Author

Nathalie Eudes

Inserm

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

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Frédérique MagdinieriD· 2 shared Jean Philippe TraniiD· 2 shared Alexandra Andrieux· 1 shared Alice NordlingeriD· 1 shared Amire Assoumani· 1 shared Anne BigotiD· 1 shared Anne DejeaniD· 1 shared Annick ToutainiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersGenetics

Frédérique MagdinierORCID

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2 papers

Recent·Most cited

Chemical inhibition of SUMOylation activates the FSHD locus

Alice Nordlinger, Loéva Morin, Alexandra Andrieux, Jean Philippe Trani, Pierre Perrin, Nathalie Eudes, Anne Bigot, Anne Dejean, Frédérique Magdinier

The paper shows that inhibiting SUMOylation with TAK981 increases DUX4 expression in human muscle cells without affecting DNA methylation or SMCHD1 activity, suggesting a new therapeutic approach for FSHD.

Scientific Reports · Jan 9, 2026Peer-reviewedGenetics

Comparison of long-read sequencing strategies for resolving complex genotypes at Facioscapulohumeral dystrophy-associated loci

Charlotte Tardy, Jean Philippe Trani, Victor Murcia Pienkowski, Loeva Morin, Christel Castro, Louis Souville, Camille Humbert, Laurène Gérard, Nathalie Eudes, Amire Assoumani, Karine Bertaux, Camille Verebi, Juliette Nectoux, Emmanuelle Salort‐Campana, Marie‐Line Jacquemont, , Frédérique Magdinier

This paper compares long-read sequencing strategies to resolve complex genotypes at FSHD-associated loci, showing that structural variants arise from intrachromosomal recombination and require high-resolution methods for accurate detection.

medRxiv · Aug 8, 2025 · PreprintGenetic & Genomic Medicine