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Stessman, H. A. F., Xiong, B., Coe, B. P., Wang, T., Hoekzema, K., Fenckova, M., et al. Turner, T. N., Coe, B. P., Dickel, D. E., Hoekzema, K., Nelson, B. J., Zody, M. C., et al. Stergiakouli, E., Davey Smith, G., Martin, J., Skuse, D. H., Viechtbauer, W., Ring, S. M., et al. Wenger, T. L., Kao, C., McDonald-McGinn, D. M., Zackai, E. H., Bailey, A., Schultz, R. T., et al. Thapar, A., and Cooper, M. (2013). Copy number variation: what’s it and what has it informed us about child psychiatric disorders? J. Am. Obstet Gynecol. 2013 Dec;122(6):1378-82. Baker, Katie (12 December 2013). “‘A Graveyard for Homosexuals’”. Schmunk, G., and Gargus, J. J. (2013). Channelopathy pathogenesis in autism spectrum disorders. Vorstman, J., van Daalen, E., Jalali, G., Schmidt, E., Pasterkamp, R., de Jonge, M., et al. Tyburczy, M. E., Jozwiak, S., Malinowska, I. A., Chekaluk, Y., Pugh, T. J., Wu, C.-L., et al. Stodgell, C. J., Ingram, J. L., O’Bara, M., Tisdale, B. K., Nau, H., and Rodier, P. M. (2006). Induction of the homeotic gene Hoxa1 via valproic acid’s teratogenic mechanism of motion.

Geoff Shupe - Friday the 13t… Sandin, S., Lichtenstein, P., Kuja-Halkola, R., Larsson, H., Hultman, C. M., and Reichenberg, A. (2014). The familial risk of autism. Strømme, P., Mangelsdorf, M. E., Scheffer, I. E., and Gécz, J. (2002). Infantile spasms, dystonia, and other X-linked phenotypes attributable to mutations in Aristaless associated homeobox gene, ARX. Szafranski, P., Schaaf, C. P., Person, R. E., Gibson, I. B., Xia, Z., Mahadevan, S., et al. Schwarz, E., Guest, P. C., Rahmoune, H., Wang, L., Levin, Y., Ingudomnukul, E., et al. Wang, W., Corominas, R., and Lin, G. N. (2019). De novo mutations from entire exome sequencing in neurodevelopmental and psychiatric disorders: from discovery to utility. The Autism Genome Project Consortium, P., Paterson, A. D., Zwaigenbaum, L., Roberts, W., Brian, J., et al. Sun, W., Poschmann, J., Cruz-Herrera del Rosario, R., Parikshak, N. N., Hajan, H. S., Kumar, V., et al. Talebizadeh, Z., Bittel, D., Miles, J., Takahashi, N., Wang, C., Kibiryeva, N., et al. Wang, C.-C., Lin, H.-C., Chan, Y.-H., Gean, P.-W., Yang, Y. K., and Chen, P. S. (2013). 5-HT1A-receptor agonist modified amygdala exercise and amygdala-associated social conduct in a valproate-induced rat autism mannequin. Werling, D. M., and Geschwind, D. H. (2013). Sex differences in autism spectrum disorders.

Short, P. J., McRae, J. F., Gallone, G., Sifrim, A., Won, H., Geschwind, D. H., et al. Sullivan, P. F., Magnusson, C., Reichenberg, A., Boman, M., Dalman, C., Davidson, M., et al. Shao, Y., Cuccaro, M. L., Hauser, E. R., Raiford, K. L., Menold, M. M., Wolpert, C. M., et al. Sarachana, T., Xu, M., Wu, R.-C., and Hu, V. W. (2011). Sex hormones in autism: androgens and estrogens differentially and reciprocally regulate RORA, a novel candidate gene for autism. 2011). A double hit implicates DIAPH3 as an autism danger gene. Smith, S. E. P., Zhou, Y.-D., Zhang, G., Jin, Z., Stoppel, D. C., and Anderson, M. P. (2011). Increased gene dosage of ube3a ends in autism traits and decreased glutamate synaptic transmission in mice. 2011). Sex-specific serum biomarker patterns in adults with Asperger’s syndrome. 2017). Association of the missense variant p.Arg203Trp in PACS1 as a trigger of intellectual disability and seizures. 2017). Targeted sequencing identifies 91 neurodevelopmental disorder threat genes with autism and developmental incapacity biases.

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