Author

Mark A Harber

Royal Free London NHS Foundation TrustORCID 0000-0002-5441-2452Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Assay:DNA methylation· 1 Organism:human· 1 Approach:machine learning (classical)· 1

Frequent Co-Authors

Austen J. J. WorthiD· 1 shared Calum ForrestiD· 1 shared Charlotte A. WilliamsiD· 1 shared Claire E. AtkinsoniD· 1 shared Cristina VenturiniiD· 1 shared Douglas ThorburniD· 1 shared Judith BreueriD· 1 shared Julia ColstoniD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Austen J. J. WorthORCID

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1 paper

Recent·Most cited

Persistent low-level variants in a subset of HCMV genes are highly predictive of poor outcome in immunocompromised patients with cytomegalovirus infection

Cristina Venturini, Julia Colston, Oscar J. Charles, Timothy Best, Claire E. Atkinson, Calum Forrest, Charlotte A. Williams, Kanchan Rao, Austen J. J. Worth, Douglas Thorburn, Mark A Harber, P. D. Griffiths, Judith Breuer

The paper identifies a viral signature from HCMV genes associated with poor outcomes in immunocompromised patients, using deep sequencing and machine learning.

medRxiv · Sep 12, 2022 · PreprintGenetic & Genomic Medicine