Author

Julie Buron

InsermORCID 0000-0002-1111-9416Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 1 Systems Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Research Focus:database / resource· 1 Assay:electronic health records· 1

Frequent Co-Authors

Clément MenuetiD· 2 shared Fabienne SchalleriD· 2 shared Françoise MuscatelliiD· 2 shared Alicia SicardiiD· 1 shared Ambre LinossieriD· 1 shared Anne‐Marie François‐BellaniD· 1 shared Catarina Santos· 1 shared Christian GestreauiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersNeuroscience

Clément MenuetORCID

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2 papers

Recent·Most cited

The oxytocin-modulated brain circuit that synchronizes heart rate with breathing

Julie Buron, Ambre Linossier, Christian Gestreau, Fabienne Schaller, Roman Tyzio, Marie‐Solenne Félix, Valery A. Matarazzo, Muriel Thoby‐Brisson, Françoise Muscatelli, Clément Menuet

This paper identifies a hypothalamus-brainstem circuit mediated by oxytocin that enhances respiratory sinus arrhythmia during calming behaviors.

Nature Neuroscience · Oct 20, 2025Peer-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