Giulia Gentile

Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway

Anna Rita Fetoni, Veronica Zorzi, Fabiola Paciello et al. · Redox Biology · 2018 · 76 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features

Piero Pavone, Andrea D. Praticò, Giulia Gentile et al. · European Journal of Medical Genetics · 2016 · 36 citations

Medicine, Dermatology, Neuroscience +15

Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without ‘hairy elbows’: expanding the phenotype of Wiedemann–Steiner syndrome

Dora Steel, Vincenzo Salpietro, Rahul Phadke et al. · Journal of Genetics · 2015 · 33 citations

Life Sciences, Genetics, Molecular Genetics +13

Splicing Players Are Differently Expressed in Sporadic Amyotrophic Lateral Sclerosis Molecular Clusters and Brain Regions

Valentina La Cognata, Giulia Gentile, Eleonora Aronica et al. · Cells · 2020 · 33 citations · Full text

Life Sciences, Molecular Biology, Neuroscience +17

A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson’s disease

Valentina La Cognata, Giovanna Morello, Giulia Gentile et al. · Neurogenetics · 2016 · 11 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17