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Plos One|December 21, 2017
RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counselingDiana Parma, Marcela Ferrer, Leonela Luce, et al.Scientific Reports|July 31, 2020
Metagenomic analysis of gut microbiota in non-treated plaque psoriasis patients stratified by disease severity: development of a new Psoriasis-Microbiome IndexIgnacio Dei-Cas, Florencia Giliberto, Leonela Luce, et al.Journal of the Neurological Sciences|October 19, 2013
Symptomatic female carriers of Duchenne muscular dystrophy (DMD): genetic and clinical characterizationFlorencia Giliberto, Claudia Pamela Radic, Leonela Luce, et al.Frontiers in Pharmacology|June 21, 2021
Theragnosis for Duchenne Muscular DystrophyLeonela Luce, Micaela Carcione, Chiara Mazzanti, et al.Genes|October 24, 2020
GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired CohortPaula Buonfiglio, Carlos D Bruque, Leonela Luce, et al.Scientific Reports|January 8, 2022
Predicting pathogenicity for novel hearing loss mutations based on genetic and protein structure approachesPaula I Buonfiglio, Carlos D Bruque, Vanesa Lotersztein, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 14, 2024
Prognostic significance of ACTN3 genotype in Duchenne muscular dystrophy: Findings from an Argentine patient cohortLeonela Luce, Chiara Mazzanti, Micaela Carcione, et al.Neurology. Genetics|January 26, 2026
Erratum: Whole-Body Skeletal Muscle MRI Patterns in Female Dystrophinopathy CarriersAlejandra P Vigliano, Leonela Luce, José Manuel Pastor Rueda, et al.Neurology. Genetics|October 6, 2025
Whole-Body Skeletal Muscle MRI Patterns in Female Dystrophinopathy CarriersAlejandra P Vigliano, Leonela Luce, José Manuel Pastor Rueda, et al.Neuromuscular Disorders : NMD|January 16, 2021
Analysis of complex structural variants in the DMD gene in one familyLeonela Luce, Martín M Abelleyro, Micaela Carcione, et al.Pageof 2