Author

Corinne Loeuillet

Centre National de la Recherche ScientifiqueORCID 0000-0001-6474-4453Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 3 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:mouse· 4 Approach:experimental assay· 3 Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:gene regulatory network inference· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Charles CouttoniD· 4 shared Christophe ArnoultiD· 4 shared Emeline LambertiD· 4 shared Guillaume MartineziD· 4 shared Jessica EscoffieriD· 4 shared Pierre F. RayiD· 4 shared Zine‐Eddine KherrafiD· 4 shared Caroline CaziniD· 3 shared

Activity by Year

2022-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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4 shared papersGenetics

Charles CouttonORCID

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4 papers

Recent·Most cited

Molecular BiologyeLifePeer-reviewedFeb 17, 2026

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…·Jessica Escoffier

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

1 citation

mouseexperimental assay

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GeneticseLifePeer-reviewedNov 7, 2023

Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function.

Denis Dacheux, Guillaume Martinez, Christine E. Broster Reix…·Charles Coutton

The paper identifies ZMYND12 as a gene associated with male infertility and flagellum function through genetic and functional studies in humans and Trypanosoma brucei.

DOI 10.7554/elife.87698.3

humanmouse

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GeneticsbioRxivPreprintFeb 27, 2023

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…·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.

1 citation

humanmouse

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GeneticseLifePeer-reviewedApr 22, 2022

Oligogenic heterozygous inheritance of sperm abnormalities in mouse

Guillaume Martinez, Charles Coutton, Corinne Loeuillet…·Christophe Arnoult

The paper investigates oligogenic inheritance of sperm abnormalities in mice, finding that increasing numbers of heterozygous mutations worsen sperm morphology and motility.

33 citationstop 3%

mousewhole-genome sequencing

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