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

  • Oates, E., Jones, K., Donkervoort, S., Charlton, A., Brammah, S., Smith III, J., Ware, J., Yau, K., Swanson, L., Whiffin, N., Peduto, A., Bournazos, A., Waddell, L., Fitzsimons, R., O'Grady, G., Sandaradura, S., Ghaoui, R., Cooper, S., Clarke, N., et al (2018). Congenital titinopathy: Comprehensive characterisation and pathogenic insights. Annals of Neurology, 83(6), 1106-1124. [More Information]
  • Sandaradura, S., Bournazos, A., Mallawaarachchi, A., Cummings, B., Waddell, L., Jones, K., Troedson, C., Sudarsanam, A., Nash, B., Peters, G., Cooper, S., et al (2018). Nemaline myopathy and distal arthrogryposis associated with an autosomal recessive�TNNT3�splice variant. Human Mutation, 39(3), 383-388. [More Information]
  • Cameron-Christie, S., Wells, C., Simon, M., Wessels, M., Tang, C., Wei, W., Takei, R., Aarts-Tesselaar, C., Sandaradura, S., Sillence, D., et al (2018). Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3. American Journal of Human Genetics, 102(6), 1115-1125. [More Information]
  • Schofield, D., Alam, K., Douglas, L., Shrestha, R., MacArthur, D., Davis, M., Laing, N., Clarke, N., Burns, J., Cooper, S., Sandaradura, S., O'Grady, G., et al (2017). Cost-effectiveness of massively parallel sequencing for diagnosis of paediatric muscle diseases. npj Genomic Medicine, 2(4), 1-7. [More Information]
  • Wojciechowski, E., Sman, A., Cornett, K., Raymond, J., Refshauge, K., Menezes, M., Burns, J., Cooper, S., North, K., Sandaradura, S., O'Grady, G. (2017). Gait patterns of children and adolescents with Charcot-Marie-Tooth disease. Gait and Posture, 56, 89-94. [More Information]
  • Cummings, B., Marshall, J., Tukiainen, T., Lek, M., Donkervoort, S., Foley, A., Bolduc, V., Waddell, L., Sandaradura, S., O'Grady, G., Bournazos, A., Oates, E., Ghaoui, R., Clarke, N., Cooper, S., et al (2017). Improving genetic diagnosis in Mendelian disease with transcriptome sequencing. Science Translational Medicine, 9(386), 1-11. [More Information]
  • O'Grady, G., Lek, M., Lamande, S., Waddell, L., Oates, E., Punetha, J., Ghaoui, R., Sandaradura, S., Best, H., Kaur, S., 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]
  • Punetha, J., Kesari, A., Uapinyoying, P., Giri, M., Clarke, N., Waddell, L., North, K., Ghaoui, R., O'Grady, G., Oates, E., Sandaradura, S., et al (2016). Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases. Journal of Neuromuscular Diseases, 3(2), 209-225. [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]

2018

  • Oates, E., Jones, K., Donkervoort, S., Charlton, A., Brammah, S., Smith III, J., Ware, J., Yau, K., Swanson, L., Whiffin, N., Peduto, A., Bournazos, A., Waddell, L., Fitzsimons, R., O'Grady, G., Sandaradura, S., Ghaoui, R., Cooper, S., Clarke, N., et al (2018). Congenital titinopathy: Comprehensive characterisation and pathogenic insights. Annals of Neurology, 83(6), 1106-1124. [More Information]
  • Sandaradura, S., Bournazos, A., Mallawaarachchi, A., Cummings, B., Waddell, L., Jones, K., Troedson, C., Sudarsanam, A., Nash, B., Peters, G., Cooper, S., et al (2018). Nemaline myopathy and distal arthrogryposis associated with an autosomal recessive�TNNT3�splice variant. Human Mutation, 39(3), 383-388. [More Information]
  • Cameron-Christie, S., Wells, C., Simon, M., Wessels, M., Tang, C., Wei, W., Takei, R., Aarts-Tesselaar, C., Sandaradura, S., Sillence, D., et al (2018). Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3. American Journal of Human Genetics, 102(6), 1115-1125. [More Information]

2017

  • Schofield, D., Alam, K., Douglas, L., Shrestha, R., MacArthur, D., Davis, M., Laing, N., Clarke, N., Burns, J., Cooper, S., Sandaradura, S., O'Grady, G., et al (2017). Cost-effectiveness of massively parallel sequencing for diagnosis of paediatric muscle diseases. npj Genomic Medicine, 2(4), 1-7. [More Information]
  • Wojciechowski, E., Sman, A., Cornett, K., Raymond, J., Refshauge, K., Menezes, M., Burns, J., Cooper, S., North, K., Sandaradura, S., O'Grady, G. (2017). Gait patterns of children and adolescents with Charcot-Marie-Tooth disease. Gait and Posture, 56, 89-94. [More Information]
  • Cummings, B., Marshall, J., Tukiainen, T., Lek, M., Donkervoort, S., Foley, A., Bolduc, V., Waddell, L., Sandaradura, S., O'Grady, G., Bournazos, A., Oates, E., Ghaoui, R., Clarke, N., Cooper, S., et al (2017). Improving genetic diagnosis in Mendelian disease with transcriptome sequencing. Science Translational Medicine, 9(386), 1-11. [More Information]

2016

  • O'Grady, G., Lek, M., Lamande, S., Waddell, L., Oates, E., Punetha, J., Ghaoui, R., Sandaradura, S., Best, H., Kaur, S., 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]
  • Punetha, J., Kesari, A., Uapinyoying, P., Giri, M., Clarke, N., Waddell, L., North, K., Ghaoui, R., O'Grady, G., Oates, E., Sandaradura, S., et al (2016). Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases. Journal of Neuromuscular Diseases, 3(2), 209-225. [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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