Author

Martin Rees

King's College LondonORCID 0000-0003-2361-5828Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Bioengineering· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:protein design· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Ay Lin KhoiD· 2 shared Heinz JungbluthiD· 2 shared Mathias GauteliD· 2 shared Adele D’AmicoiD· 1 shared Aishwarya Dhall· 1 shared Alan H. BeggsiD· 1 shared Alessandro MussaiD· 1 shared Alicia Cuber CaballeroiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersBioengineering

Ay Lin KhoORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

BioengineeringCommunications BiologyPeer-reviewedSep 23, 2026

The generation and validation of a de novo-designed titin binder for use in fluorescence microscopy

Martin Rees, Andrew J. Beavil, Melissa A. B. Amerudin…·Mathias Gautel

The paper designs and validates a de novo protein binder for the titin M10 domain, demonstrating its utility in fluorescence microscopy without antibodies.

DOI 10.1038/s42003-026-10988-1

humanproteomics

𝕏 PostBluesky

Genetic & Genomic MedicineGenome MedicinePeer-reviewedFeb 26, 2026

A comprehensive framework for the interpretation of TTN missense variants

Maria Francesca Di Feo, Martin Rees, Victoria Lillback…·Marco Savarese

The paper presents a framework for interpreting TTN missense variants by integrating clinical, computational, and functional evidence, identifying two variants as likely pathogenic.

2 citationstop 4%

humanwhole-exome sequencing

𝕏 PostBluesky