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  • Hamdan, F. F., Daoud, H., Piton, A., Gauthier, J., Dobrzeniecka, S., et al. De novo SYNGAP1 mutations in nonsyndromic intellectual disability and autism. Biological Psychiatry, published online in advance of print.
  • Hamdan, F.F., Gauthier, J., Spiegelman, D., Noreau, A., Yang, Y., et al. (2009). Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation. New England Journal of Medicine, 360, 599605.
  • Pinto, D., Pagnamenta, A.T., Klei, L., Anney, R., Merico, D., et al. (2010). Functional impact of global rare copy number variation in autism spectrum disorders. Nature, 466, 368372.