Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomaliesErsilia Barbato, Viviana Caputo, Andrea Ciolfi et al.|Archives of Oral Biology|2018Cited by 19
GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlationsMaria Luce Genovesi, Viviana Caputo, Agnese Giovannetti et al.|Bone|2020Cited by 14
Small RNAs and tooth development: The role of microRNAs in tooth agenesis and impactionAgnese Giovannetti, Viviana Caputo, Rosanna Guarnieri et al.|Journal of Dental Sciences|2024Cited by 9
Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological CiliogenesisGiulia Di Napoli, Viviana Caputo, Noemi Panzironi et al.|Molecular Neurobiology|2022Cited by 9
Prenatal whole exome sequencing detects a new homozygous fukutin <i>(FKTN)</i> mutation in a fetus with an ultrasound suspicion of familial Dandy–Walker malformationAlice Traversa, Antonio Pizzuti, Silvia Bernardo et al.|Molecular Genetics & Genomic Medicine|2019Cited by 6