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Preview	Issue Date	Title	Author(s)
	2008	Gene expression analysis in absence epilepsy using a monozygotic twin design	Helbig, I.; Matigian, N.; Vadlamudi, L.; Lawrence, K.; Bayly, M.; Bain, S.; Diyagama, D.; Scheffer, I.; Mulley, J.; Holloway, A.; Berkovic, S.; Hayward, N.
	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.
	2014	Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations	Scheffer, I.; Heron, S.; Regan, B.; Mandelstam, S.; Crompton, D.; Hodgson, B.; Licchetta, L.; Provini, F.; Bisulli, F.; Vadlamudi, L.; Gecz, J.; Connelly, A.; Tinuper, P.; Ricos, M.; Berkovic, S.; Dibbens, L.
	2007	Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines	McRae, A.; Matigian, N.; Vadlamudi, L.; Mulley, J.; Mowry, B.; Martin, N.; Berkovic, S.; Hayward, N.; Visscher, P.
	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.
	2010	Timing of de novo mutagenesis - A twin study of sodium-channel mutations	Vadlamudi, L.; Dibbens, L.; Lawrence, K.; Iona, X.; McMahon, J.; Murrell, W.; Mackay-Sim, A.; Scheffer, I.; Berkovic, S.

Showing results 2 to 7 of 7 < previous