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Dr Ramesh Narayanan
Lecturer (Education)
School of Medical Sciences
Faculty of Medicine and Health
School of Medical Sciences
Faculty of Medicine and Health
Publications
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Journals
- Fellner, A., Wali, G., Mahant, N., Grosz, B., Ellis, M., Narayanan, R., Ng, K., Davis, R., Tchan, M., Kotschet, K., et al (2024). Genome sequencing reanalysis increases the diagnostic yield in dystonia. Parkinsonism and Related Disorders, 124. [More Information]
- Hunt, N., Lockwood, G., Heffernan, S., Daymond, J., Ngu, M., Narayanan, R., Westwood, L., Mohanty, B., Esser, L., Williams, C., Kuncic, Z., McCourt, P., Le Couteur, D., Cogger, V. (2024). Oral nanotherapeutic formulation of insulin with reduced episodes of hypoglycaemia. Nature Nanotechnology, 19(4), 534-544. [More Information]
- Cutrupi, A., Narayanan, R., Perez-Siles, G., Grosz, B., Lai, K., Boyling, A., Ellis, M., Lin, R., Neumann, B., Mao, D., Nicholson, G., Vucic, S., Kennerson, M., et al (2023). Novel gene-intergenic fusion involving ubiquitin E3 ligase UBE3C causes distal hereditary motor neuropathy. Brain, 146(3), 880-897. [More Information]
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2024
- Fellner, A., Wali, G., Mahant, N., Grosz, B., Ellis, M., Narayanan, R., Ng, K., Davis, R., Tchan, M., Kotschet, K., et al (2024). Genome sequencing reanalysis increases the diagnostic yield in dystonia. Parkinsonism and Related Disorders, 124. [More Information]
- Hunt, N., Lockwood, G., Heffernan, S., Daymond, J., Ngu, M., Narayanan, R., Westwood, L., Mohanty, B., Esser, L., Williams, C., Kuncic, Z., McCourt, P., Le Couteur, D., Cogger, V. (2024). Oral nanotherapeutic formulation of insulin with reduced episodes of hypoglycaemia. Nature Nanotechnology, 19(4), 534-544. [More Information]
2023
- Cutrupi, A., Narayanan, R., Perez-Siles, G., Grosz, B., Lai, K., Boyling, A., Ellis, M., Lin, R., Neumann, B., Mao, D., Nicholson, G., Vucic, S., Kennerson, M., et al (2023). Novel gene-intergenic fusion involving ubiquitin E3 ligase UBE3C causes distal hereditary motor neuropathy. Brain, 146(3), 880-897. [More Information]
- Nishide, M., Le Marquand, K., Davis, M., Halmagyi, G., Fellner, A., Narayanan, R., Kennerson, M., Reddel, S., Worgan, L., Panegyres, P., Kumar, K. (2023). Two New Families and a Literature Review of ELOVL4-Associated Spinocerebellar Ataxia Type 34. Cerebellum. [More Information]
2021
- Narayanan, R., Brewer, M., Perez-Siles, G., Ellis, M., Ly, C., Burgess, A., Neumann, B., Nicholson, G., Vucic, S., Kennerson, M. (2021). Charcot-Marie-tooth disease causing mutation (p.R158H) in pyruvate dehydrogenase kinase 3 (PDK3) affects synaptic transmission, ATP production and causes neurodegeneration in a CMTX6 C. elegans model. Human Molecular Genetics, 31(1), 133-145. [More Information]