Home › Researcher directory › Cyril Gitiaux

Cyril Gitiaux

Affiliation : Hôpital Necker-Enfants Malades · Université Paris Cité · Assistance Publique – Hôpitaux de Paris

• 5Publications (affiliation in France)
• 219Total publications
• 3855Citations
• 31h-index

ORCIDOpenAlex

Research profile

Cyril Gitiaux has 5 indexed publications (2017–2026). Their work appears mainly in “medRxiv”, “Proceedings of the National Academy of Sciences” and “Frontiers in Pediatrics”. Their most cited article, “Autosomal recessive primary microcephaly due to ASPM mutations: An update” (2017), has been cited 71 times. 3 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, United Kingdom, Colombia.

Is this you? Get your research seen

Create your free DzCademia profile and add your articles: they will show up more easily on Google and in AI assistants like ChatGPT, so more people can read and cite your work.

Create my free profile Add my publications

Research areas

• Inflammatory Myopathies and Dermatomyositis
• Muscle Physiology and Disorders
• Systemic Sclerosis and Related Diseases
• Myasthenia Gravis and Thymoma
• Peripheral Neuropathies and Disorders

Publications (5)

• 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
• Case Report: Pediatric immune-mediated necrotizing myopathies mimicking inherited muscle disorders: clinical, paraclinical, and genetic insights from two cases
  2026 · Frontiers in Pediatrics
• Deciphering the natural history of SCA7 in children
  2020 · European Journal of Neurology · cited 20 times
• Autosomal recessive primary microcephaly due to ASPM mutations: An update
  2017 · Human Mutation · cited 71 times

Publication venues

• medRxiv × 1
• Proceedings of the National Academy of Sciences × 1
• Frontiers in Pediatrics × 1
• European Journal of Neurology × 1
• Human Mutation × 1

Publications per year

• 20263
• 20201
• 20171

Collaborations

Partner institutions : Inserm · Institut des Maladies Génétiques Imagine · Sorbonne Université · ERN EURO-NMD · Human Genetic of Infectious Diseases

Co-authors’ countries : United States · United Kingdom · Colombia

Co-authors

• Emilie Rocher
• Marie‐Céline Fleury
• Rocío N. Villar‐Quiles
• Laurent Abel
• Nicolas Girard
• Karolina Hankiewicz
• Shahram Attarian
• Thierry Jo Molina
• Florent Wallet
• Vivien Béziat
• Kahina Saker
• Alexis Maillard

Bibliographic data from OpenAlex (open database).