Xenia Iona
Publications by Year
Research Areas
Epilepsy research and treatment, Genomics and Rare Diseases, Genetics and Neurodevelopmental Disorders, Ion channel regulation and function, Neuroscience and Neuropharmacology Research
Most-Cited Works
- → The spectrum of SCN1A-related infantile epileptic encephalopathies(2007)527 cited
- → Mutations in DEPDC5 cause familial focal epilepsy with variable foci(2013)359 cited
- → De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study(2006)293 cited
- → PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome(2012)258 cited
- → A variant of KCC 2 from patients with febrile seizures impairs neuronal Cl − extrusion and dendritic spine formation(2014)188 cited
- → SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis(2009)170 cited
- → Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study(2010)140 cited
- → Timing of De Novo Mutagenesis — A Twin Study of Sodium-Channel Mutations(2010)104 cited
- → A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A(2006)100 cited
- → PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures(2012)83 cited