# Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/diagnostic-exome-sequencing-provides-a-molecular-diagnosis-for-a-significant/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Katherine L. Helbig,Kelly D. Farwell Hagman,Deepali N. Shinde,Cameron Mroske,Zöe Powis,Shuwei Li,Sha Tang,Ingo Helbig |
| Citations | 368 |
| DOI | 10.1038/gim.2015.186 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | true |
| OA Status | bronze |
| OA URL | https://www.nature.com/articles/gim2015186.pdf |
| OpenAlex ID | https://openalex.org/W2281890638 |
| PMID | 26795593 |
| Type | article |
| Year | 2016 |

## Paper authors

- [Sha Tang](https://scholariq.org/researchers/sha-tang/)

## 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/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-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.