Publications by authors named "M Benkirane"

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Type and position of repeat interruptions as determinants of disease severity and expansion size in Friedreich ataxia.
Mehdi Benkirane, Cecilia Marelli, Ariane Choumert, Cyril Goizet, Olivier Patat

Genet Med· December 2025

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Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy.
Pritha Bisarad, Yung-Chun Wang, Peter T Skidmore, Carolina I Galaz-Montoya, Sara A Lewis, Mehdi Benkirane

medRxiv· November 2025

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Unintegrated HIV-1 DNA recruits cGAS via its histone-binding domain to escape innate immunity.
Cyprien Jahan, Lucie Bonnet-Madin, Shinichi Machida, Bijan Sobhian, Suzie Thenin-Houssier, Monsef Benkirane

Proc Natl Acad Sci U S A· March 2025

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AP4B1 hypomorphic variants cause autosomal recessive adult-onset ataxia.
Quentin Sabbagh, Natalia Hernandez Poblete, Chloé Angelini, Clément Hersent, Mehdi Benkirane

J Neurol· January 2025

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Phenotypic variability related to dominant UCHL1 mutations: about three families with optic atrophy and ataxia.
C Marelli, F Ramond, C Vignal, C Blanchet, S Frost, M Benkirane

J Neurol· September 2024

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