Centre National de la Recherche Scientifique
ORCID: 0000-0002-5825-5319Also affiliated with Université de Bordeaux, Inserm, Centre Hospitalier Universitaire de Bordeaux, Institut des Maladies Neurodégénératives, Maladies Rares: Génétique et Métabolisme
Pilot corpus only
This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.
Driven by 2 papers. Top paper: “De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability”.
Margot A. Cousin, Nikita R. Dsouza, Thomas D. Challman, Karen E. Wain, Zöe Powis +67 more
Chloé Angelini, Claire Bar, Wahiba Amer El Khedoud, Christine Barnérias, Razika Boulariah‐Hadjou +15 more