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 · 312 citations · Full text

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

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 · 48 citations · Full text

Genetics, Pathology, Gene Cause Brachyolmia +16

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 · 45 citations · Full text

Sedation with 50% nitrous oxide/oxygen for outpatient dental treatment in individuals with intellectual disability

Denise Faulks, Martine Hennèquin, Sylvie Albecker-Grappe et al. · Developmental Medicine & Child Neurology · 2007 · 42 citations · Full text