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Brain : a Journal of Neurology|September 25, 2010
Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritanceDouglas E Crompton, Ingrid E Scheffer, Isabella Taylor, et al.
Neurology|October 19, 2012
PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizuresIngrid E Scheffer, Bronwyn E Grinton, Sarah E Heron, et al.
EMBO Reports|March 27, 2014
A variant of KCC2 from patients with febrile seizures impairs neuronal Cl- extrusion and dendritic spine formationMartin Puskarjov, Patricia Seja, Sarah E Heron, et al.
Annals of Neurology|March 30, 2004
Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathySamuel F Berkovic, Sarah E Heron, Lucio Giordano, et al.
American Journal of Human Genetics|October 26, 2022
A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressureBronwyn E Grinton, Erandee Robertson, Liam G Fearnley, et al.
Brain : a Journal of Neurology|October 6, 2006
Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutationsIngrid E Scheffer, Louise A Harkin, Bronwyn E Grinton, et al.
Epilepsy Research|January 9, 2021
Contribution of rare genetic variants to drug response in absence epilepsyKenneth A Myers, Mark F Bennett, Bronwyn E Grinton, et al.
Epilepsia|April 23, 2004
Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex familiesCarla Marini, Ingrid E Scheffer, Kathryn M Crossland, et al.
Annals of Neurology|August 19, 2023
Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic ArchitectureRebekah V Harris, Karen L Oliver, Piero Perucca, et al.
Neurology|May 26, 2021
Association of SLC32A1 Missense Variants With Genetic Epilepsy With Febrile Seizures PlusSarah E Heron, Brigid M Regan, Rebekah V Harris, et al.
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