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NPJ Genomic Medicine|March 23, 2024
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidatesMarta Viggiano, Fabiola Ceroni, Paola Visconti, et al.Journal of Cellular and Molecular Medicine|January 21, 2021
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorderCinzia Cameli, Marta Viggiano, Magali J Rochat, et al.Annals of Clinical and Translational Neurology|March 27, 2019
Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsiesTommaso Pippucci, Laura Licchetta, Sara Baldassari, et al.Frontiers in Genetics|November 24, 2022
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorderLeonardo Caporali, Claudio Fiorini, Flavia Palombo, et al.Pageof 2