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Benjamin Cogné

Affiliation : Centre National de la Recherche Scientifique · Inserm · Centre Hospitalier Universitaire de Nantes · Institut du Thorax · Nantes Université

• 1Publications (affiliation in France)
• 299Total publications
• 4923Citations
• 42h-index

ORCIDOpenAlex

Research profile

Benjamin Cogné has 1 indexed publication (2025). Their work appears in “Nature Genetics”. Their most cited article, “Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption” (2025), has been cited 57 times. Their work is co-authored with at least 12 researchers.

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Research areas

• Genomics and Rare Diseases
• Genetics and Neurodevelopmental Disorders
• Genomic variations and chromosomal abnormalities
• RNA Research and Splicing
• Fetal and Pediatric Neurological Disorders

Publications (1)

• Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption
  2025 · Nature Genetics · cited 57 times

Collaborations

Partner institutions : Assistance Publique – Hôpitaux de Paris · Sorbonne Université · Pitié-Salpêtrière Hospital · Université de Rouen Normandie · Université Paris Cité

Co-authors

• Amandine Santini
• Victoria Granier
• Samuel Fennelly
• Abhilasha Jakhar
• Fouzia Benkerdou
• Benjamin Ganne
• Martine Doco‐Fenzy
• Hamza Hadj Abdallah
• Alexandra Afenjar
• Marie‐Noëlle Bonnet‐Dupeyron
• Odile Boute
• Yannis Duffourd

Bibliographic data from OpenAlex (open database).