Corinne Collet
9PUBLICATIONS
56CO-AUTHORS
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Publications (9)
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|Apr 09, 2026
Identification of an episignature for CHD3-related Snijders Blok-Campeau syndrome reveals heterogeneity in the CHARGE syndrome episignature: towards a better characterisation of chromatinopathies.Amandine Santini, Angelo Tognon, Anne-Claire Richard
|Nov 08, 2024
Genetics and Bone Mineral Density Predict the Fractures in Adults With Osteogenesis Imperfecta: A Prospective Study.Camille Blandin, Corinne Collet, Agnes Ostertag
|Sep 24, 2024
Early-Onset Osteoporosis: Molecular Analysis in Large Cohort and Focus on the PLS3 Gene.Maxence Mancini, Roland Chapurlat, Bertrand Isidor
|Feb 02, 2023
Clinical interest of molecular study in cases of isolated midline craniosynostosis.Federico Di Rocco, Massimiliano Rossi, Isabelle Verlut
|May 03, 2021
More severe phenotype of early-onset osteoporosis associated with recessive form of LRP5 and combination with DKK1 or WNT3A.Caroline Caetano da Silva, Manon Ricquebourg, Philippe Orcel
|Aug 10, 2020
A novel deep intronic variant in ATP7B in five unrelated families affected by Wilson disease.France Woimant, Aurelia Poujois, Adrien Bloch
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Frequent Collaborators
2 joint publications
Alice Goldenberg
2 joint publications
Martine Cohen-Solal
2 joint publications
Thomas Funck-Brentano
2 joint publications
Nicolas Chatron
1 joint publications
E Brischoux-Boucher
1 joint publications
A Trimouille
1 joint publications
G Baujat
1 joint publications
S Baer
1 joint publications
E Weber
1 joint publications
Maud de Dieuleveult
