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Guilhem Solé

Affiliation : Université de Bordeaux · Centre Hospitalier Universitaire de Bordeaux · Hôpital Pellegrin

• 6Publications (affiliation in France)
• 248Total publications
• 4513Citations
• 32h-index

ORCIDOpenAlex

Research profile

Guilhem Solé has 6 indexed publications (2011–2026). Their work appears mainly in “Journal of the Neurological Sciences”, “medRxiv” and “Proceedings of the National Academy of Sciences”. Their most cited article, “REEP1 mutations in SPG31: Frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunction” (2011), has been cited 94 times. 2 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in United States, Tunisia.

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Research areas

• Muscle Physiology and Disorders
• Hereditary Neurological Disorders
• Peripheral Neuropathies and Disorders
• Genomics and Rare Diseases
• Neurogenetic and Muscular Disorders Research

Publications (6)

• High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies
  2026 · medRxiv
• High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies
  2026 · Proceedings of the National Academy of Sciences
• A multicenter retrospective study of charcot‐marie‐tooth disease type 4B (CMT4B) associated with mutations in myotubularin‐related proteins (MTMRs)
  2019 · Annals of Neurology · cited 41 times
• Some new proposals for the classification of inherited myopathies
  2018 · Journal of the Neurological Sciences · cited 2 times
• History and current difficulties in classifying inherited myopathies and muscular dystrophies
  2017 · Journal of the Neurological Sciences · cited 22 times
• REEP1 mutations in SPG31: Frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunction
  2011 · Human Mutation · cited 94 times

Publication venues

• Journal of the Neurological Sciences × 2
• medRxiv × 1
• Proceedings of the National Academy of Sciences × 1
• Annals of Neurology × 1
• Human Mutation × 1

Publications per year

• 20262
• 20191
• 20181
• 20171
• 20111

Collaborations

Partner institutions : Inserm · Hôpital Necker-Enfants Malades · Institut des Maladies Génétiques Imagine · Assistance Publique – Hôpitaux de Paris · Pitié-Salpêtrière Hospital

Co-authors’ countries : United States · Tunisia

Co-authors

• Cyril Goizet
• Emilie Rocher
• Marie‐Céline Fleury
• Rocío N. Villar‐Quiles
• Laurent Abel
• Nicolas Girard
• Stéphane Mathis
• Karolina Hankiewicz
• Shahram Attarian
• Fanny Duval
• Thierry Jo Molina
• Cyril Gitiaux

Bibliographic data from OpenAlex (open database).