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Research Outputs

  • 134 Citations
  • 3 h-Index
  • 8 Article
  • 1 Chapter
  • 1 Letter

Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 mice

McCann, E. P., Fifita, J. A., Grima, N., Galper, J., Mehta, P., Freckleton, S. E., Zhang, K. Y., Henden, L., Hogan, A. L., Chan Moi Fat, S., Wu, S. S. L., Jagaraj, C. J., Berning, B. A., Williams, K. L., Twine, N. A., Bauer, D., Piguet, O., Hodges, J., Kwok, J. B. J., Halliday, G. M. & 7 others, Kiernan, M. C., Atkin, J., Rowe, D. B., Nicholson, G. A., Walker, A. K., Blair, I. P. & Yang, S., 1 Feb 2020, In : Journal of Neurology, Neurosurgery and Psychiatry. 91, 2, p. 162-171 10 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutations

Konopka, A., Whelan, D. R., Jamali, M. S., Perri, E., Shahheydari, H., Toth, R. P., Parakh, S., Robinson, T., Cheong, A., Mehta, P., Vidal, M., Ragagnin, A. M. G., Khizhnyak, I., Jagaraj, C. J., Galper, J., Grima, N., Deva, A., Shadfar, S., Nicholson, G. A., Yang, S. & 6 others, Cutts, S. M., Horejsi, Z., Bell, T. D. M., Walker, A. K., Blair, I. P. & Atkin, J. D., 9 Sep 2020, In : Molecular Neurodegeneration. 15, 1, p. 1-28 28 p., 51.

Research output: Contribution to journalArticle

Open Access
3 Downloads (Pure)

Riluzole does not ameliorate disease caused by cytoplasmic TDP-43 in a mouse model of amyotrophic lateral sclerosis

Wright, A. L., Le, S., Mehta, P., Gatta, P. D., Berning, B. A., Jacobs, K. R., Gul, H., Gil, R. S., Hedl, T. J., Riddell, W. R., Watson, O., Keating, S. S., Chung, R. S., Atkin, J. D., Lee, A., Shi, B., Blizzard, C. A., Morsch, M. & Walker, A. K., 29 Aug 2019, (In preparation) In : bioRxiv.

Research output: Contribution to journalArticle


The isolation of pure populations of neurons by laser capture microdissection: methods and application in neuroscience

Morris, R. & Mehta, P., 2018, Laser capture microdissection: methods and protocols. Murray, G. I. (ed.). New York, NY: Humana Press Inc., Vol. 1723. p. 223-233 11 p. (Methods in Molecular Biology; vol. 1723).

Research output: Chapter in Book/Report/Conference proceedingChapter


"Dancing feet dyskinesias": A clue to parkin gene mutations

Chang, F. C. F., Mehta, P., Koentjoro, B., Latt, M., Blair, N., Nicholson, G., Sue, C. M. & Fung, V. S. C., Apr 2012, In : Movement Disorders. 27, 4, p. 587-588 2 p.

Research output: Contribution to journalLetter

2 Citations (Scopus)

Pathogenic effects of novel mutations in the P-Type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb Syndrome, a form of early-onset Parkinsonism

Park, J-S., Mehta, P., Cooper, A. A., Veivers, D., Heimbach, A., Stiller, B., Kubisch, C., Fung, V. S., Krainc, D., Mackay-Sim, A. & Sue, C. M., Aug 2011, In : Human mutation. 32, 8, p. 956-964 9 p.

Research output: Contribution to journalArticle

87 Citations (Scopus)

Mitochondrial DNA haplogroups J and K are note protective for Parkinson's disease in the Australian community

Mehta, P., Mellick, G. D., Rowe, D. B., Halliday, G. M., Jones, M. M., Manwaring, N., Vandebona, H., Silburn, P. A., Wang, J. J., Mitchell, P. & Sue, C. M., 30 Jan 2009, In : Movement Disorders. 24, 2, p. 290-292 3 p.

Research output: Contribution to journalArticle

21 Citations (Scopus)

Population prevalence and incidence of Parkinson's disease in an Australian community

Mehta, P., Kifley, A., Wang, J. J., Rochtchina, E., Mitchell, P. & Sue, C. M., Dec 2007, In : Internal Medicine Journal. 37, 12, p. 812-814 3 p.

Research output: Contribution to journalArticle

20 Citations (Scopus)