# Targeted next generation sequencing as a diagnostic tool in epileptic disorders

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/targeted-next-generation-sequencing-as-a-diagnostic-tool-in-epileptic-disorders/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Johannes R. Lemke,Erik Riesch,Tim Scheurenbrand,Max Schubach,Christian Wilhelm,Isabelle Steiner,Jörg Hansen,Carolina Courage,Sabina Gallati,Sarah Bürki,Susi Strozzi,Barbara Goeggel Simonetti,Sebastian Grunt,Maja Steinlin,Michael Alber,Markus Wolff,Thomas Klopstock,Eva Christina Prott,Rüdiger Lorenz,Christiane Spaich,Sabine Rona,Maya Lakshminarasimhan,Judith F. Kroll,Thomas Dorn,Günter Krämer,Matthis Synofzik,Felicitas Becker,Yvonne Weber,Holger Lerche,Detlef Böhm,Saskia Biskup |
| Citations | 332 |
| DOI | 10.1111/j.1528-1167.2012.03516.x |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine,Neuroscience |
| Open Access | true |
| OA Status | bronze |
| OA URL | https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/j.1528-1167.2012.03516.x |
| OpenAlex ID | https://openalex.org/W1673813955 |
| PMID | 22612257 |
| Type | article |
| Year | 2012 |

## Paper authors

- [Thomas Klopstock](https://scholariq.org/researchers/thomas-klopstock/)

## Paper journal

- [Epilepsia](https://scholariq.org/journals/epilepsia/)

## Paper primary topic

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Paper topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Epilepsy research and treatment](https://scholariq.org/topics/epilepsy-research-and-treatment/)
- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)

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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.