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Naïg Guéguen

Affiliation : Centre National de la Recherche Scientifique · Inserm · Centre Hospitalier Universitaire d'Angers · Mitochondrial and Cardiovascular Physiopathology · Université d'Angers

• 6Publications (affiliation in France)
• 122Total publications
• 4372Citations
• 42h-index

ORCIDOpenAlex

Research profile

Naïg Guéguen has 6 indexed publications (2015–2026). Their work appears mainly in “Scientific Reports”, “Genes” and “Brain Communications”. Their most cited article, “Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies” (2015), has been cited 75 times. Their work is co-authored with at least 12 researchers, including institutions in Morocco.

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Research areas

• Mitochondrial Function and Pathology
• Metabolism and Genetic Disorders
• Hereditary Neurological Disorders
• Autophagy in Disease and Therapy
• Adipose Tissue and Metabolism

Publications (6)

• Pathophysiological insights into ACO2-related inherited disorders through combined functional and multi-omic analyses of ACO2 patient-derived fibroblasts
  2026 · Scientific Reports
• Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy
  2022 · Genes · cited 5 times
• DominantACO2mutations are a frequent cause of isolated optic atrophy
  2021 · Brain Communications · cited 38 times
• Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy
  2020 · Neurology Genetics · cited 52 times
• Loss of function of Ywhah in mice induces deafness and cochlear outer hair cells' degeneration
  2016 · Cell Death Discovery · cited 16 times
• Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies
  2015 · The American Journal of Human Genetics · cited 75 times

Publication venues

• Scientific Reports × 1
• Genes × 1
• Brain Communications × 1
• Neurology Genetics × 1
• Cell Death Discovery × 1
• The American Journal of Human Genetics × 1

Publications per year

• 20261
• 20221
• 20211
• 20201
• 20161
• 20151

Collaborations

Partner institutions : Mohamed I University · Université de Montpellier · Institute for Neurosciences of Montpellier · Institut des Maladies Génétiques Imagine · Hôpital Gui de Chauliac

Co-authors’ countries : Morocco

Co-authors

• Guy Lenaers
• Patrizia Amati‐Bonneau
• Pascal Reynier
• Dominique Bonneau
• Arnaud Chevrollier
• Majida Charif
• Isabelle Meunier
• Valérie Desquiret‐Dumas
• Céline Bris
• David Goudenège
• Vincent Procaccio
• Xavier Zanlonghi

Bibliographic data from OpenAlex (open database).