-
Mulley, JC, Scheffer, IE, Desai, T, Bayly, MA, Grinton, BE, Vears, DF, Berkovic, SF, Dibbens, LM.
Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes.
Epilepsia
52(10)
:
e139 -e142
2011
view publication
-
Corbett, MA, Schwake, M, Bahlo, M, Dibbens, LM, Lin, M, Gandolfo, LC, Vears, DF, O'Sullivan, JD, Robertson, T, Bayly, MA, et al.
A Mutation in the Golgi Qb-SNARE Gene GOSR2 Causes Progressive Myoclonus Epilepsy with Early Ataxia.
American Journal of Human Genetics
88(5)
:
657 -663
2011
view publication
-
Arsov, T, Smith, KR, Damiano, J, Franceschetti, S, Canafoglia, L, Bromhead, CJ, Andermann, E, Vears, DF, Cossette, P, Rajagopalan, S, et al.
Kufs Disease, the Major Adult Form of Neuronal Ceroid Lipofuscinosis, Caused by Mutations in CLN6.
American Journal of Human Genetics
88(5)
:
566 -573
2011
view publication
-
Crompton, DE, Scheffer, IE, Taylor, I, Cook, MJ, McKelvie, PA, Vears, DF, Lawrence, KM, McMahon, JM, Grinton, BE, McIntosh, AM, et al.
Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance.
Brain
133(11)
:
3221 -3231
2010
view publication
-
Lillywhite, LM, Saling, MM, Harvey, AS, Abbott, DF, Archer, JS, Vears, DF, Scheffer, IE, Jackson, GD.
Neuropsychological and functional MRI studies provide converging evidence of anterior language dysfunction in BECTS.
Epilepsia
50(10)
:
2276 -2284
2009
view publication