Author

Federica Begalli

Queen Mary University of LondonORCID 0000-0002-7478-0252Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:cancer & tumor microenvironment· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alexandra CsábiiD· 1 shared Anne BarlieriD· 1 shared Ashutosh RaiiD· 1 shared Attila PatócsiD· 1 shared Barbara JarząbiD· 1 shared Carmen S. Martin· 1 shared Caroline E BrainiD· 1 shared Charlotte Louise HalliD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexandra CsábiORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintFeb 27, 2026

Familial medullary thyroid carcinoma secondary to an SLC30A9 intragenic deletion and translation reinitiation

Donato Iacovazzo, Federica Begalli, Oniz Suleyman…·Márta Korbonits

The paper identifies an SLC30A9 deletion causing familial medullary thyroid carcinoma through translation reinitiation and shows its oncogenic effects.

DOI 10.64898/2026.02.26.26346165

humanwhole-exome sequencing