Author

Quentin Raas

Hôpital Necker-Enfants MaladesORCID 0000-0002-8380-8990Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:metabolomics· 1 Assay:proteomics· 1 Approach:statistical model· 1 Organism:zebrafish· 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 Arnaud Hubas· 1 shared Christel TraniD· 1 shared Clémence Labasse· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. Madelaine

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1 paper

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