Author

Alessandro Bertini

Fondazione IRCCS Istituto Neurologico Carlo BestaORCID 0009-0004-4987-7898Unclaimed ORCID profile · follow to get notified of new preprints

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Alessandro Bertini1 paper · Fondazione IRCCS Istituto Neurologico Carlo Besta

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Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Approach:statistical model· 1

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Alix de BecdelièvreiD· 1 shared Amandine Pauset· 1 shared André MégarbanéiD· 1 shared Andrea CorteseiD· 1 shared Anne‐Sophie LiaiD· 1 shared Camille Humbert· 1 shared Chiara PisciottaiD· 1 shared Christel Castro· 1 shared

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2025-2025 · peak 1/yr

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Alix de BecdelièvreORCID

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintJun 30, 2025

Bi-allelic mutations in KCTD11 cause a new form of autosomal recessive intermediate Charcot-Marie-Tooth disease

Jihane Gadacha, Zahraa Haidar, Nathalie Roëckel…·Valérie Delague

This paper identifies bi-allelic mutations in KCTD11 as a cause of autosomal recessive intermediate Charcot-Marie-Tooth disease and elucidates its role in myelin homeostasis through molecular mechanisms.

DOI 10.1101/2025.06.30.661538

mousestatistical model

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