Associate Professor Jonathan Payne is co-lead of the Brain & Mind Research Group at the Murdoch Children's Research Institute, where he leads the Genetics and Neurodevelopment Team and sits on the steering committee of the Neurodevelopment Flagship. He is a practicing senior clinical neuropsychologist at the Royal Children's Hospital and an Honorary Principal Research Fellow in the Department of Paediatrics, University of Melbourne.
Associate Professor Payne's research draws on a range of cognitive, behavioural, neuroimaging, and laboratory protocols to understand how genetic variants can affect brain development and increase the risk for neurodevelopmental disorders. He is also an experienced trialist and leads several pharmacological and non-pharmacological clinical trials.
Associate Professor Jonathan Payne is co-lead of the Brain & Mind Research Group at the Murdoch Children's Research Institute, where he leads the Genetics and Neurodevelopment Team and sits on the steering committee of the Neurodevelopment Flagship....
Associate Professor Jonathan Payne is co-lead of the Brain & Mind Research Group at the Murdoch Children's Research Institute, where he leads the Genetics and Neurodevelopment Team and sits on the steering committee of the Neurodevelopment Flagship. He is a practicing senior clinical neuropsychologist at the Royal Children's Hospital and an Honorary Principal Research Fellow in the Department of Paediatrics, University of Melbourne.
Associate Professor Payne's research draws on a range of cognitive, behavioural, neuroimaging, and laboratory protocols to understand how genetic variants can affect brain development and increase the risk for neurodevelopmental disorders. He is also an experienced trialist and leads several pharmacological and non-pharmacological clinical trials.
Top Publications
Payne, JM.
Bridging the Gap Between Mouse Behavior and Human Cognition in Neurofibromatosis Type 1..
EBioMedicine
2(10)
:
1290 -1291
2015
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Summers, MA, Quinlan, KG, Payne, JM, Little, DG, North, KN, Schindeler, A.
Skeletal muscle and motor deficits in Neurofibromatosis Type 1..
J Musculoskelet Neuronal Interact
15(2)
:
161 -170
2015
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Champion, JA, Rose, KJ, Payne, JM, Burns, J, North, KN.
Relationship between cognitive dysfunction, gait, and motor impairment in children and adolescents with neurofibromatosis type 1..
Dev Med Child Neurol
56(5)
:
468 -474
2014
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Pride, NA, Korgaonkar, MS, Barton, B, Payne, JM, Vucic, S, North, KN.
The genetic and neuroanatomical basis of social dysfunction: lessons from neurofibromatosis type 1..
Hum Brain Mapp
35(5)
:
2372 -2382
2014
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Payne, JM, Pickering, T, Porter, M, Oates, EC, Walia, N, Prelog, K, North, KN.
Longitudinal assessment of cognition and T2-hyperintensities in NF1: an 18-year study..
Am J Med Genet A
164A(3)
:
661 -665
2014
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