Author

Arnaud Hubas

Hôpital Cochin

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Assay:metabolomics· 1

Frequent Co-Authors

A. Madelaine· 1 shared Aleksandra Nadaj‐PaklezaiD· 1 shared Anaïs Chanut· 1 shared Anne‐Sophie ArmandiD· 1 shared Apolline ImbardiD· 1 shared Bénédicte ChazaudiD· 1 shared Christel TraniD· 1 shared Clémence Labasse· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. Madelaine

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Novel variants in ryanodine receptor type 3 predispose to acute rhabdomyolysis due to impaired autophagy

Hortense de Calbiac, Laure Caccavelli, Solène Renault, Marine Madrange, Quentin Raas, Marjolène Straube, Guy Brochier, Emmanuelle Lacène, Anaïs Chanut, A. Madelaine, Clémence Labasse, Lylia Mekzine, Sebastián Montealegre, Nicolas Goudin, Aleksandra Nadaj‐Pakleza, , Pascale de Lonlay

This study identifies rare RYR3 variants causing recurrent rhabdomyolysis by impairing autophagy and mitochondrial function, highlighting RyR3's role in muscle stress adaptation.

medRxiv · Mar 3, 2026 · PreprintGenetic & Genomic Medicine

Epigenetic control of myogenic identity of human muscle stem cells in Duchenne Muscular Dystrophy

Jimmy Massenet, Michèle Weiss‐Gayet, Hina Bandukwala, Wilhelm Bouchereau, Stéphanie Gobert, Mélanie Magnan, Arnaud Hubas, Patrick Nusbaum, Isabelle Desguerre, Cyril Gitiaux, Francis Jeffrey Dilworth, Bénédicte Chazaud

The paper investigates how epigenetic changes in muscle stem cells from Duchenne Muscular Dystrophy patients lead to loss of myogenic identity and identifies MEF2B as a key mediator.

iScience · Nov 8, 2024Peer-reviewedGenomics