# Sanjay M. Sisodiya

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/sanjay-m-sisodiya/

## Facts

| Field | Value |
| --- | --- |
| Citations | 41,185 |
| Field | Epilepsy research and treatment |
| h-index | 101 |
| i10-index | 373 |
| Last Known Institution | Epilepsy Research UK |
| OpenAlex ID | https://openalex.org/A5074816207 |
| ORCID iD | https://orcid.org/0000-0002-1511-5893 |
| Works | 573 |

## Researcher papers

- [Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery](https://scholariq.org/papers/histopathological-findings-in-brain-tissue-obtained-during-epilepsy-surgery/)
- [Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study](https://scholariq.org/papers/structural-brain-abnormalities-in-the-common-epilepsies-assessed-in-a-worldwide/)
- [De novo mutations in ATP1A3 cause alternating hemiplegia of childhood](https://scholariq.org/papers/de-novo-mutations-in-atp1a3-cause-alternating-hemiplegia-of-childhood/)
- [De novo variants in neurodevelopmental disorders with epilepsy](https://scholariq.org/papers/de-novo-variants-in-neurodevelopmental-disorders-with-epilepsy/)
- [Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations](https://scholariq.org/papers/heterozygous-mutations-of-otx2-cause-severe-ocular-malformations/)
- [Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals](https://scholariq.org/papers/ultra-rare-genetic-variation-in-the-epilepsies-a-whole-exome-sequencing-study-of/)
- [White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study](https://scholariq.org/papers/white-matter-abnormalities-across-different-epilepsy-syndromes-in-adults-an/)
- [<i>SOX2</i> anophthalmia syndrome](https://scholariq.org/papers/i-sox2-i-anophthalmia-syndrome/)
- [Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism](https://scholariq.org/papers/genetic-heterogeneity-in-cornelia-de-lange-syndrome-cdls-and-cdls-like/)
- [Consensus on diagnosis and management of JME: From founder's observations to current trends](https://scholariq.org/papers/consensus-on-diagnosis-and-management-of-jme-from-founder-s-observations-to/)

## 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/)
- [Neuroscience and Neuropharmacology Research](https://scholariq.org/topics/neuroscience-and-neuropharmacology-research/)
- [Pharmacological Effects and Toxicity Studies](https://scholariq.org/topics/pharmacological-effects-and-toxicity-studies/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## Researcher university

- [Epilepsy Research UK](https://scholariq.org/institutions/epilepsy-research-uk/)

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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.