Marie‐Cécile Manière

Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases

Céline Cluzeau, S. Hadj‐Rabia, Marguerite Jambou et al. · Human Mutation · 2010 · 316 citations

Medicine, Genetics, Molecular Genetics +15

Orodental phenotype and genotype findings in all subtypes of hypophosphatasia

Amélie Reibel, Marie‐Cécile Manière, François Clauss et al. · Orphanet Journal of Rare Diseases · 2009 · 121 citations · Full text

Dentistry, Oral Biology, Oral Pathology +14

Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop’s classification

Agnès Bloch‐Zupan, Tristan Rey, Alexandra Jimenez-Armijo et al. · Frontiers in Physiology · 2023 · 59 citations · Full text

Dentistry, Oral Biology, Oral Pathology +17

Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta

Mathilde Huckert, Corinne Stoetzel, Supawich Morkmued et al. · Human Molecular Genetics · 2015 · 49 citations · Full text

Dentistry, Craniofacial Biology, Oral Biology +17

Amelogenesis imperfecta: therapeutic strategy from primary to permanent dentition across case reports

Steve Toupenay, Benjamin Fournier, Marie‐Cécile Manière et al. · BMC Oral Health · 2018 · 46 citations · Full text

Dentistry, Pediatric Dentistry, Dentoalveolar Surgery +13