Author

Amire Assoumani

Hôpital de la Timone

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

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Annick ToutainiD· 1 shared Camille HumbertiD· 1 shared Camille VerebiiD· 1 shared Céline TardiD· 1 shared Charlotte Tardy· 1 shared Christel Castro· 1 shared Emmanuelle Salort‐CampanaiD· 1 shared Frédérique MagdinieriD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Annick ToutainORCID

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1 paper

Recent·Most cited

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