Area of research
Pediatrics, Perinatology and Child Health · Psychiatry and Mental health
Research interest
Research interests include Cerebral Palsy and Movement Disorders, Neonatal and fetal brain pathology, Genomics and Rare Diseases, and Infant Development and Preterm Care.
Incidence of Childhood Stroke and Association With Recent Infection: A Population-Based Study Using Linked Data.
Exomes in Paediatrics: Co-Design and Implementation of Interventions to Support Paediatricians to Provide Genomic Care.
Safety and Feasibility of Autologous Cord Blood Infusion for Cerebral Palsy: A Case Report With Ethical and Translational Considerations.
Implementing Publicly Funded Fetal Exome Sequencing: A Statewide Multidisciplinary Model for Equitable Integration of Genomics Into Perinatal Care.
A description and a diagnostic framework: Synergy for practical cerebral palsy diagnosis and care.
KCNQ2 neonatal epilepsy: Impact of prompt diagnosis and treatment, and early predictors of outcome severity.
Effectiveness and tolerability of cannabidiol in paediatric epilepsy: a one-year multisite prospective study
Investigating the impact of severe maternal SARS-CoV-2 infection on infant DNA methylation and neurodevelopment.
Genetic testing in cerebral palsy with clinical and neuroimaging variables.
The Australian Genomics Mitochondrial Flagship: A national program delivering mitochondrial diagnoses.
Pregnancy in women with mitochondrial disease-A literature review and suggested guidance for preconception and pregnancy care.
Paediatric Fever Management Practices and Antipyretic Use Among Doctors and Nurses in Australian Emergency Departments.
Targeted long-read sequencing enables comprehensive analysis of the genetic and epigenetic landscape of inherited myopathies
Australian Emergency Department Doctors and Nurses' Perspectives on the Duration of Persistent Tachycardia in Children
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.
Uncertainties Regarding Cerebral Palsy Diagnosis: Opportunities to Clarify the Consensus Definition.
Clinical Actionability of Genetic Findings in Cerebral Palsy
Kawasaki Disease and Respiratory Viruses: Ecological Spatiotemporal Analysis
Hypotonic cerebral palsy.
Investigating the impact of severe maternal SARS-CoV-2 infection on infant DNA methylation and neurodevelopment
Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.
Redefining cerebral palsies as a diverse group of neurodevelopmental disorders with genetic aetiology.
Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic <i>MRPL39</i> variants as a cause of pediatric onset mitochondrial disease
Developmental regression in children: Current and future directions
Uncertainties regarding cerebral palsy diagnosis: opportunities to operationalize the consensus definition
Safety and efficacy of orally administered full-spectrum medicinal cannabis plant extract 0.08% THC (NTI-164) in children with autism spectrum disorder: An open-label study
Clinical actionability of genetic findings in cerebral palsy
Developmental outcomes for survivors of placental laser photocoagulation for the management of twin-to-twin transfusion syndrome.