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Valentina Sardone

Hexanucleotide Repeats in ALS/FTD Form Length-Dependent RNA Foci, Sequester RNA Binding Proteins, and Are Neurotoxic
2013 · Youn-Bok Lee, Han-Jou Chen, et al. · Cell Reports · 523
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Increased dystrophin production with golodirsen in patients with Duchenne muscular dystrophy
2020 · Diane E. Frank, Frederick J. Schnell, et al. · Neurology · 344
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Differential roles of the ubiquitin proteasome system (UPS) and autophagy in the clearance of soluble and aggregated TDP-43 species
2014 · Emma L Scotter, Caroline Vance, et al. · Journal of Cell Science · 296
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Delivery is key: lessons learnt from developing splice‐switching antisense therapies
2017 · Caroline Godfrey, Lourdes R Desviat, et al. · EMBO Molecular Medicine · 158
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Long-Term Safety and Efficacy Data of Golodirsen in Ambulatory Patients with Duchenne Muscular Dystrophy Amenable to Exon 53 Skipping: A First-in-human, Multicenter, Two-Part, Open-Label, Phase 1/2 Trial
2021 · Laurent Servais, Eugenio Mercuri, et al. · Nucleic Acid Therapeutics · 135
Antisense Oligonucleotide-Based Therapy for Neuromuscular Disease
2017 · Valentina Sardone, Haiyan Zhou, et al. · Molecules · 110
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Retention of hexanucleotide repeat-containing intron in C9orf72 mRNA: implications for the pathogenesis of ALS/FTD
2016 · Michael Niblock, Bradley N. Smith, et al. · Acta Neuropathologica Communications · 65
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TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations
2015 · Viviana Pensato, Cinzia Tiloca, et al. · Journal of Neurology · 59
Allele-Specific Knockdown of ALS-Associated Mutant TDP-43 in Neural Stem Cells Derived from Induced Pluripotent Stem Cells
2014 · Agnes L. Nishimura, Carole Shum, et al. · PLoS ONE · 52
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Posttranscriptional regulation of SOD1 gene expression under oxidative stress: Potential role of ELAV proteins in sporadic ALS
2013 · Pamela Milani, Marialaura Amadio, et al. · Neurobiology of Disease · 44
Hydrogen peroxide-mediated induction of SOD1 gene transcription is independent from Nrf2 in a cellular model of neurodegeneration
2015 · Michela Dell'Orco, Pamela Milani, et al. · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · 38
HuD regulates SOD1 expression during oxidative stress in differentiated neuroblastoma cells and sporadic ALS motor cortex
2020 · Michela Dell'Orco, Valentina Sardone, et al. · Neurobiology of Disease · 27
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A multicenter comparison of quantification methods for antisense oligonucleotide-induced DMD exon 51 skipping in Duchenne muscular dystrophy cell cultures
2018 · Monika Hiller, Maria Sofia Falzarano, et al. · PLoS ONE · 27
A novel high-throughput immunofluorescence analysis method for quantifying dystrophin intensity in entire transverse sections of Duchenne muscular dystrophy muscle biopsy samples
2018 · Valentina Sardone, Matthew Ellis, et al. · PLoS ONE · 27
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From Transcriptome to Noncoding RNAs: Implications in ALS Mechanism
2012 · Stella Gagliardi, Pamela Milani, et al. · Neurology Research International · 21
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Golodirsen Induces Exon Skipping Leading to Sarcolemmal Dystrophin Expression in Duchenne Muscular Dystrophy Patients With Mutations Amenable to Exon 53 Skipping (S22.001)
2018 · Francesco Muntoni, Diane Frank, et al. · Neurology · 19
High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients
2021 · Silvia Torelli, Domenic Scaglioni, et al. · Journal of Neuropathology & Experimental Neurology · 12
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Expanded G4C2 repeats linked to C9ORF72ALS and FTD form length-dependent RNA foci, sequester RNA binding proteins and are neurotoxic
2013 · Youn-Bok Lee, Han-Jou Chen, et al. · Molecular Neurodegeneration · 7
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HuD regulates SOD1 expression during oxidative stress in differentiated neuroblastoma cells and sporadic ALS motor cortex
2022 · Michela, Dell'Orco, Valentina, Sardone, et al. · Zenodo (CERN European Organization for Nuclear Research)
P.143Correlation between dystrophin espression and clinical phenotype using high-throughput digital immunoanalysis in Duchenne and Becker muscular dystrophy patients
2019 · S. Torelli, D. Scaglioni, et al. · Neuromuscular Disorders
Next Generation Sequencing and Experimental Myology
2018 · M. Ellis, V. Sardone, et al. · Neuromuscular Disorders
Dystrophin quantification in Duchenne and Becker muscular dystrophy: correlation between dystrophin protein and clinical phenotype
2018 · V. Sardone, J. Domingos, et al. · Neuromuscular Disorders
A semi-automated image processing method for quantify dystrophin coverage at the sarcolemma membrane of each individual muscle fibre
2017 · V. Sardone, A. Jones, et al. · Neuromuscular Disorders
Dystrophin quantification on Western blotting: comparative analysis of different methods
2017 · A. Jones, V. Sardone, et al. · Neuromuscular Disorders
Optimizing dystrophin quantification in DMD and BMD patients: A new semi-automated acquisition and analysis method
2016 · V. Sardone, M. Ellis, et al. · Neuromuscular Disorders
Works count: 30
Citation count: 1,964
H-index: 16
I10-index: 17
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