Author

Elizabeth L. Christie

The University of MelbourneORCID 0000-0002-9959-7024Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Developmental Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Organism:Drosophila· 1 Research Focus:drug response / drug discovery· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1

Frequent Co-Authors

Amanda J. CompadreiD· 1 shared Besaiz J. Sánchez-SáncheziD· 1 shared Brian Marc StrameriD· 1 shared Callum Dark· 1 shared Daniel BakopoulosiD· 1 shared Danielle Kemper· 1 shared Deanna H. WongiD· 1 shared Dineo KhabeleiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCancer Biology

Amanda J. CompadreORCID

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2 papers

Recent·Most cited

Cancer BiologybioRxivPreprintMar 4, 2026

Targeting ALC1 can safely expand the therapeutic utility of PARP inhibitors across high-grade serous ovarian cancers

Lindsey N Aubuchon, Deanna H. Wong, Natasha Ramakrishnan…·Priyanka Verma

This study shows that targeting ALC1 can enhance PARP inhibitor effectiveness in ovarian cancers, particularly in HRD and CCNE1-amplified tumors, with minimal toxicity.

DOI 10.64898/2025.12.04.692458

humanbulk RNA-seq

Developmental BiologyEMBO ReportsPeer-reviewedNov 28, 2023

Convergent Insulin and TGF-β signalling drives cancer cachexia by promoting aberrant fatbody ECM accumulation in a Drosophila tumour model

Daniel Bakopoulos, Sofya Golenkina, Callum Dark…·Louise Y Cheng

This study identifies insulin and TGF-β signaling convergence in Drosophila adipose tissue that drives ECM accumulation and muscle wasting in a tumor model.

19 citations

Drosophilastatistical model