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Nicolas Chatron

Affiliation : Lyon 1 Université · Centre National de la Recherche Scientifique · Inserm · Hospices Civils de Lyon · Institut NeuroMyoGène · Laboratoire Physiopathologie et Génétique du Neurone et du Muscle

• 5Publications (affiliation in France)
• 207Total publications
• 2557Citations
• 28h-index

ORCIDOpenAlex

Research profile

Nicolas Chatron has 5 indexed publications (2015–2025). Their work appears mainly in “Clinical Genetics”, “Journal of Thrombosis and Haemostasis” and “Genetics in Medicine”. Their most cited article, “Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverag” (2015), has been cited 32 times. 4 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in Tunisia, Algeria.

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Research areas

• Genomics and Rare Diseases
• Genetics and Neurodevelopmental Disorders
• Genomic variations and chromosomal abnormalities
• Epilepsy research and treatment
• Genome Rearrangement Algorithms

Publications (5)

• Transcript Long‐Read Sequencing Unveils the Molecular Complexity of a Novel ROGDI Splicing Variant in a Tunisian Family With Kohlschütter‐Tönz Syndrome
  2025 · Clinical Genetics · cited 3 times
• Whole F8 gene sequencing identified pathogenic structural variants in the remaining unsolved patients with severe hemophilia A
  2024 · Journal of Thrombosis and Haemostasis · cited 8 times
• Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders
  2024 · Genetics in Medicine · cited 5 times
• Clinical and molecular cytogenetic studies of five new patients with 20q11q12 deletion and review of the literature: Proposition of two critical regions
  2024 · American Journal of Medical Genetics Part A · cited 3 times
• Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA
  2015 · Applied & Translational Genomics · cited 32 times

Publication venues

• Clinical Genetics × 1
• Journal of Thrombosis and Haemostasis × 1
• Genetics in Medicine × 1
• American Journal of Medical Genetics Part A × 1
• Applied & Translational Genomics × 1

Publications per year

• 20251
• 20243
• 20151

Collaborations

Partner institutions : Centre de Recherche en Neurosciences de Lyon · Laboratoire de Biométrie et Biologie Evolutive · CHU Dijon Bourgogne · Hémostase & Thrombose · École Normale Supérieure de Lyon

Co-authors’ countries : Tunisia · Algeria

Co-authors

• Damien Sanlaville
• Gaëtan Lesca
• Audrey Labalme
• Dorothee M. Ville
• Louis Januel
• Estelle Lafont
• Natalie Stieltjes
• Claire Bardel
• Mad‐Hélénie Elsensohn
• Nadia Boutry‐Kryza
• Souad Bensaid
• Miriam Essid

Bibliographic data from OpenAlex (open database).