Author

Felix Omnes

Inserm

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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Neuroscience· 1 Systems Biology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Catarina Santos· 2 shared Fabienne SchalleriD· 2 shared Françoise MuscatelliiD· 2 shared Pierre-Yves BarelleiD· 2 shared Sébastien G. BouretiD· 2 shared Alessandra BertoniiD· 1 shared Alicia SicardiiD· 1 shared Anne‐Marie François‐BellaniD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersNeuroscience

Catarina Santos

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Author profile →

2 papers

Recent·Most cited

Inhibition of oxytocin neurons during key periods of development has long-term behavioural and body composition effects.

Fabienne Schaller, Marie-Sophie Alifrangis, Pierre-Yves Barelle, Catarina Santos, Roman Tyzio, Alessandra Bertoni, Felix Omnes, Yasmine Belaïdouni, Francesca Bader, Emilie Pallesi‐Pocachard, Jean‐Luc Gaïarsa, Sébastien G. Bouret, Françoise Muscatelli

This study inhibits oxytocin neurons during different developmental stages in mice, revealing long-term behavioral and metabolic effects depending on timing and sex.

Molecular Autism · Sep 9, 2026Peer-reviewedNeuroscience

Investigation of a Novel Mouse Model of Prader-Willi Syndrome with Invalidation of Necdin and Magel2

Pierre-Yves Barelle, Alicia Sicardi, Fabienne Schaller, Julie Buron, Denis Becquet, Felix Omnes, Françoise Watrin A, Catarina Santos, Clément Menuet, Anne‐Marie François‐Bellan, Émilie Caron, Jessica Klucznik, Vincent Prévot, Sébastien G. Bouret, Françoise Muscatelli

This study creates a novel mouse model with deletion of Necdin and Magel2 genes, revealing functional interactions and phenotypes relevant to Prader-Willi Syndrome.

bioRxiv · Jul 24, 2024 · PreprintSystems Biology