Epilepsy is a common disease in the Australian population affecting 3 percent of individuals. It incurs lifelong medical, social and educational costs, and in some cases can be fatal. It is a large burden on public healthcare in Australia. Focal epilepsies are the most common type of seizure that arise from specific parts of the brain. This study has two aims and a future strategy relevant to gene discovery and clinical testing for focal epilepsy.
Vulnerability to cocaine use: discovering common mechanisms conserved across animal phyla. Drug abuse costs Australia an estimated $ 20 billion each year, and research is urgently needed to understand how drugs cause long-term behavioural dysfunction. Our research will identify the basal cellular mechanisms underlying drug abuse and addiction, which are likely to be the best targets for therapies to prevent and cure addiction. Our findings are also relevant to other neuropsychiatric disorders r ....Vulnerability to cocaine use: discovering common mechanisms conserved across animal phyla. Drug abuse costs Australia an estimated $ 20 billion each year, and research is urgently needed to understand how drugs cause long-term behavioural dysfunction. Our research will identify the basal cellular mechanisms underlying drug abuse and addiction, which are likely to be the best targets for therapies to prevent and cure addiction. Our findings are also relevant to other neuropsychiatric disorders related to drug abuse (e.g. depression, anxiety) that are on the increase in Australia. Our work will enhance Australia's reputation for neuroscience research, and will provide training for students in neuropharmacology and molecular neurobiology.Read moreRead less
Unravelling The Genetics Of The Common Epilepsies Using Discordant Monozygotic Twins
Funder
National Health and Medical Research Council
Funding Amount
$673,778.00
Summary
Epilepsy is a common disease in the Australian population affecting 3% of individuals that has a significant genetic contribution. To improve patient care we will study a unique set of identical twins discordant for different types of common genetic epilepsies. Identification of novel genes involved in common epilepsies will provide information relevant to prognosis, recurrence risks and treatment options for patients and their families. It will enhance long established Australian clinical and r ....Epilepsy is a common disease in the Australian population affecting 3% of individuals that has a significant genetic contribution. To improve patient care we will study a unique set of identical twins discordant for different types of common genetic epilepsies. Identification of novel genes involved in common epilepsies will provide information relevant to prognosis, recurrence risks and treatment options for patients and their families. It will enhance long established Australian clinical and research expertise in epilepsy.Read moreRead less
The Clinical Features, Causes And Diagnosis Of Severe Epilepsies Of Infancy: A Population-based Study
Funder
National Health and Medical Research Council
Funding Amount
$227,261.00
Summary
Severe epilepsies of infancy (SEI) are characterised by frequent seizures and are often resistant to treatment. The prognosis is typically poor. The cause is unknown in many infants. This study will identify genes and brain malformations causing SEI, determine the frequency and clinical features of each cause, and measure the diagnostic yield of genetic testing and brain imaging. The findings will improve timely diagnosis of SEI and guide research priorities for development of novel therapies.
I am a developmental neurobiologist interested in finding out how neurons in the brain are assembled and wired together. I am also interested in finding a cure for patients who have brain damage from trauma or stroke by preventing damaged neurons from dea