Author

Quentin Fort

Lyon 1 UniversitéORCID 0000-0002-5534-7154Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:scRNA-seq· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Abdoulaye Diallo· 1 shared Aïcha BoughalemiD· 1 shared Anne-Laure Bougé· 1 shared Armelle Luscan· 1 shared Arnaud BonnaffouxiD· 1 shared Bérangère Robert· 1 shared Cynthia FourgeuxiD· 1 shared David GenevièveiD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abdoulaye Diallo

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2 papers

Recent·Most cited

Inference and validation of a dynamic gene regulatory network influencing cell fate during Duchenne muscular dystrophy initiation

Elsa Gratianne Guillot, Quentin Fort, Elise Mozin, Bérangère Robert, Matteo Bouvier, Cynthia Fourgeux, Paul Simon, Sara Munoz, Matthew Carter Childers, Jérémie Poschmann, Oumeya Adjali, David L. Mack, Arnaud Bonnaffoux, Jean-Baptiste Dupont

The paper identifies a dynamic gene regulatory network in Duchenne muscular dystrophy that controls cell fate decisions and shows how disease mutations disrupt this network.

bioRxiv · Nov 19, 2025 · PreprintBioinformatics

Genome Alert!: a standardized procedure for genomic variant reinterpretation and automated genotype-phenotype reassessment in clinical routine

Kévin Yauy, François Lecoquierre, Stéphanie Baert‐Desurmont, Detlef Trost, Aïcha Boughalem, Armelle Luscan, Jean‐Marc Costa, Vanna Géromel, Laure Raymond, Pascale Richard, Sophie Coutant, Mélanie Broutin, Raphaël Lanos, Quentin Fort, Stenzel Cackowski, , Nicolas Philippe

Genome Alert! automatically detects changes in variant classifications and gene-disease associations over time, improving clinical interpretation of genomic data with minimal human effort.

Genetics in Medicine · Mar 17, 2022Peer-reviewedGenetic & Genomic Medicine