Arianna Vino

A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development

Else Eising, Amaia Carrión-Castillo, Arianna Vino et al. · Molecular Psychiatry · 2018 · 175 citations · Full text

Brain Development, Genetics, Genetic Epidemiology +25

Identification and functional characterization of<i>de novo FOXP1</i>variants provides novel insights into the etiology of neurodevelopmental disorder

Elliot Sollis, Sarah A. Graham, Arianna Vino et al. · Human Molecular Genetics · 2015 · 91 citations · Full text

Neurogenomics, Brain Development, Genetics +20

Rare variants in axonogenesis genes connect three families with sound–color synesthesia

Amanda K. Tilot, Katerina S. Kucera, Arianna Vino et al. · Proceedings of the National Academy of Sciences · 2018 · 65 citations · Full text

Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders

Sara B. Estruch, Sarah A. Graham, Martí Quevedo et al. · Human Molecular Genetics · 2018 · 64 citations · Full text

A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment

Reymundo Lozano, Arianna Vino, Cristina Lozano et al. · European Journal of Human Genetics · 2015 · 51 citations · Full text

Neurodevelopmental Disorders, Foxp1 Variant, Mendelian Disorder +11