Associate Professor Ellie Smith

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

Telephone 98453222
Fax 98453238

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Selected grants

2010

  • Oxytocin treatment for Prader-Willi Syndrome; Einfeld S, Smith A, Guastella A, Smith A; National Health and Medical Research Council (NHMRC)/Project Grants.

2009

  • A Trial of Oxytocin To Improve Behaviour and Cognition in Prader-Willi Syndrome; Einfeld S, McGregor I, Guastella A, Smith A; Foundation for Prader-Willi Research/Research Grant.

Selected publications

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Journals

  • Prabhu, S., Gottlieb, D., Varikatt, W., St Heaps, L., Diaz, S., Smith, A. (2010). Adult B-cell acute lymphoblastic leukemia with two unrelated abnormal cytogenetic clones. Cancer Genetics and Cytogenetics, 201(1), 24-27. [More Information]
  • Alexander, S., Smith, N., Hu, M., Verran, D., Shun, A., Dorney, S., Smith, A., Webster, B., Shaw, P., Lammi, A., Stormon, M. (2008). Chimerism and Tolerance in a Recipient of a Deceased-Donor Liver Transplant. New England Journal of Medicine, 358(4), 369-374. [More Information]
  • Hung, D., St Heaps, L., Benson, W., Mirochnik, O., Sharma, P., Smith, A. (2007). Deletion of 3'CBFbeta in an inv(16)(p13.lq22) ascertained by fluorescence in situ hybridization and reverse-transcriptase polymerase chain reaction. Cancer Genetics and Cytogenetics, 172(1), 92-94. [More Information]
  • Storlazzi, C., Fioretos, T., Surace, C., Lonoce, A., Mastrorilli, A., Strombeck, B., D’Addabbo, P., Iacovelli, F., Minervini, C., Aventin, A., Smith, A., et al (2006). MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene. Human Molecular Genetics, 15(6), 933-942. [More Information]
  • Smith, A., Das, P., O'Reilly, J., Patsouris, C., Campbell, L. (2006). Three adults with acute lymphoblastic leukemia and dic(7;9)(p11.2;p11). Cancer Genetics and Cytogenetics, 166(1), 86-88. [More Information]
  • Durrant, E., Diaz, S., Greenaway, S., Smith, A. (2005). A novel cytogenetic abnormality in Burkitt lymphoma associated with treatment resistant disease. Clinical and Laboratory Haematology, 27, 5.

2010

  • Prabhu, S., Gottlieb, D., Varikatt, W., St Heaps, L., Diaz, S., Smith, A. (2010). Adult B-cell acute lymphoblastic leukemia with two unrelated abnormal cytogenetic clones. Cancer Genetics and Cytogenetics, 201(1), 24-27. [More Information]

2008

  • Alexander, S., Smith, N., Hu, M., Verran, D., Shun, A., Dorney, S., Smith, A., Webster, B., Shaw, P., Lammi, A., Stormon, M. (2008). Chimerism and Tolerance in a Recipient of a Deceased-Donor Liver Transplant. New England Journal of Medicine, 358(4), 369-374. [More Information]

2007

  • Hung, D., St Heaps, L., Benson, W., Mirochnik, O., Sharma, P., Smith, A. (2007). Deletion of 3'CBFbeta in an inv(16)(p13.lq22) ascertained by fluorescence in situ hybridization and reverse-transcriptase polymerase chain reaction. Cancer Genetics and Cytogenetics, 172(1), 92-94. [More Information]

2006

  • Storlazzi, C., Fioretos, T., Surace, C., Lonoce, A., Mastrorilli, A., Strombeck, B., D’Addabbo, P., Iacovelli, F., Minervini, C., Aventin, A., Smith, A., et al (2006). MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene. Human Molecular Genetics, 15(6), 933-942. [More Information]
  • Smith, A., Das, P., O'Reilly, J., Patsouris, C., Campbell, L. (2006). Three adults with acute lymphoblastic leukemia and dic(7;9)(p11.2;p11). Cancer Genetics and Cytogenetics, 166(1), 86-88. [More Information]

2005

  • Durrant, E., Diaz, S., Greenaway, S., Smith, A. (2005). A novel cytogenetic abnormality in Burkitt lymphoma associated with treatment resistant disease. Clinical and Laboratory Haematology, 27, 5.

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