Author

Linda van Bijsterveldt

MRC Laboratory of Molecular BiologyORCID 0000-0003-3183-4633Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Genomics· 1 Synthetic Biology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Organism:E. coli· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Charalampos P. TriantafyllidisiD· 2 shared Francesca Meteora BuffaiD· 2 shared Adrian Llewellyn HarrisiD· 1 shared Alan McIntyreiD· 1 shared Alessandro BarberisiD· 1 shared Ana MiariD· 1 shared Andrew DhawaniD· 1 shared Askar A. KleefeldtiD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersCancer Biology

Charalampos P. TriantafyllidisORCID

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3 papers

Recent·Most cited

Synthetic BiologySciencePeer-reviewedJul 31, 2025

Escherichia coli with a 57-codon genetic code

Wesley E. Robertson, Fabian B. H. Rehm, Martin Spinck…·Jason W. Chin

This paper describes the creation of a synthetic Escherichia coli strain with a 57-codon genetic code by recoding 105 codons in a 4 Mb synthetic genome.

38 citationstop 1%

E. coliexperimental assay

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Cancer BiologybioRxivPreprintJun 23, 2022

Reconstructing the functional effect of TP53 somatic mutations on its regulon using causal signalling network modelling

Charalampos P. Triantafyllidis, Alessandro Barberis, Ana Miar…·Francesca Meteora Buffa

The paper uses network modeling to analyze how TP53 mutations affect gene regulation across cancer types and samples.

DOI 10.1101/2022.06.23.497293

humanbulk RNA-seq

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GenomicsbioRxivPreprintAug 30, 2021

Dicer-to-Argonaute switch controls biogenesis of oncogenic miRNA

Laura M. Winchester, Linda van Bijsterveldt, Andrew Dhawan…·Francesca Meteora Buffa

The paper identifies a switch from DICER-dependent to Argonaute-mediated miRNA biogenesis in cancer, showing that non-canonical processing of oncogenic miRNAs promotes cancer progression.

1 citation

humanbulk RNA-seq

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