Author

Jessica Klucznik

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

Click to filter author papers

Neuroscience· 1 Systems Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

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

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersNeuroscience

Émilie CaronORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Vesicle-mediated oxytocin release drives melanocortin circuit maturation during a neonatal critical period

Pierre-Yves Barelle, Fabienne Schaller, Soyoung Park, Émilie Caron, Jessica Klucznik, Phillipe Ciofi, Françoise Muscatelli, Sébastien G. Bouret

This study shows that oxytocin release during a neonatal critical period is essential for melanocortin circuit development and metabolic function.

bioRxiv · Apr 10, 2025 · PreprintNeuroscience

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