Dr Christopher Hahn
Centre for Cancer Biology
College of Health
Eligible to supervise Masters and PhD - email supervisor to discuss availability.
Dr Christopher N Hahn, PhDSA Pathology Department of Genetics and Molecular Pathology Frome Rd, Adelaide.Molecular Pathology Research Laboratory: All disease processes in humans have a genetic component, either inherited or acquired by somatic mutation during cell division. It is important to identify genes and mutations that cause disease, predispose families to diseases, or are acquired during disease progression as these are important diagnostic and prognostic markers. They also provide direct targets and biological pathways for therapeutic intervention.We are interested in how and why genetic mutations occur, how these changes cause diseases or disease predisposition such as cancer and autoimmunity, and ways of better treating and monitoring these diseases. Our model diseases are typically, blood cell diseases, such as leukaemias, lymphomas and autoimmunity (such as arthritis). We also work on rare or orphan diseases with unmet clinical needs, such as genetic diagnoses for family planning.Our department is co-located with the ACRF Cancer Genomics Facility, which provides access to powerful cutting edge genetic/genomic technologies including bioinformatics, next-generation sequencing and sample preparation robotics. The Department performs both basic and translational research, which includes implementing these new technologies into its diagnostic tests for personalized medicine.
Germline mutations in familial haematopoietic malignancies identifies new pan-cancer predisposition genes and may alter clinical decision making, including for known cancer genes.
https://www.youtube.com/watch?v=Ep8_eA2meM0&feature=youtu.be
Biological characterisation and therapeutic options for high risk, DDX41 mutated, haematological malignancies. Beat Cancer Research Project Grant.
| Date | Position | Institution name |
|---|---|---|
| 2020 - ongoing | Adjunct Associate Professor | University of South Australia |
| 2019 - ongoing | Affiliate Senior Lecturer | University of Adelaide |
| 2018 - ongoing | Associate Member of the Centre for Cancer Biology Faculty | Centre for Cancer Biology |
| 2008 - ongoing | Section Head - Molecular Pathology Research Laboratory | SA Pathology |
| Language | Competency |
|---|---|
| English | Can read, write, speak, understand spoken and peer review |
| Date | Institution name | Country | Title |
|---|---|---|---|
| 1987 - 1991 | University of Adelaide | Australia | PhD |
| Year | Citation |
|---|---|
| 2023 | Shah, M. V., Kutyna, M., Shah, S., Tran, E. N. H., Baranwal, A., Ladon, D., . . . Hiwase, D. (2023). Comparison of World Health Organization and International Consensus Classification Guidelines for Myeloid Neoplasms Harboring TP53-Mutations Using an Independent International Cohort. In BLOOD Vol. 142 (pp. 4 pages). CA, San Diego: ELSEVIER. DOI WoS4 |
| 2023 | Scott, H. S., Zerella, J., Homan, C., Arts, P., Lin, S., Spinelli, S. J., . . . Hahn, C. N. (2023). ERG Is a New Predisposition Gene for Bone Marrow Failure and Hematological Malignancy. In BLOOD Vol. 144 (pp. LBA8). CA, San Diego: ELSEVIER. DOI WoS2 |
| 2023 | Hong, L. E., Kok, C. H., Kutyna, M., Li, J. J., Chhetri, R., Ross, D. M., . . . Hiwase, D. (2023). High Prevalence of IDH Mutation in Myeloid Neoplasm with Concomitant Autoimmune Rheumatic Disorders. In BLOOD Vol. 142 (pp. 4 pages). CA, San Diego: ELSEVIER. DOI |
| 2023 | Hiwase, D., Baranwal, A., Shah, S., Kutyna, M., Hahn, C. N., Abdelmajid, M., . . . Shah, M. V. (2023). Single-Hit TP53 mut Is Associated with Poor Outcomes in Therapy-Related but Not De Novo Myelodysplastic Syndromes: Importance of Clinical History. In BLOOD Vol. 142 (pp. 4 pages). CA, San Diego: ELSEVIER. DOI |
| 2022 | Coenen, N., Dachselt, R., Finkbeiner, B., Frenkel, H., Hahn, C., Horak, T., . . . Siber, J. (2022). Explaining Hyperproperty Violations. In S. Shoham, & Y. Vizel (Eds.), COMPUTER AIDED VERIFICATION (CAV 2022), PT I Vol. 13371 (pp. 407-429). ISRAEL, Haifa: SPRINGER INTERNATIONAL PUBLISHING AG. DOI WoS10 |
| 2022 | Saygin, C., Roloff, G. W., Hahn, C. N., Chhetri, R., Gill, S., Elmariah, H., . . . Godley, L. A. (2022). Allogeneic Hematopoietic Stem Cell Transplant Outcomes in Adults with Inherited Myeloid Malignancies. In BLOOD Vol. 140 (pp. 10542-10544). LA, New Orleans: ELSEVIER. DOI |
| 2022 | Hahn, C., Levy, A., Zapata, C., & Sutphin, R. (2022). DESMOPLASTIC SMALL ROUND CELL TUMOR (DSRCT) OF THE MAJOR SALIVARY GLAND: CASE REPORT. In PEDIATRIC BLOOD & CANCER Vol. 69 (pp. 1 page). WILEY. |
| 2021 | Hansen, M., & Hahn, C. (2021). Autoimmune Encephalitis: Modifiable and Non-modifiable Predictors of Relapse. In NEUROLOGY Vol. 96 (pp. 2 pages). LIPPINCOTT WILLIAMS & WILKINS. |
| 2021 | Berenbrink, P., Friedetzky, T., Hahn, C., Hintze, L., Kaaser, D., Kling, P., & Nagel, L. (2021). Infinite Balanced Allocation via Finite Capacities. In 2021 IEEE 41ST INTERNATIONAL CONFERENCE ON DISTRIBUTED COMPUTING SYSTEMS (ICDCS 2021) (pp. 965-975). ELECTR NETWORK: IEEE COMPUTER SOC. DOI WoS1 |
| 2021 | Coenen, N., Finkbeiner, B., Hahn, C., Hofmann, J., & Schillo, Y. (2021). Runtime Enforcement of Hyperproperties. In Z. Hou, & V. Ganesh (Eds.), AUTOMATED TECHNOLOGY FOR VERIFICATION AND ANALYSIS, ATVA 2021 Vol. 12971 (pp. 283-299). ELECTR NETWORK: SPRINGER INTERNATIONAL PUBLISHING AG. DOI WoS4 |
| 2021 | Hahn, C. N., Feurstein, S. K., Singhal, D., Kutyna, M. M., Chhetri, R., Wee, A., . . . Hiwase, D. (2021). Unexpected High Frequency of Pathogenic Germline Variants in Older Adults with Primary Myelodysplastic Syndrome. In BLOOD Vol. 138 (pp. 4 pages). GA, Atlanta: ELSEVIER. DOI WoS1 |
| 2021 | Schmitt, F., Hahn, C., Rabe, M. N., & Finkbeiner, B. (2021). Neural Circuit Synthesis from Specification Patterns. In M. Ranzato, A. Beygelzimer, Y. Dauphin, P. S. Liang, & J. W. Vaughan (Eds.), ADVANCES IN NEURAL INFORMATION PROCESSING SYSTEMS 34 (NEURIPS 2021) Vol. 34 (pp. 13 pages). ELECTR NETWORK: NEURAL INFORMATION PROCESSING SYSTEMS (NIPS). WoS5 |
| 2020 | Finkbeiner, B., Hahn, C., Hofmann, J., & Tentrup, L. (2020). Realizing ω-regular Hyperproperties. In S. K. Lahiri, & C. Wang (Eds.), COMPUTER AIDED VERIFICATION, PT II Vol. 12225 (pp. 40-63). ELECTR NETWORK: SPRINGER INTERNATIONAL PUBLISHING AG. DOI WoS11 |
| 2019 | Hahn, C. (2019). Algorithms for Monitoring Hyperproperties. In B. Finkbeiner, & L. Mariani (Eds.), RUNTIME VERIFICATION, RV 2019 Vol. 11757 (pp. 70-90). PORTUGAL, Porto: SPRINGER INTERNATIONAL PUBLISHING AG. DOI WoS2 |
| 2019 | Homan, C., Armstrong, M., Dobbins, J., Lawrence, D., Wang, P., Arts, P., . . . Brown, A. (2019). DEVELOPMENT OF A DATA PORTAL FOR AGGREGATION AND ANALYSIS OF GENOMICS DATA IN FAMILIAL PLATELET DISORDER WITH PREDISPOSITION TO MYELOID MALIGNANCY - THE RUNX1.DB. In EXPERIMENTAL HEMATOLOGY Vol. 76 (pp. S69). ELSEVIER SCIENCE INC. |
| 2019 | Venugopal, P., Babic, M., Barnett, C., Bray, S., Brown, A., Cheah, J., . . . Young, C. C. (2019). IMPLICATIONS OF REVERTANT SOMATIC MOSAICISM IN BONE MARROW FAILURE SYNDROMES. In EXPERIMENTAL HEMATOLOGY Vol. 76 (pp. S90). ELSEVIER SCIENCE INC. DOI |
| 2019 | Cheah, J., Brown, A., Eshraghi, L., Feng, J., Schreiber, A., Babic, M., . . . Scott, H. (2019). AN INTEGRATIVE GENOMIC APPROACH TO EXAMINE MUTATIONS AND BIOLOGICAL PATHWAYS ASSOCIATED WITH HAEMATOLOGICAL MALIGNANCY DEVELOPMENT IN DDX41 MUTATED FAMILIES. In EXPERIMENTAL HEMATOLOGY Vol. 76 (pp. S61). ELSEVIER SCIENCE INC. |
| 2019 | Singhal, D., Hahn, C. N., Moma, L. D., Wee, L. Y. A., Chhetri, R., Babic, M., . . . Hiwase, D. K. (2019). Deleterious Germline Variants, Especially in the DNA Repair Pathway, Are Common in Patients with Non-Related Multiple Cancers, One of Them Being Hematological Malignancy. In BLOOD Vol. 134 (pp. 3 pages). FL, Orlando: ELSEVIER. DOI WoS1 |
| 2019 | Venugopal, P., Cheah, J. J. C., Eshraghi, L., Shahrin, N. H., Homan, C., Feng, J., . . . Scott, H. S. (2019). An Integrative Genomic Approach to Examine Mutations and Biological Pathways Associated with Hematological Malignancy Development in DDX41 Mutated Families. In BLOOD Vol. 134 (pp. 3 pages). FL, Orlando: ELSEVIER. DOI WoS2 |
| 2019 | Brown, A. L., Babic, M., Schreiber, A., Feng, J., Dobbins, J., Arts, P., . . . Scott, H. S. (2019). Familial Clustering of Hematological Malignancies: Harbingers of Wider Germline Cancer Susceptibility. In BLOOD Vol. 134 (pp. 3 pages). FL, Orlando: ELSEVIER. DOI |
| 2019 | Hahn, C. N., Babic, M., Brautigan, P. J., Venugopal, P., Phillips, K., Dobbins, J., . . . Scott, H. S. (2019). Australian Familial Haematological Cancer Study - Findings from 15 Years of Aggregated Clinical, Genomic and Transcriptomic Data. In BLOOD Vol. 134 (pp. 4 pages). FL, Orlando: ELSEVIER. DOI WoS2 |
| 2019 | Coenen, N., Finkbeiner, B., Hahn, C., & Hofmann, J. (2019). The Hierarchy of Hyperlogics. In 2019 34TH ANNUAL ACM/IEEE SYMPOSIUM ON LOGIC IN COMPUTER SCIENCE (LICS) (pp. 13 pages). CANADA, Vancouver: IEEE. DOI WoS39 |
| 2019 | Hahn, C., Stenger, M., & Tentrup, L. (2019). Constraint-Based Monitoring of Hyperproperties. In T. Vojnar, & L. Zhang (Eds.), TOOLS AND ALGORITHMS FOR THE CONSTRUCTION AND ANALYSIS OF SYSTEMS, PT II Vol. 11428 (pp. 115-131). CZECH REPUBLIC, Prague: SPRINGER INTERNATIONAL PUBLISHING AG. DOI WoS24 |
| 2018 | Finkbeiner, B., Hahn, C., Stenger, M., & Tentrup, L. (2018). RVHyper: A Runtime Verification Tool for Temporal Hyperproperties. In D. Beyer, & M. Huisman (Eds.), TOOLS AND ALGORITHMS FOR THE CONSTRUCTION AND ANALYSIS OF SYSTEMS, TACAS 2018, PT II Vol. 10806 (pp. 194-200). GREECE, Thessaloniki: SPRINGER INTERNATIONAL PUBLISHING AG. DOI WoS34 |
| 2018 | Finkbeiner, B., Hahn, C., Lukert, P., Stenger, M., & Tentrup, L. (2018). Synthesizing Reactive Systems from Hyperproperties. In H. Chockler, & G. Weissenbacher (Eds.), COMPUTER AIDED VERIFICATION (CAV 2018), PT I Vol. 10981 (pp. 289-306). ENGLAND, Oxford: SPRINGER INTERNATIONAL PUBLISHING AG. DOI WoS25 |
| 2018 | Finkbeiner, B., Hahn, C., & Torfah, H. (2018). Model Checking Quantitative Hyperproperties. In H. Chockler, & G. Weissenbacher (Eds.), COMPUTER AIDED VERIFICATION (CAV 2018), PT I Vol. 10981 (pp. 144-163). ENGLAND, Oxford: SPRINGER INTERNATIONAL PUBLISHING AG. DOI WoS33 |
| 2018 | Hahn, C., Huntgeburth, J., & Zarnekow, R. (2018). Leverage Once, Earn Repeatedly-Capabilities for Creating and Appropriating Value in Cloud Platform Ecosystems. In R. Lamboglia, A. Cardoni, R. P. Dameri, & D. Mancini (Eds.), NETWORK, SMART AND OPEN: THREE KEYWORDS FOR INFORMATION SYSTEMS INNOVATION Vol. 24 (pp. 143-164). ITALY, Verona: SPRINGER INTERNATIONAL PUBLISHING AG. DOI WoS1 |
| 2018 | Finkbeiner, B., Hahn, C., & Hans, T. (2018). MGHyper: Checking Satisfiability of HyperLTL Formulas Beyond the ∃*∀* Fragment. In S. K. Lahiri, & C. Wang (Eds.), AUTOMATED TECHNOLOGY FOR VERIFICATION AND ANALYSIS (ATVA 2018) Vol. 11138 (pp. 521-527). CA, Los Angeles: SPRINGER INTERNATIONAL PUBLISHING AG. DOI WoS15 |
| 2017 | Finkbeiner, B., Hahn, C., Stenger, M., & Tentrup, L. (2017). Monitoring Hyperproperties. In S. Lahiri, & G. Reger (Eds.), RUNTIME VERIFICATION (RV 2017) Vol. 10548 (pp. 190-207). WA, Seattle: SPRINGER INTERNATIONAL PUBLISHING AG. DOI WoS25 |
| 2017 | Finkbeiner, B., Hahn, C., & Stenger, M. (2017). EAHyper: Satisfiability, Implication, and Equivalence Checking of Hyperproperties. In R. Majumdar, & V. Kuncak (Eds.), COMPUTER AIDED VERIFICATION (CAV 2017), PT II Vol. 10427 (pp. 564-570). GERMANY, Heidelberg: SPRINGER INTERNATIONAL PUBLISHING AG. DOI WoS36 |
| 2017 | Singhal, D., Wee, A., Parker, W., Moore, S., Babic, M., Feng, J., . . . Hiwase, D. K. (2017). Presence of Rare Germline Variants in Fanconi Anaemia Pathway Genes Confers a Poor Prognosis Comparable to <i>TP53</i> Mutations in Therapy-Related Myeloid Neoplasms. In BLOOD Vol. 130 (pp. 3 pages). Atlanta, GA: AMER SOC HEMATOLOGY. WoS2 |
| 2017 | Branford, S., Wang, P., Yeung, D., Purins, A., Marum, J. E., Nataren, N., . . . Hughes, T. P. (2017). Integrative Genomics Reveals Cancer Associated Mutations Are Common at Diagnosis of CML in Patients with Poor Response to TKI Therapy. In BLOOD Vol. 130 (pp. 4 pages). GA, Atlanta: AMER SOC HEMATOLOGY. |
| 2017 | Hahn, C. N., Wee, A., Babic, M., Feng, J., Wang, P., Kutyna, M. M., . . . Scott, H. S. (2017). Duplication on Chromosome 14q Identified in Familial Predisposition to Myeloid Malignancies and Myeloproliferative Neoplasms. In BLOOD Vol. 130 (pp. 2 pages). Atlanta, GA: AMER SOC HEMATOLOGY. WoS3 |
| 2017 | Brown, A. L., Churpek, J., Hahn, C. N., & Scott, H. S. (2017). Clonal Evolution in the Setting of Germline Predisposition. In BLOOD Vol. 130 (pp. 1 page). GA, Atlanta: AMER SOC HEMATOLOGY. WoS3 |
| 2016 | Singhal, D., Wee, L. A., Parker, W. T., Moore, S., Babic, M., Feng, J., . . . Hiwase, D. K. (2016). The Frequency of Genetic Mutations in T-MN Is High and Comparable to Primary MDS but the Spectrum Is Different. In BLOOD Vol. 128 (pp. 5 pages). San Diego, CA: AMER SOC HEMATOLOGY. DOI |
| 2016 | Bassal, M. A., Leo, P., Samaraweera, S. E., Maung, K. Z. Y., Babic, M., Venugopal, P., . . . D'Andrea, R. (2016). Metabolic Profiling of Adult Acute Myeloid Leukemia (AML). In BLOOD Vol. 128 (pp. 6 pages). San Diego, CA: AMER SOC HEMATOLOGY. DOI WoS1 |
| 2016 | Brown, A. L., Hahn, C. N., Carmichael, C., Wilkins, E., Babic, M., Chong, C. -E., . . . Scott, H. S. (2016). Expanded Phenotypic and Genetic Heterogeneity in the Clinical Spectrum of FPD-AML: Lymphoid Malignancies and Skin Disorders Are Common Features in Carriers of Germline <i>RUNX1</i> Mutations. In BLOOD Vol. 128 (pp. 6 pages). San Diego, CA: AMER SOC HEMATOLOGY. DOI WoS2 |
| 2015 | Hahn, C. N., Babic, M., Schreiber, A. W., Kutyna, M. M., Wee, L. A., Brown, A. L., . . . Hiwase, D. (2015). Rare and Common Germline Variants Contribute to Occurrence of Myelodysplastic Syndrome. In BLOOD Vol. 126 (pp. 4 pages). Orlando, FL: AMER SOC HEMATOLOGY. DOI WoS3 |
| 2015 | Branford, S., Wang, P. P. S., Parker, W. T., Yeung, D., Marum, J. E., Stangl, D., . . . Hughes, T. P. (2015). High Incidence of Mutated Cancer-Associated Genes at Diagnosis in CML Patients with Early Transformation to Blast Crisis. In BLOOD Vol. 126 (pp. 4 pages). Orlando, FL: AMER SOC HEMATOLOGY. |
| 2015 | Labes, S., Hahn, C., & Zarnekow, R. (2015). The Value of Community Clouds for Collaboration in the Public Sector. In AMCIS 2015 PROCEEDINGS (pp. 13 pages). PR, Fajardo: ASSOC INFORMATION SYSTEMS. |
| 2015 | Hahn, C., Zarnekow, R., & Roeher, D. (2015). A value proposition oriented typology of electronic marketplaces for B2B SaaS applications. In AMCIS 2015 PROCEEDINGS (pp. 15 pages). PR, Fajardo: ASSOC INFORMATION SYSTEMS. |
| 2014 | Reichert, M., Bakir, B., Hahn, C., Rhim, A. D., Vonderheide, R. H., Reynolds, A. B., . . . Rustgi, A. K. (2014). P120catenin Facilitates Pancreatic Regeneration and Monoallelic Loss Accelerates Kras-Driven Carcinogenesis and Metastasis. In GASTROENTEROLOGY Vol. 146 (pp. S173). IL, Chicago: W B SAUNDERS CO-ELSEVIER INC. |
| 2014 | Heeg, S., Das, K. K., Reichert, M., Takano, S., Bakir, B., Lieberman, A. E., . . . Rustgi, A. K. (2014). The ETS Transcription Factor ETV5 Regulates Ductal Morphogenesis and Differentiation in Association With SOX9. In GASTROENTEROLOGY Vol. 146 (pp. S138). IL, Chicago: W B SAUNDERS CO-ELSEVIER INC. |
| 2014 | Heeg, S., Das, K. K., Reichert, M., Takano, S., Bakir, B., Hahn, C., . . . Rustgi, A. K. (2014). The ETS-Transcription Factor Etv1 Is an Important Regulator of Pancreatic Carcinogenesis and Invasion. In GASTROENTEROLOGY Vol. 146 (pp. S15). IL, Chicago: W B SAUNDERS CO-ELSEVIER INC. |
| 2014 | Ling, K., Lee, H., Brautigan, P., Moore, S., Fraser, R., Cheah, P., . . . Scott, H. (2014). Deciphering the secret role of Sox4 gene locus during mouse cerebral corticogenesis. In Journal of Neurochemistry Vol. 130 (pp. 8). Kaohsiung, Taiwan: Wiley. |
| 2013 | Reichert, M., Takano, S., von Burstin, J., Heeg, S., Kim, S. -B., Lee, J. -S., . . . Rustgi, A. K. (2013). The Prrx1 Homeodomain Transcription Factor Plays a Central Role in Pancreatic Regeneration and Carcinogenesis. In GASTROENTEROLOGY Vol. 144 (pp. S143). FL, Orlando: W B SAUNDERS CO-ELSEVIER INC. |
| 2013 | Heeg, S., Reichert, M., Takano, S., Wu, K. K., Botta, G. P., Bakir, B., . . . Rustgi, A. K. (2013). The Ets-Transcription Factor Etv1 Induces Invasion and Enhances Self Renewal Capacity in PanIN and Pdac. In GASTROENTEROLOGY Vol. 144 (pp. S12-S13). FL, Orlando: W B SAUNDERS CO-ELSEVIER INC. |
| 2013 | Reichert, M., Bakir, B., Hahn, C., Rhim, A. D., Vonderheide, R. H., Adsay, V., & Rustgi, A. K. (2013). Inactivation of a Single Allele of P120catenin Dramatically Accelerates KRAS-Driven Carcinogenesis in the Pancreas. In GASTROENTEROLOGY Vol. 144 (pp. S81). FL, Orlando: W B SAUNDERS CO-ELSEVIER INC. |
| 2013 | Hahn, C., Repschlager, J., Erek, K., & Zarnekow, R. (2013). An Exploratory Study on Cloud Strategies. In AMCIS 2013 PROCEEDINGS (pp. 9 pages). IL, Chicago: ASSOC INFORMATION SYSTEMS. |
| 2011 | Hahn, C., Recker, J., & Mendling, J. (2011). An Exploratory Study of IT-Enabled Collaborative Process Modeling. In M. ZurMuehlen, & J. W. Su (Eds.), BUSINESS PROCESS MANAGEMENT WORKSHOPS Vol. 66 (pp. 61-+). NJ, Stevens Inst Technol, Hoboken: SPRINGER-VERLAG BERLIN. WoS11 |
| 2011 | Rao, N., Butcher, C., Neufing, P., Bray, S., Hahn, C., Scott, H., . . . D'Andrea, R. (2011). Mechanisms of Co-operation of DNMT3A Mutations with JAK2 V617F Through Histone H4 Arginine 3 Provides New Insights in MPN Disease Pathogenesis. In 53rd ASH Annual Meeting and Exposition Vol. 118 (pp. 1). Washington DC: AMER SOC HEMATOLOGY. WoS1 |
| 2003 | Hime, N., Wee, K., Barter, P., & Rye, K. A. (2003). <i>In vivo</i> formation of high density lipoproteins containing both apolipoprotein A-I and apolipoprotein A-II in the rabbit. In ATHEROSCLEROSIS SUPPLEMENTS Vol. 4 (pp. 222). KYOTO, JAPAN: ELSEVIER IRELAND LTD. |
| 2003 | Hime, N., Drew, K., Hahn, C., & Rye, K. A. (2003). Influence of apolipoprotein E isoforms on hepatic lipase-mediated phospholipid and triacylglycerol hydrolysis in reconstituted high density lipoproteins. In ATHEROSCLEROSIS SUPPLEMENTS Vol. 4 (pp. 222). KYOTO, JAPAN: ELSEVIER IRELAND LTD. |
| 1999 | De Geest, N., Mann, L., De Sousa-Hitzler, J., Hahn, C., Rottier, R., & D'Azzo, A. (1999). Lysosomal neuraminidase deficiency in mice: a model for sialidosis.. In AMERICAN JOURNAL OF HUMAN GENETICS Vol. 65 (pp. A26). UNIV CHICAGO PRESS. WoS1 |
| - | Hagen, R., Mc Lean, K., Hahn, C. N., & Penny, C. (n.d.). RADIOGRAPHIC, CT AND MRI FEATURES OF COMPRESSIVE CERVICAL MYELOPATHY IN YOUNG TEXEL AND BELTEX SHEEP. In VETERINARY RADIOLOGY & ULTRASOUND Vol. 51 (pp. 200). WILEY-BLACKWELL PUBLISHING, INC. |
| Year | Citation |
|---|---|
| 2022 | Shah, M. V., Hahn, C. N., Chhetri, R., Tran, E. N. H., & Hiwase, D. (2022). Integrated personalized prediction model identifies a subgroup of wild-type tp53therapy-related myeloid neoplasm patients with poor outcome. Poster session presented at the meeting of Blood. US: American Society of Hematology. DOI |
| 2022 | Brown, A. L., Homan, C., Drazer, M. W., Yu, K., Lawrence, D., Feng, J., . . . Godley, L. A. (2022). Somatic Mutational Landscape of Hereditary Hematopoietic Malignancies Associated with Germline Variants in <i>RUNX1</i>, <i>GATA2</i> and <i>DDX41</i>. Poster session presented at the meeting of BLOOD. US: AMER SOC HEMATOLOGY. DOI WoS5 |
| 2018 | Singhal, D., Wee, A., Kutyna, M. M., Babic, M., Chhetri, R., Parker, W., . . . Hiwase, D. K. (2018). Therapy-Related Myeloid Neoplasms (T-MN) and Primary MDS (PMDS) Patients with Very Low (VL) or Low (L) IPSS-R Score Share Clinical and Biological Characteristics and Have Similar Outcome. Poster session presented at the meeting of BLOOD. CA, San Diego: AMER SOC HEMATOLOGY. DOI |
| 2017 | Oftedal, B. E., Lundgren, B. A., Bratland, E., Wolff, A. B., Hamm, D., Gan, P. -Y., . . . Scott, H. S. (2017). T cell receptor assessment in autoimmune disease requires access to the most adjacent immunologically active organ. Poster session presented at the meeting of SCANDINAVIAN JOURNAL OF IMMUNOLOGY. Stockholm, SWEDEN: WILEY. |
| 2017 | Singhal, D., Wee, L. A., Babic, M., Parker, W., Moore, S., Feng, J., . . . Hiwase, D. (2017). THERAPY RELATED MYELOID NEOPLASMS (T-MN) SHOW HIGH MUTATION FREQUENCY AND A SPECTRUM DIFFERENT FROM PRIMARY MDS. Poster session presented at the meeting of LEUKEMIA RESEARCH. Valencia, SPAIN: PERGAMON-ELSEVIER SCIENCE LTD. DOI |
| 2017 | de Sousa, S. M. C., Stowasser, M., Feng, J., Schreiber, A. W., Hahn, C. N., Torpy, D. J., . . . Scott, H. S. (2017). Sequence variants in ARMC5 are not implicated in familial hyperaldosteronism type II. Poster session presented at the meeting of Clinical endocrinology. UK: Wiley-Blackwell Publishing. |
| 2016 | Beck, D., Thoms, J., Palu, C., Herold, T., Shah, A., Olivier, J., . . . Pimanda, J. (2016). INTEGRATIVE ANALYSIS OF LINCRNA EXPRESSION IN 922 ACUTE MYELOID LEUKEMIA PATIENTS REVEALS MULTIPLE PROGNOSTIC GENE SIGNATURES. Poster session presented at the meeting of HAEMATOLOGICA. Copenhagen, DENMARK: FERRATA STORTI FOUNDATION. |
| 2014 | Casolari, D. A., Iarossi, D. G., Butcher, C. M., Bray, S. C., Parker, W. T., Hahn, C. N., . . . D'Andrea, R. J. (2014). Aberrant activation of epidermal growth factor receptor in MPN may respond to the kinase inhibitor gefitinib. Poster session presented at the meeting of Blood. US: American Society of Hematology. |
- Germline mutations in familial haematopoietic malignancies identifies new pan-cancer predisposition genes and may alter clinical decision making, including for known cancer genes, NHMRC - Project Grant, 01/01/2019 - 31/12/2022
- Biological characterisation and therapeutic options for high risk, DDX41 mutated, haematological malignancies, Cancer Council SA - Beat Cancer, 01/01/2018 - 31/12/2018
| Date | Role | Research Topic | Program | Degree Type | Student Load | Student Name |
|---|---|---|---|---|---|---|
| 2025 | Principal Supervisor | Genomic Drivers and Therapeutic Vulnerabilities in Hematologic Malignancy Progression | Doctor of Philosophy | Doctorate | Full Time | Ms Yang Zhang |
| 2025 | Principal Supervisor | Genomic Drivers and Therapeutic Vulnerabilities in Hematologic Malignancy Progression | Doctor of Philosophy | Doctorate | Full Time | Ms Yang Zhang |
| 2023 | Co-Supervisor | Multiplex assay of variant effect (MAVE) to measure functional effects following saturation mutagenesis of GATA2 and RUNX1. | Doctor of Philosophy | Doctorate | Full Time | Mr Wen Teng |
| 2023 | Co-Supervisor | Genomic Mechanisms Influencing Outcome In Chronic Myeloid Leukaemia | Doctor of Philosophy | Doctorate | Part Time | Miss Adelina Catherina B. Fernandes |
| 2023 | Co-Supervisor | 111117 - Examining the role of the pathogenic bone marrow microenvironment and hematopoietic stem cell stress in the development of leukaemia in blood cancer predisposition | Doctor of Philosophy | Doctorate | Full Time | Saman Ghalamkari |
| 2023 | Co-Supervisor | Genomic Mechanisms Influencing Outcome In Chronic Myeloid Leukaemia | Doctor of Philosophy | Doctorate | Part Time | Miss Adelina Catherina B. Fernandes |
| 2023 | Co-Supervisor | Multiplex assay of variant effect (MAVE) to measure functional effects following saturation mutagenesis of GATA2 and RUNX1. | Doctor of Philosophy | Doctorate | Full Time | Mr Wen Teng |
| 2023 | Principal Supervisor | 109455 - Examining the impact of environmental stressors and mutant microenvironment on disease development in models of inherited predisposition to haematological malignancies | Doctor of Philosophy | Doctorate | Full Time | Mr An Thanh Dung Nguyen |
| Date | Role | Research Topic | Program | Degree Type | Student Load | Student Name |
|---|---|---|---|---|---|---|
| 2023 - 2025 | Co-Supervisor | The Genetic Landscape of Therapy-related Myeloid Neoplasms | Doctor of Philosophy | Doctorate | Full Time | Dr Deepak Singhal |
| 2022 - 2025 | Co-Supervisor | Germline ERG Haploinsufficiency in Predisposition to Disease | Doctor of Philosophy | Doctorate | Full Time | Miss Jiarna Zerella |
| 2012 - 2016 | Co-Supervisor | Identification and Characterisation of Genetic Lesions that Predispose to and Gene Expression Patterns that Contribute to Myeloid Malignancies | Doctor of Philosophy | Doctorate | Full Time | Ms Parvathy Venugopal |
| 2009 - 2013 | Co-Supervisor | Genetics and Functional Characterization of GATA2, a Novel Cancer Gene in Familial Leukaemia | Doctor of Philosophy | Doctorate | Full Time | Mr Chan Eng Chong |
| 2000 - 2005 | Co-Supervisor | Characterisation of a novel gene p73RhoGAP in angiogenesis | Doctor of Philosophy | Doctorate | Full Time | Mrs Zhi Su |