I aim to understand the genetics of the epilepsies. Through detailed analysis of different types of epilepsy, and associated features such as intellectual disability and autism, I will describe new epilepsy syndromes, and together with gene discovery, implement novel targeted therapies. This translational program will transform clinical practice by informing diagnosis, prognostic and genetic counseling, and lead to targeted precision therapies to improve outcomes for each patient.
I am a clinician researcher in paediatric emergency medicine. My research focus is acute neurological problems and includes both high volume and rare but life threatening conditions in children. Award of an NHMRC Practitioner Fellowship will allow me to address major evidence gaps in the acute care of children presenting to the emergency department with head injuries and brain attacks (acute neurological dysfunction), and to translate the findings into widespread practice.