Author

Margot Jarrige

InsermORCID 0000-0002-5877-2615Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Hélène PolvècheiD· 2 shared Alan R.L. DorvaliD· 1 shared Angélique Terray· 1 shared Anthony Brureau· 1 shared Antigoni ManousopoulouiD· 1 shared Cécile MartinatiD· 1 shared Célia VasliniD· 1 shared Céline BrugeiD· 1 shared

Activity by Year

2021-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

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2 shared papersMolecular Biology

Hélène PolvècheORCID

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Author profile →

3 papers

Recent·Most cited

DAB2 as a biomarker and mechanistic link between lipid dysregulation and disease progression in LGMD R2

Céline Bruge, Nathalie Bourg, Emilie Pellier, Quentin Miagoux, Manon Benabidès, Noëlla Grossi, Margot Jarrige, Hélène Polvèche, Valeria Agostini, Anthony Brureau, Stéphane Vassilopoulos, Teresinha Evangelista, Gorka Fernández‐Eulate, Tanya Stojkovic, Isabelle Richard, Xavier Nissan

bioRxiv · Sep 11, 2025 · PreprintMolecular Biology

Dynamic extrinsic pacing of the HOX clock in human axial progenitors controls motor neuron subtype specification

Vincent Mouilleau, Célia Vaslin, Rémi Robert, Simona Gribaudo, Nour Nicolas, Margot Jarrige, Angélique Terray, Léa Lesueur, Mackenzie W. Mathis, Gist F. Croft, Mathieu Daynac, V. Rouiller, Hynek Wichterle, Vanessa Ribes, Cécile Martinat, Stéphane Nedelec

This study shows that the HOX clock in human axial progenitors is dynamically paced by extrinsic cues like FGF signaling, enabling controlled motor neuron subtype specification.

Development · Mar 15, 2021Peer-reviewedDevelopmental Biology

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

Virginie Mournetas, Emmanuelle Massouridès, Jean‐Baptiste Dupont, Étienne Kornobis, Hélène Polvèche, Margot Jarrige, Alan R.L. Dorval, Maxime R.F. Gosselin, Antigoni Manousopoulou, Spiros D. Garbis, Dariusz C. Górecki, Christian Pinset

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

Journal of Cachexia Sarcopenia and Muscle · Feb 1, 2021Peer-reviewedDevelopmental Biology