Author

Mounia Bensaid

InsermORCID 0000-0001-7322-0627Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 3

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Organism:mouse· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:DNA methylation· 1

Frequent Co-Authors

Aude-Marie Lepagnol-BesteliD· 3 shared Michel SimonneauiD· 3 shared Yann Loe-MieiD· 3 shared Antoine TrilleriD· 1 shared Arnaud DuchoniD· 1 shared Céline Reverdy· 1 shared Christine PlançoniD· 1 shared Futoshi SuizuiD· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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3 shared papersNeuroscience

Aude-Marie Lepagnol-BestelORCID

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3 papers

Recent·Most cited

NeuroscienceGenes & DiseasesPeer-reviewedOct 19, 2024

AUTS2 expression within mammalian lineage: a predictor of neural networks involved in Autism Spectrum Disorders

Aude-Marie Lepagnol-Bestel, Yann Loe-Mie, Mounia Bensaid, Michel Simonneau

The paper investigates AUTS2 expression across mammalian species to identify phenotypes linked to Autism Spectrum Disorders.

2 citations

𝕏 PostBluesky

NeurosciencebioRxivPreprintDec 1, 2022

AUTS2 gene dosage affects synaptic AMPA receptors via a local dendritic spine AUTS2-TTC3-AKT-mTORC1 signaling dysfunction

Aude-Marie Lepagnol-Bestel, Arnaud Duchon, Julia Viard…·Michel Simonneau

This study shows that AUTS2 gene dosage affects synaptic AMPA receptors through the AUTS2-TTC3-AKT-mTORC1 pathway, leading to behavioral and cognitive impairments in mice.

1 citation

mouseexperimental assay

𝕏 PostBluesky

NeurosciencebioRxivPreprintSep 11, 2019

Multi-hit autism genomic architecture evidenced from consanguineous families with involvement of FEZF2 and mutations in high-risk genes

Mounia Bensaid, Yann Loe-Mie, Aude-Marie Lepagnol-Bestel…·Michel Simonneau

The paper identifies a multi-hit genomic architecture for ASD in consanguineous families, involving FEZF2 deletions and mutations in high-risk genes.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky