Author

T. Maher

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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Biochemistry· 1 Cancer Biology· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:differential expression· 2 Approach:experimental assay· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Assay:DNA methylation· 1

Frequent Co-Authors

A. Blanchard· 1 shared A. Fisher· 1 shared A. M. Valdes· 1 shared A. Taylor· 1 shared C. Menni· 1 shared D. Guillotin· 1 shared G. Flint· 1 shared G. Hadjigeorgiou· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperCell Biology

A. Blanchard

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

G-quadruplex structures regulate long-range transcriptional reprogramming to promote drug resistance in ovarian cancer

J. Robinson, G. Flint, I. Garner, S. Galli, T. Maher, M. Kuimova, R. Vilar, I. McNeish, R. Brown, H. C. Keun, M. Di Antonio

This study identifies G-quadruplex structures as regulators of long-range transcriptional reprogramming in drug-resistant ovarian cancer, showing their role in promoting resistance and potential as therapeutic targets.

bioRxiv · Jun 24, 2024 · PreprintCancer Biology

Characterisation of fasting and postprandial NMR metabolites: insights from the ZOE PREDICT 1 Study

K. M. Bermingham, M. Mazidi, P. W. Franks, T. Maher, A. M. Valdes, I. Linenberg, J. Wolf, G. Hadjigeorgiou, T. D. Spector, C. Menni, J. M. Ordovas, S. E. Berry, W. L. Hall

This study characterizes postprandial NMR metabolites in the ZOE PREDICT 1 cohort, showing significant inter- and intra-individual variability and strong correlations between fasting and postprandial measurements.

bioRxiv · Nov 14, 2022 · PreprintBiochemistry

Transcriptome analysis of IPF fibroblastic foci identifies key pathways involved in fibrogenesis

D. Guillotin, A. Taylor, M. Plate, P. Mercer, L. Edwards, R. Haggart, G. Miele, R. McAnulty, T. Maher, R. E. Hynds, M. Jamal-Hanjani, R. Marshall, A. Fisher, A. Blanchard, R. Chambers

This study identifies key transcriptional pathways in IPF fibroblastic foci using RNA-seq and bioinformatics, highlighting the TSC2/RHEB axis as a potential therapeutic target for fibrosis.

bioRxiv · Mar 10, 2020Cell Biology