Author

Thomas Stervinou

Centre National de la Recherche ScientifiqueORCID 0009-0006-9079-4597Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Pathology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:human· 2 Organism:mouse· 2 Assay:spatial transcriptomics· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Assay:electronic health records· 1

Frequent Co-Authors

Guillaume LamiraultiD· 2 shared Nathalie GaboritiD· 2 shared Agnès TessieriD· 1 shared Alice BoissardiD· 1 shared Arie O. VerkerkiD· 1 shared Arthur A.M. WildeiD· 1 shared Bastiaan J. BoukensiD· 1 shared Bastien CimarostiiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersPathology

Guillaume LamiraultORCID

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2 papers

Recent·Most cited

Desmin p.R406W mutation is associated with arrhythmias through structural and electrophysiological remodeling

Michelle Geryk, Thomas Stervinou, Martin Bouaud, Bastien Cimarosti, Jérôme Montnach, Agnès Tessier, Charlène Jouve, Pierre Lindenbaum, Florence Kyndt, Alice Boissard, Cécile Henry, Mélèze Hocini, Sabrina Batonnet‐Pichon, Benjamin Lauzier, Guillaume Lamirault, , Flavien Charpentier

This study investigates the pathogenic effects of the DES p.R406W mutation, showing it causes electrical and structural heart remodeling linked to arrhythmias and sudden cardiac death.

bioRxiv · Aug 11, 2026 · PreprintPathology

The Brugada syndrome associated gene WT1 impacts on SCN5A expression and cardiac conduction

E. Madelief Marsman, Joost Allard Offerhaus, Thomas Stervinou, Isabella Mengarelli, Leander Beekman, Lisanne M.W. Wilde, Simona Casini, T J Streef, Maurice J.B. van den Hoff, Marie‐José Goumans, Arie O. Verkerk, Sean Joseph Jurgens, Arthur A.M. Wilde, Guillaume Lamirault, Nathalie Gaborit, , Fernanda M. Bosada

This study shows WT1 regulates SCN5A expression and cardiac conduction in Brugada syndrome through a regulatory element in the RV.

bioRxiv · Jan 16, 2025 · PreprintGenetics