| Mitochondrial dysfunction as a cause of optic neuropathies V Carelli, FN Ross-Cisneros, AA Sadun Progress in retinal and eye research 23 (1), 53-89, 2004 | 979 | 2004 |
| Disturbed mitochondrial dynamics and neurodegenerative disorders F Burté, V Carelli, PF Chinnery, P Yu-Wai-Man Nature reviews neurology 11 (1), 11-24, 2015 | 786 | 2015 |
| The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool A Achilli, C Rengo, C Magri, V Battaglia, A Olivieri, R Scozzari, F Cruciani, ... The American Journal of Human Genetics 75 (5), 910-918, 2004 | 659 | 2004 |
| 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 |
| Proteolytic cleavage of Opa1 stimulates mitochondrial inner membrane fusion and couples fusion to oxidative phosphorylation P Mishra, V Carelli, G Manfredi, DC Chan Cell metabolism 19 (4), 630-641, 2014 | 582 | 2014 |
| Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the … A Torroni, M Petrozzi, L D'Urbano, D Sellitto, M Zeviani, F Carrara, ... American journal of human genetics 60 (5), 1107, 1997 | 559 | 1997 |
| Multi-system neurological disease is common in patients with OPA1 mutations P Yu-Wai-Man, PG Griffiths, GS Gorman, CM Lourenco, AF Wright, ... Brain 133 (3), 771-786, 2010 | 496 | 2010 |
| 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 |
| The clinical maze of mitochondrial neurology S DiMauro, EA Schon, V Carelli, M Hirano Nature Reviews Neurology 9 (8), 429-444, 2013 | 441 | 2013 |
| 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 |
| OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion C Zanna, A Ghelli, AM Porcelli, M Karbowski, RJ Youle, S Schimpf, ... Brain 131 (2), 352-367, 2008 | 433 | 2008 |
| Complex I deficiency primes Bax-dependent neuronal apoptosis through mitochondrial oxidative damage C Perier, K Tieu, C Guégan, C Caspersen, V Jackson-Lewis, V Carelli, ... Proceedings of the National Academy of Sciences 102 (52), 19126-19131, 2005 | 376 | 2005 |
| Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors G Gasparre, AM Porcelli, E Bonora, LF Pennisi, M Toller, L Iommarini, ... Proceedings of the National Academy of Sciences 104 (21), 9001-9006, 2007 | 358 | 2007 |
| Optic nerve degeneration and mitochondrial dysfunction: genetic and acquired optic neuropathies V Carelli, FN Ross-Cisneros, AA Sadun Neurochemistry international 40 (6), 573-584, 2002 | 344 | 2002 |
| Efficient mitochondrial biogenesis drives incomplete penetrance in Leber’s hereditary optic neuropathy C Giordano, L Iommarini, L Giordano, A Maresca, A Pisano, ML Valentino, ... Brain 137 (2), 335-353, 2014 | 336 | 2014 |
| Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy J Guy, X Qi, F Pallotti, EA Schon, G Manfredi, V Carelli, A Martinuzzi, ... Annals of Neurology: Official Journal of the American Neurological …, 2002 | 333 | 2002 |
| An international classification of inherited metabolic disorders (ICIMD) CR Ferreira, S Rahman, M Keller, J Zschocke, ICIMD Advisory Group, ... Journal of inherited metabolic disease 44 (1), 164-177, 2021 | 316 | 2021 |
| The glutamate/cystine xCT antiporter antagonizes glutamine metabolism and reduces nutrient flexibility CS Shin, P Mishra, JD Watrous, V Carelli, M D’Aurelio, M Jain, DC Chan Nature communications 8 (1), 15074, 2017 | 313 | 2017 |
| Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy P Barboni, G Savini, ML Valentino, P Montagna, P Cortelli, AM De Negri, ... Ophthalmology 112 (1), 120-126, 2005 | 303 | 2005 |
| Oestrogens ameliorate mitochondrial dysfunction in Leber’s hereditary optic neuropathy C Giordano, M Montopoli, E Perli, M Orlandi, M Fantin, FN Ross-Cisneros, ... Brain 134 (1), 220-234, 2011 | 299 | 2011 |
