Author

Rosie K. A. Bunton-Stasyshyn

Mary Lyon Centre at MRC HarwellORCID 0000-0002-1895-2240Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Neuroscience· 1 Physiology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:mouse· 3 Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Research Focus:cell type annotation· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Michelle E. StewartiD· 3 shared Lydia TebouliD· 2 shared Sara E. WellsiD· 2 shared Abraham Acevedo‐ArozenaiD· 1 shared Adam P GiessiD· 1 shared Alana Luzzio· 1 shared Alasdair J. AllaniD· 1 shared Alessandro Marrero‐GagliardiiD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersPhysiology

Michelle E. StewartORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Placental defects revealed by modelling PWS in mice

Anna E. Webberley, Raquel Boqué-Sastre, Lauren Bailey, Cerys Charles, R. Jones, Rosie K. A. Bunton-Stasyshyn, Michelle E. Stewart, Sara E. Wells, David S. Chatelet, Stephanie Robinson, Matthew J. Higgs, Rosalind M. John, Anthony R Isles

The paper shows reduced PWS gene expression in mouse placenta leads to a 25% loss of fetal endothelial cells critical for nutrient transfer.

bioRxiv · Jul 1, 2026 · PreprintPhysiology

Mendelian gene identification through mouse embryo viability screening

Pilar Cacheiro, Carl Henrik Westerberg, Jesse Mager, Mary E. Dickinson, Lauryl M. J. Nutter, Violeta Muñoz‐Fuentes, Chih‐Wei Hsu, Ignatia B. Van den Veyver, Ann Marie Flenniken, Colin McKerlie, Stephen A. Murray, Lydia Teboul, Jason D. Heaney, K. C. Kent Lloyd, Louise Lanoue, , John Pullinger

The paper identifies novel Mendelian genes by analyzing mouse embryo lethality and linking them to human disease phenotypes and genetic variants.

Genome Medicine · Oct 13, 2022Peer-reviewedGenetic & Genomic Medicine

Generation, quality control, and analysis of the first genomically humanised knock-in mice for the ALS/FTD genes SOD1, TARDBP (TDP-43), and FUS

Anny Devoy, Georgia Price, Francesca De Giorgio, Rosie K. A. Bunton-Stasyshyn, David Thompson, Samanta Gasco, Alasdair J. Allan, Gemma F. Codner, R. Nair, Charlotte Tibbit, Ross McLeod, Zeinab Ali, Judith Noda, Alessandro Marrero‐Gagliardi, José Miguel Brito Armas, , Thomas J. Cunningham

The paper creates genomically humanised knock-in mice for ALS/FTD genes SOD1, TARDBP, and FUS, showing they express human proteins at endogenous levels and are phenotypically normal.

bioRxiv · Jul 5, 2021 · PreprintNeuroscience