grant

Defining FMR1 and SNRPN epigenetic signatures associated with neurodevelopmental disorders [ 2017 - 2021 ]

Research Grant

[Cite as https://purl.org/au-research/grants/nhmrc/1120561]

Brief description Fragile X Syndrome and imprinting disorders such as Prader-Willi Syndrome and Angelman Syndrome are characterised by variable penetrance for intellectual disability, motor delay and autism spectrum disorder. This project aims to investigate the prognostic value of using blood-based biomarker tests and sensitive neuroscience informed measures to predict risk and severity of neuropsychological problems in children affected by these disorders.

Funding Amount $AUD 326,352.65

Funding Scheme Early Career Fellowships

Notes Peter Doherty Biomedical ECF

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Identifiers
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ACN 633 798 857