# Dick Lindhout

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/dick-lindhout/

## Facts

| Field | Value |
| --- | --- |
| Citations | 24,076 |
| Field | Epilepsy research and treatment |
| h-index | 67 |
| i10-index | 164 |
| Last Known Institution | University Medical Center Utrecht |
| OpenAlex ID | https://openalex.org/A5023585572 |
| ORCID iD | https://orcid.org/0000-0001-9580-624X |
| Works | 299 |

## Researcher papers

- [Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4](https://scholariq.org/papers/familial-hemiplegic-migraine-and-episodic-ataxia-type-2-are-caused-by-mutations/)
- [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/)
- [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/)

## Researcher topics

- [Epilepsy research and treatment](https://scholariq.org/topics/epilepsy-research-and-treatment/)
- [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/)
- [Pregnancy and Medication Impact](https://scholariq.org/topics/pregnancy-and-medication-impact/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Researcher university

- [University Medical Center Utrecht](https://scholariq.org/institutions/university-medical-center-utrecht/)

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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.