Laura Licchetta
Istituto delle Scienze Neurologiche di Bologna(IT)Istituti di Ricovero e Cura a Carattere Scientifico(IT)
Publications by Year
Research Areas
Epilepsy research and treatment, Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Glycogen Storage Diseases and Myoclonus, Neuroscience and Neuropharmacology Research
Most-Cited Works
- → Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy(2012)408 cited
- → Mutations in DEPDC5 cause familial focal epilepsy with variable foci(2013)359 cited
- → A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy(2014)313 cited
- → Definition and diagnostic criteria of sleep-related hypermotor epilepsy(2016)293 cited
- → The landscape of epilepsy-related GATOR1 variants(2018)237 cited
- → Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy(2015)232 cited
- → Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations