Author

Elizabeth L. Anderson

Wellcome Sanger Institute

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:statistical model· 2 Assay:whole-genome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

David J. AdamsiD· 2 shared Alastair DroopiD· 1 shared Albrecht StenzingeriD· 1 shared Alexandra SapetschnigiD· 1 shared Andrea CiolfiiD· 1 shared Andrea GuarracinoiD· 1 shared Anne CzechanskiiD· 1 shared Antonella LauriiD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenomics

David J. AdamsORCID

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2 papers

Recent·Most cited

The mouse pangenome reveals the structural complexity of the murine protein coding landscape

Mohab Helmy, Jin U. Li, Xinyu F. Yan, Rachel K. Meade, Elizabeth L. Anderson, Patrick B. Chen, Anne Czechanski, Tomás Di Domenico, Jonathan Flint C, Erik P. Garrison, Marco Túlio Pardini Gontijo, Andrea Guarracino, Leanne S. Haggerty, Édith Heard, Kerstin Howe, , Thomas Keane

The paper presents a mouse pangenome with 17 strains, resolving structural complexity and improving RNA-Seq analysis by identifying non-reference genes and VNTR polymorphisms.

Cell Genomics · Dec 1, 2025Peer-reviewedGenomics

Activation of Wnt/β-catenin signalling by mutually exclusive FBXW11 and CTNNB1 hotspot mutations drives salivary gland basal cell adenoma

Kim Wong, Justin A. Bishop, Ilan Weinreb, Marialetizia Motta, Martin Del Castillo Velasco‐Herrera, Emanuele Bellacchio, Ingrid Ferreira, Louise van der Weyden, Jacqueline Marcia Boccacino, Antonella Lauri, Giovannina Rotundo, Andrea Ciolfi, Saamin Cheema, Rebeca Olvera-León, Victoria Offord, , David J. Adams

Exome and transcriptome sequencing of salivary basal cell adenomas reveals a recurrent FBXW11 p.F517S mutation, exclusive with CTNNB1 p.I35T, together accounting for 94% of cases.

Nature Communications · May 19, 2025Peer-reviewedCancer Biology✦ In-depth digest