Lieve Claes
Publications by Year
Research Areas
Epilepsy research and treatment, Ion channel regulation and function, Neuroscience and Neuropharmacology Research, Ion Transport and Channel Regulation, Genomics and Rare Diseases
Most-Cited Works
- → De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy(2001)1,257 cited
- → KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy(2011)503 cited
- → Early‐onset absence epilepsy caused by mutations in the glucose transporter GLUT1(2009)296 cited
- → novoSNP, a novel computational tool for sequence variation discovery(2005)288 cited
- → A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome(2009)263 cited
- → A Functional Null Mutation ofSCN1Bin a Patient with Dravet Syndrome(2009)249 cited
- → De novoSCN1Amutations are a major cause of severe myoclonic epilepsy of infancy(2003)202 cited
- → Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy(2010)184 cited
- → Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy(2004)131 cited
- → TheSCN1Avariant database: a novel research and diagnostic tool(2009)127 cited