Nicolas Chassaing
8PUBLICATIONS
30CO-AUTHORS
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Publications (8)
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|Jan 22, 2026
Expanding the Phenotypic Spectrum Associated With Loss-of-Function SMARCA4 Variants to Eye Developmental Anomalies.Bertrand Chesneau, Marjolaine Willems, Abdelhakim Bouazzaoui
|Oct 25, 2024
Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development.Fabiola Ceroni, Munevver B Cicekdal, Richard Holt
|Feb 28, 2024
A founder variant expands the phenotype of WNT7B-related PDAC syndrome.Lama AlAbdi, Zuhair Rahbeeni, Sateesh Maddirevula
|Aug 16, 2023
Clinical, genetic and biochemical signatures of RBP4-related ocular malformations.Julie Plaisancié, Jelena Martinovic, Bertrand Chesneau
|Aug 14, 2023
Low risk of embryonic and other cancers in PIK3CA-related overgrowth spectrum: Impact on screening recommendations.Laurence Faivre, Jean-Charles Crépin, Manon Réda
|Jul 05, 2022
Bi-allelic variants in WNT7B disrupt the development of multiple organs in humans.Samir Bouasker, Nisha Patel, Rebecca Greenlees
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Frequent Collaborators
3 joint publications
Marjolaine Willems
3 joint publications
Bertrand Chesneau
2 joint publications
Florence Petit
2 joint publications
Clémence Vanlerberghe
2 joint publications
Salima El Chehadeh
2 joint publications
Fowzan S Alkuraya
1 joint publications
Aurore Garde
1 joint publications
Olivia Boccara
1 joint publications
Arthur Sorlin
1 joint publications
Marion Aubert-Mucca
