Franco Carrara
Fondazione IRCCS Istituto Neurologico Carlo Besta(IT)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, RNA modifications and cancer, Genetic Neurodegenerative Diseases
Most-Cited Works
- → MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion(2006)416 cited
- → Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNA Ser(UCN) gene(1995)209 cited
- → Identification of an X-Chromosomal Locus and Haplotype Modulating the Phenotype of a Mitochondrial DNA Disorder(2005)191 cited
- → Haplogroup Effects and Recombination of Mitochondrial DNA: Novel Clues from the Analysis of Leber Hereditary Optic Neuropathy Pedigrees(2006)182 cited
- → Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy(2007)180 cited
- → RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy(2015)111 cited
- → A novel mtDNA mutation in the ND5 subunit of complex I in two MELAS patients(2001)110 cited
- → A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function(2008)102 cited
- → A novel nonsense mutation (Q352X) in the mitochondrial cytochrome b gene associated with a combined deficiency of complexes I and III(2002)102 cited
- → Identification of novel mutations in five patients with mitochondrial encephalomyopathy(2008)101 cited