Dr Sue Heatley

Project Manager

School of Public Health

College of Health


Dr Sue Heatley Environmental Change & Health OutcomesSchool of Public HealthPrevious:Postdoctoral Research Fellow, South Australian Health & Medical Research InstituteThe Kids Cancer Project Postdoctoral Fellow (2016-2022)Centre for Cancer Biology, Australian Red Cross Blood Service, St Jude Children's Research Hospital Education:University of Melbourne Experience:Post-doctoral FellowSouth Australian Health & Medical Research InstituteJuly 2013 - March 2025Genomics Research Team LeaderSouth Australian Health & Medical Research InstituteJuly 2013 – Dec 2016|AdelaidePostdoctoral ScientistCentre for Cancer BiologyAugust 2011 – June 2013 (1 year 11 months)|AdelaideMedical Education Project OfficerAustralian Red Cross Blood ServiceJuly 2009 – August 2011 (2 years 2 months)|AdelaideVisiting Postdoctoral FellowSt Jude Children's Research HospitalJune 2010 – February 2011 (9 months)|Memphis, TN, USAMedical Scientist, Research & DevelopmentAustralian Red Cross Blood ServiceJanuary 1998 – June 2009 (11 years 6 months)|AdelaideMedical Scientist/Technical Officer/Nurse attendantAustralian Red Cross Blood ServiceOctober 1984 – December 1997 (13 years 3 months)|Adelaide

Dr Sue Heatley gained her PhD in Transplant Immunology from the University of Melbourne in 2011. She also has a Masters in Education (Educational Leadership). In 2010 she was awarded a New Investigator Scholarship by the Haematology Society of Australia & New Zealand (HSANZ) to undertake a visiting fellow position in the laboratory of Prof Charles Mullighan at the St Jude’s Children’s Research Hospital, Memphis, TN, USA. In 2013, Sue accepted her current position at SAHMRI in the Leukaemia Research group of Prof Deb White and Prof Tim Hughes in the Cancer Theme. She is a member of several professional societies including HSANZ and the Australian & New Zealand Children’s Haematology and Oncology Group.

Sue has extensive laboratory experience having worked at the Australian Red Cross Blood Service for over 25 years including over 12 years in the Research Department and 2 years in Medical Education. She has presented her research at both national and international meetings, being awarded the prestigious Albert Baikie Memorial Medal in 2015 for best presentation by a new investigator. Sue has authored over 30 publications with over 3000 career citations and is the current Kids Cancer Project Postdoctoral Fellow. Her current research interests are focussed on the genomic landscape of ALL and improving patient outcome through personalised medicine.

Date Position Institution name
2025 - ongoing Project Manager University of Adelaide
2013 - ongoing Affiliate Senior Lecturer University of Adelaide

Date Type Title Institution Name Country Amount
2016 Award HSANZ Travel Award Haematology Society of Australia and New Zealand Australia $1000
2016 Fellowship The Kids Cancer Project Postdoctoral Fellow - Australia $170,932
2015 Award Albert Baikie Memorial Award Haematology Society of Australia and New Zealand Australia $3000
2009 Award ASHI International Scholar American Society for Histocompatability and Immunogenetics United States -
2009 Achievement Presidential Symposium Haematology Society of Australia and New Zealand Australia -
2009 Scholarship New Investigator Scholarship Haematology Society of Australia and New Zealand Australia $30,000

Date Institution name Country Title
2011 - 2012 Charles Sturt University Australia Master of Education
2004 - 2011 University of Melbourne Australia PhD
2002 - 2004 Charles Sturt University Australia Bachelor of Medical Science (Honours)
1996 - 1999 Charles Sturt University Australia Bachelor of Medical Science (Pathology)

Date Title Institution Country
2010 - 2011 Visting Postdoctoral Fellow St Jude Children's Research Hospital United States

Year Citation
2025 Lagonik, E., Page, E. C., Bruning, J. B., Eadie, L. N., Heatley, S. L., Greenwood, M., . . . White, D. L. (2025). Activity of STAMP inhibitors in ABL2 rearranged Acute Lymphoblastic Leukemia is dependent on the Abl2 SH3 domain. Blood Neoplasia, 2(3), 100109.
DOI Scopus1 Europe PMC1
2025 Quinlan, L., Page, E. C., Rehn, J., McClure, B. J., Osborn, M. P., Moore, A. S., . . . Heatley, S. L. (2025). High Expression of NTRK1 in ETV6::RUNX1 Positive Acute Lymphoblastic Leukaemia Drives Factor Independence and Sensitivity to Larotrectinib.. Pediatric Blood and Cancer, 72(11), e31983-1-e31983-7.
DOI
2024 Eadie, L. N., Lagonik, E., Page, E. C., Schutz, C. E., Heatley, S. L., McClure, B. J., . . . White, D. L. (2024). Asciminib is a novel inhibitor of ABL1 and ABL2 gene fusions in ALL but requires the ABL SH3 domain for efficacy. Blood, 144(9), 1022-1026.
DOI Scopus6 WoS6 Europe PMC6
2024 Yeung, D. T., Eadie, L. N., Rehn, J., Heatley, S. L., McClure, B. J., Page, E. C., . . . White, D. L. (2024). Diagnostic Genomic Analysis is Prognostic in AYA ALL Patients Treated on a MRD-Stratified Pediatric Protocol. Blood Neoplasia, 2(1), 100041.
DOI Scopus1
2023 Eadie, L. N., Rehn, J. A., Breen, J., Osborn, M. P., Jessop, S., Downes, C. E. J., . . . White, D. L. (2023). Case Report: Rare IKZF1 Gene Fusions Identified in Neonate with Congenital KMT2A-Rearranged Acute Lymphoblastic Leukemia. Genes, 14(2), 264-1-264-11.
DOI Scopus1 WoS1 Europe PMC1
2023 Page, E. C., Heatley, S. L., Rehn, J., Thomas, P. Q., Yeung, D. T., & White, D. L. (2023). Gain of chromosome 21 increases the propensity for P2RY8: :CRLF2 acute lymphoblastic leukemia via increased HMGN1 expression. Frontiers in Oncology, 13(1177871), 1177871.
DOI Scopus8 WoS9 Europe PMC8
2023 Eadie, L. N., Rehn, J. A., Schutz, C. E., Heatley, S. L., Kutyna, M. M., Hiwase, D. K., . . . Yeung, D. T. (2023). Case report: Rare case of donor cell-derived T-cell acute lymphoblastic leukaemia in a female patient after receiving an allo-transplant from her male sibling. British Journal of Haematology, 203(2), 282-287.
DOI Europe PMC1
2023 Thomson, A. J., Rehn, J. A., Heatley, S. L., Eadie, L. N., Page, E. C., Schutz, C., . . . White, D. L. (2023). Reproducible Bioinformatics Analysis Workflows for Detecting IGH Gene Fusions in B-Cell Acute Lymphoblastic Leukaemia Patients. Cancers, 15(19), 4731-1-4731-13.
DOI Scopus6 WoS6 Europe PMC6
2022 Downes, C. E. J., Rehn, J., Heatley, S. L., Yeung, D., McClure, B. J., & White, D. L. (2022). Identification of a novel GOLGA4–JAK2 fusion gene in B-cell acute lymphoblastic leukaemia. British Journal of Haematology, 196(3), 700-705.
DOI Scopus5 WoS5 Europe PMC5
2022 Rehn, J., Mayoh, C., Heatley, S. L., McClure, B. J., Eadie, L. N., Schutz, C., . . . White, D. L. (2022). Rascall: Rapid (Ra) screening (Sc) of RNA-seq data for prognostically significant genomic alterations in acute lymphoblastic leukaemia (ALL). PLoS Genetics, 18(10), 1-23.
DOI Scopus18 WoS16 Europe PMC19
2022 Page, E. C., Heatley, S. L., Eadie, L. N., McClure, B. J., de Bock, C. E., Omari, S., . . . White, D. L. (2022). HMGN1 plays a significant role in CRLF2 driven Down Syndrome leukemia and provides a potential therapeutic target in this high-risk cohort. Oncogene, 41(6), 797-808.
DOI Scopus18 WoS17 Europe PMC15
2022 McClure, B. J., Pal, M., Heatley, S. L., Rehn, J., Schutz, C., Breen, J., . . . White, D. L. (2022). Two novel cases of NUTM1-rearranged B-cell acute lymphoblastic leukaemia presenting with high-risk features. British Journal of Haematology, 196(6), 1407-1411.
DOI Scopus9 WoS8 Europe PMC7
2022 Shirazi, P. T., Eadie, L. N., Heatley, S. L., Page, E. C., François, M., Hughes, T. P., . . . White, D. L. (2022). Exploring the oncogenic and therapeutic target potential of the MYB-TYK2 fusion gene in B-cell acute lymphoblastic leukemia. Cancer Gene Therapy, 29(8-9), 1140-1152.
DOI Scopus7 WoS7 Europe PMC7
2022 Heatley, S. L., Page, E. C., Eadie, L. N., McClure, B. J., Rehn, J., Yeung, D. T., . . . White, D. L. (2022). Case Report: Precision Medicine Target Revealed by In Vitro Modeling of Relapsed, Refractory Acute Lymphoblastic Leukemia From a Child With Neurofibromatosis. Frontiers in Oncology, 12(851572), 851572-1-851572-6.
DOI Scopus3 WoS2 Europe PMC3
2022 Venn, N. C., Huang, L., Hovorková, L., Muskovic, W., Wong, M., Law, T., . . . Sutton, R. (2022). Measurable residual disease analysis in paediatric acute lymphoblastic leukaemia patients with ABL-class fusions. British Journal of Cancer, 127(5), 908-915.
DOI Scopus8 WoS7 Europe PMC7
2022 Downes, C. E., McClure, B. J., McDougal, D. P., Heatley, S. L., Bruning, J. B., Thomas, D., . . . White, D. L. (2022). JAK2 Alterations in Acute Lymphoblastic Leukemia: Molecular Insights for Superior Precision Medicine Strategies. Frontiers in Cell and Developmental Biology, 10(942053), 1-34.
DOI Scopus27 WoS24 Europe PMC22
2021 Tavakoli Shirazi, P., Eadie, L. N., Page, E. C., Heatley, S. L., Bruning, J. B., & White, D. L. (2021). Constitutive JAK/STAT signaling is the primary mechanism of resistance to JAKi in TYK2-rearranged acute lymphoblastic leukemia. Cancer Letters, 512, 28-37.
DOI Scopus11 WoS12 Europe PMC12
2021 Tavakoli Shirazi, P., N Eadie, L., L Heatley, S., & L White, D. (2021). TYK2 Activating Alterations in Acute Lymphoblastic Leukemia: Novel Driver Oncogenes with Potential Avenues for Precision Medicine?. Journal of Cancer Science and Clinical Therapeutics, 05(02).
DOI
2021 Heatley, S. L., Asari, K., Schutz, C. E., Leclercq, T. M., McClure, B. J., Eadie, L. N., . . . White, D. L. (2021). In-vitro modeling of TKI resistance in the high-risk B-cell acute lymphoblastic leukemia fusion gene RANBP2-ABL1 - implications for targeted therapy. Leukemia and Lymphoma, 62(5), 1157-1166.
DOI Scopus4 WoS3 Europe PMC3
2021 Sutton, R., Pozza, L. D., Khaw, S. L., Fraser, C., Revesz, T., Chamberlain, J., . . . Kotecha, R. S. (2021). Outcomes for Australian children with relapsed/refractory acute lymphoblastic leukaemia treated with blinatumomab. Pediatric Blood and Cancer, 68(5), 1-7.
DOI Scopus20 WoS17 Europe PMC17
2020 McClure, B. J., Heatley, S. L., Rehn, J., Breen, J., Sutton, R., Hughes, T. P., . . . White, D. L. (2020). High-risk B-cell acute lymphoblastic leukaemia presenting with hypereosinophilia and acquiring a novel PAX5 fusion on relapse. British Journal of Haematology, 191(2), 301-304.
DOI Scopus4 WoS3 Europe PMC3
2019 Tavakoli Shirazi, P., Eadie, L. N., Heatley, S. L., Hughes, T. P., Yeung, D. T., & White, D. L. (2019). The effect of co-occurring lesions on leukaemogenesis and drug response in T-ALL and ETP-ALL.. British journal of cancer, 122(4), 455-464.
DOI Scopus12 WoS12 Europe PMC10
2018 McClure, B., Heatley, S., Kok, C., Sadras, T., An, J., Hughes, T., . . . White, D. (2018). Pre-B acute lymphoblastic leukaemia recurrent fusion, EP300-ZNF384, is associated with a distinct gene expression. British Journal of Cancer, 118(7), 1000-1004.
DOI Scopus33 WoS29 Europe PMC26
2018 Page, E. C., Heatley, S. L., Yeung, D. T., Thomas, P. Q., & White, D. L. (2018). Precision medicine approaches may be the future for CRLF2 rearranged Down Syndrome Acute Lymphoblastic Leukaemia patients. Cancer Letters, 432, 69-74.
DOI Scopus6 WoS6 Europe PMC5
2018 Heatley, S. L., Mullighan, C. G., Doherty, K., Danner, S., O'Connor, G. M., Hahn, U., . . . Brooks, A. G. (2018). Activating killer-cell immunoglobulin-like receptor haplotype influences clinical outcome following HLA-matched sibling haematopoietic stem cell transplantation. HLA, 92(2), 74-82.
DOI Scopus13 WoS12 Europe PMC9
2017 Heatley, S. L., Sadras, T., Kok, C. H., Nievergall, E., Quek, K., Dang, P., . . . White, D. L. (2017). High prevalence of relapse in children with Philadelphia-like acute lymphoblastic leukemia despite risk-adapted treatment. Haematologica, 102(12), e490-e493.
DOI Scopus56 WoS55 Europe PMC52
2017 Pagani, I. S., Kok, C. H., Saunders, V. A., Van der Hoek, M. B., Heatley, S. L., Schwarer, A. P., . . . Ross, D. M. (2017). A method for next-generation sequencing of paired diagnostic and remission Samples to detect mitochondrial DNA mutations associated with leukemia. The Journal of molecular diagnostics : JMD, 19(5), 711-721.
DOI Scopus6 WoS5 Europe PMC7
2017 Sadras, T., Heatley, S., Kok, C., McClure, B., Yeung, D., Hughes, T., . . . White, D. (2017). A novel somatic JAK2 kinase-domain mutation in pediatric acute lymphoblastic leukemia with rapid on-treatment development of LOH. Cancer Genetics, 216-217, 86-90.
DOI Scopus13 WoS13 Europe PMC13
2017 Sadras, T., Heatley, S., Kok, C., Dang, P., Galbraith, K., McClure, B., . . . White, D. (2017). Differential expression of MUC4, GPR110 and IL2RA defines two groups of CRLF2-rearranged acute lymphoblastic leukemia patients with distinct secondary lesions. Cancer Letters, 408, 92-101.
DOI Scopus19 WoS21 Europe PMC18
2016 White, D. (2016). Acute sensitivity of Ph-like acute lymphoblastic leukemia to the SMAC-mimetic birinapant. Cancer Research, 76(15), 4579-4591.
DOI Scopus19 WoS19 Europe PMC17
2016 Lopes, B., Meyer, C., Barbosa, T., Stadt, U., Horstmann, M., Venn, N., . . . Emerenciano, M. (2016). COBL is a novel hotspot for IKZF1 deletions in childhood acute lymphoblastic leukemia. Oncotarget, 7(33), 53064-53073.
DOI Scopus9 WoS9 Europe PMC7
2016 Trahair, T., Lock, R., Sutton, R., Sia, K., Evans, K., Richmond, J., . . . Revesz, T. (2016). Xenograft-directed personalized therapy for a patient with post-transplant relapse of ALL. Bone Marrow Transplantation, 51(9), 1279-1282.
DOI Scopus5 WoS5 Europe PMC5
2016 Dolai, S., Sia, K., Robbins, A., Zhong, L., Heatley, S., Vincent, T., . . . Lock, R. (2016). Quantitative phosphotyrosine profiling of patient-derived xenografts identifies therapeutic targets in pediatric leukemia. Cancer Research, 76(9), 2766-2777.
DOI Scopus14 WoS14 Europe PMC15
2015 Yeung, D. T., Moulton, D. J., Heatley, S. L., Nievergall, E., Dang, P., Braley, J., . . . White, D. L. (2015). Relapse of BCR-ABL1-like ALL mediated by the ABL1 kinase domain mutation T315I following initial response to dasatinib treatment. Leukemia, 29(1), 230-232.
DOI Scopus27 WoS22 Europe PMC21
2014 Sadras, T., Perugini, M., Kok, C., Iarossi, D., Heatley, S., Brumatti, G., . . . D'Andrea, R. (2014). Interleukin-3-mediated regulation of β-catenin in myeloid transformation and acute myeloid leukemia. Journal of Leukocyte Biology, 96(1), 83-91.
DOI Scopus18 WoS17 Europe PMC13
2014 Dolai, S., Sia, K. C. S., Robbins, A. K., Zhong, L., Heatley, S., Vincent, T., . . . Lock, R. B. (2014). Targeted Cancer Therapy in High-Risk Pediatric Leukemia Using Global Phosphotyrosine Profiling. BLOOD, 124(21), 3 pages.
2013 Heatley, S., Pietra, G., Lin, J., Widjaja, J., Harpur, C., Lester, S., . . . Brooks, A. (2013). Polymorphism in human cytomegalovirus UL40 impacts on recognition of human leukocyte antigen-E (HLA-E) by natural killer cells. Journal of Biological Chemistry, 288(12), 8679-8690.
DOI Scopus105 WoS107 Europe PMC94
2013 To, L. (2013). The genomic landscape of hypodiploid acute lymphoblastic leukemia. Nature Genetics, 45(3), 242-252.
DOI Scopus587 WoS525 Europe PMC486
2012 Zhang, J., Ding, L., Holmfeldt, L., Wu, G., Heatley, S., Payne-Turner, D., . . . Mullighan, C. (2012). The genetic basis of early T-cell precursor acute lymphoblastic leukaemia. Nature, 481(7380), 157-163.
DOI Scopus1399 WoS1304 Europe PMC1251
2011 Wang, J., Mullighan, C., Easton, J., Roberts, S., Heatley, S., Ma, J., . . . Zhang, J. (2011). CREST maps somatic structural variation in cancer genomes with base-pair resolution. Nature Methods, 8(8), 652-654.
DOI Scopus405 WoS389 Europe PMC389
2011 Mullighan, C., Zhang, J., Kasper, L., Lerach, S., Payne-Turner, D., Phillips, L., . . . Downing, J. (2011). CREBBP mutations in relapsed acute lymphoblastic leukaemia. Nature, 471(7337), 235-241.
DOI Scopus548 WoS497 Europe PMC470
2011 Carroll, K., Dean, M., Heatley, S., Meehan, A., Mifsud, N., Kotsimbos, T., . . . Westall, G. (2011). High levels of mannose-binding lectin are associated with poor outcomes after lung transplantation. Transplantation, 91(9), 1044-1049.
DOI Scopus25 WoS23 Europe PMC20
2009 Worthley, D., Johnson, D., Eisen, D., Dean, M., Heatley, S., Tung, J., . . . Mullighan, C. (2009). Donor Mannose - Binding Lectin Deficiency Increases the Likelihood of Clinically Significant Infection after Liver Transplantation. Clinical Infectious Diseases, 48(4), 410-417.
DOI Scopus51 WoS50 Europe PMC46
2008 Mullighan, C., Heatley, S., Danner, S., Dean, M., Doherty, K., Hahn, H., . . . Bardy, P. (2008). Mannose-binding lectin status is associated with risk of major infection following myeloablative sibling allogeneic hematopoietic stem cell transplantation. Blood, 112(5), 2120-2128.
DOI Scopus40 WoS39 Europe PMC34
2008 Worthley, D. L., Johnson, D. F., Eisen, D. P., Dean, M. M., Heatley, S., Tung, J. -P., . . . Bardy, P. G. (2008). Donor-derived mannose-binding lectin deficiency increases the risk of infection after liver transplantation. JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 23, A307.
2008 Eisen, D. P., Dean, M. M., O'Sullivan, M. V. N., Heatley, S., & Minchinton, R. M. (2008). Mannose-binding lectin deficiency does not appear to predispose to cryptococcosis in non-immunocompromised patients. Medical Mycology, 46(4), 371-375.
DOI Scopus18 WoS18 Europe PMC17
2007 Worthley, D., Mullighan, C., Dean, M., Gordon, D., Phillips, P., Heatley, S., . . . Bardy, P. (2007). Mannose-binding lectin deficiency does not increase the prevalence of Helicobacter pylori seropositivity. European Journal of Gastroenterology & Hepatology, 19(2), 147-152.
DOI Scopus10 WoS8 Europe PMC7
2006 Dean, M. M., Heatley, S., & Minchinton, R. M. (2006). Heteroligomeric forms of codon 54 mannose binding lectin (MBL) in circulation demonstrate reduced in vitro function. Molecular Immunology, 43(7), 950-961.
DOI Scopus27 WoS24 Europe PMC23
2006 Eisen, D. P., Dean, M. M., Thomas, P., Marshall, P., Gerns, N., Heatley, S., . . . Lipman, J. (2006). Low mannose-binding lectin function is associated with sepsis in adult patients. FEMS Immunology and Medical Microbiology, 48(2), 274-282.
DOI Scopus55 WoS50 Europe PMC41
2005 Dean, M. M., Minchinton, R. M., Heatley, S., & Eisen, D. P. (2005). Mannose binding lectin acute phase activity in patients with severe infection. Journal of Clinical Immunology, 25(4), 346-352.
DOI Scopus87 WoS76 Europe PMC66
2005 Annells, M., Hart, P., Mullighan, C., Heatley, S., Robinson, J., & McDonald, H. (2005). Polymorphisms in immunoregulatory genes and the risk of histologic chorioamnionitis in Caucasoid women: a case control study. BMC Pregnancy and Childbirth, 5(1), WWW1-WWW9.
DOI Scopus35 Europe PMC33
2004 Annells, M., Hart, P., Mullighan, C., Heatley, S., Robinson, J., Bardy, P., & McDonald, H. (2004). Interleukins-1, 4, -6, -10, tumor necrosis factor, transforming growth factor-β, FAS, and mannose-binding protein C gene polymorphisms in Australian women: risk of preterm birth. American Journal of Obstetrics and Gynecology, 191(6), 2056-2067.
DOI Scopus139 WoS130 Europe PMC117
2004 Mullighan, C., Heatley, S., Doherty, K., Szabo, F., Grigg, A., Hughes, T., . . . Bardy, P. (2004). Non-HLA immunogenetic polymorphisms and the risk of complications after allogeneic hemopoietic stem-cell transplantation. Transplantation, 27(4), 587-596.
DOI Scopus80 WoS73 Europe PMC64
2004 Mullighan, C., Heatley, S., Lester, S., Rischmueller, M., Gordon, T., & Bardy, P. (2004). Fas gene promoter polymorphisms in primary Sjogren's syndrome. Annals of the Rheumatic Diseases, 63(1), 98-101.
DOI Scopus22 WoS23 Europe PMC31
2003 Helbig, K., Heatley, S., Harris, R., Mullighan, C., Bardy, P., & Marmion, B. (2003). Variation in immune response genes and chronic Q fever. Concepts: preliminary test with post-Q fever fatigue syndrome. Genes and Immunity, 4(1), 82-85.
DOI Scopus31 WoS27 Europe PMC19
2002 Mullighan, C., Heatley, S., Doherty, K., Szabo, F., Grigg, A., Hughes, T., . . . Bardy, P. (2002). Mannose-binding lectin gene polymorphisms are associated with major infection following allogeneic hemopoietic stem cell transplantation. Blood, 99(10), 3524-3529.
DOI Scopus188 WoS168 Europe PMC140
2002 Minchinton, R. M., Dean, M. M., Clark, T. R., Heatley, S., & Mullighan, C. G. (2002). Analysis of the relationship between mannose-binding lectin (MBL) genotype, MBL levels and function in an Australian blood donor population. Scandinavian Journal of Immunology, 56(6), 630-641.
DOI Scopus176 WoS167 Europe PMC144
2001 Mullighan, C. G., Heatley, S., Doherty, K., Szabo, F., Grigg, A. P., Hughes, T. P., . . . Bardy, P. G. (2001). Non-HLA genetic polymorphisms influence risk of acute and chronic graft-versus-host disease, early death and infection following allogeneic haemopoietic stem cell transplantation.. BLOOD, 98(11), 739A-740A.
WoS1
2001 Tait, B. D., Maddison, R., McCluskey, J., Deayton, S., Heatley, S., Lester, S., . . . Holdsworth, R. (2001). Clinical relevance of the minor histocompatibility antigen HA-1 in allogeneic bone marrow transplantation between HLA identical siblings. Transplantation Proceedings, 33(1-2), 1760-1761.
DOI Scopus10 WoS12 Europe PMC10
2000 Mullighan, C. G., Heatley Sue, B., Bardy, P. G., Lester, S., Rischmueller, M., & Gordon, T. P. (2000). Lack of association between mannose-binding lectin gene polymorphisms and primary Sjogren's syndrome. Arthritis and Rheumatism, 43(12), 2851-2852.
DOI Scopus14 WoS15 Europe PMC10
2000 Turner, M., Dinan, L., Heatley, S., Jack, D., Boettcher, B., Lester, S., . . . Roberton, D. (2000). Restricted polymorphism of the mannose-binding lectin gene of indigenous Australians. Human Molecular Genetics, 9(10), 1481-1486.
DOI Scopus69 WoS59 Europe PMC42
1999 Lester, S., Heatley, S., Bardy, P., Bahnisch, J., Bannister, K., Faull, R., & Clarkson, A. (1999). The DD genotype of the angiotensin-converting enzyme gene occurs in very low frequency in Australian Aboriginals. Nephrology, Dialysis and Transplantation, 14(4), 887-890.
DOI Scopus29 WoS27 Europe PMC18

Year Citation
2020 Tavakoli, P. S., Eadie, L., Heatley, S. L., Yeung, D. T., & White, D. L. (2020). The MYB-TYK2 gene fusion induces B-cell acute lymphoblastic leukaemia in in vitro and in vivo models and can be effectively targeted by the dual SYK/JAK inhibitor, cerdulatinib (Vol. 4). Lippincott, Williams & Wilkins.
DOI

Year Citation
2023 White, D. L., Rehn, J. A., Schutz, C. E., Heatley, S. L., Eadie, L. N., Thomson, A., . . . Greenwood, M. (2023). Improved MRD Negativity Rates in Adverse Genomic Risk B-ALL Patients with Chemotherapy / Blinatumomab Induction: Experience from the Australasian Leukaemia Lymphoma Group (ALLG) ALL06/09 Studies. In BLOOD Vol. 142 (pp. 6 pages). CA, San Diego: AMER SOC HEMATOLOGY.
DOI
2023 Eadie, L. N., Schutz, C. E., Page, E. C., Conlin, T. S., Heatley, S. L., Lagonik, E., . . . White, D. L. (2023). Asciminib Is Effective Against ABL1 Gene Fusions in Acute Lymphoblastic Leukemia but Only When the ABL1 SH3 Domain Is Present. In BLOOD Vol. 142 (pp. 4 pages). CA, San Diego: AMER SOC HEMATOLOGY.
DOI WoS4
2021 Page, E. C., Heatley, S. L., Rehn, J., Yeung, D. T., Thomas, P. Q., & White, D. L. (2021). <i>HMGN1</i> expression Predisposes Down Syndrome Patients to Develop <i>P2RY8-CRLF2</i> acute Lymphoblastic Leukemia. In BLOOD Vol. 138 (pp. 4 pages). GA, Atlanta: ELSEVIER.
DOI
2019 Dean, M. M., Lopez, G. H., Liley, H. G., Heatley, S. L., & Minchinton, R. M. (2019). Development of functional mannose binding lectin is delayed in extremely low birth weight infants. In JOURNAL OF IMMUNOLOGY Vol. 202 (pp. 3 pages). San Diego, CA: AMER ASSOC IMMUNOLOGISTS.
2016 Asari, K., Heatley, S. L., Sadras, T., Leclercq, T. M., Fitter, S., Kok, C. H., . . . White, D. L. (2016). <i>In Vitro</i> Modeling of Ph-like ALL Fusions Identifies Novel Kinase-Domain Mutations As Mode of TKI-Resistance Implications for Targeted Therapy. In BLOOD Vol. 128 (pp. 5 pages). San Diego, CA: AMER SOC HEMATOLOGY.
DOI WoS1
2016 Pagani, I. S., Kok, C. H., Saunders, V., Goyne, J., McLean, J., VanderHoek, M., . . . Ross, D. M. (2016). The genomic landscape of mitochondrial DNA mutations in chronic myeloid leukaemia.. In European Journal of Human Genetics. Barcelona: Natue Publishing Group.
2016 Pagani, I. S., Kok, C. H., Wang, J., Saunders, V., Goyne, J., McLean, J., . . . Ross, D. M. (2016). MITOCHONDRIAL DNA MUTATIONS IDENTIFY CLONAL HETEROGENEITY IN CHRONIC MYELOID LEUKAEMIA. In HAEMATOLOGICA Vol. 101 (pp. 234). Copenhagen, DENMARK: FERRATA STORTI FOUNDATION.
2016 Zaliova, M., Moorman, A. V., Cazzaniga, G., Stanulla, M., Harvey, R. C., Roberts, K. G., . . . Zuna, J. (2016). Characterization of leukemias with ETV6-ABL1 fusion. In Proceedings of the 57th Annual Meeting of the American-Society-of-Hematology, as published in Haematologica Vol. 101 (pp. 1082-1093). Orlando, FL: Ferrata Storti Foundation.
DOI Scopus81 WoS74 Europe PMC65
2015 Hiwase, D., Hahn, C., Babic, M., Moore, S., Singhal, D., Kutyna, M., . . . Scott, H. (2015). MULTIPLE MUTATIONS IN THE SAME GENE SUGGEST CLONAL DIVERSITY AND IS ASSOCIATED WITH POOR PROGNOSIS IN MDS. In LEUKEMIA RESEARCH Vol. 39 (pp. S77-S78). Washington, DC: PERGAMON-ELSEVIER SCIENCE LTD.
DOI
2011 Zhang, J., Ding, L., Holmfeldt, L., Wu, G., Heatley, S. L., Payne-Turner, D., . . . Mullighan, C. G. (2011). Discovery of Novel Recurrent Mutations in Childhood Early T-Cell Precursor Acute Lymphoblastic Leukemia by Whole Genome Sequencing - a Report From the St Jude Children's Research Hospital - Washington University Pediatric Cancer Genome Project. In BLOOD Vol. 118 (pp. 32-33). San Diego, CA: AMER SOC HEMATOLOGY.
2010 Mullighan, C., Zhang, J., Kasper, L. H., Lerach, S., Payne-Turner, D., Phillips, L. A., . . . Downing, J. R. (2010). <i>CREBBP</i> Mutations In Relapsed Acute Lymphoblastic Leukemia. In BLOOD Vol. 116 (pp. 184). Orlando, FL: AMER SOC HEMATOLOGY.
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2010 Heatley, S. L., Mullighan, C. G., Sullivan, L. C., Brooks, A. G., Szer, J., Bradstock, K., . . . Bardy, P. G. (2010). KIR HAPLOTYPE MAY INFLUENCE CLINICAL OUTCOME FOLLOWING HLA-MATCHED SIBLING HAEMOPOIETIC STEM CELL TRANSPLANTATION. In BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION Vol. 16 (pp. S270). ELSEVIER SCIENCE INC.
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2009 Heatley, S., Sullivan, L., Pietra, G., Lin, J., Jordan, J., Mingari, M. C., . . . Brooks, A. (2009). RECOGNITION OF HLA-E BY NATURAL KILLER CELLS IS IMPACTED BY VARIATION IN CYTOMEGALOVIRUS UL40 SEQUENCES IN HAEMOPOIETIC STEM CELL TRANSPLANTATION. In HUMAN IMMUNOLOGY Vol. 70 (pp. S167). CA, San Francisco: ELSEVIER SCIENCE INC.
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2009 Heatley, S., Mullighan, C., Sullivan, L., Brooks, A., & Bardy, P. (2009). THE EFFECT OF KIR HAPLOTYPE ON CLINICAL OUTCOME FOLLOWING HLA-MATCHED SIBLING HAEMOPOIETIC STEM CELL TRANSPLANTATION. In HUMAN IMMUNOLOGY Vol. 70 (pp. S169). San Francisco, CA: ELSEVIER SCIENCE INC.
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2007 Hurst, N., Mullighan, C. G., Heatley, S. L., Robinson, K., Danner, S., Hahn, U., . . . Bardy, P. G. (2007). Risk factors for blood product usage following sibling allogeneic haemopoietic stem cell transplantation (allo-HCT). In BLOOD Vol. 110 (pp. 856A). Atlanta, GA: AMER SOC HEMATOLOGY.
DOI
2007 Worthley, D. L., Mullighan, C. G., Dean, M. M., Gordon, D. L., Phillips, P., Heatley, S., . . . Bardy, P. G. (2007). Mannose-binding lectin deficiency does not predispose to <i>Helicobacter pylori</i> infection. In GASTROENTEROLOGY Vol. 132 (pp. A709). DC, Washington: W B SAUNDERS CO-ELSEVIER INC.
2006 Mullighan, C., Heatley, S. L., Villalta, N. R., Doherty, K. V., Danner, S., Hahn, U., . . . Bardy, P. G. (2006). Extended <i>TNF</i> genotyping identifies <i>TNF</i>-857T as a risk factor for acute graft-versus-host disease following allogeneic hematopoietic stem cell transplantation.. In BLOOD Vol. 108 (pp. 16A). Orlando, FL: AMER SOC HEMATOLOGY.
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2006 Mullighan, C. G., Heatley, S. E., Danner, S., Dean, M., Doherty, K. V., Hahn, U., . . . Bardy, P. G. (2006). Mannose-binding lectin status is associated with risk of major infection following myeloalblative sibling allogeneic hematopoietic stem cell transplantation.. In BLOOD Vol. 108 (pp. 829A). Orlando, FL: AMER SOC HEMATOLOGY.
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2003 Eisen, D., Dean, M., Heatley, S., O'Sullivan, M., & Minchinton, R. (2003). Mannose binding lectin insufficiency predisposes to cryptococcal infection in HIV negative patients. In TRENDS IN MEDICAL MYCOLOGY (pp. 17-20). NETHERLANDS, AMSTERDAM: MEDIMOND S R L.
2002 Heatley, S., Humphreys, I., & Doherty, K. (2002). Polymorphisms in <i>HFE</i> and <i>DMT1</i>:: Their frequency and effect on iron stores in blood donors.. In TRANSFUSION Vol. 42 (pp. 69S-70S). FLORIDA, ORLANDO: AMER ASSOC BLOOD BANKS.
2000 Bardy, P., Grigg, A. P., Szer, J., Roberts, A., Schwarer, A. P., Spencer, A., . . . Hughes, T. P. (2000). Successful engraftment with disease response following sibling allograft with reduced conditioning, T-cell depletion and delayed incremental DLI in CML and MM.. In BLOOD Vol. 96 (pp. 783A). AMER SOC HEMATOLOGY.

Year Citation
2024 Rehn, J., Heatley, S., Page, E., Eadie, L., Schutz, C., Thomson, A., . . . White, D. (2024). Acquired copy number variants are highly correlated with Ph+ALL subgroups identified by transcriptomic analysis. Poster session presented at the meeting of Blood Annual Scientific Meeting.
2024 Rehn, J., Page, E., Heatley, S., Eadie, L., Schutz, C., Thomson, A., . . . White, D. (2024). Genomic characterisation of PAX5alt B-cell acute lymphoblastic leukaemia reveals novel PAX5 fusions. Poster session presented at the meeting of Australian and New Zealand Children’s Haematology/Oncology Group (ANZCHOG) Scientific Meeting.
2023 Rehn, J., Schutz, C., Page, E., Heatley, S., Eadie, L., McClure, B., . . . White, D. (2023). High expression of DUX4 mRNA is a reliable indicator of DUX4-rearranged acute lymphoblastic leukaemia. Poster session presented at the meeting of Australian and New Zealand Children’s Haematology/Oncology group (ANZCHOG) Scientific Meeting.
2022 Thomson, A., Rehn, J., Heatley, S., Eadie, L., McClure, B., Page, E., . . . White, D. (2022). Benchmarking the detection rate of IGH gene fusions in B-cell Acute Lymphoblastic Leukaemia. Poster session presented at the meeting of Australian Bioinformatics and Computational Biology Society (ABACBS) Conference.
2021 Heatley, S. L., Page, E. C., Eadie, L. N., McClure, B. J., Rehn, J., Yeung, D. T., . . . White, D. L. (2021). Modeling Relapsed, Refractory Acute Lymphoblastic Leukemia from a Child with Neurofibromatosis. Poster session presented at the meeting of BLOOD. GA, Atlanta: AMER SOC HEMATOLOGY.
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2021 Eadie, L., Heatley, S., McClure, B., Rehn, J., Schutz, C., Breen, J., . . . White, D. (2021). Next Generation Genomic Analyses Inform Druggable Targets In T-All Patients. Poster session presented at the meeting of 4th International T-ALL/T-NHL conference: T-ALL2020: Omics, genetics and therapy.
2021 McClure, B., Heatley, S., Grose, R., & White, D. (2021). Activation of the immune cell repertoire in B-cell acute lymphoblastic leukaemia. Poster session presented at the meeting of 12th Biennial Childhood Leukemia and Lymphoma Symposium (CLLS).
2021 Eadie, L., Heatley, S., McClure, B., Rehn, J., Schutz, C., Breen, J., . . . White, D. (2021). Next Generation Genomic Analyses Inform Druggable Targets In T-All Patients. Poster session presented at the meeting of 12th Biennial Childhood Leukemia and Lymphoma Symposium (CLLS).
2021 Heatley, S., Rehn, J., Breen, J., Moore, A., Sutton, R., Osborn, M., & White, D. (2021). Using single cell mRNAseq to interrogate the genomic consequences of Ph-like acute lymphoblastic leukaemia in adolescents. Poster session presented at the meeting of 12th Biennial Childhood Leukemia and Lymphoma Symposium (CLLS).
2020 Page, E., Heatley, S., Thomas, P., & White, D. (2020). HMGN1 is necessary for Down Syndrome leukaemic cell proliferation and cooperates with CRLF2 for leukaemic transformation. Poster session presented at the meeting of The 59th ASMR National Scientific Conference.
2020 Eadie, L. N., Rehn, J., Heatley, S. L., McClure, B. J., Schutz, C. S., Breen, J., . . . White, D. L. (2020). Next Generation Genomic Analyses in T-ALL Patients Identify Recurrent and Novel Genomic Abnormalities. Poster session presented at the meeting of BLOOD. ELECTR NETWORK: ELSEVIER.
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2020 Tavakoli, P., Eadie, L. N., Heatley, S. L., Bruning, J. B., & White, D. L. (2020). Persistent Activation of JAK/STAT Signaling Plays an Important Role in<i>in Vitro</i>Jaki Resistance in <i>TYK2</i>-rearranged B-Cell Acute Lymphoblastic Leukaemia. Poster session presented at the meeting of BLOOD. ELECTR NETWORK: ELSEVIER.
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2020 Tavakoli, P. S., Eadie, L. N., Heatley, S. L., Yeung, D. T., & White, D. L. (2020). The MYB-TYK2 gene fusion induces B-cell acute lymphoblastic leukaemia in in vitro and in vivo models and can be effectively targeted by the dual SYK/JAK inhibitor, cerdulatinib. Poster session presented at the meeting of 25th Congress of The European Hematology Association. Frankfurt, Germany (virtual meeting).
2020 Rehn, J. A., Breen, J., Heatley, S. L., McClure, B. J., Eadie, L. N., Schutz, C. E., . . . White, D. L. (2020). Targeted pseudo-alignment technique for rapid and accurate identification of disease-causing variants in acute lymphoblastic leukaemia. Poster session presented at the meeting of 14th Annual Florey Postgraduate Conference. Adelaide, South Australia.
2020 Rehn, J. A., Breen, J., Heatley, S. L., McClure, B. J., Eadie, L. N., Schutz, C. E., . . . White, D. L. (2020). Pseudo-alignment technique for accurate detection of disease-causing variants in acute lymphoblastic leukaemia. Poster session presented at the meeting of Australian Bioinformatics and Computational Biology Society (ABACBS) 2020 National Conference. Canberra, ACT.
2020 Tavakoli, P. S., Eadie, L. N., Heatley, S. L., Yeung, D. T., & White, D. L. (2020). Vorinostat treatment demonstrated efficacy against MYB-TYK2 altered B-cell acute lymphoblastic leukaemia in in vitro and in vivo models. Poster session presented at the meeting of ASMR Annual Scientific Meeting. Adelaide, South Australia.
2020 Tavakoli, P. S., Eadie, L. N., Heatley, S. L., Bruning, J. B., & White, D. L. (2020). Persistent activation of JAK/STAT signaling plays an important role in in vitro Jaki resistance in TYK2-rearranged B-Cell Acute Lymphoblastic Leukaemia. Poster session presented at the meeting of 62nd Annual Meeting of the American Society of Hematology. San Diego, California (virtual conference).
2020 Eadie, L., Heatley, S., McClure, B., Schutz, C., Breen, J., Hughes, T., . . . White, D. (2020). Next Generation Genomic Analyses Inform Druggable Targets In T-All Patients. Poster session presented at the meeting of Australian & New Zealand Children’s Haematology/Oncology Group.
2020 McClure, B., Heatley, S., Grose, R., Yeung, D., & White, D. (2020). Activation of the immune cell repertoire in B-cell acute lymphoblastic leukaemia.. Poster session presented at the meeting of Australian & New Zealand Children’s Haematology/Oncology Group.
2020 Page, E. C., Heatley, S. L., Thomas, P. Q., & White, D. L. (2020). Inducible Knockout of <i>HMGN1</i> in an <i>In Vivo</i> xenograft Model Reduces Down Syndrome Leukemic Burden and Increases Survival Outcomes. Poster session presented at the meeting of BLOOD. ELECTR NETWORK: ELSEVIER.
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2019 Yeung, D., Greenwood, M., Rehn, J., Heatley, S., McClure, B., Eadie, L., . . . White, D. (2019). High risk genomic alterations identified at the time of diagnosis are strongly associated with MRD and subsequent poor outcomes in AYA ALL patients treated on a pediatric inspired chemotherapy regimen. Poster session presented at the meeting of Blood. Orlando, CA: American Society of Hematology.
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2019 Page, E. C., Heatley, S. L., Yeung, D. T., Thomas, P. Q., & White, D. L. (2019). A Novel Role for <i>HMGN1</i> in Down Syndrome Acute Lymphoblastic Leukemia. Poster session presented at the meeting of BLOOD. FL, Orlando: ELSEVIER.
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2019 Tavakoli, P. S., Eadie, L., Heatley, S. L., & White, D. L. (2019). The dual SYK/JAK inhibitor cerdulatinib demonstrates in vitro efficacy against a novel MYB-TYK2 fusion protein in acute lymphoblastic leukaemia cells. Poster session presented at the meeting of Australian and New Zealand Children’s Haematology/Oncology Group (ANZCHOG) Scientific Meeting 2019. Christchurch, New Zealand.
2019 Eadie, L., Heatley, S. L., McClure, B. J., Rehn, J. A., Breen, J., Hughes, T. P., . . . White, D. L. (2019). Exploration of the Genomic Diversity in T-ALL Patients Using mRNA Sequencing. Poster session presented at the meeting of 1st European Society of Haematology (ESH) Translational Conference on ALL. Berlin, Germany.
2019 Eadie, L., Heatley, S. L., McClure, B. J., Rehn, J. A., Breen, J., Hughes, T. P., . . . White, D. L. (2019). Exploration of the Genomic Diversity in T-ALL Patients Using mRNA Sequencing. Poster session presented at the meeting of ASMR Annual Scientific Meeting. Adelaide, South Australia.
2019 Rehn, J. A., Breen, J., Heatley, S. L., McClure, B. J., Eadie, L., Schutz, C. E., . . . White, D. L. (2019). Investigating “alignment-free” computational techniques for the accurate identification of Acute Lymphoblastic Leukaemia (ALL) gene fusion events. Poster session presented at the meeting of SAHMRI Annual Scientific Meeting. Adelaide, South Australia.
2019 Heatley, S. L., McClure, B. J., Eadie, L. N., Rehn, J. A., Breen, J., Hughes, T. P., . . . White, D. L. (2019). Exploring the genomic diversity of AYA and adult high-risk B-ALL cases by mRNA sequencing. Poster session presented at the meeting of SAHMRI Annual Scientific Meeting. Adelaide, South Australia.
2019 Toomes, C., McClure, B., Mayne, B., Bruning, J., Heatley, S., Kok, C., . . . White, D. (2019). Identification and characterisation of ruxolitinib resistant mutations in JAK2-rearranged B-cell acute lymphoblastic leukaemia. Poster session presented at the meeting of Poster, Australian Society for Medical Research (ASMR) SA Meeting.
2018 Asari, K., Leclercq, T., Srihari, S., Fitter, S., Yeung, D., Hughes, T., . . . White, D. L. (2018). in vitro modelling of Ph-like ALL uncovers novel genomic alterations associated with TKI-resistance as a consequence of targeted therapy. Poster session presented at the meeting of Childhood Leukaemia and Lymphoma Symposium. Helsinki, Finland.
2018 Heatley, S. L., Mayne, B. T., McClure, B. J., Kok, C., Sadras, T., Dang, P., . . . White, D. L. (2018). Exploring the genomic diversity of AYA and adult high-risk B-ALL cases by mRNA sequencing. Poster session presented at the meeting of 23rd Congress of European Hematology Association. Stockholm, Sweden.
2018 Downes, C. E., McClure, B. J., Heatley, S. L., Yeung, D. T., & White, D. L. (2018). Identification of ruxolitinib resistance mutations in Pro-B cells driven by a high-risk B-ALL JAK2-fusion. Poster session presented at the meeting of Poster, New Directions in Leukaemia Research (NDLR).
2018 Heatley, S. L., McClure, B. J., Kok, C., Sadras, T., Dang, P., Galbraith, K., . . . White, D. L. (2018). Exploring the genomic diversity of adult and AYA cases with high-risk B-ALL by mRNA sequencing. Poster session presented at the meeting of NDLR.
2018 Downes, C. E., McClure, B. J., Mayne, B. T., Bruning, J. B., Heatley, S. L., Kok, C., . . . White, D. L. (2018). Identification and computational modelling of ruxolitinib resistant mutations in JAK2-rearranged B-cell acute lymphoblastic leukaemia. Poster session presented at the meeting of Poster, Adelaide Protein Group (APG) Student Awards.
2018 Page, E. C., Heatley, S. L., Thomas, P., & White, D. L. (2018). Precision medicine approaches may be the future for CRLF2 rearranged Down Syndrome Acute Lymphoblastic Leukaemia. Poster session presented at the meeting of ASMR.
2018 Downes, C. E., McClure, B. J., Mayne, B. T., Bruning, J. B., Heatley, S. L., Kok, C., . . . White, D. L. (2018). Identification of ruxolitinib resistance mutations in Pro-B cells driven by a high-risk JAK2 fusion in B-cell acute lymphoblastic leukaemia. Poster session presented at the meeting of Oral, Australian Society for Medical Research (ASMR) SA Meeting.
2018 Tavakoli Shiraz, P., Eadie, L. N., Heatley, S. L., & White, D. L. (2018). The dual SYK/JAK inhibitor cerdulatinib demonstrates in vitro efficacy against a novel MYB-TYK2 fusion protein in acute lymphoblastic leukaemia cells. Poster session presented at the meeting of ASMR.
2018 Downes, C. E., McClure, B. J., Mayne, B. T., Bruning, J. B., Heatley, S. L., Kok, C., . . . White, D. L. (2018). Identification and Characterisation of Ruxolitinib Resistant Mutations in JAK2-rearranged B-cell Acute Lymphoblastic Leukaemia. Poster session presented at the meeting of Poster, Australasian Genomic Technologies Association (AGTA) Annual Conference.
2018 Downes, C. E., McClure, B. J., Mayne, B. T., Bruning, J. B., Heatley, S. L., Kok, C., . . . White, D. L. (2018). Identification of ruxolitinib resistance mutations in Pro-B cells driven by a high-risk B-ALL JAK2-fusion. Poster session presented at the meeting of Poster, Australian and New Zealand Children's Haematology/Oncology Group (ANZCHOG) Annual Scientific Meeting.
2018 Tavakoli Shiraz, P., Eadie, L. N., Heatley, S. L., & White, D. L. (2018). The dual SYK/JAK inhibitor cerdulatinib demonstrates in vitro efficacy against a novel MYB-TYK2 fusion protein in acute lymphoblastic leukaemia cells. Poster session presented at the meeting of SAHMRI Scientific Seminar.
2018 Downes, C. E., McClure, B. J., Mayne, B. T., Bruning, J. B., Heatley, S. L., Kok, C., . . . White, D. L. (2018). Identification and computational modelling of ruxolitinib resistant mutations in JAK2-rearranged B-cell acute lymphoblastic leukaemia. Poster session presented at the meeting of Poster, South Australian Health and Medical Research Institute (SAHMRI) Annual Scientific Meeting.
2018 Tavakoli Shiraz, P., Eadie, L. N., Heatley, S. L., & White, D. L. (2018). The dual SYK/JAK inhibitor cerdulatinib demonstrates in vitro efficacy against a novel MYB-TYK2 fusion protein in acute lymphoblastic leukaemia cells. Poster session presented at the meeting of 12th Annual Florey postgraduate Conference.
2018 Downes, C. E., McClure, B. J., Mayne, B. T., Bruning, J. B., Heatley, S. L., Kok, C., . . . White, D. L. (2018). Identification and computational modelling of ruxolitinib resistant mutations in JAK2-rearranged B-cell acute lymphoblastic leukaemia. Poster session presented at the meeting of Poster, European Molecular Biology Laboratory (EMBL) Australia Postgraduate Symposium.
2018 Tavakoli Shiraz, P., Eadie, L. N., Heatley, S. L., & White, D. L. (2018). The dual SYK/JAK inhibitor cerdulatinib demonstrates in vitro efficacy against a novel MYB-TYK2 fusion protein in acute lymphoblastic leukaemia cells. Poster session presented at the meeting of EMBL Australia Postgraduate Symposium.
2017 McClure, B. J., Heatley, S. L., Kok, C., Sadras, T., An, J., Quek, K., . . . White, D. L. (2017). EP300-ZNF384 is a recurrent fusion gene with distinct gene expression in adolescent/young adult pre-B-ALL patients. Poster session presented at the meeting of ANZCHOG.
2017 Heatley, S. L., Sadras, T., Kok, C., Nievergall, E., Quek, K., Dang, P., . . . White, D. L. (2017). High Prevalence of Relapse in Australian Children with Ph-like Acute Lymphoblastic Leukemia Despite Risk-Adapted Treatment. Poster session presented at the meeting of ANZCHOG.
2017 Asari, K., Sadras, T., Srihari, S., Fitter, S., An, J., Zannettino, A. C., . . . White, D. L. (2017). in vitro Modelling of Ph-like ALL Fusions Uncovers Novel Kinase-domain Mutations as a Mode of TKI-resistance and Potential Consequence of Targeted TKI Therapy. Poster session presented at the meeting of ANZCHOG.
2017 McClure, B. J., Heatley, S. L., Sadras, T., Sutton, R., & White, D. L. (2017). EP300-ZNF384 is a recurrent fusion gene with distinct gene expression in adolescent/young adult Australian pre-B-acute lymphoblastic leukaemia. Poster session presented at the meeting of IBFM.
2017 Heatley, S., Sadras, T., Kok, C., Nievergall, E., Quek, K., Dang, P., . . . White, D. (2017). High prevalence of relapse in children with Philadelphia-like acute lymphoblastic leukemia despite risk-adapted treatment. Poster session presented at the meeting of Abstracts of the 57th Annual Meeting of the American Society of Hematology, as published in Blood. Orlando, FL: American Society of Hematology.
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2017 Downes, C. E., McClure, B. M., Heatley, S. H., Sadras, T. S., Hughes, T. H., Kok, C. K., . . . White, D. W. (2017). Identification and cloning of a novel GOLGA4-JAK2 fusion from an adult patient with B-cell Acute Lymphoblastic Leukaemia. Poster session presented at the meeting of Poster, Australian Society for Medical Research (ASMR) SA Meeting. Adelaide.
2016 Heatley, S., Sadras, T., kok, C., Venn, N., Revesz, T., Osborn, M., . . . White, D. L. (2016). Australian Children with Ph-like ALL enrolled to ANZCHOG ALL8 had a high prevalence of relapse despite risk adapted treatment. Poster session presented at the meeting of CLS SCIENTIFIC PROGRAMME, Refractory Leukemia and Miscellaneous. Athens.
2016 Sadras, T., Heatley, S., Dang, P., Kok, C., Quek, K., Nievergall, E., . . . White, D. L. (2016). A nine-gene signature defines 2 groups of CRLF2 rearranged B-ALL patients with distinctive genetic features. Poster session presented at the meeting of .. Athens.
2016 Pagani, I. S., Kok, C., Saunders, V., Goyne, J., McLean, J., Vanderhoek, M., . . . Ross, D. (2016). The genomic landscape of mitochondrial DNA mutations in chronic myeloid leukaemia. Poster session presented at the meeting of .. Barcelona, Spain.
2016 Sadras, T., Heatley, S., Kok, C., Quek, K., Dang, P., Nievergall, E., . . . White, D. L. (2016). CRLF2 rearranged B-ALL cases with a Ph-like gene signature are enriched for JAK2 mutations. Poster session presented at the meeting of .. Noosa, QLD.
2016 McClure, B., Heatley, S., Sadras, T., Nievergall, E., Kok, C., Dang, P., . . . White, D. L. (2016). Identification of a significantly high prevalence of relapse in Australian children with Ph-like ALL. Poster session presented at the meeting of .. Noosa, QLD.
2016 Asari, K., Heatley, S., Leclercq, T., Fitter, S., Zannettino, A., Hughes, T., & White, D. L. (2016). In vitro Modelling of Therapeutic Resistance to Elucidate Mechanisms of TKI-Resistant High-Risk ALL. Poster session presented at the meeting of .. Noosa, QLD.
2016 Pagani, I., Kok, C., Saunders, V., Goyne, J., McLean, J., Vanderhoek, M., . . . White, D. L. (2016). Do mitochondrial mutations in chronic myeloid leukaemia identify a pre-leukemic clone?. Poster session presented at the meeting of .. Noosa, QLD.
2016 White, D. L., McClure, B., Heatley, S., Sadras, T., Quek, K., & Hughes, T. (2016). Investigation of the transforming capacity of a recently identified EP300-ZNF384 fusion gene in adult acute lymphoblastic leukaemia. Poster session presented at the meeting of Poster Session. Adelaide, SA.
2016 Asari, K., Heatley, S., Leclercq, T., Fitter, S., Kok, C. H., Zannettino, A., . . . White, D. L. (2016). Investigating Modes of Therapeutic Resistance via In Vitro Modelling of TKI-resistant High-Risk Philadelphia-chromosome-positive and Philadelphia-chromosome-like Acute Lymphoblastic Leukaemia. Poster session presented at the meeting of Poster Session. Adelaide, SA.
2016 Galbraith, K., Sadras, T., McClure, B., Heatley, S., & White, D. L. (2016). Identification of novel therapeutic targets in CRLF2 rearranged acute lymphoblastic leukaemia. Poster session presented at the meeting of Poster Session. Adelaide, SA.
2016 Heatley, S., Sadras, T., McClure, B., Kok, C. H., Dang, P., Nievergall, E., . . . White, D. L. (2016). The Incidence of Ph-like Acute Lymphoblastic Leukaemia (ALL) Increases with Age and is Characterised by Poor Outcome. Poster session presented at the meeting of Poster Session. Melbourne, VIC.
2016 Pagani, I. S., Kok, C. H., Wang, J., Saunders, V., Van der Hoek, M., Heatley, S., . . . Ross, D. (2016). Mitochondrial DNA Mutations at Diagnosis are Linked to Response in TKI treated Chronic Myeloid Leukaemia Patients. Poster session presented at the meeting of Poster Session. Melbourne, VIC.
2015 Zaliova, M., Moorman, A., Cazzaniga, G., Stanulla, M., Harvey, R., Roberts, K., . . . Zuna, J. (2015). Characterization of Leukemias with ETV6-ABL1 Fusion. Poster session presented at the meeting of BLOOD. Orlando, FL: AMER SOC HEMATOLOGY.
2015 Sadras, T., Heatley, S., Nievergall, E., Kok, C., Dang, P., Yeung, D., . . . White, D. (2015). JAK2 MUTATIONS ARE HIGHLY ENRICHED IN CRLF2-REARRANGED B-ALL CASES WITH A PH-LIKE GENE SIGNATURE. Poster session presented at the meeting of HAEMATOLOGICA. Vienna, AUSTRIA: FERRATA STORTI FOUNDATION.
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2014 Nievergall, E., Heatley, S., Kok, C., Dang, P., Frede, A., Moore, S., . . . White, D. (2014). THE INCIDENCE OF THE HIGH-RISK PH-LIKE ALL SUBTYPE MAY ACCOUNT FOR THE MAJORITY OF NON BCR-ABL1+B ALL CASES IN ADULTS. Poster session presented at the meeting of HAEMATOLOGICA. Milan, ITALY: FERRATA STORTI FOUNDATION.

Grant Funding:

2024 Channel 7 Children’s Research Foundation $100,000: Using Single Cell Sequencing to Elucidate the Clonal Evolution of Acute Lymphoblastic Leukaemia to Prevent Relapse in Children and Improve Outcomes.

July 1 2016- June 30 2018 & July 1 2019- Dec 2022 The Kids Cancer Project $436,015 Elucidating drug sensitivity and clonal evolution of Ph-like ALL in adolescents. 

Fellowship: Susan Heatley

2015 Channel 7 Children’s Research Foundation $75,000

Developing a robust screening tool to identify children with high risk “Ph-like” Acute Lymphoblastic Leukaemia (ALL) that will lead to improved outcomes through the use of targeted therapies.

CIA Susan Heatley, CIB Deborah White, CIC Charles Mullighan

Date Role Research Topic Program Degree Type Student Load Student Name
2024 External Supervisor Identifying Predictors of CNS involvement in Acute Lymphoblastic Leukaemia Doctor of Philosophy Doctorate Full Time Mr Luke Jacob Quinlan
2024 External Supervisor Identifying Predictors of CNS involvement in Acute Lymphoblastic Leukaemia Doctor of Philosophy Doctorate Full Time Mr Luke Jacob Quinlan
2023 External Supervisor Interrogating the DUX4 rearranged subtype of B cell Acute Lymphoblastic Leukaemia Doctor of Philosophy Doctorate Full Time Mr Thomas Oliver McGovern
2023 External Supervisor Interrogating the DUX4 rearranged subtype of B cell Acute Lymphoblastic Leukaemia Doctor of Philosophy Doctorate Full Time Mr Thomas Oliver McGovern

Date Role Research Topic Program Degree Type Student Load Student Name
2018 - 2021 Co-Supervisor Exploring the cooperation and targetability of CRLF2 and HMGN1 in Down Syndrome Acute Lymphoblastic Leukaemia Doctor of Philosophy Doctorate Full Time Miss Elyse Chenae Page
2017 - 2021 Co-Supervisor Characterising the novel MYB-TYK2 fusion gene in high-risk acute lymphoblastic leukaemia: oncogenic potential, effective therapeutic strategies and In vitro modelling of drug resistance mechanisms Doctor of Philosophy Doctorate Full Time Miss Paniz Tavakoli Shirazi
2015 - 2018 Co-Supervisor In vitro Modelling of High-risk ALL Fusions Uncovers Genomic Alterations and Non-canonical Signalling Pathways as a Mode of TKI-Resistance - Implications for Targeted Therapy Doctor of Philosophy Doctorate Full Time Miss Kartini Asari

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