Karen L Oliver

14PUBLICATIONS
72CO-AUTHORS
Aboriginal and Torres Strait Islander artefactsEpigenetics (incl. genome methylation and epigenomics)Major global burdens of diseaseSocial epidemiologyNeurology and neuromuscular diseases
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Publications (14)

|Sep 18, 2026
SLC7A6OS Founder Mutation: A Rare Cause of Progressive Myoclonus Epilepsy Dated to 1100 Years Ago.

|Mar 08, 2026
Genetic testing for familial epilepsies: Diagnostic yield and genetic findings.

Colin A Ellis, Juliette Copeland, Isabella Velez

|Aug 28, 2025
WWOX-Related Developmental and Epileptic Encephalopathy: Expanding the Clinical Spectrum and Deciphering the Genotype-Phenotype.

Kelley Gao, Lisa G Riley, Jacques Raubenheimer

|Mar 06, 2025
Phenotypic heterogeneity in familial epilepsies is influenced by polygenic risk for generalized and focal epilepsies.

Colin A Ellis, Ruth Ottman, Michael P Epstein

|Feb 14, 2025
Psychoses of Epilepsy: Unravelling the Phenotypic and Genotypic Features.

Genevieve Rayner, Eliza Honybun, Melanie Bahlo

|Aug 03, 2024
Solving the Etiology of Developmental and Epileptic Encephalopathy with Spike-Wave Activation in Sleep (D/EE-SWAS).

Sindhu Viswanathan, Karen L Oliver, Brigid M Regan

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Frequent Collaborators

8 joint publications

Samuel F Berkovic

7 joint publications

Ingrid Scheffer

6 joint publications

Melanie Bahlo

3 joint publications

Colin A Ellis