Isabelle Bailleul‐Forestier

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

Sebastian Köhler, Sandra C. Doelken, Chris Mungall et al. · Nucleic Acids Research · 2013 · 837 citations · Full text

Medicine, Biomedical Informatics, Pathology +14

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 · 135 citations · Full text

Dentistry, Oral Biology, Dentin Biology +10

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

Graciana Jaureguiberry, Muriel de La Dure‐Molla, David Parry et al. · Nephron Physiology · 2013 · 103 citations · Full text

Medicine, Genetics, Nephrology +16

Caries experience in a severely obese adolescent population

Isabelle Bailleul‐Forestier, Karine Lopes, M. Souames et al. · International Journal of Paediatric Dentistry · 2007 · 91 citations

Dentistry, Pediatric Dentistry, Preventive Dentistry +17

Mutations in <i>WNT10A</i> are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

Julie Plaisancié, Isabelle Bailleul‐Forestier, Véronique Gaston et al. · American Journal of Medical Genetics Part A · 2013 · 58 citations

Medicine, Genetics, Molecular Genetics +17