Author

Marc Naven

University of Cambridge

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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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

A. Heather EliasseniD· 1 shared Alison M. DunningiD· 1 shared Alpa V. PateliD· 1 shared Amy Trentham‐DietziD· 1 shared Andreas HadjisavvasiD· 1 shared Anna González‐NeiraiD· 1 shared Anna JakubowskaiD· 1 shared Antonis C. AntoniouiD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. Heather EliassenORCID

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Author profile →

1 paper

Recent·Most cited

Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification

Maria Zanti, Denise G O'Mahony, Michael T. Parsons, Leila Dorling, Joe Dennis, Nicholas James Boddicker, Wenan Chen, Chunling Hu, Marc Naven, Kristia Yiangou, Thomas U. Ahearn, Christine B. Ambrosone, Irene Louise Andrulis, Antonis C. Antoniou, Paul Livermore Auer, , Gary Zirpoli

The paper uses case-control data from over 400,000 women to classify BRCA1 and BRCA2 variants, finding high consistency with ClinVar annotations for 785 previously unclassified variants.

Nature Communications · May 24, 2025Peer-reviewedGenetic & Genomic Medicine