# Pasquale Striano

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/pasquale-striano/

## Facts

| Field | Value |
| --- | --- |
| Citations | 34,064 |
| Field | Epilepsy research and treatment |
| h-index | 89 |
| i10-index | 577 |
| Last Known Institution | Istituto Giannina Gaslini |
| OpenAlex ID | https://openalex.org/A5088309302 |
| Works | 1,014 |

## Researcher papers

- [Mapping the human genetic architecture of COVID-19](https://scholariq.org/papers/mapping-the-human-genetic-architecture-of-covid-19/)
- [Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders](https://scholariq.org/papers/genetic-and-phenotypic-heterogeneity-suggest-therapeutic-implications-in-scn2a/)
- [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 variants in neurodevelopmental disorders with epilepsy](https://scholariq.org/papers/de-novo-variants-in-neurodevelopmental-disorders-with-epilepsy/)
- [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/)
- [AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders](https://scholariq.org/papers/ampa-receptor-glua2-subunit-defects-are-a-cause-of-neurodevelopmental-disorders/)
- [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/)
- [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/)
- [Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32](https://scholariq.org/papers/genome-wide-association-analysis-of-genetic-generalized-epilepsies-implicates/)
- [A second update on mapping the human genetic architecture of COVID-19](https://scholariq.org/papers/a-second-update-on-mapping-the-human-genetic-architecture-of-covid-19/)

## Researcher topics

- [Epilepsy research and treatment](https://scholariq.org/topics/epilepsy-research-and-treatment/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Pharmacological Effects and Toxicity Studies](https://scholariq.org/topics/pharmacological-effects-and-toxicity-studies/)
- [Glycogen Storage Diseases and Myoclonus](https://scholariq.org/topics/glycogen-storage-diseases-and-myoclonus/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Researcher university

- [Istituto Giannina Gaslini](https://scholariq.org/institutions/istituto-giannina-gaslini/)

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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.