Clauss, François

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

Cluzeau, C., Hadj-Rabia, S., Jambou, M., Mansour, S., Guigue, P., Masmoudi, S., Bal, E., Chassaing, N., Vincent, M.-C., Viot, G., et al. (2011) · Human Mutation

dental development and anomaliesGenetic and rare skin diseases.

Cited by 311

Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders

de La Dure‐Molla, M., Fournier, B. P., Manzanares, M. C., Acevedo, A. C., Hennekam, R. C., Friedlander, L., Boy‐Lefèvre, M., Kerner, S., Toupenay, S., Garrec, P., et al. (2019) · American Journal of Medical Genetics Part A

dental development and anomaliesCleft Lip and Palate Research

Cited by 85

Cytokines during periodontal wound healing: potential application for new therapeutic approach

Morand, D., Davideau, J., Clauss, F., Jessel, N., Tenenbaum, H., & Huck, O. (2017) · Oral Diseases

Periodontal Regeneration and TreatmentsOral microbiology and periodontitis research

Cited by 80

Deficiency of the SMOC2 matricellular protein impairs bone healing and produces age-dependent bone loss

Morkmued, S., Clauss, F., Schuhbaur, B., Fraulob, V., Mathieu, E., Hemmerlé, J., Clevers, H., Koo, B.-K., Dollé, P., Bloch-Zupan, A., et al. (2020) · Scientific Reports

Bone and Dental Protein Studiesdental development and anomalies

Cited by 25