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Outcome assessment in a statewide screening cohort with genetically linked intellectual disability

Description 
This project aims to assess outcomes in a statewide screening cohort by examining conditions genetically linked to intellectual disability. It seeks to determine how these conditions can be identified as part of the comprehensive Victorian newborn screening program. It will assess how early detection through screening impacts long-term outcomes across the lifespan.
Essential criteria: 
Minimum entry requirements can be found here: https://www.monash.edu/admissions/entry-requirements/minimum
Keywords 
Newborn screening; Intellectual disability; Fragile X syndrome ; Prader-Willi syndrome, Systematic Reviews; Meta-analysis; Evidence synthesis
School 
School of Clinical Sciences at Monash Health / Hudson Institute of Medical Research » Paediatrics
Available options 
PhD/Doctorate
Masters by research
Honours
BMedSc(Hons)
Time commitment 
Full-time
Part-time
Top-up scholarship funding available 
No
Physical location 
Monash Children's Hospital
Co-supervisors 
Prof 
Katrina Williams
Assoc Prof 
David Godler
(External)

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