Author

Riccardo Bonfanti

IRCCS Ospedale San RaffaeleORCID 0000-0002-4104-2763Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cell Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Approach:experimental assay· 1 Assay:scRNA-seq· 1 Approach:statistical model· 1

Frequent Co-Authors

Fabio ManentiiD· 2 shared Federica CuozzoiD· 2 shared Gabriel SiracusanoiD· 2 shared Giulio FrontinoiD· 2 shared Lorenzo PiemontiiD· 2 shared Raniero ChimientiiD· 2 shared Valentina ZamarianiD· 2 shared Valeria SordiiD· 2 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersCell Biology

Fabio ManentiORCID

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2 papers

Recent·Most cited

Cell BiologyDiabetesPeer-reviewedApr 9, 2025

Liraglutide treatment reverses unconventional cellular defects in induced pluripotent stem cell-derived β cells harboring a partially functional WFS1 variant

Silvia Torchio, Gabriel Siracusano, Federica Cuozzo…·Lorenzo Piemonti

This study shows liraglutide treatment restores glucose-stimulated insulin secretion and reduces apoptosis in WFS1 mutant iPSC-derived β cells.

7 citations

𝕏 PostBluesky

GeneticsbioRxivPreprintDec 29, 2023

A WFS1 variant disrupting acceptor splice site uncovers the impact of alternative splicing on β cell apoptosis in a patient with Wolfram syndrome.

Raniero Chimienti, Silvia Torchio, Gabriel Siracusano…·Lorenzo Piemonti

This study investigates how a WFS1 splice site mutation affects β cell apoptosis in Wolfram syndrome by analyzing alternative splicing and functional consequences in patient-derived iPSCs.

1 citation

humanbulk RNA-seq

𝕏 PostBluesky