Rikke S. Møller
University of Southern Denmark(DK)Epilepsy Action(GB)Centre For Irish and European Security(IE)Epilepsy Foundation(AU)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Epilepsy research and treatment, Genomic variations and chromosomal abnormalities, Ion channel regulation and function
Most-Cited Works
- → Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1(2013)686 cited
- → Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders(2017)566 cited
- → 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy(2009)555 cited
- → Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies(2018)499 cited
- → Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies(2009)448 cited
- → Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes(2013)437 cited