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, Pietro Palumbo et al.|Bone|2020Cited by 14
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
Heterozygous nonsense <i>ARX</i> mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co‐inheritanceAlice Traversa, Viviana Caputo, Katia Margiotti et al.|Molecular Genetics & Genomic Medicine|2020Cited by 4