Author

Gaëlle Hayot

Centre National de la Recherche ScientifiqueORCID 0000-0001-8113-7399Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Neuroscience· 1 Pathology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 3 Organism:zebrafish· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1

Frequent Co-Authors

Christelle GolzioiD· 2 shared Agathe KahniD· 1 shared Aida Bytyci TelegrafiiD· 1 shared Albane A. BizetiD· 1 shared Alexandre BenmerahiD· 1 shared Alexia Mahuzier· 1 shared Alica M. GoldmaniD· 1 shared Alicia Boughton· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersNeuroscience

Christelle GolzioORCID

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3 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

𝕏 PostBluesky

NeurosciencebioRxivPreprintOct 6, 2021

CHD8-associated gastrointestinal complaints are caused by impaired vagal neural crest development and intestinal homeostatic imbalance

Gaëlle Hayot, Mathieu Massonot, Céline Keime…·Christelle Golzio

1 citation

zebrafishspatial transcriptomics

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