# Samuel F. Berkovic

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/samuel-f-berkovic/

## Facts

| Field | Value |
| --- | --- |
| Citations | 80,691 |
| Field | Epilepsy research and treatment |
| h-index | 147 |
| i10-index | 648 |
| Last Known Institution | The University of Melbourne |
| OpenAlex ID | https://openalex.org/A5054067653 |
| ORCID iD | https://orcid.org/0000-0003-4580-841X |
| Works | 1,136 |

## Researcher papers

Showing 12 of 19.

- [<scp>ILAE</scp> classification of the epilepsies: Position paper of the <scp>ILAE</scp> Commission for Classification and Terminology](https://scholariq.org/papers/scp-ilae-scp-classification-of-the-epilepsies-position-paper-of-the-scp-ilae-scp/)
- [Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009](https://scholariq.org/papers/revised-terminology-and-concepts-for-organization-of-seizures-and-epilepsies/)
- [A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy](https://scholariq.org/papers/a-missense-mutation-in-the-neuronal-nicotinic-acetylcholine-receptor-4-subunit/)
- [doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein](https://scholariq.org/papers/doublecortin-a-brain-specific-gene-mutated-in-human-x-linked-lissencephaly-and/)
- [Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B](https://scholariq.org/papers/febrile-seizures-and-generalized-epilepsy-associated-with-a-mutation-in-the-na/)
- [The spectrum of SCN1A-related infantile epileptic encephalopathies](https://scholariq.org/papers/the-spectrum-of-scn1a-related-infantile-epileptic-encephalopathies/)
- [<i>KCNQ2</i> encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy](https://scholariq.org/papers/i-kcnq2-i-encephalopathy-emerging-phenotype-of-a-neonatal-epileptic/)
- [Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies](https://scholariq.org/papers/genome-wide-mega-analysis-identifies-16-loci-and-highlights-diverse-biological/)
- [ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology](https://scholariq.org/papers/ilae-classification-of-the-epilepsies-position-paper-of-the-ilae-commission-for/)
- [High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies](https://scholariq.org/papers/high-rate-of-recurrent-de-novo-mutations-in-developmental-and-epileptic/)
- [Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy](https://scholariq.org/papers/missense-mutations-in-the-sodium-gated-potassium-channel-gene-kcnt1-cause-severe/)
- [Somatic Mutations in Cerebral Cortical Malformations](https://scholariq.org/papers/somatic-mutations-in-cerebral-cortical-malformations/)

## Researcher topics

- [Epilepsy research and treatment](https://scholariq.org/topics/epilepsy-research-and-treatment/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Neuroscience and Neuropharmacology Research](https://scholariq.org/topics/neuroscience-and-neuropharmacology-research/)
- [Glycogen Storage Diseases and Myoclonus](https://scholariq.org/topics/glycogen-storage-diseases-and-myoclonus/)

## Researcher university

- [The University of Melbourne](https://scholariq.org/institutions/the-university-of-melbourne/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.