Author

Christine Plançon

Commissariat à l'Énergie Atomique et aux Énergies AlternativesORCID 0000-0003-4065-1337Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:protein structure prediction· 1 Assay:proteomics· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aude-Marie Lepagnol-BesteliD· 2 shared Jean‐François DeleuzeiD· 2 shared Michel SimonneauiD· 2 shared Yann Loe-MieiD· 2 shared Anne BolandiD· 1 shared Clotilde MircheriD· 1 shared Eugene Y. YuiD· 1 shared Eunjoon KimiD· 1 shared

Activity by Year

2019-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersNeuroscience

Aude-Marie Lepagnol-BestelORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintDec 11, 2019

Chr21 protein-protein interactions: enrichment in products involved in intellectual disabilities, autism and Late Onset Alzheimer Disease

Julia Viard, Yann Loe-Mie, Rachel Daudin…·Aude-Marie Lepagnol-Bestel

The paper identifies protein-protein interactions on Chr21 linked to intellectual disabilities, autism, and Alzheimer's by analyzing yeast two-hybrid screens and synaptic localization.

DOI 10.1101/2019.12.11.872606

humanproteomics

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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