Author

Gregory Bruce Mann

Royal Women's HospitalORCID 0000-0002-2508-9203Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ian G CampbelliD· 2 shared Lisa M. DevereuxiD· 2 shared Sunil R. LakhaniiD· 2 shared Amanda B. SpurdleiD· 1 shared Amy E. McCart ReediD· 1 shared Andrew R. GreeniD· 1 shared Anita Rohini SkandarajahiD· 1 shared Cristina FortuñoiD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersCancer Biology

Ian G CampbellORCID

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2 papers

Recent·Most cited

Cancer BiologyThe Journal of PathologyPeer-reviewedOct 30, 2025

Phylogenetic analysis of paired breast carcinomas identifies genetic events associated with clonal recurrence and invasive progression

Tanjina Kader, Maia Zethoven, Sakshi Mahale…·Kylie L. Gorringe

The paper analyzes paired breast carcinomas to determine if recurrences are clonal or new tumors, finding 7% are non-clonal by whole exome sequencing.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJun 12, 2025

Integrating breast tumor homologous recombination deficiency status to aid germline BRCA1 and BRCA2 variant classification

Cristina Fortuño, Jia Zhang, Lambros T. Koufariotis…·Nicola Waddell

This paper integrates tumor homologous recombination deficiency status with germline BRCA1 and BRCA2 variant classification to improve pathogenicity prediction.

DOI 10.1101/2025.06.12.25329237

humanwhole-genome sequencing

𝕏 PostBluesky