Manuela Fadda

SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function

Anna Fassio, Lysanne Patry, Sonia Congia et al. · Human Molecular Genetics · 2011 · 236 citations · Full text

Life Sciences, Genetics, Neuroscience +17

PRRT2 Is a Key Component of the Ca2+-Dependent Neurotransmitter Release Machinery

Pierluigi Valente, Enrico Castroflorio, Pia Rossi et al. · Cell Reports · 2016 · 152 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity

Floriana Fruscione, Pierluigi Valente, Bruno Sterlini et al. · Brain · 2018 · 137 citations · Full text

Life Sciences, Genetics, Neuroscience +16

TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathway

Antonio Falace, Emmanuelle Buhler, Manuela Fadda et al. · Proceedings of the National Academy of Sciences · 2014 · 96 citations · Full text

Life Sciences, Developmental Biology, Neuroscience +16

SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth

Anna Corradi, Manuela Fadda, Amélie Piton et al. · Human Molecular Genetics · 2013 · 89 citations · Full text

Life Sciences, Genetics, Neuroscience +17