Author

Joël Fluss

University Hospital of GenevaORCID 0000-0002-6413-162XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Aldo S. BaderiD· 1 shared Alexandre G. DayeriD· 1 shared Anirban MajumdariD· 1 shared Aude Molinard‐ChenuiD· 1 shared Christopher J. CarnieiD· 1 shared Damian P. SmedleyiD· 1 shared Emma M. ClementiD· 1 shared Estelle ColiniD· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetics

Aldo S. BaderORCID

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2 papers

Recent·Most cited

Loss of CTLH component MAEA impairs DNA repair and replication and leads to developmental delay

Soren H. Hough, Satpal S. Jhujh, Samah W. Awwad, Oliver Lewis, Simon Lam, John Christopher Thomas, Thorsten Mosler, Aldo S. Bader, Lauren E. Bartik, Shane A McKee, Shivarajan Manickavasagam Amudhavalli, Estelle Colin, Nadirah S. Damseh, Emma M. Clement, Pilar Cacheiro, , Stephen P. Jackson

The paper identifies MAEA as a critical regulator of DNA repair and replication, with loss of function causing developmental delay and neurodevelopmental deficits.

EMBO Molecular Medicine · Dec 19, 2025Peer-reviewedGenetics

MCF2 is linked to a complex perisylvian syndrome and affects cortical lamination

Aude Molinard‐Chenu, Joël Fluss, Sacha Laurent, Méryle Laurent, Michel Guipponi, Alexandre G. Dayer

The paper identifies a mutation in the MCF2 gene linked to congenital bilateral perisylvian syndrome and shows it impairs cortical neuronal migration in mice.

Annals of Clinical and Translational Neurology · Dec 17, 2019Peer-reviewedNeuroscience