Biallelic <i>SQSTM1</i> mutations in early-onset, variably progressive neurodegenerationValentina Muto, Marco Tartaglia, Elisabetta Flex et al.|Neurology|2018Cited by 52
Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomaliesErsilia Barbato, Viviana Caputo, Alice Traversa 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, Pietro Palumbo et al.|Bone|2020Cited by 14
Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological CiliogenesisGiulia Di Napoli, Viviana Caputo, Noemi Panzironi et al.|Molecular Neurobiology|2022Cited by 9
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