Olivia Jayne Henry

Karolinska Institutet

Sweden

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Articles (10)

Year:

2025

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2025

Year:

2024

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2024

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2024

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2024

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2023

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2022

Year:

2022

Year:

2022

Collaborators (8)

Heidi Kirsch

Professor of Clinical Neurology and Radiology & Biomedical Imaging

UCSF Medical Center

UNITED STATES

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Kazunori Nakajima

JAPAN

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Nathan Fountain

UNITED STATES

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Rebekah V Harris

University of Melbourne

AUSTRALIA

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Ruth Ottman

Professor

Columbia University

UNITED STATES

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Rhys Thomas

Newcastle University Faculty of Medical Sciences

UNITED KINGDOM

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Samuel Berkovic

University of Melbourne

AUSTRALIA

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Saul Mullen

University of Melbourne

AUSTRALIA

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Olivia Jayne Henry

Research Interests

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Articles (10)

Phenotypic heterogeneity in familial epilepsies is influenced by polygenic risk for generalized and focal epilepsies

Clinical whole genome sequencing in pediatric epilepsy: Genetic and phenotypic spectrum of 733 individuals

The role of copy number variants in the genetic architecture of common familial epilepsies.

De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanism

Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ families

Familial aggregation of seizure outcomes in four familial epilepsy cohorts

Individualised human phenotype ontology gene panels improve clinical whole exome and genome sequencing analytical efficacy in a cohort of developmental and epileptic encephalopathies

Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery

Outcome at age 7 of epilepsy presenting in the first 2 years of life. A population-based study.

Evidence for a Dual-Pathway, 2-Hit Genetic Model for Focal Cortical Dysplasia and Epilepsy.

Collaborators (8)

Heidi Kirsch

Kazunori Nakajima

Nathan Fountain

Rebekah V Harris

Ruth Ottman

Rhys Thomas

Samuel Berkovic

Saul Mullen

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