Valérie Benoit
5PUBLICATIONS
96CO-AUTHORS
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Publications (5)
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|May 23, 2025
Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic loci.Mathis Hildonen, Andrea Ciolfi, Marco Ferilli
|Jan 04, 2023
Clinical and Neurophysiologic Phenotypes in Neonates With <i>BRAT1</i> Encephalopathy.Evelina Carapancea, Marie-Coralie Cornet, Mathieu Milh
|May 26, 2022
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder.Maria B Christensen, Amanda M Levy, Nazanin A Mohammadi
|Jul 13, 2021
Frequency of Participation in External Quality Assessment Programs Focused on Rare Diseases: Belgian Guidelines for Human Genetics Centers.Joséphine Lantoine, Anne Brysse, Vinciane Dideberg
|May 04, 2021
Broadening the phenotypic spectrum and physiological insights related to EIF2S3 variants.Stephanie Moortgat, Isabelle Manfroid, Hélène Pendeville
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Frequent Collaborators
2 joint publications
Marco Tartaglia
2 joint publications
Zeynep Tümer
2 joint publications
Kristof Van Schil
2 joint publications
Reza Maroofian
2 joint publications
Paulino Gomez-Puertas
2 joint publications
Matthias De Wachter
2 joint publications
Bert Callewaert
1 joint publications
Isabelle Manfroid
1 joint publications
Laurence Faivre
1 joint publications
Isabelle Maystadt
