Author

Jean-Marc Plaza

Centre National de la Recherche ScientifiqueORCID 0000-0001-6130-8867Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 1 Pathology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Approach:experimental assay· 1 Assay:multiome· 1 Assay:proteomics· 1

Frequent Co-Authors

Agathe KahniD· 1 shared Albane A. BizetiD· 1 shared Alexandre BenmerahiD· 1 shared Alexia Mahuzier· 1 shared Amandine ViauiD· 1 shared Andreas W. SaileriD· 1 shared Aude-Marie Lepagnol-BesteliD· 1 shared Bertrand KnebelmanniD· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperPathology

Agathe KahnORCID

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2 papers

Recent·Most cited

PathologybioRxivPreprintApr 18, 2024

The ANKS3/BICC1 protein complex is a master post-transcriptional regulator of NPHP1 ciliopathy gene transcripts

Alexia Mahuzier, Gweltas Odye, Valentina Grampa…·Sophie Saunier

The paper identifies ANKS3/BICC1 as a post-transcriptional regulator of NPHP1 transcripts, linking it to ciliopathy phenotypes through transcript decay and ciliary dysfunction.

4 citations

zebrafishrat

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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