# Holger Lerche

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/holger-lerche/

## Facts

| Field | Value |
| --- | --- |
| Citations | 28,832 |
| Field | Epilepsy research and treatment |
| h-index | 91 |
| i10-index | 286 |
| Last Known Institution | University Children's Hospital Tübingen |
| OpenAlex ID | https://openalex.org/A5034571694 |
| ORCID iD | https://orcid.org/0000-0002-1783-8710 |
| Works | 1,115 |

## Researcher papers

- [Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery](https://scholariq.org/papers/histopathological-findings-in-brain-tissue-obtained-during-epilepsy-surgery/)
- [Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders](https://scholariq.org/papers/genetic-and-phenotypic-heterogeneity-suggest-therapeutic-implications-in-scn2a/)
- [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/)
- [Efficient generation of neural stem cell-like cells from adult human bone marrow stromal cells](https://scholariq.org/papers/efficient-generation-of-neural-stem-cell-like-cells-from-adult-human-bone-marrow/)
- [Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes](https://scholariq.org/papers/mutations-in-grin2a-cause-idiopathic-focal-epilepsy-with-rolandic-spikes/)
- [Targeted next generation sequencing as a diagnostic tool in epileptic disorders](https://scholariq.org/papers/targeted-next-generation-sequencing-as-a-diagnostic-tool-in-epileptic-disorders/)
- [A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy](https://scholariq.org/papers/a-recurrent-de-novo-mutation-in-kcnc1-causes-progressive-myoclonus-epilepsy/)
- [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/)

## Researcher topics

- [Epilepsy research and treatment](https://scholariq.org/topics/epilepsy-research-and-treatment/)
- [Ion channel regulation and function](https://scholariq.org/topics/ion-channel-regulation-and-function/)
- [Neuroscience and Neuropharmacology Research](https://scholariq.org/topics/neuroscience-and-neuropharmacology-research/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Cardiac electrophysiology and arrhythmias](https://scholariq.org/topics/cardiac-electrophysiology-and-arrhythmias/)

## Researcher university

- [University Children's Hospital Tübingen](https://scholariq.org/institutions/university-children-s-hospital-tubingen/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.