Author

Céline Brochier‐Armanet

Lyon 1 UniversitéORCID 0000-0003-4669-3589Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Organism:bacteria (other)· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Research Focus:phylogenetics / evolution· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alexandre DupreyiD· 1 shared Alexandre FabreiD· 1 shared Ange‐Line BrueliD· 1 shared Arnaud Blanchard· 1 shared Arnauld Delarue· 1 shared Aurélie Bourchany· 1 shared Bertrand RoquelaureiD· 1 shared Caroline Lacoste· 1 shared

Activity by Year

2017-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenomics

Alexandre DupreyORCID

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2 papers

Recent·Most cited

The phytopathogenic nature of Dickeya aquatica 174/2 and the dynamic early evolution of Dickeya pathogenicity

Alexandre Duprey, Najwa Taïb, Simon Léonard, Tiffany Garin, Jean‐Pierre Flandrois, William Nasser, Céline Brochier‐Armanet, Sylvie Reverchon

This paper sequenced the genome of Dickeya aquatica, showing its pathogenic potential and revealing evolutionary dynamics in Dickeya species.

Environmental Microbiology · Apr 10, 2019Peer-reviewedGenomics

Osteo-Oto-Hepato-Enteric Syndrome (O2HE) is caused by loss of function mutations in UNC45A

Clothilde Estève, Ludmila Francescatto, Perciliz L. Tan, Aurélie Bourchany, Cécile de Leusse, Evelyne Marinier, Arnaud Blanchard, Patrice Bourgeois, Céline Brochier‐Armanet, Ange‐Line Bruel, Arnauld Delarue, Yannis Duffourd, Emmanuelle Ecochard‐Dugelay, Geraldine Hery, Frédéric Huet, , Alexandre Fabre

The paper identifies biallelic UNC45A mutations as the cause of O2HE syndrome, characterized by cholestasis, congenital diarrhea, hearing loss, and bone fragility.

bioRxiv · Oct 26, 2017 · PreprintGenetics