Author

Tamara Cameron

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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Biochemistry· 1 Genetics· 1 Genomics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Organism:mouse· 2 Assay:ATAC-seq· 1 Assay:ChIP-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Assay:CUT&Tag· 1

Frequent Co-Authors

Kelsey A. BresliniD· 3 shared Marnie E. BlewittiD· 3 shared Megan IminitoffiD· 3 shared Quentin A. GouiliD· 3 shared Andrew KeniryiD· 2 shared Hannah Kate VanyaiiD· 2 shared Iromi Wickramasinghe· 2 shared James M. MurphyiD· 2 shared

Activity by Year

2026-2026 · peak 4/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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3 shared papersGenomics

Kelsey A. BreslinORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

SMCHD1's DNA binding activity enables its stable retention on chromatin

Ruifeng Hu, Julissa J. Sánchez‐Velásquez, Jieqiong Lou, Kelsey A. Breslin, Tamara Cameron, Ashleigh N. Solano, Iromi Wickramasinghe, Quentin A. Gouil, Andrew J. Kueh, Tracy Willson, Andrew Keniry, Niall D. Geoghegan, Elizabeth Hinde, Marnie E. Blewitt

This study shows that SMCHD1's weak DNA binding is essential for its chromatin retention and function, revealing how DNA binding affects its localization and gene repression.

bioRxiv · Sep 20, 2026 · PreprintGenomics

Regulation of Human Erythroferrone Expression

Gemma Moir-Meyer, Robert Sertori, Cavan Bennett, Martin Pál, Anne Pettikiriarachchi, Jim R. Hughes, Hal Drakesmith, James O. J. Davies, Damien J. Downes, Matthew E. Gosden, Mohsin Badat, Danielle B. Clucas, Christian Babbs, Ryo Kurita, Connie S.N. Li Wai Suen, , Sant‐Rayn Pasricha

This study identifies the transcriptional regulatory mechanisms governing ERFE expression in human erythroblasts using genomic approaches.

bioRxiv · Jul 3, 2026 · PreprintMolecular Biology

SMCHD1 is a novel target for gene-activation therapy to treat Prader-Willi Syndrome

Megan Iminitoff, Anna K. Le Fevre, Tamara Cameron, Hannah Kate Vanyai, Caleb Chew, Sarah Kinkel, Kelsey A. Breslin, Susanne Theiß, Quentin A. Gouil, Merlin C. Thomas, James M. Murphy, Christian Patrick Schaaf, Andrew Keniry, Marnie E. Blewitt

This study identifies SMCHD1 as a target for gene-activation therapy in Prader-Willi Syndrome by showing its role in repressing the PWS gene cluster and demonstrating gene activation in mouse models.

bioRxiv · May 14, 2026 · PreprintGenetics

DNA binding by ATPase-adjacent domains stimulates SMCHD1 ATPase activity

Alexandra D. Gurzau, Richard W. Birkinshaw, Andrew P. Leis, Tamara Cameron, Megan Iminitoff, Kelsey A. Breslin, Iromi Wickramasinghe, Samantha Eccles, Hannah Kate Vanyai, Quentin A. Gouil, Peter E. Czabotar, James M. Murphy, Marnie E. Blewitt

This study identifies a second DNA-binding site in SMCHD1 and shows that DNA binding stimulates its ATPase activity, revealing a mechanism for gene silencing.

bioRxiv · Feb 5, 2026 · PreprintBiochemistry