Dr Maree Flaherty

Clinical Senior Lecturer
Clinical Ophthalmology & Eye Health
Central Clinical School

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Selected publications

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Journals

  • Jayanetti, V., Klistorner, A., Graham, S., Dexter, M., Flaherty, M., Jones, K., Billson, F., Wilson, M., North, K., Grigg, J., Fraser, C. (2018). Monitoring of optic nerve function in Neurofibromatosis 2 children with optic nerve sheath meningiomas using multifocal visual evoked potentials. Journal of Clinical Neuroscience, 50, 262-267. [More Information]
  • Ma, A., Grigg, J., Prokudin, I., Flaherty, M., Bennetts, B., Jamieson, R. (2018). New mutations in GJA8 expand the phenotype to include total sclerocornea. Clinical Genetics, 93(1), 155-159. [More Information]
  • Flaherty, M., Geering, K., Crofts, S., Grigg, J. (2017). Ocular and electrophysiological findings in a patient with Sly syndrome. Ophthalmic Genetics, 38(4), 376-379. [More Information]
  • Ma, A., Grigg, J., Ho, G., Prokudin, I., Farnsworth, E., Holman, K., Cheng, A., Billson, F., Martin, F., Fraser, C., Christodoulou, J., Flaherty, M., Bennetts, B., Jamieson, R., et al (2016). Sporadic and Familial Congenital Cataracts: Mutational Spectrum and new Diagnoses using Next-Generation Sequencing. Human Mutation, 37(4), 371-384. [More Information]

2018

  • Jayanetti, V., Klistorner, A., Graham, S., Dexter, M., Flaherty, M., Jones, K., Billson, F., Wilson, M., North, K., Grigg, J., Fraser, C. (2018). Monitoring of optic nerve function in Neurofibromatosis 2 children with optic nerve sheath meningiomas using multifocal visual evoked potentials. Journal of Clinical Neuroscience, 50, 262-267. [More Information]
  • Ma, A., Grigg, J., Prokudin, I., Flaherty, M., Bennetts, B., Jamieson, R. (2018). New mutations in GJA8 expand the phenotype to include total sclerocornea. Clinical Genetics, 93(1), 155-159. [More Information]

2017

  • Flaherty, M., Geering, K., Crofts, S., Grigg, J. (2017). Ocular and electrophysiological findings in a patient with Sly syndrome. Ophthalmic Genetics, 38(4), 376-379. [More Information]

2016

  • Ma, A., Grigg, J., Ho, G., Prokudin, I., Farnsworth, E., Holman, K., Cheng, A., Billson, F., Martin, F., Fraser, C., Christodoulou, J., Flaherty, M., Bennetts, B., Jamieson, R., et al (2016). Sporadic and Familial Congenital Cataracts: Mutational Spectrum and new Diagnoses using Next-Generation Sequencing. Human Mutation, 37(4), 371-384. [More Information]

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