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Genome Medicine|June 10, 2017
brain-coX: investigating and visualising gene co-expression in seven human brain transcriptomic datasetsSaskia Freytag, Rosemary Burgess, Karen L Oliver, et al.
Neurology. Genetics|July 19, 2017
ExACtly zero or once: A clinically helpful guide to assessing genetic variants in mild epilepsiesCaitlin A Bennett, Slavé Petrovski, Karen L Oliver, et al.
Annals of Neurology|February 14, 2025
Psychoses of Epilepsy: Unravelling the Phenotypic and Genotypic FeaturesGenevieve Rayner, Eliza Honybun, Melanie Bahlo, et al.
Human Genetics|August 18, 2014
Using familial information for variant filtering in high-throughput sequencing studiesMelanie Bahlo, Rick Tankard, Vesna Lukic, et al.
Epilepsia|March 6, 2025
Phenotypic heterogeneity in familial epilepsies is influenced by polygenic risk for generalized and focal epilepsiesColin A Ellis, Ruth Ottman, Michael P Epstein, et al.
Brain : a Journal of Neurology|September 25, 2025
Epilepsy concordance in monozygotic twins: the role of common genetic variantsYew Li Dang, Karen L Oliver, Kate Esnault, et al.
Neurology. Genetics|April 12, 2016
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discoveryKaren L Oliver, Vesna Lukic, Saskia Freytag, et al.
Plos One|July 12, 2014
Harnessing gene expression networks to prioritize candidate epileptic encephalopathy genesKaren L Oliver, Vesna Lukic, Natalie P Thorne, et al.
Epilepsy Research|February 14, 2017
SCN1A clinical spectrum includes the self-limited focal epilepsies of childhoodSara Kivity, Karen L Oliver, Zaid Afawi, et al.
Epilepsia|February 22, 2023
Genes4Epilepsy: An epilepsy gene resourceKaren L Oliver, Ingrid E Scheffer, Mark F Bennett, et al.
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