Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes by Epi25 Collaborative, Chen, S, Neale, BM, Berkovic, SF, Kariuki, SM, Newton, CRJC

Development of a rapid functional assay that predicts GLUT1 disease severity by Zaman, SM, Mullen, SA, Petrovski, S, Maljevic, S, Gazina, EV, Phillips, AM, Jones, GD, Hildebrand, MS, Damiano, J, Auvin, S, Lerche, H, Weber, YG, Berkovic, SF, Scheffer, IE, Reid, CA, Petrou, S