| Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway AR Fetoni, V Zorzi, F Paciello, G Ziraldo, C Peres, M Raspa, F Scavizzi, ... Redox Biology 19, 301-317, 2018 | 69 | 2018 |
| Is this the real time for genomics? M Guarnaccia, G Gentile, E Alessi, C Schneider, S Petralia, S Cavallaro Genomics 103 (2-3), 177-182, 2014 | 41 | 2014 |
| A neurocutaneous phenotype with paired hypo-and hyperpigmented macules, microcephaly and stunted growth as prominent features P Pavone, AD Praticò, G Gentile, R Falsaperla, R Iemmolo, M Guarnaccia, ... European Journal of Medical Genetics 59 (5), 283-9, 2016 | 40 | 2016 |
| Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without ‘hairy elbows’: expanding the phenotype of Wiedemann–Steiner syndrome D Steel, V Salpietro, R Phadke, M Pitt, G Gentile, A Massoud, L Batten, ... Journal of Genetics 94 (4), 755-8, 2015 | 34 | 2015 |
| Dysregulated miRNAs as Biomarkers and Therapeutical Targets in Neurodegenerative Diseases G Gentile, G Morello, V La Cognata, M Guarnaccia, FL Conforti, ... Journal of Personalized Medicine 12 (5), 770, 2022 | 30 | 2022 |
| Splicing Players Are Differently Expressed in Sporadic Amyotrophic Lateral Sclerosis Molecular Clusters and Brain Regions V La Cognata, G Gentile, E Aronica, S Cavallaro Cells 9 (1), 159, 2020 | 26 | 2020 |
| The contribution of CNVs to the most common aging-related neurodegenerative diseases G Gentile, V La Cognata, S Cavallaro Aging Clin Exp Res 33 (5), 1187-1195, 2021 | 24 | 2021 |
| A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson's disease V La Cognata, G Morello, G Gentile, V D'Agata, C Criscuolo, F Cavalcanti, ... Neurogenetics, 1-12, 2016 | 12 | 2016 |
| Individual Oligogenic Background in p. D91A-SOD1 Amyotrophic Lateral Sclerosis Patients G Gentile, B Perrone, G Morello, IL Simone, S Andò, S Cavallaro, ... Genes 12 (12), 1843, 2021 | 7 | 2021 |
| miRNA and mRNA profiling links connexin deficiency to deafness via early oxidative damage in the mouse stria vascularis G Gentile, F Paciello, V Zorzi, AG Spampinato, M Guarnaccia, G Crispino, ... Frontiers in Cell and Developmental Biology 8, 1754, 2021 | 6 | 2021 |
| ALS and CHARGE syndrome: a clinical and genetic study C Ungaro, L Citrigno, F Trojsi, T Sprovieri, G Gentile, M Muglia, ... Acta Neurologica Belgica, 2018 | 6 | 2018 |
| Tumor Growth in the High Frequency Medulloblastoma Mouse Model Ptch1+/−/Tis21KO Has a Specific Activation Signature of the PI3K/AKT/mTOR Pathway and Is Counteracted by the PI3K … M Ceccarelli, G D’Andrea, L Micheli, G Gentile, S Cavallaro, G Merlino, ... Frontiers in Oncology, 2021 | 5 | 2021 |
| Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 Family G Morello, G Gentile, R Spataro, AG Spampinato, M Guarnaccia, ... Journal of Personalized Medicine 10 (4), 262, 2020 | 5 | 2020 |
| Functional Genomics Identifies Tis21-Dependent Mechanisms and Putative Cancer Drug Targets Underlying Medulloblastoma Shh-Type Development G Gentile, M Ceccarelli, L Micheli, F Tirone, S Cavallaro Front Pharmacol 7 (449), 2016 | 5 | 2016 |
| Transcriptional Profiles of Cell Fate Transitions Reveal Early Drivers of Neuronal Apoptosis and Survival G Morello, A Villari, AG Spampinato, V La Cognata, M Guarnaccia, ... Cells 10 (11), 3238, 2021 | 4 | 2021 |
| NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders V La Cognata, G Morello, G Gentile, F Cavalcanti, R Cittadella, ... Current Genomics 19 (6), 431-443, 2018 | 4 | 2018 |
| Translational Medicine in Neurological Disorders: A Genomic Perspective G Gentile, S Cavallaro Current Genomics 20 (3), 151, 2019 | 2 | 2019 |
| A genomic screening platform highlighting differences and overlaps in neurodegenerative diseases G Gentile, LC Valentina, G Morello, M Guarnaccia, AG Spampinato, ... PROGETTO DI INTERESSE "INVECCHIAMENTO" Convegno Finale - CNR -Roma, Poster …, 2019 | | 2019 |
| Copy Number Variants in Neurological Disorder G Gentile, S Cavallaro Current genomics 19 (6), 411, 2018 | | 2018 |
| Una piattaforma array CGH custom per l’identificazione di CNV in pazienti affetti da Sindromi Neurocutanee ed altri disordini neurologici: validazione della regione d’interesse … G Gentile, V La Cognata, G Morello, M Muglia, A Magariello, A Patitucci, ... XIX congresso SIGU - 23-26 novembre 2016, 2016 | | 2016 |
Sebastiano CavallaroCnr在 cnr.it 的电子邮件经过验证
