| OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes P Amati-Bonneau, ML Valentino, P Reynier, ME Gallardo, B Bornstein, ... Brain 131 (2), 338-351, 2008 | 612 | 2008 |
| Melanopsin retinal ganglion cell loss in A lzheimer disease C La Morgia, FN Ross‐Cisneros, Y Koronyo, J Hannibal, R Gallassi, ... Annals of neurology 79 (1), 90-109, 2016 | 450 | 2016 |
| Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA–haplogroup background G Hudson, V Carelli, L Spruijt, M Gerards, C Mowbray, A Achilli, A Pyle, ... The American Journal of Human Genetics 81 (2), 228-233, 2007 | 440 | 2007 |
| Artificial intelligence to detect papilledema from ocular fundus photographs D Milea, RP Najjar, Z Jiang, D Ting, C Vasseneix, X Xu, M Aghsaei Fard, ... New England Journal of Medicine 382 (18), 1687-1695, 2020 | 360 | 2020 |
| Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders V Carelli, C La Morgia, ML Valentino, P Barboni, FN Ross-Cisneros, ... Biochimica et Biophysica Acta (BBA)-Bioenergetics 1787 (5), 518-528, 2009 | 297 | 2009 |
| Idebenone treatment in Leber's hereditary optic neuropathy V Carelli, C La Morgia, ML Valentino, G Rizzo, M Carbonelli, AM De Negri, ... Brain 134 (9), e188-e188, 2011 | 283 | 2011 |
| International consensus statement on the clinical and therapeutic management of Leber hereditary optic neuropathy V Carelli, M Carbonelli, IF De Coo, A Kawasaki, T Klopstock, WA Lagrèze, ... Journal of Neuro-Ophthalmology 37 (4), 371-381, 2017 | 266 | 2017 |
| Bilateral visual improvement with unilateral gene therapy injection for Leber hereditary optic neuropathy P Yu-Wai-Man, NJ Newman, V Carelli, ML Moster, V Biousse, AA Sadun, ... Science translational medicine 12 (573), eaaz7423, 2020 | 252 | 2020 |
| Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder AJ Abrams, RB Hufnagel, A Rebelo, C Zanna, N Patel, MA Gonzalez, ... Nature genetics 47 (8), 926-932, 2015 | 246 | 2015 |
| Melanopsin retinal ganglion cells are resistant to neurodegeneration in mitochondrial optic neuropathies C La Morgia, FN Ross-Cisneros, AA Sadun, J Hannibal, A Munarini, ... Brain 133 (8), 2426-2438, 2010 | 221 | 2010 |
| 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 | 207 | 2015 |
| Efficacy and safety of intravitreal gene therapy for Leber hereditary optic neuropathy treated within 6 months of disease onset NJ Newman, P Yu-Wai-Man, V Carelli, ML Moster, V Biousse, ... Ophthalmology 128 (5), 649-660, 2021 | 201 | 2021 |
| Retinal imaging in Alzheimer's and neurodegenerative diseases PJ Snyder, J Alber, C Alt, LJ Bain, BE Bouma, FH Bouwman, DC DeBuc, ... Alzheimer's & Dementia 17 (1), 103-111, 2021 | 198 | 2021 |
| Leber’s hereditary optic neuropathy AA Sadun, CL Morgia, V Carelli Current treatment options in neurology 13 (1), 109-117, 2011 | 192 | 2011 |
| A neurodegenerative perspective on mitochondrial optic neuropathies P Yu-Wai-Man, M Votruba, F Burté, C La Morgia, P Barboni, V Carelli Acta neuropathologica 132 (6), 789-806, 2016 | 191 | 2016 |
| Leber’s hereditary optic neuropathy with childhood onset P Barboni, G Savini, ML Valentino, C La Morgia, C Bellusci, AM De Negri, ... Investigative Ophthalmology & Visual Science 47 (12), 5303-5309, 2006 | 188 | 2006 |
| M itochondrial DNA and primary mitochondrial dysfunction in P arkinson's disease MP Giannoccaro, C La Morgia, G Rizzo, V Carelli Movement Disorders 32 (3), 346-363, 2017 | 166 | 2017 |
| Patterns of retinal ganglion cell damage in neurodegenerative disorders: parvocellular vs magnocellular degeneration in optical coherence tomography studies C La Morgia, L Di Vito, V Carelli, M Carbonelli Frontiers in neurology 8, 710, 2017 | 160 | 2017 |
| Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern? C La Morgia, P Barboni, G Rizzo, M Carbonelli, G Savini, C Scaglione, ... European journal of neurology 20 (1), 198-201, 2013 | 160 | 2013 |
| Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy SL Stenton, NL Sheremet, CB Catarino, NA Andreeva, Z Assouline, ... The Journal of Clinical Investigation 131 (6), 2021 | 159 | 2021 |
Gaetano CantalupoDepartment of Engineering for Innovation Medicine, University of Verona, ItalyVerified email at univr.it
