# Andreas Brunklaus

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/andreas-brunklaus/

## Facts

| Field | Value |
| --- | --- |
| Citations | 4,442 |
| Field | Epilepsy research and treatment |
| h-index | 32 |
| i10-index | 52 |
| Last Known Institution | Royal Hospital for Children |
| OpenAlex ID | https://openalex.org/A5021769497 |
| ORCID iD | 0000-0002-7728-6903 |
| Works | 107 |

## Researcher papers

- [Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort](https://scholariq.org/papers/incidence-and-phenotypes-of-childhood-onset-genetic-epilepsies-a-prospective/)
- [Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome](https://scholariq.org/papers/prognostic-clinical-and-demographic-features-in-scn1a-mutation-positive-dravet/)
- [Genotype–phenotype associations in <i>SCN1A</i> -related epilepsies](https://scholariq.org/papers/genotype-phenotype-associations-in-i-scn1a-i-related-epilepsies/)
- [Early childhood epilepsies: epidemiology, classification, aetiology, and socio-economic determinants](https://scholariq.org/papers/early-childhood-epilepsies-epidemiology-classification-aetiology-and-socio/)
- [Evidence for oxidative stress in the frontal cortex in patients with recurrent depressive disorder—a postmortem study](https://scholariq.org/papers/evidence-for-oxidative-stress-in-the-frontal-cortex-in-patients-with-recurrent/)
- [Dravet syndrome and its mimics: Beyond <i><scp>SCN</scp>1A</i>](https://scholariq.org/papers/dravet-syndrome-and-its-mimics-beyond-i-scp-scn-scp-1a-i/)
- [Dravet syndrome—From epileptic encephalopathy to channelopathy](https://scholariq.org/papers/dravet-syndrome-from-epileptic-encephalopathy-to-channelopathy/)
- [A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variants](https://scholariq.org/papers/a-catalogue-of-new-incidence-estimates-of-monogenic-neurodevelopmental-disorders/)
- [The gain of function <i>SCN1A</i> disorder spectrum: novel epilepsy phenotypes and therapeutic implications](https://scholariq.org/papers/the-gain-of-function-i-scn1a-i-disorder-spectrum-novel-epilepsy-phenotypes-and/)
- [Predicting functional effects of missense variants in voltage-gated sodium and calcium channels](https://scholariq.org/papers/predicting-functional-effects-of-missense-variants-in-voltage-gated-sodium-and/)
- [Caregiver burden and therapeutic needs in Dravet syndrome - A national UK cross-sectional questionnaire study](https://scholariq.org/papers/caregiver-burden-and-therapeutic-needs-in-dravet-syndrome-a-national-uk-cross/)

## 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/)
- [Ion channel regulation and function](https://scholariq.org/topics/ion-channel-regulation-and-function/)
- [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

- [Royal Hospital for Children](https://scholariq.org/institutions/royal-hospital-for-children/)

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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.