Author

Jean-Baptiste Dupont

InsermORCID 0000-0001-5706-8178Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Jean-Baptiste Dupont1 paper · Inserm

Biology Disciplines

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Bioengineering· 1 Bioinformatics· 1 Developmental Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

Bérangère Robert· 2 shared David L. MackiD· 2 shared Oumeya AdjaliiD· 2 shared Alan R.L. DorvaliD· 1 shared Antigoni ManousopoulouiD· 1 shared Arnaud BonnaffouxiD· 1 shared Bodvael FraysseiD· 1 shared Caroline Le GuineriD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersBioengineering

Bérangère Robert

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Author profile →

3 papers

Recent·Most cited

BioengineeringbioRxivPreprintJan 14, 2026

Engineered muscle tissues with enhanced maturation enable the identification of clinically relevant rAAV capsids

Clémence Lièvre, Bérangère Robert, Giada Mainieri…·Jean-Baptiste Dupont

This study uses engineered human muscle tissues to evaluate AAV capsid efficiency, finding that more mature tissues show improved transduction by AAV9 and MyoAAV variants.

DOI 10.64898/2026.01.13.699271

humanbulk RNA-seq

𝕏 PostBluesky

BioinformaticsbioRxivPreprintNov 19, 2025

Inference and validation of a dynamic gene regulatory network influencing cell fate during Duchenne muscular dystrophy initiation

Elsa Gratianne Guillot, Quentin Fort, Elise Mozin…·Jean-Baptiste Dupont

The paper identifies a dynamic gene regulatory network in Duchenne muscular dystrophy that controls cell fate decisions and shows how disease mutations disrupt this network.

DOI 10.1101/2025.11.19.689189

𝕏 PostBluesky

Developmental BiologyJournal of Cachexia Sarcopenia and MusclePeer-reviewedFeb 1, 2021

Myogenesis modelled by human pluripotent stem cells uncovers Duchenne muscular dystrophy phenotypes prior to skeletal muscle commitment

Virginie Mournetas, Emmanuelle Massouridès, Jean‐Baptiste Dupont…·Christian Pinset

This study uses hiPSCs from DMD patients to model myogenesis and identifies early disease phenotypes before skeletal muscle commitment.

60 citations

humanbulk RNA-seq

𝕏 PostBluesky