| Interaction of COMT Val108/158 Met Genotype and Olanzapine Treatment on Prefrontal Cortical Function in Patients With Schizophrenia A Bertolino, G Caforio, G Blasi, M De Candia, V Latorre, V Petruzzella, ... American Journal of Psychiatry 161 (10), 1798-1805, 2004 | 396 | 2004 |
| The oxidative phosphorylation system in mammalian mitochondria S Papa, PL Martino, G Capitanio, A Gaballo, D De Rasmo, A Signorile, ... Advances in Mitochondrial Medicine, 3-37, 2012 | 316 | 2012 |
| Additive effects of genetic variation in dopamine regulating genes on working memory cortical activity in human brain A Bertolino, G Blasi, V Latorre, V Rubino, A Rampino, L Sinibaldi, ... Journal of Neuroscience 26 (15), 3918-3922, 2006 | 294 | 2006 |
| Reduced transcription of mitochondrial DNA in the senescent rat: Tissue dependence and effect of l‐carnitine MN Gadaleta, V Petruzzella, M Renis, F Fracasso, P Cantatore European Journal of Biochemistry 187 (3), 501-506, 1990 | 230 | 1990 |
| Prefrontal-hippocampal coupling during memory processing is modulated by COMT val158met genotype A Bertolino, V Rubino, F Sambataro, G Blasi, V Latorre, L Fazio, G Caforio, ... Biological psychiatry 60 (11), 1250-1258, 2006 | 222 | 2006 |
| Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions CT Moraes, E Ricci, V Petruzzella, S Shanske, S DiMauro, EA Schon, ... Nature genetics 1 (5), 359-367, 1992 | 200 | 1992 |
| Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex I A Iuso, S Scacco, C Piccoli, F Bellomo, V Petruzzella, R Trentadue, ... Journal of Biological Chemistry 281 (15), 10374-10380, 2006 | 171 | 2006 |
| Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial … V Petruzzella, V Tiranti, P Fernandez, P Ianna, R Carrozzo, M Zeviani Genomics 54 (3), 494-504, 1998 | 168 | 1998 |
| A nonsense mutation in the NDUFS4 gene encoding the 18 kDa (AQDQ) subunit of complex I abolishes assembly and activity of the complex in a patient with Leigh … V Petruzzella, R Vergari, I Puzziferri, D Boffoli, E Lamantea, M Zeviani, ... Human molecular genetics 10 (5), 529-536, 2001 | 155 | 2001 |
| Pathological mutations of the human NDUFS4 gene of the 18-kDa (AQDQ) subunit of complex I affect the expression of the protein and the assembly and function of the complex S Scacco, V Petruzzella, S Budde, R Vergari, R Tamborra, D Panelli, ... Journal of Biological Chemistry 278 (45), 44161-44167, 2003 | 144 | 2003 |
| Extremely high levels of mutant mtDNAs co-localize with cytocohrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243 V Petruzzella, CT Moraes, MC Sano, SE Bonilla, S DiMauro, EA Schon Human molecular genetics 3 (3), 449-454, 1994 | 142 | 1994 |
| HmtDB, a genomic resource for mitochondrion-based human variability studies F Rubino, R Piredda, FM Calabrese, D Simone, M Lang, C Calabrese, ... Nucleic acids research 40 (D1), D1150-D1159, 2012 | 116 | 2012 |
| Pontocerebellar hypoplasia type 6 caused by mutations in RARS2: definition of the clinical spectrum and molecular findings in five patients D Cassandrini, MR Cilio, M Bianchi, M Doimo, M Balestri, A Tessa, ... Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2013 | 95 | 2013 |
| Minireview: The NADH: Ubiquinone Oxidoreductase (Complex I) of the Mammalian Respiratory Chain and the cAMP Cascade S Papa, AM Sardanelli, S Scacco, V Petruzzella, Z Technikova-Dobrova, ... Journal of bioenergetics and biomembranes 34, 1-10, 2002 | 85 | 2002 |
| Reduced synthesis of mtRNA in isolated mitochondria of senescent rat brain P Fernandez-Silva, V Petruzzella, F Fracasso, MN Badaleta, P Cantatore Biochemical and biophysical research communications 176 (2), 645-653, 1991 | 85 | 1991 |
| Respiratory chain complex I, a main regulatory target of the cAMP/PKA pathway is defective in different human diseases S Papa, D De Rasmo, Z Technikova-Dobrova, D Panelli, A Signorile, ... FEBS letters 586 (5), 568-577, 2012 | 84 | 2012 |
| Prefrontal dysfunction in schizophrenia controlling for COMT Val158Met genotype and working memory performance A Bertolino, G Caforio, V Petruzzella, V Latorre, V Rubino, S Dimalta, ... Psychiatry Research: Neuroimaging 147 (2-3), 221-226, 2006 | 84 | 2006 |
| New morphological approaches to the study of mitochondrial encephalomyopathies E Bonilla, M Sciacco, K Tanji, M Sparaco, V Petruzzella, CT Moraes Brain Pathology 2 (2), 113-119, 1992 | 84 | 1992 |
| Lipid composition in synaptic and nonsynaptic mitochondria from rat brains and effect of aging FM Ruggiero, F Cafagna, V Petruzzella, MN Gadaleta, E Quagliariello Journal of neurochemistry 59 (2), 487-491, 1992 | 81 | 1992 |
| Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex I SMS Budde, L van den Heuvel, RJP Smeets, D Skladal, JA Mayr, ... Journal of inherited metabolic disease 26, 813-815, 2003 | 80 | 2003 |
