Holger Lerche

Hoppe Seyler Str. 3
Tuebingen, BW 72076, Germany

Last Updated: 09/26/2026

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Found 234 publications

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Journal: medRxiv : the preprint server for health sciences

Published: March 13, 2026

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Journal: medRxiv : the preprint server for health sciences

Published: March 13, 2026

Uncovering targets and molecular pathways for personalizing treatment in epilepsy.

Uncovering targets and molecular pathways for personalizing treatment in epilepsy.

Journal: Expert opinion on therapeutic targets

Published: March 01, 2026

Correlation of polygenic risk score and clinical phenotype in patients with genetic generalized epilepsy.

Correlation of polygenic risk score and clinical phenotype in patients with genetic generalized epilepsy.

Journal: Epilepsia

Published: February 25, 2026

9.4-Tesla magnetic resonance imaging in focal epilepsy patients with high-resolution surface-based profiling of focal cortical dysplasias.

9.4-Tesla magnetic resonance imaging in focal epilepsy patients with high-resolution surface-based profiling of focal cortical dysplasias.

Journal: Epilepsia

Published: February 16, 2026

Accurate prediction of gain- and loss-of-function missense variants in GABAA receptors.

Accurate prediction of gain- and loss-of-function missense variants in GABAA receptors.

Journal: EBioMedicine

Published: January 05, 2026

Antineuronal antibody titres in autoimmune encephalitis: clinical implications for diagnosis and long-term immunotherapy.

Antineuronal antibody titres in autoimmune encephalitis: clinical implications for diagnosis and long-term immunotherapy.

Journal: Frontiers in immunology

Published: December 19, 2025

Sleep magnetoencephalography enhances detection and source imaging of seizures and fast oscillations in focal cortical dysplasia.

Sleep magnetoencephalography enhances detection and source imaging of seizures and fast oscillations in focal cortical dysplasia.

Journal: Epilepsia

Published: December 16, 2025

Genetic risk factor identification for common epilepsies guided by integrative omics data analysis.

Genetic risk factor identification for common epilepsies guided by integrative omics data analysis.

Journal: Epilepsia

Published: September 09, 2025

Ketogenic Diet in Super-Refractory Status Epilepticus: A Retrospective Cohort Study with Severity-Matched Controls in Critically Ill Adults.

Ketogenic Diet in Super-Refractory Status Epilepticus: A Retrospective Cohort Study with Severity-Matched Controls in Critically Ill Adults.

Journal: Neurocritical care

Published: September 03, 2025

STX1B variant-specific synaptic dysfunction is associated with network hyperexcitability in human iPSC-derived neurons.

STX1B variant-specific synaptic dysfunction is associated with network hyperexcitability in human iPSC-derived neurons.

Journal: EBioMedicine

Published: August 28, 2025

To the editors: SCN1A gain-of-function effects in Dravet syndrome: Insights into clinical phenotypes and therapeutic implications.

To the editors: SCN1A gain-of-function effects in Dravet syndrome: Insights into clinical phenotypes and therapeutic implications.

Journal: Epilepsia open

Published: August 06, 2025

Showing 1-12 of 234

Last Updated: 09/26/2026