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PreviewIssue DateTitleAuthor(s)
2002Generalized epilepsy with febrile seizures plus: Mutation of the sodium channel subunit SCN1BWallace, R.; Scheffer, I.; Parasivam, G.; Barnett, S.; Wallace, G.; Sutherland, G.; Berkovic, S.; Mulley, J.
1995A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsySteinlein, O.; Mulley, J.; Propping, P.; Wallace, R.; Phillips, H.; Sutherland, G.; Scheffer, I.; Berkovic, S.
1996Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21Wallace, R.; Berkovic, S.; Howell, R.; Sutherland, G.; Mulley, J.
1997FMR2 expression in families with FRAXE mental retardationGecz, J.; Oostra, B.; Hockey, A.; Carbonell, P.; Turner, G.; Haan, E.; Sutherland, G.; Mulley, J.
1995Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to 20q13.2Phillips, H.; Scheffer, I.; Berkovic, S.; Hollway, G.; Sutherland, G.; Mulley, J.
2004GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsiesDibbens, L.; Feng, H.; Richards, M.; Harkin, L.; Hodgson, B.; Scott, D.; Jenkins, M.; Petrou, S.; Sutherland, G.; Scheffer, I.; Berkovic, S.; Mcdonald, R.; Mulley, J.
1996FRAGILE X SYNDROME AND FRAGILE XE MENTAL RETARDATION [Review]Sutherland, G.; Mulley, J.
2007NEDD4-2 as a potential candidate susceptibility gene for epileptic photosensitivityDibbens, L.; Ekberg, J.; Taylor, I.; Hodgson, B.; Conroy, S.; Lensink, I.; Kumar, S.; Zielinski, M.; Harkin, L.; Sutherland, G.; Adams, D.; Berkovic, S.; Scheffer, I.; Mulley, J.; Poronnik, P.

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