Concepedia

Author

Camille Peron

Fondazione IRCCS Istituto Neurologico Carlo BestaORCID

Also Known As

Camille Peron, PERON, Camille, Peron, Camille

25

Publications

295

Citations

8

H-Index

23

Concepts

All Affiliations

Fondazione IRCCS Istituto Neurologico Carlo BestaIstituto delle Scienze Neurologiche di BolognaUniversity of BolognaNational Research CouncilSan Raffaele University of Rome
CP

About

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

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

148

2

Molecular Biology

2

2

138

3

Natural Sciences

1

1

47

4

Biology

1

1

47

5

Cell Biology

1

1

10

Camille Peron

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8

Publications

283

Citations

8

H-Index

YearCitations

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

Valentina Del Dotto, Farid Ullah, Ivano Di Meo,

Journal of Clinical Investigation

2019

91

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

Alberto Danese, Simone Patergnani, Alessandra Maresca,

Cell Reports

2022

60

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

Andrea Legati, Nadia Zanetti, Alessia Nasca,

Journal of Molecular Diagnostics

2021

47

TFG binds LC3C to regulate ULK1 localization and autophagosome formation

Marianna Carinci, Beatrice Testa, Matteo Bordi,

The EMBO Journal

2021

24

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,

Cell Reports Medicine

2024

21

Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives

Camille Peron, Alessandra Maresca, Andrea Cavaliere,

Frontiers in Neurology

2021

16

Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber’s Hereditary optic Neuropathy (LHON)

Camille Peron, Roberta Mauceri, Tommaso Cabassi,

Stem Cell Research

2020

14

The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs

Flavia Palombo, Camille Peron, Leonardo Caporali,

Stem Cell Reports

2021

10

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