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Karen Oliver

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Senior Research Fellow

University of Melbourne

Australia

Research Interests

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Grant: Open

Integrating monogenic and polygenic epilepsy risk factors to advance molecular diagnoses and to understand disease risk

Open Date: 2026-01-01

Close Date: 2031-12-01

Articles (16)

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Collaborators (23)

Heidi Kirsch

Professor of Clinical Neurology and Radiology & Biomedical Imaging

UCSF Medical Center

UNITED STATES

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Caren Armstrong

Assistant Professor of clinical neurology

university of california davis medical center

UNITED STATES

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Roland Krause

Research Scientist

University of Luxembourg

LUXEMBOURG

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Nathan Fountain

Professor

University of Virginia School of Medicine

UNITED STATES

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Anna-Elina Lehesjoki

Professor

University of Helsinki

FINLAND

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Gianpiero Cavalleri

Professor of Human Genetics

IRELAND

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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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Caroline Cusick

Broad Institute

UNITED STATES

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Rhys Thomas

Reader in Epilepsy

Newcastle University Faculty of Medical Sciences

UNITED KINGDOM

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Toshimitsu Suzuki

Lecturer

Nagoya University

JAPAN

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Ingrid Scheffer

University of Melbourne

AUSTRALIA

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Mark Fitzgerald

Associate Professor of Clinical Neurology

UNITED STATES

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Kazuhiro Yamakawa

Professor

Nagoya University

JAPAN

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Samuel Berkovic

University of Melbourne

AUSTRALIA

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Heather Mefford

Member

St. Jude Children's Research Hospital

UNITED STATES

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Piero Perucca

AUSTRALIA

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Deepak Gill

Clinical Senior lecturer

University of Sydney

AUSTRALIA

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Olivia Jayne Henry

Karolinska Institutet

SWEDEN

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Gloria Hoi-Yee Li

Assistant Professor

The Hong Kong Polytechnic University

HONG KONG

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Angelo Labate

Full Professor of Neurology

University of Messina

ITALY

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Saul Mullen

University of Melbourne

AUSTRALIA

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Doug Speed

Professor at Aarhus University

Aarhus University

DENMARK

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ApplyKite TwinLearns as you apply

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Karen Oliver

Research Interests

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Recent Grants

Articles (16)

Genetic testing for familial epilepsies: Diagnostic yield and genetic findings.

Epilepsy concordance in monozygotic twins: the role of common genetic variants

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

WWOX -Related Developmental and Epileptic Encephalopathy

Psychoses of Epilepsy: Unravelling the Phenotypic and Genotypic Features

Inflation of polygenic risk scores caused by sample overlap and relatedness: Examples of a major risk of bias.

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

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

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

Familial aggregation of seizure outcomes in four familial epilepsy cohorts

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Familial mesial temporal lobe epilepsy: clinical spectrum and genetic evidence for a polygenic architecture.

Recognition and epileptology of protracted CLN3 disease

IRF2BPL: A new genotype for progressive myoclonus epilepsies

Genes4Epilepsy: An epilepsy gene resource

WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk

Collaborators (23)

Heidi Kirsch

Caren Armstrong

Roland Krause

Nathan Fountain

Anna-Elina Lehesjoki

Gianpiero Cavalleri

Rebekah V Harris

Ruth Ottman

Caroline Cusick

Rhys Thomas

Toshimitsu Suzuki

Ingrid Scheffer

Mark Fitzgerald

Kazuhiro Yamakawa

Samuel Berkovic

Heather Mefford

Piero Perucca

Deepak Gill

Olivia Jayne Henry

Gloria Hoi-Yee Li

Angelo Labate

Saul Mullen

Doug Speed

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