Author

Julie Riviere

Centre National de la Recherche Scientifique

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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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:electronic health records· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:phylogenetics / evolution· 1 Approach:statistical model· 1

Frequent Co-Authors

Jérôme CavailléiD· 2 shared Laure VerretiD· 2 shared Virginie MartyiD· 2 shared Baptiste Grand· 1 shared Christophe AudouardiD· 1 shared Eva Maria NovoaiD· 1 shared Ivan MilenkoviciD· 1 shared Jade Hebras· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Jérôme CavailléORCID

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2 papers

Recent·Most cited

Evolutionary and biological insights into the paternally expressed Snord116-Ipw-Snord115 gene array at the imprinted Prader-Willi syndrome domain

Virginie Marty, Jade Hebras, Raphaël Boursereau, Baptiste Grand, Julie Riviere, Sophie Le Gonidec, Ivan Milenkovic, Christophe Audouard, Pascale Mercier, Jean Personnaz, Eva Maria Novoa, Laure Verret, Jean‐Philippe Pradère, Jérôme Cavaillé

The paper investigates the role of Snord116 and Snord115 genes in Prader-Willi syndrome using knockout mice and comparative genomics, finding their impact on growth, metabolism, and gene regulation.

bioRxiv · Jul 30, 2026 · PreprintGenetics

Loss of SNORD115 mitigates SNORD116-driven sleep abnormalities in mouse models of Prader-Willi syndrome

Julie Riviere, Virginie Marty, Jérôme Cavaillé, Laure Verret

This study shows that deleting SNORD115 reduces REM sleep abnormalities caused by SNORD116 deletion in PWS mouse models, revealing complex interactions between these SNORDs.

Neurobiology of Disease · Jul 30, 2026Peer-reviewedNeuroscience