Rikke S. Møller

Analysis of shared heritability in common disorders of the brain

Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane et al. · Science · 2018 · 2K citations · Full text

Brain Function, Psychiatric Disorders, Genetics +23

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

Gemma L. Carvill, Sinéad B. Heavin, Simone C. Yendle et al. · Nature Genetics · 2013 · 683 citations · Full text

Genetics, Novo Mutations, Neurotransmission +5

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Markus Wolff, Katrine M. Johannesen, Ulrike B. S. Hedrich et al. · Brain · 2017 · 558 citations · Full text

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

Heather C. Mefford, Andrew J. Sharp, Michel Guipponi et al. · Nature Genetics · 2009 · 553 citations · Full text

Neurobiology Of Disease, Psychiatric Genetics, Neurology +5

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

Bassel Abou‐Khalil, Pauls Auce, Andreja Avberšek et al. · Nature Communications · 2018 · 493 citations · Full text

Epilepsy Therapies, Genetics, Genetic Epidemiology +22