Author

C. Hertz-Fowler

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Microbiology· 2 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Assay:whole-genome sequencing· 2 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Organism:multiple species· 1 Research Focus:phylogenetics / evolution· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

A. Bragin· 1 shared A. Pavlov· 1 shared A. Polyakov· 1 shared A. Shanmugasundram· 1 shared C. Clemente· 1 shared C. Halliday· 1 shared C. Tomlinson· 1 shared D. E. Dobson· 1 shared

Activity by Year

2016-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 16 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

1 shared paperGenomics

A. Bragin

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genome-wide subcellular protein localisation in the flagellate parasite Trypanosoma brucei

K. Billington, C. Halliday, R. Madden, P. Dyer, M. Carrington, S. Vaughan, C. Hertz-Fowler, S. Dean, J. D. Sunter, R. J. Wheeler, K. Gull

The paper maps subcellular protein localization in Trypanosoma brucei using fluorescence microscopy, revealing functional insights and organelle adaptations.

bioRxiv · Jun 9, 2022 · PreprintMicrobiology

Genome assemblies across the diverse evolutionary spectrum of Leishmania protozoan parasites

W. C. Warren, N. Akopyants, D. E. Dobson, C. Hertz-Fowler, L.-F. Lye, P. J. Myler, G. Ramasamy, A. Shanmugasundram, F. Silva-Franco, S. Steinbiss, C. Tomlinson, R. K. Wilson, S. M. Beverley

The paper provides high-quality genome assemblies and gene annotations for 13 Leishmania and related species to study the origins of parasitism.

bioRxiv · May 29, 2021Microbiology

NGS-based assay for frequent newborn inherited diseases: from development to implementation

T. Simakova, A. Bragin, M. Zaytseva, C. Clemente, M. Lewicka, J.C. Machado, J.L. Costa, M. Hughes, C. Hertz-Fowler, N. Petrova, A. Polyakov, R. Zinchenko, E. Kondratyeva, A. Pavlov

The paper develops and validates an NGS-based assay for diagnosing common newborn inherited diseases and reports its successful clinical implementation.

bioRxiv · Apr 26, 2016 · PreprintGenomics