:10.1016/j.neuron.2023.06.010.

Wigdor EM, Weiner DJ, Grove J, et al. The female protective effect against autism spectrum disorder. Cell genomics. 2022;2(6):100134. doi:10.1016/j.xgen.2022.100134.