Corinne Collet (C Collet)

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 6

Top Topics

Autism Spectrum Disorder

Transforming Growth Factor

Staphylococcus Aureus

Top Venues

Molecular genetics & genomic medicine

European journal of human genetics : EJHG

BMC medical genetics

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Federico Di Rocco, Massimiliano Rossi, Isabelle Verlut, Alexandru Szathmari, Pierre Aurélien Beuriat, Nicolas Chatron, Julie Chauvel-Picard, Carmine Mottolese, Pauline Monin, Matthieu Vinchon, Sofia Guernouche, Corinne Collet
Clinical interest of molecular study in cases of isolated midline craniosynostosis. European journal of human genetics : EJHG (2023)
Federico Di Rocco, Massimiliano Rossi, Isabelle Verlut, Alexandru Szathmari, Pierre Aurélien Beuriat, Nicolas Chatron, Julie Chauvel-Picard, Carmine Mottolese, Pauline Monin, Matthieu Vinchon, Sofia Guernouche, Corinne Collet
Clinical interest of molecular study in cases of isolated midline craniosynostosis. European journal of human genetics : EJHG (2023)
Caroline Caetano Silva, Manon Ricquebourg, Philippe Orcel, Stéphanie Fabre, Thomas Funck-Brentano, Martine Cohen-Solal, Corinne Collet
More severe phenotype of early-onset osteoporosis associated with recessive form of LRP5 and combination with DKK1 or WNT3A. Molecular genetics & genomic medicine 9 (6) (2021)
France Woimant, Aurelia Poujois, Adrien Bloch, Tabaras Jordi, Jean-Louis Laplanche, Hélène Morel, Corinne Collet
A novel deep intronic variant in ATP7B in five unrelated families affected by Wilson disease. Molecular genetics & genomic medicine 8 (10) (2020)
Elise Brischoux-Boucher, Aurélien Trimouille, Genevieve Baujat, Alice Goldenberg, E Schaefer, B Guichard, P Hannequin, G Paternoster, Sarah Baer, C Cabrol, E Weber, G Godfrin, Marion Lenoir, Didier Lacombe, Corinne Collet, Lionel Van Maldergem
IL11RA-related Crouzon-like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differences. Clinical genetics 94 (3-4) (2018)
Corinne Collet, Jean-Louis Laplanche, Justine Page, Hélène Morel, France Woimant, Aurélia Poujois
High genetic carrier frequency of Wilson's disease in France: discrepancies with clinical prevalence. BMC medical genetics 19 (1) (2018)