| OPA1 isoforms in the hierarchical organization of mitochondrial functions V Del Dotto, P Mishra, S Vidoni, M Fogazza, A Maresca, L Caporali, ... Cell reports 19 (12), 2557-2571, 2017 | 194 | 2017 |
| Syndromic parkinsonism and dementia associated with OPA1 missense mutations V Carelli, O Musumeci, L Caporali, C Zanna, C La Morgia, V Del Dotto, ... Annals of neurology 78 (1), 21-38, 2015 | 180 | 2015 |
| Eight human OPA1 isoforms, long and short: What are they for? V Del Dotto, M Fogazza, V Carelli, M Rugolo, C Zanna Biochimica et Biophysica Acta (BBA)-Bioenergetics 1859 (4), 263-269, 2018 | 153 | 2018 |
| Cigarette toxicity triggers Leber’s hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways L Giordano, S Deceglie, P d'Adamo, ML Valentino, C La Morgia, ... Cell death & disease 6 (12), e2021-e2021, 2015 | 135 | 2015 |
| SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder V Del Dotto, F Ullah, I Di Meo, P Magini, M Gusic, A Maresca, L Caporali, ... The Journal of clinical investigation 130 (1), 108-125, 2020 | 75 | 2020 |
| Incomplete penetrance in mitochondrial optic neuropathies L Caporali, A Maresca, M Capristo, V Del Dotto, F Tagliavini, ... Mitochondrion 36, 130-137, 2017 | 71 | 2017 |
| Expanding and validating the biomarkers for mitochondrial diseases A Maresca, V Del Dotto, M Romagnoli, C La Morgia, L Di Vito, M Capristo, ... Journal of Molecular Medicine 98, 1467-1478, 2020 | 56 | 2020 |
| OPA1: How much do we know to approach therapy? V Del Dotto, M Fogazza, G Lenaers, M Rugolo, V Carelli, C Zanna Pharmacological research 131, 199-210, 2018 | 56 | 2018 |
| Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber’s hereditary optic neuropathy L Caporali, L Iommarini, C La Morgia, A Olivieri, A Achilli, A Maresca, ... PLoS genetics 14 (2), e1007210, 2018 | 52 | 2018 |
| Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome C La Morgia, A Maresca, G Amore, LL Gramegna, M Carbonelli, ... Scientific reports 10 (1), 4785, 2020 | 43 | 2020 |
| Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models V Del Dotto, M Fogazza, F Musiani, A Maresca, SJ Aleo, L Caporali, ... Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1864 (10 …, 2018 | 43 | 2018 |
| ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy L Caporali, S Magri, A Legati, V Del Dotto, F Tagliavini, F Balistreri, ... Annals of neurology 88 (1), 18-32, 2020 | 34 | 2020 |
| Pathological mitophagy disrupts mitochondrial homeostasis in Leber’s hereditary optic neuropathy A Danese, S Patergnani, A Maresca, C Peron, A Raimondi, L Caporali, ... Cell Reports 40 (3), 2022 | 26 | 2022 |
| Metabolomics hallmarks OPA1 variants correlating with their in vitro phenotype and predicting clinical severity JM Chao de la Barca, M Fogazza, M Rugolo, S Chupin, V Del Dotto, ... Human molecular genetics 29 (8), 1319-1329, 2020 | 21 | 2020 |
| DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism A Maresca, V Del Dotto, M Capristo, E Scimonelli, F Tagliavini, L Morandi, ... Human Molecular Genetics 29 (11), 1864-1881, 2020 | 20 | 2020 |
| Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations SJ Aleo, V Del Dotto, M Fogazza, A Maresca, T Lodi, P Goffrini, A Ghelli, ... Human Molecular Genetics 29 (22), 3631-3645, 2020 | 13 | 2020 |
| Mitochondrial mass assessment in a selected cell line under different metabolic conditions A Costanzini, G Sgarbi, A Maresca, V Del Dotto, G Solaini, A Baracca Cells 8 (11), 1454, 2019 | 12 | 2019 |
| Dominant Optic Atrophy (DOA): modeling the kaleidoscopic roles of OPA1 in mitochondrial homeostasis V Del Dotto, V Carelli Frontiers in Neurology 12, 681326, 2021 | 11 | 2021 |
| The pro-oncogenic protein IF1 does not contribute to the Warburg effect and is not regulated by PKA in cancer cells G Sgarbi, R Righetti, V Del Dotto, S Grillini, V Giorgio, A Baracca, ... Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1870 (1), 166879, 2024 | 5 | 2024 |
| Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome C La Morgia, A Maresca, G Amore, LL Gramegna, M Carbonelli, ... Scientific Reports 10, 2020 | 5 | 2020 |
