François Clauss

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

A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement

Megana Prasad, Véronique Geoffroy, Serge Vicaire et al. · Journal of Medical Genetics · 2015 · 134 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

Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations

Graciana Jaureguiberry, Muriel de La Dure‐Molla, David Parry et al. · Nephron Physiology · 2013 · 102 citations · Full text

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

Muriel de La Dure‐Molla, Benjamin Fournier, María Cristina Manzanares‐Céspedes et al. · American Journal of Medical Genetics Part A · 2019 · 79 citations · Full text

Genetics, Genetic Epidemiology, Diagnosis +19