Laurent Villard
20PUBLICATIONS
85CO-AUTHORS
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Publications (20)
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|Aug 08, 2025
The Clinical and Genetic Landscape of a French Multicenter Cohort of 2563 Epilepsy Patients Referred for Genetic Diagnosis.Jean-Madeleine de Sainte Agathe, Pauline Monin, Florence Riccardi
|Jul 09, 2025
Long-term treatment with carbamazepine restores cognitive abilities in a mouse model of KCNQ2 developmental and epileptic encephalopathy.Jordane Louis, Natalia Doudka, Marie-Solenne Félix
|Dec 21, 2023
Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability.Elham Khosrowabadi, Cécile Mignon-Ravix, Florence Riccardi
|Jun 21, 2023
BRAT1-related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients.Camille Engel, Stéphanie Valence, Geoffroy Delplancq
|Apr 04, 2023
NAPB and developmental and epileptic encephalopathy: Description of the electroclinical profile associated with a novel pathogenic variant.Cécile Mignon-Ravix, Florence Riccardi, Géraldine Daquin
|Nov 03, 2022
Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X.Elsa Leitão, Christopher Schröder, Ilaria Parenti
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Frequent Collaborators
4 joint publications
Mathieu Milh
4 joint publications
Gaetan Lesca
3 joint publications
Florence Molinari
2 joint publications
Emilie Borloz
2 joint publications
Pasquale Striano
2 joint publications
Dorothée Ville
2 joint publications
Jozef Gecz
2 joint publications
Juliette Piard
2 joint publications
Elise Brischoux-Boucher
2 joint publications
Jean-Christophe Roux
