Author

Alasdair Russell

University of Cambridge

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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Cancer Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:drug response / drug discovery· 1 Assay:proteomics· 1

Frequent Co-Authors

Chandra Sekhar Reddy ChilamakuriiD· 2 shared Jason S. CarrolliD· 2 shared Abigail R. EdwardsiD· 1 shared Anne PajoniD· 1 shared Barbara Gruenwald· 1 shared Catarina PelicanoiD· 1 shared Clive S. D’SantosiD· 1 shared Elizabeth Mannion· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersCancer Biology

Chandra Sekhar Reddy ChilamakuriORCID

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Author profile →

2 papers

Recent·Most cited

IL-1-activated cancer-associated fibroblasts promote STAT1-driven transcriptional reprogramming of pancreatic tumour cells

Catarina Pelicano, Igor V. Chernukhin, Marleen Woelke, Priscilla S.W. Cheng, Lisa Young, Abigail R. Edwards, Elizabeth Mannion, Yi Cheng, Maureen Crowshaw, Steven Kupczak, Sara Pinto Teles, Muntadher Jihad, Kamal Kishore, Chandra Sekhar Reddy Chilamakuri, Valar Nila Roamio Franklin, , Shalini V. Rao

This paper shows that IL-1-activated cancer-associated fibroblasts (iCAFs) promote STAT1-driven transcriptional reprogramming in pancreatic tumour cells, leading to chemoresistance and identifying STAT1 as a therapeutic target.

bioRxiv · May 29, 2026 · PreprintCancer Biology

GenEditID: an open-access platform for the high-throughput identification of CRISPR edited cell clones

Ying Xue, Y. C. Loraine Tung, Rasmus Siersbæk, Anne Pajon, Chandra Sekhar Reddy Chilamakuri, Rubén Álvarez-Fernández, Richard Bowers, Jason S. Carroll, Matthew Eldridge, Alasdair Russell, Florian T. Merkle

GenEditID is a platform for identifying CRISPR-edited cell clones using deep sequencing and proteomic data, enabling scalable and sensitive gene editing analysis.

bioRxiv · Jun 13, 2019 · PreprintGenomics