Author

Alice Pebay

The University of Melbourne

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioengineering· 1 Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:clustering· 1 Organism:mouse· 1

Frequent Co-Authors

Alex Hewitt· 2 shared Maciej DaniszewskiiD· 2 shared Alison Conquest· 1 shared Amy Fan Li· 1 shared Anna E King· 1 shared Bang V Bui· 1 shared Camden Lo· 1 shared Damian Hernandez· 1 shared

Activity by Year

2016-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersBioengineering

Alex Hewitt

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Autonomic neurons are intrinsically hyperexcitable in a Friedreich ataxia iPSC model

Jarmon G. Lees, Haoxiang Zhang, Li Li, Mirella Dottori, Alice Pebay, Louise Corben, Martin Delatycki, Stephen Wilcox, Jeffrey M. Pullin, Jarny Choi, Davis McCarthy, Jill S. Napierala, Jill Napierala, Shiang Yong Lim

This paper establishes that FRDA autonomic neurons are hyperexcitable and exhibit mitochondrial dysfunction using iPSC-derived models.

bioRxiv · Oct 11, 2026 · PreprintNeuroscience

Development of a modular automated system for maintenance and differentiation of adherent human pluripotent stem cells.

Duncan E Crombie, Maciej Daniszewski, Helena H Liang, Tejal Kulkarni, Fan Li, Grace E Lidgerwood, Alison Conquest, Damian Hernandez, Sandy S Hung, Katherine P Gill, Elisabeth De Smit, Lisa S Kearns, Linda Clarke, Valentin M Sluch, Xitiz Chamling, , Alice Pebay

This paper develops an automated system for maintaining and differentiating human pluripotent stem cells, enabling large-scale culture and reducing variability.

bioRxiv · Oct 5, 2016Bioengineering

AAV-mediated CRISPR/Cas gene editing of retinal cells in vivo.

Sandy SC Hung, Vicki Chrysostomou, Amy Fan Li, Jeremiah KH Lim, Jiang-Hui Wang, Joseph E Powell, Leilei Tu, Maciej Daniszewski, Camden Lo, Raymond C Wong, Jonathan G Crowston, Alice Pebay, Anna E King, Bang V Bui, Guei-Sheung Liu, Alex Hewitt

This study uses AAV2 to deliver CRISPR/Cas components to retinal cells in Thy1-YFP mice, achieving an 84% reduction in YFP-positive cells without affecting retinal function.

Investigative Opthalmology & Visual Science · Jun 29, 2016Peer-reviewedGenomics