Samuel Berkovic

University of Melbourne

Australia

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Articles (20)

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Collaborators (21)

Heidi Kirsch

Professor of Clinical Neurology and Radiology & Biomedical Imaging

UCSF Medical Center

UNITED STATES

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Zhibin Chen

MONASH UNIVERSITY

AUSTRALIA

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Gianpiero Cavalleri

Professor of Human Genetics

IRELAND

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Marina AJ Tijssen

professor Movement Disorders

University of Groningen

NETHERLANDS

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Rebekah V Harris

University of Melbourne

AUSTRALIA

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Yue Huang

Assistant Professor

Harvard Medical School

UNITED STATES

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Sanjay Sisodiya

University College London

UNITED KINGDOM

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Michael Lardelli

Lecturer, then Senior Lecturer, then Associate Professor in Genetics

University of Adelaide

AUSTRALIA

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Caroline Cusick

Broad Institute

UNITED STATES

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Patrick Kwan

AUSTRALIA

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Toshimitsu Suzuki

Lecturer

Nagoya University

JAPAN

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Murat Gunel

Sterling Professor and Chair, Dept. of Neurosurgery

Yale University

UNITED STATES

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Ingrid Scheffer

University of Melbourne

AUSTRALIA

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Helen Cross

University College London

UNITED KINGDOM

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H. Westley Phillips

Stanford University

UNITED STATES

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Kazuhiro Yamakawa

Professor

Nagoya University

JAPAN

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Jozef Gecz

AUSTRALIA

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Mark Corbett

AUSTRALIA

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Olivia Jayne Henry

Karolinska Institutet

SWEDEN

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Hirsch Edouard

Professor

University of Strasbourg

FRANCE

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Doug Speed

Professor

Aarhus University

DENMARK

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Samuel Berkovic

Research Interests

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Articles (20)

Is there really evidence for neurodegeneration in Dravet syndrome? Commentary on the publication by Selvarajah et al.

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

Toxoplasma gondii seropositivity as a risk factor for epilepsy: A discordant monozygotic twin study

Improving genetic diagnostic yield in familial and sporadic cerebral cavernous malformations: detection of copy number and deep Intronic variants

SUDEP risk is influenced by longevity genomics: a polygenic risk score study

Sleep‐related hypermotor epilepsy—No longer controversial

Phenotypic Spectrum in Individuals with Pathogenic GABRG2 Loss- and Gain-of-Function Variants

Twins with temporal lobe epilepsy: genetic contributions to hippocampal sclerosis and other subtypes

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

Progressive Myoclonus Epilepsy: Distinctive MRI Changes in Cerebellar and Motor Networks

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

Aicardi Syndrome Is a Genetically Heterogeneous Disorder

Recognition and epileptology of protracted CLN3 disease

Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy

Risk of sudden unexpected death in epilepsy (SUDEP) with lamotrigine and other sodium channel‐modulating antiseizure medications

The Muddle of Myoclonus

The Muddle of Myoclonus

ILAE Genetics Literacy series: Progressive myoclonus epilepsies

IRF2BPL: A new genotype for progressive myoclonus epilepsies

History of familial adult myoclonus epilepsy/benign adult familial myoclonic epilepsy around the world

Collaborators (21)

Heidi Kirsch

Zhibin Chen

Gianpiero Cavalleri

Marina AJ Tijssen

Rebekah V Harris

Yue Huang

Sanjay Sisodiya

Michael Lardelli

Caroline Cusick

Patrick Kwan

Toshimitsu Suzuki

Murat Gunel

Ingrid Scheffer

Helen Cross

H. Westley Phillips

Kazuhiro Yamakawa

Jozef Gecz

Mark Corbett

Olivia Jayne Henry

Hirsch Edouard

Doug Speed

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