Author

Nicolas Charlet‐Berguerand

Centre National de la Recherche ScientifiqueORCID 0000-0002-4423-4920Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Animal Behavior & Cognition· 1 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Research Focus:protein structure prediction· 1

Frequent Co-Authors

Aida Bytyci TelegrafiiD· 1 shared Alica M. GoldmaniD· 1 shared Alicia Boughton· 1 shared Amélie PitoniD· 1 shared Angélique QuartieriD· 1 shared Bertrand IsidoriD· 1 shared Biyu Yang· 1 shared Candace Gamble· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 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

1 shared paperGenetics

Aida Bytyci TelegrafiORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Animal Behavior & CognitionbioRxivPreprintFeb 12, 2026

A novel uN2CpolyG Transgenic Mouse Model Recapitulates Multisystemic polyG Proteinopathy Pathology of Neuronal Intranuclear Inclusion Disease

Yalan Wan, Yilei Zheng, Chao Gao…·Jianwen Deng

This study develops a transgenic mouse model that recapitulates the multisystemic pathology of neuronal intranuclear inclusion disease through polyG protein aggregates.

1 citation

mouseexperimental assay

𝕏 PostBluesky

GeneticsbioRxivPreprintDec 4, 2019

Highly clustered de novo frameshift variants in the neuronal splicing factor NOVA2 result in a specific abnormal C terminal part and cause a severe form of intellectual disability with autistic features.

Francesca Mattioli, Gaëlle Hayot, Nathalie Drouot…·Amélie Piton

The paper identifies de novo frameshift variants in NOVA2 causing a severe neurodevelopmental disorder with intellectual disability and autistic features, and shows altered RNA splicing and functional deficits.

DOI 10.1101/858696

humanzebrafish

𝕏 PostBluesky