Author

Sarah Flannery

University of Oxford

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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Cell Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Benedikt Mathias KessleriD· 2 shared Iolanda VendrelliD· 2 shared Milad ShademaniD· 2 shared Vered RaziD· 2 shared Adán Pinto-FernándeziD· 1 shared Alberto MalerbaiD· 1 shared Geertje van der HorstiD· 1 shared March· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersCell Biology

Benedikt Mathias KesslerORCID

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2 papers

Recent·Most cited

N-terminal truncation diversifies USP18 function during early myogenesis

Tom I. Nijssen, Simeon D. Draganov, Milad Shademan, Sarah Flannery, Iolanda Vendrell, Benedikt Mathias Kessler, Adán Pinto-Fernández, Vered Raz

This study shows that the N-terminal truncation of USP18 generates a short isoform (SF) with distinct functions in muscle differentiation compared to the long isoform (LF).

bioRxiv · Oct 18, 2026 · PreprintCell Biology

Domain-specific regulation of PABPN1 uncouples aggregation from function and enables therapeutic rescue

Milad Shademan, Iolanda Vendrell, Alberto Malerba, s Khoshbash, Sarah Flannery, March, Geertje van der Horst, Silvère M. van der Maarel, Benedikt Mathias Kessler, Vered Raz

This study identifies a stabilized PABPN1 variant, trPAB, that reduces aggregation and restores function in OPMD and bladder cancer models, supporting its potential as a gene therapy.

bioRxiv · Jun 16, 2026 · PreprintNeuroscience