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Preview	Issue Date	Title	Author(s)
	2002	Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome	Lower, K.; Turner, G.; Kerr, B.; Mathews, K.; Shaw, M.; Gedeon, A.; Schelley, S.; Hoyme, H.; White, S.; Delatycki, M.; Lampe, A.; Clayton-Smith, J.; Stewart, H.; van Ravenswaay, C.; de Vries, B.; Cox, B.; Grompe, M.; Ross, S.; Thomas, P.; Mulley, J.; et al.
	2002	Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy	Stromme, P.; Mangelsdorf, M.; Shaw, M.; Lower, K.; Lewis, S.; Bruyere, H.; Lutcherath, V.; Gedeon, A.; Wallace, R.; Scheffer, I.; Turner, G.; Partington, M.; Frints, S.; Fryns, J.; Sutherland, G.; Mulley, J.; Gecz, J.
	2007	A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channel	Xu, R.; Thomas, E.; Jenkins, M.; Gazina, E.; Chiu, C.; Heron, S.; Mulley, J.; Scheffer, I.; Berkovic, S.; Petrou, S.
	2007	Association studies and functional validation or functional validation alone?	Heron, S.; Sanchez, L.; Scheffer, I.; Berkovic, S.; Mulley, J.
	2007	Channelopathies in idiopathic epilepsy	Heron, S.; Scheffer, I.; Berkovic, S.; Dibbens, L.; Mulley, J.
	2007	Is photosensitive epilepsy less common in males due to variation in X chromosome photopigment genes?	Taylor, I.; Hodgson, B.; Scheffer, I.; Mulley, J.; Berkovic, S.; Dibbens, L.
	2005	Is variation in the GABA(B) receptor 1 gene associated with temporal lobe epilepsy ?	Tan, N.; Heron, S.; Scheffer, I.; Berkovic, S.; Mulley, J.
	2007	SCN2A mutations and benign familial neonatal-infantile seizures: The phenotypic spectrum	Herlenius, E.; Heron, S.; Grinton, B.; Keay, D.; Scheffer, I.; Mulley, J.; Berkovic, S.
	2007	A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy	Cavalleri, G.; Walley, N.; Soranzo, N.; Mulley, J.; Doherty, C.; Kapoor, A.; Depondt, C.; Lynch, J.; Scheffer, I.; Heils, A.; Gehrmann, A.; Kinirons, P.; Gandhi, S.; Satishchandra, P.; Wood, N.; Anand, A.; Sander, T.; Berkovic, S.; Delanty, N.; Goldstein, D.; et al.
	2006	Severe myoclonic epilepsy of infancy (Dravet syndrome): Recognition and diagnosis in adults	Jansen, F.; Sadleir, L.; Harkin, L.; Vadlamudi, L.; McMahon, J.; Mulley, J.; Scheffer, I.; Berkovic, S.