Élise Lebigot
5PUBLICATIONS
47CO-AUTHORS
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Publications (5)
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|Feb 08, 2025
Mitochondrial DNA or Genomic DNA Variant(s): Utility of Exhaustive Sequencing in Leigh Syndrome.Pauline Gaignard, Pierre-Hadrien Becker, Anne-Frederique Dessein
|Jan 02, 2025
E4F1 coordinates pyruvate metabolism and the activity of the elongator complex to ensure translation fidelity during brain development.Michela Di Michele, Aurore Attina, Pierre-François Roux
|Sep 28, 2023
Author Correction: CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder.Aurélie de Thonel, Johanna K Ahlskog, Kevin Daupin
|Nov 17, 2022
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder.Aurélie de Thonel, Johanna K Ahlskog, Kevin Daupin
|Feb 01, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.Holger Hengel, Célia Bosso-Lefèvre, George Grady
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Frequent Collaborators
2 joint publications
Anna L Aalto
2 joint publications
Michel Petitjean
2 joint publications
Federico Miozzo
2 joint publications
Matthieu Sanial
2 joint publications
Laurent David
2 joint publications
Carole Chaput
2 joint publications
Pierre Gressens
2 joint publications
Anniina Vihervaara
2 joint publications
Kevin Daupin
2 joint publications
Aurélie de Thonel
