Author

Lisa Redford

Newcastle University

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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Research Focus:variant calling· 2 Assay:bulk RNA-seq· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Anca OniscuiD· 2 shared Ghanim Alhilal· 2 shared John BurniD· 2 shared Ottie O’Brien· 2 shared Richard GalloniD· 2 shared Sira Moreno Laguna· 2 shared Amanda Waltham· 1 shared Ángel AlonsoiD· 1 shared

Activity by Year

2018-2018 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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2 shared papersGenomics

Anca OniscuORCID

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2 papers

Recent·Most cited

A novel panel of short mononucleotide repeats linked to informative polymorphisms enabling effective high volume low cost discrimination between mismatch repair deficient and proficient tumours

Lisa Redford, Ghanim Alhilal, Stephanie J. Needham, Ottie O’Brien, Julie Coaker, John R. Tyson, Leonardo Maldaner Amorim, Iona Middleton, Osagie G. Izuogu, Mark Johan Arends, Anca Oniscu, Ángel Alonso, Sira Moreno Laguna, Richard Gallon, Harsh J. Sheth, , John Burn

The paper introduces a panel of short mononucleotide repeats for MSI testing, showing high concordance with traditional methods and potential for scalable, cost-effective tumor classification.

PLoS ONE · Aug 29, 2018Peer-reviewedGenomics

A molecular inversion probe and sequencing-based microsatellite instability assay for high throughput cancer diagnostics and Lynch syndrome screening

Richard Gallon, Christine Hayes, Lisa Redford, Ghanim Alhilal, Ottie O’Brien, Amanda Waltham, Stephanie Needham, Mark Arends, Anca Oniscu, Angel Miguel Alonso, Sira Moreno Laguna, Harsh Sheth, Mauro Santibanez-Koref, Michael S Jackson, John Burn

This paper develops a sequencing-based assay using molecular inversion probes to detect microsatellite instability and BRAF V600E mutations in colorectal cancer, enabling high-throughput diagnostics and Lynch syndrome screening.

bioRxiv · Aug 1, 2018 · PreprintCancer Biology