Author

Elsa Giordani

Centre National de la Recherche Scientifique

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genetics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Organism:human· 1 Assay:proteomics· 1

Frequent Co-Authors

Charles CouttoniD· 2 shared Christophe ArnoultiD· 2 shared Corinne LoeuilletiD· 2 shared Emeline LambertiD· 2 shared Geneviève Chevalier· 2 shared Guillaume MartineziD· 2 shared Jessica EscoffieriD· 2 shared Lisa De Macedo· 2 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersMolecular Biology

Charles CouttonORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Sperm motility restoration in mice suffering from oligo-astheno-teratozoospermia by in vivo injection and electroporation of naked mRNA

Charline Vilpreux, Paul Fourquin, Guillaume Martinez, Magali Court, Florence Appaix, Jean-Luc Duteyrat, Maxime Henry, Julien Vollaire, Camille Ayad, Altan Yavuz, Geneviève Chevalier, Lisa De Macedo, Sofia Andrade Rebelo, Edgar Del Llano, Célia Tebbakh, , Jessica Escoffier

This study uses in vivo mRNA electroporation to restore sperm motility in ARMC2-deficient mice, demonstrating a potential treatment for male infertility.

eLife · Feb 17, 2026Peer-reviewedMolecular Biology

Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse

Jana Muroňová, Zine‐Eddine Kherraf, Elsa Giordani, Emeline Lambert, Simon Eckert, Caroline Cazin, Amir Amiri‐Yekta, Magali Court, Geneviève Chevalier, Guillaume Martinez, Yasmine Neirijnck, Françoise Kühne, Lydia Wehrli, Nikolai Klena, Virginie Hamel, , Christophe Arnoult

This study identifies bi-allelic CCDC146 mutations as a cause of non-syndromic male infertility in humans and mice, showing its role in sperm flagellum structure and microtubule organization.

bioRxiv · Feb 27, 2023 · PreprintGenetics