- Unequal Impact of COL1A1 and COL1A2 Variants on Dentinogenesis Imperfecta . J Dent Res. 2023 Mar 23. doi: 10.1177/00220345231154569. PMID: 36951356
- The dental triage method at Rothschild Hospital during the first lockdown due to the COVID-19 pandemic. PLoS One. 2023 Feb. doi: 10.1371/journal.pone.0281390.
- Oral Phenotype of Singleton-Merten Syndrome: A Systematic Review Illustrated With a Case Report. Front Genet. 2022. PMID: 35754802
- International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia. Nat Rev Endocrinol. 2022 Mar. PMID: 34837063
- Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti. JEADV 2020, doi: 10.1111/jdv.16403.
- Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders. Am J Med Genet A. 2019. doi: 10.1002/ajmg.a.61316
- Oral health related quality of life of children and adolescents affected by rare orofacial diseases: a questionnaire-based cohort study. MD. Orphanet J Rare Dis. 2019. PMID: 31164137
- Management of rare diseases of the Head, Neck and Teeth: results of a French population-based prospective 8-year study. Orphanet J Rare Dis. 2017. PMID: 28526043
- Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations. J Med Genet 2017. PMID: 27530400