Author

Naïg Guéguen

Observed names: GUEGUEN, Naïg, Gueguen, Naig, Gueguen, Naïg, N Gueguen, N. GUEGUEN, N. Gueguen, Naig Gueguen, Naïg Gueguen

Institutions: Centre National de la Recherche Scientifique, Inserm, Centre Hospitalier Universitaire d'Angers, Centre hospitalier universitaire d'Orléans, Mitochondrial and Cardiovascular Physiopathology, Université d'Angers

Observed institutions: Centre National de la Recherche Scientifique, Inserm, Université de Montpellier, Université Nantes Angers Le Mans, Centre Hospitalier Universitaire de Nantes, Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement, Mohamed I University, Centre Hospitalier Universitaire d'Angers, Centre hospitalier universitaire d'Orléans, Université Montpellier 1, Institut National de la Recherche Agronomique, Université Montpellier 2, Mitochondrial and Cardiovascular Physiopathology, Université d'Angers

ORCID: 0000-0002-3094-8121

Observed ORCID: 0000-0002-3094-8121

OpenAlex ID: A5018701159

New Insights into Muscle Fiber Types in the Pig

2002 · Louis Lefaucheur, Patrick Ecolan, et al. · Journal of Histochemistry & Cytochemistry · 197

Mitochondrial coupling defect in Charcot–Marie–Tooth type 2A disease

2007 · Dominique Loiseau, Arnaud Chevrollier, et al. · Annals of Neurology · 156

OPA1-associated disorders: Phenotypes and pathophysiology

2009 · Patrizia Amati-Bonneau, Dan Milea, et al. · The International Journal of Biochemistry & Cell Biology · 151

Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome

2014 · Estelle Colin, Evelyne Huynh Cong, et al. · The American Journal of Human Genetics · 142

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Resveratrol Induces a Mitochondrial Complex I-dependent Increase in NADH Oxidation Responsible for Sirtuin Activation in Liver Cells

2013 · Valérie Desquiret-Dumas, Naïg Gueguen, et al. · Journal of Biological Chemistry · 141

Hereditary optic neuropathies share a common mitochondrial coupling defect

2008 · Arnaud Chevrollier, Virginie Guillet, et al. · Annals of Neurology · 133

Methyl donor deficiency induces cardiomyopathy through altered methylation/acetylation of PGC‐1α by PRMT1 and SIRT1

2011 · Maira Moreno Garcia, Rosa‐Maria Guéant‐Rodriguez, et al. · The Journal of Pathology · 127

The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse

2012 · Emmanuelle Sarzi, Claire Angebault, et al. · Brain · 121

Methyl donor deficiency impairs fatty acid oxidation through PGC-1α hypomethylation and decreased ER-α, ERR-α, and HNF-4α in the rat liver

2012 · Shabnam Pooya, Sébastien Blaise, et al. · Journal of Hepatology · 119

Mitochondrial dysfunction and pathophysiology of Charcot–Marie–Tooth disease involving GDAP1 mutations

2010 · Julien Cassereau, Arnaud Chevrollier, et al. · Experimental Neurology · 101

A Mitochondria-Specific Isoform of FASTK Is Present In Mitochondrial RNA Granules and Regulates Gene Expression and Function

2015 · Alexis A. Jourdain, Mirko Koppen, et al. · Cell Reports · 100

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Resveratrol Directly Binds to Mitochondrial Complex I and Increases Oxidative Stress in Brain Mitochondria of Aged Mice

2015 · Naïg Gueguen, Valérie Desquiret-Dumas, et al. · PLoS ONE · 93

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Early-onset Behr syndrome due to compound heterozygous mutations in OPA1

2014 · Dominique Bonneau, Estelle Colin, et al. · Brain · 91

AK2 deficiency compromises the mitochondrial energy metabolism required for differentiation of human neutrophil and lymphoid lineages

2015 · E Six, C Lagresle-Peyrou, et al. · Cell Death and Disease · 86

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Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)

2008 · Julien Cassereau, Arnaud Chevrollier, et al. · Neurogenetics · 86

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies

2015 · Claire Angebault, Pierre-Olivier Guichet, et al. · The American Journal of Human Genetics · 76

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Acute intermittent porphyria causes hepatic mitochondrial energetic failure in a mouse model

2014 · Chadi Homedan, Jihane Laafi, et al. · The International Journal of Biochemistry & Cell Biology · 71

The addition of ketone bodies alleviates mitochondrial dysfunction by restoring complex I assembly in a MELAS cellular model

2016 · Samuel Frey, Guillaume Geffroy, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 68

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2010 · Delphine Mirebeau‐Prunier, Soazig Le Pennec, et al. · FEBS Journal · 68

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Comparison of Spheroids Formed by Rat Glioma Stem Cells and Neural Stem Cells Reveals Differences in Glucose Metabolism and Promising Therapeutic Applications

2012 · Marie Morfouace, Lisenn Lalier, et al. · Journal of Biological Chemistry · 67

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Overexpression of the Mitochondrial T3 Receptor p43 Induces a Shift in Skeletal Muscle Fiber Types

2008 · François Casas, Laurence Pessemesse, et al. · PLoS ONE · 65

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Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity

2009 · Virginie Guillet, Arnaud Chevrollier, et al. · Mitochondrion · 61

Phenotypic spectrum of MFN2 mutations in the Spanish population

2009 · C Casasnovas, I Banchs, et al. · Journal of Medical Genetics · 61

Multiple Sclerosis–like Disorder in Opa1-related Autosomal Dominant Optic Atrophy

2008 · C. Verny, D. Loiseau, et al. · Neurology · 61

2015 · Juan Manuel Chao de la Barca, Delphine Prunier-Mirebeau, et al. · Neurobiology of Disease · 59

Works count: 123

Citation count: 4,377

H-index: 42

I10-index: 81