Eléonore Viora-Dupont
5PUBLICATIONS
51CO-AUTHORS
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Publications (5)
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|Jul 23, 2025
The Arrival of Exome Sequencing in French Prenatal Diagnosis: An Exploratory Qualitative Study Among Professionals in Prenatal Diagnosis Centers: Prenatome-SHS.Charlène Daval, Nicolas Meunier-Beillard, Eléonore Viora-Dupont
|May 27, 2024
Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study).Eléonore Viora-Dupont, Françoise Robert, Aline Chassagne
|Sep 12, 2023
Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndrome.E Viora-Dupont, A Denommé-Pichon, M Chevarin
|Feb 06, 2023
The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant.Mio Aerden, Anne-Sophie Denommé-Pichon, Dominique Bonneau
|Feb 10, 2022
Copy number variants calling from WES data through eXome hidden Markov model (XHMM) identifies additional 2.5% pathogenic genomic imbalances smaller than 30 kb undetected by array-CGH.Emilie Tisserant, Antonio Vitobello, Davide Callegarin
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Frequent Collaborators
4 joint publications
Anne-Sophie Denommé-Pichon
4 joint publications
Laurence Faivre
4 joint publications
Antonio Vitobello
4 joint publications
Frédéric Tran-Mau-Them
4 joint publications
Ange-Line Bruel
4 joint publications
Christophe Philippe
3 joint publications
Christel Thauvin-Robinet
2 joint publications
Julian Delanne
2 joint publications
Sophie Nambot
2 joint publications
Sébastien Moutton
