Karen L. Oliver
245 Burgundy St
Heidelberg, VIC 3084, Australia
Heidelberg, VIC 3084, Australia
Last Updated: 09/26/2026
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Found 51 publications
Genetic testing for familial epilepsies: Diagnostic yield and genetic findings.
Journal: Epilepsia
Published: December 02, 2025
WWOX-Related Developmental and Epileptic Encephalopathy: Expanding the Clinical Spectrum and Deciphering the Genotype-Phenotype.
Journal: Neurology
Published: August 28, 2025
Epilepsy concordance in monozygotic twins: the role of common genetic variants.
Journal: Brain : a journal of neurology
Published: June 01, 2025
Novel, complex configurations of the MARCHF6 repeat expansion associated with progressive myoclonic epilepsy and familial adult myoclonic epilepsy.
Journal: Brain communications
Published: January 19, 2025
Identifying individuals with rare disease variants by inferring shared ancestral haplotypes from SNP array data.
Journal: NAR genomics and bioinformatics
Published: November 20, 2024
Psychoses of Epilepsy: Unravelling the Phenotypic and Genotypic Features.
Journal: Annals of neurology
Published: July 01, 2024
Investigating the effect of polygenic background on epilepsy phenotype in 'monogenic' families.
Journal: EBioMedicine
Published: June 05, 2024
Inflation of polygenic risk scores caused by sample overlap and relatedness: Examples of a major risk of bias.
Journal: American journal of human genetics
Published: April 24, 2024
Familial aggregation of seizure outcomes in four familial epilepsy cohorts.
Journal: Epilepsia
Published: September 12, 2023
Last Updated: 09/26/2026