Dr Sarah Sandaradura

Clinical Associate Lecturer
Paediatrics & Child Health, Children's Hospital, Westmead

Telephone +61 2 9845 3273

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Clinical Specialty

Paediatrics

Selected publications

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Journals

  • O'Grady, G., Lek, M., Lamande, S., Waddell, L., Oates, E., Punetha, J., Ghaoui, R., Sandaradura, S., Best, H., Clarke, N., Cooper, S., et al (2016). Diagnosis and etiology of congenital muscular dystrophy: We are halfway there. Annals of Neurology, 80(1), 101-111. [More Information]
  • Sandaradura, S., North, K. (2015). LMOD3: the missing link "in nemaline myopathy?". Oncotarget, 6(29), 26548-26549. [More Information]
  • Yuen, M., Sandaradura, S., Dowling, J., Kostyukova, A., Moroz, N., Quinlan (nee Edwards), K., Lehtokari, V., Ravenscroft, G., Todd, E., Ceyhan-Birsoy, O., Houweling, P., Waddell, L., Clarke, N., et al (2014). Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy. Journal of Clinical Investigation, 124(11), 4693-4708. [More Information]
  • Lehtokari, V., Kiiski, K., Sandaradura, S., Laporte, J., Repo, P., Frey, J., Donner, K., Marttila, M., Saunders, C., Barth, P., Clarke, N., et al (2014). Mutation Update: The Spectra of Nebulin Variants and Associated Myopathies. Human Mutation, 35(12), 1418-1426. [More Information]
  • Gupta, V., Ravenscroft, G., Shaheen, R., Todd, E., Swanson, L., Shiina, M., Ogata, K., Hsu, C., Clarke, N., Darras, B., Sandaradura, S., et al (2013). Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy. American Journal of Human Genetics, 93(6), 1108-1117. [More Information]
  • Romero, N., Sandaradura, S., Clarke, N. (2013). Recent advances in nemaline myopathy. Current Opinion In Neurology, 26(5), 519-526. [More Information]

2016

  • O'Grady, G., Lek, M., Lamande, S., Waddell, L., Oates, E., Punetha, J., Ghaoui, R., Sandaradura, S., Best, H., Clarke, N., Cooper, S., et al (2016). Diagnosis and etiology of congenital muscular dystrophy: We are halfway there. Annals of Neurology, 80(1), 101-111. [More Information]

2015

  • Sandaradura, S., North, K. (2015). LMOD3: the missing link "in nemaline myopathy?". Oncotarget, 6(29), 26548-26549. [More Information]

2014

  • Yuen, M., Sandaradura, S., Dowling, J., Kostyukova, A., Moroz, N., Quinlan (nee Edwards), K., Lehtokari, V., Ravenscroft, G., Todd, E., Ceyhan-Birsoy, O., Houweling, P., Waddell, L., Clarke, N., et al (2014). Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy. Journal of Clinical Investigation, 124(11), 4693-4708. [More Information]
  • Lehtokari, V., Kiiski, K., Sandaradura, S., Laporte, J., Repo, P., Frey, J., Donner, K., Marttila, M., Saunders, C., Barth, P., Clarke, N., et al (2014). Mutation Update: The Spectra of Nebulin Variants and Associated Myopathies. Human Mutation, 35(12), 1418-1426. [More Information]

2013

  • Gupta, V., Ravenscroft, G., Shaheen, R., Todd, E., Swanson, L., Shiina, M., Ogata, K., Hsu, C., Clarke, N., Darras, B., Sandaradura, S., et al (2013). Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy. American Journal of Human Genetics, 93(6), 1108-1117. [More Information]
  • Romero, N., Sandaradura, S., Clarke, N. (2013). Recent advances in nemaline myopathy. Current Opinion In Neurology, 26(5), 519-526. [More Information]

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