The Genetic Metabolics Disorders Research Team
> Professor John Christodoulou, Research Team Leader
John is a Clinical Geneticist and a world leading clinician-scientist renowned for his research program investigating the genetics causes of rare childhood diseases. His has a strong track record in research of Rett Syndrome, Phenylketonuria (PKU) and other metabolic diseases. Please visit John's University of Sydney profile page for more information.
> Dr Wendy Gold, Senior Research Fellow, email: Wendy Gold
Wendy's primary research goal is to better understand the molecular genetics of Rett Syndrome and find a way to halt the onset of this disease. More information can be found on Wendy's University of Sydney profile page.
> Dr Lisa Riley, Senior Research Officer, email Lisa Riley
Lisa leads a research program focused on gene discovery and functional characterisation of novel mitochondrial respiratory chain disorders (MRCD). Lisa's University of Sydney profile page has more information about her research.
> Other Research Team Members
- Associate Professor Kevin Carpenter, Dept Head and Principal Scientist, NSW Biochemical Genetics Service
- Dr Naz Al-Hafid, Research Officer, PKU
- Dr Minal Menezes, Research Officer
- Nasim Bahram Sangani, PhD Student