Fry, A., Fawcett, K., Zelnik, N., Yuan, H., Thompson, B., Shemer-Meiri, L., … Pilz, D. (2018). De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain : A Journal of Neurology. https://doi.org/10.1093/brain/awx358 (Original work published 2018)

Vlaskamp, D., Shaw, B., Burgess, R., Mei, D., Montomoli, M., Xie, H., … Scheffer, I. (2019). <i>SYNGAP1</i> encephalopathy: A distinctive generalized developmental and epileptic encephalopathy. Neurology, 92(2), e96-e107. https://doi.org/10.1212/WNL.0000000000006729 (Original work published 2019)