| 2020 |
Cottard M, Vignot E, Fontanges E, Merle B, Collet C, Chapurlat R. Genetic testing is useful in adults with limited phenotypes of genetic skeletal conditions. Bone. May 2020;134:115218. |
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| 2020 |
Morice A, Cornette R, Giudice A, Collet C, Paternoster G, Arnaud É, Galliani E, Picard A, Legeai-Mallet L, Khonsari R. Early mandibular morphological differences in patients with FGFR2 and FGFR3-related syndromic craniosynostoses: a 3D comparative study. Bone. December 2020;141:115600. |
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| 2021 |
Pickering M-E, Ltaief-Boudrigua A, Feurer E, Collet C, Chapurlat R. A new lrp6 variant and camurati-engelmann-like disease. Bone. February 2021;143:115706. |
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| 2023 |
Hendrickx G, Boudin E, Steenackers E, Collet C, Mortier GR, Geneviève D, Van Hul W. A recessive form of craniodiaphyseal dysplasia caused by a homozygous missense variant in SP7/Osterix. Bone. February 2023;167:116633. |
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| 2023 |
Cohen-Solal M, Collet C, Bizot P, Pavis C, Funck-Brentano T. Osteopetrosis: the patient point of view and medical challenges. Bone. February 2023;167:116635. |
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