Author

Jean‐Baptiste Gourraud

Centre National de la Recherche ScientifiqueORCID 0000-0002-6961-2131Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Pathology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Jean‐Jacques SchottiD· 2 shared Jérôme MontnachiD· 2 shared Pierre LindenbaumiD· 2 shared Vincent ProbstiD· 2 shared Agnès TessieriD· 1 shared Ahmad S. AminiD· 1 shared Alex LipoviD· 1 shared Alice BoissardiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersPathology

Jean‐Jacques SchottORCID

Mutual co-authors in cluster

Author profile →

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

Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome

Alex Lipov, Manon Baudic, Pierre Lindenbaum, Isabella Mengarelli, Matthew J. O’Neill, Fernanda M. Bosada, Yanushi Dullewe Wijeyeratne, Luis de la Higuera Romero, Maarten Kooyman, Marion Gaudin, Graziella Aquilina, Leander Beekman, Estelle Baron, Mathilde Bertrand, Zoya Kingsbury, , Connie R. Bezzina

This study identifies rare and low-frequency non-coding variants at the SCN5A locus associated with Brugada syndrome using whole-genome sequencing and functional assays.

medRxiv · Jul 10, 2026 · PreprintGenetic & Genomic Medicine