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Preview	Issue Date	Title	Author(s)
	2014	Genetics of epilepsy: the testimony of twins in the molecular era	Vadlamudi, L.; Milne, R.; Lawrence, K.; Heron, S.; Eckhaus, J.; Keay, D.; Connellan, M.; Torn-Broers, Y.; Howell, R.; Mulley, J.; Scheffer, I.; Dibbens, L.; Hopper, J.; Berkovic, S.
	2013	Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome	Mulley, J.; Hodgson, B.; McMahon, J.; Iona, X.; Bellows, S.; Mullen, S.; Farrell, K.; Mackay, M.; Sadleir, L.; Bleasel, A.; Gill, D.; Webster, R.; Wirrell, E.; Harbord, M.; Sisodiya, S.; Andermann, E.; Kivity, S.; Berkovic, S.; Scheffer, I.; Dibbens, L.
	2012	Rare protein sequence variation in SV2A gene does not affect response to levetiracetam	Dibbens, L.; Hodgson, B.; Helbig, K.; Oliver, K.; Mulley, J.; Berkovic, S.; Scheffer, I.
	2010	Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study	McIntosh, A.; McMahon, J.; Dibbens, L.; Iona, X.; Mulley, J.; Scheffer, I.; Berkovic, S.
	2012	Familial focal epilepsy with variable foci mapped to chromosome 22q12: Expansion of the phenotypic spectrum	Klein, K.; O'Brien, T.; Praveen, K.; Heron, S.; Mulley, J.; Foote, S.; Berkovic, S.; Scheffer, I.
	2010	Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3	Heron, S.; Scheffer, I.; Grinton, B.; Eyre, H.; Oliver, K.; Bain, S.; Berkovic, S.; Mulley, J.
	2011	Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes	Mulley, J.; Scheffer, I.; Desai, T.; Bayly, M.; Grinton, B.; Vears, D.; Berkovic, S.; Dibbens, L.
	2010	Neonatal seizures and Long QT Syndrome: A cardiocerebral channelopathy?	Heron, S.; Hernandez, M.; Edwards, C.; Edkins, E.; Jansen, F.; Scheffer, I.; Berkovic, S.; Mulley, J.
	2010	De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin	Heron, S.; Scheffer, I.; Iona, X.; Zuberi, S.; Birch, R.; McMahon, J.; Bruce, C.; Berkovic, S.; Mulley, J.
	2011	De novo SCN1A mutations in migrating partial seizures of infancy	Carranza Rojo, D.; Hamiwka, L.; McMahon, J.; Dibbens, L.; Arsov, T.; Suls, A.; Stodberg, T.; Kelley, K.; Wirrell, E.; Appleton, B.; Mackay, M.; Freeman, J.; Yendle, S.; Berkovic, S.; Bienvenu, T.; De Jonghe, P.; Thorburn, D.; Mulley, J.; Mefford, H.; Scheffer, I.