Giulia Valvo

Fondazione Stella Maris — Italy

Biochemistry, Genetics and Molecular Biology · Life Sciences

11h-index414citations15works0.02yr avg
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Research Topics

Genetics and Neurodevelopmental Disorders(9), Epilepsy research and treatment(4), Autism Spectrum Disorder Research(4), Child and Adolescent Psychosocial and Emotional Development(2), Ion channel regulation and function(2)

Publications15 total

Customized multigene panels in epilepsy: the best things come in small packages
Neurogenetics·2019· 10 cited
Electrophysiological features of sleep in children with Kir4.1 channel mutations and Autism–Epilepsy phenotype: a preliminary study
SLEEP·2019· 11 citedOpen Access
Clinical and electroencephalographic correlates of psychiatric features in children with frontal lobe epilepsy
Epilepsy & Behavior·2019· 7 cited
Internalizing and externalizing symptoms in preschool and school-aged children with epilepsy: Focus on clinical and EEG features
Epilepsy & Behavior·2017· 23 cited
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy
Scientific Reports·2016· 71 citedOpen Access
The Revolution in Migraine Genetics: From Aching Channels Disorders to a Next-Generation Medicine
Frontiers in Cellular Neuroscience·2016· 25 citedOpen Access
Focal cortical dysplasia, microcephaly and epilepsy in a boy with 1q21.1-q21.3 duplication
European Journal of Medical Genetics·2016· 11 cited
Targeted Gene Resequencing (Astrochip) to Explore the Tripartite Synapse in Autism–Epilepsy Phenotype with Macrocephaly
NeuroMolecular Medicine·2015· 24 cited
Temporal lobe connects regression and macrocephaly to autism spectrum disorders
European Child & Adolescent Psychiatry·2015· 28 citedOpen Access
Late-Onset Epileptic Spasms
Journal of Child Neurology·2014· 18 cited
Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism–epilepsy phenotype
Human Molecular Genetics·2014· 83 citedOpen Access
Autism-epilepsy phenotype with macrocephaly suggests PTEN, but not GLIALCAM, genetic screening
BMC Medical Genetics·2014· 61 citedOpen Access
Somatic Overgrowth Predisposes to Seizures in Autism Spectrum Disorders
PLoS ONE·2013· 22 citedOpen Access
22q11.2 Microduplication syndrome and epilepsy with continuous spikes and waves during sleep (CSWS). A case report and review of the literature
Epilepsy & Behavior·2012· 20 cited
I disturbi depressivi nell'età prescolare
CNR Solar (Scientific Open-access Literature Archive and Repository) (Consiglio Nazionale delle Ricerche)·2008

Frequent Co-authors

Federico Sicca(14), Filippo M. Santorelli(8), Anna Rita Ferrari(6), Francesca Moro(5), Renzo Guerrini(5), Maria Marchese(4), Simona Pellacani(4), Sara Baldini(3), Filippo Muratori(3), Raffaella Tancredi(3), Elena Ambrosini(2), Maria Stefania Brignone(2), Maria Cristina D’Adamo(2), Ilenio Servettini(2), Angela Lanciotti(2), Luigi Catacuzzeno(2), Fabio Franciolini(2), Paola Molinari(2), Alessandro Grottesi(2), Mauro Pessia(2)