Concepedia

Camille Peron

CP

8

Publications

283

Citations

8

H-Index

2019

Active since

Affiliations

Fondazione IRCCS Istituto Neurologico Carlo Besta(Current)

Istituto delle Scienze Neurologiche di Bologna

University of Bologna

National Research Council

San Raffaele University of Rome

Camille Peron is an author at Fondazione IRCCS Istituto Neurologico Carlo Besta specializing in molecular genetics, medicine, and mitochondrial function.

ORCID

Top concepts

Publications per year

2019–2024

8

Publications

8

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

Valentina Del Dotto, Farid Ullah, Ivano Di Meo et al. · Journal of Clinical Investigation · 2019 · 91 citations · Full text

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Pathological mitophagy disrupts mitochondrial homeostasis in Leber’s hereditary optic neuropathy

Alberto Danese, Simone Patergnani, Alessandra Maresca et al. · Cell Reports · 2022 · 60 citations · Full text

Current and New Next-Generation Sequencing Approaches to Study Mitochondrial DNA

Andrea Legati, Nadia Zanetti, Alessia Nasca et al. · Journal of Molecular Diagnostics · 2021 · 47 citations

, , +13

TFG binds LC3C to regulate ULK1 localization and autophagosome formation

Marianna Carinci, Beatrice Testa, Matteo Bordi et al. · The EMBO Journal · 2021 · 24 citations · Full text

Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy

Serena J. Aleo, Valentina Del Dotto, Martina Romagnoli et al. · Cell Reports Medicine · 2024 · 21 citations · Full text

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