Author

Anne Robert

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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Biochemistry· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:mouse· 2 Assay:proteomics· 2 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:multiome· 1 Research Focus:protein structure prediction· 1

Frequent Co-Authors

Asmae Maachi· 1 shared Audrey Thevenin· 1 shared Bruno CharpentieriD· 1 shared Catherine BuiiD· 1 shared Déborah HelleiD· 1 shared Hélène Marty· 1 shared Hervé MoineiD· 1 shared Isabelle LebarsiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperMolecular Biology

Asmae Maachi

Mutual co-authors in cluster

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2 papers

Recent·Most cited

The DGKK mRNA is a primary target of the Prader-Willi syndrome-associated snoRNA SNORD116

Soline Louis, Oktay Cakil, Audrey Thevenin, Hélène Marty, Asmae Maachi, Virginie Marty, Anne Robert, Marie-Eve Chagot, Bruno Charpentier, Xavier Manival, Isabelle Lebars, Hervé Moine, Stephane Labialle

The paper identifies DGKK as the primary target of SNORD116, showing increased DGKK RNA and protein levels upon SNORD116 depletion in human and mouse models.

bioRxiv · Oct 21, 2026 · PreprintMolecular Biology

P4HA1 and P4HA2 accept both shared and isoenzyme-specific substrate residues in type I collagen to directly and indirectly orchestrate its post-translational modification landscape

Déborah Helle, Anne Robert, Nick Ramalanjaona, Catherine Bui, Sandrine Gulberti, Jean‐Baptiste Vincourt

This study investigates the substrate specificity of P4HA1 and P4HA2 in collagen post-translational modifications using proteomic and peptide analysis in mouse cells.

bioRxiv · Oct 15, 2026 · PreprintBiochemistry