Roland Coras

13PUBLICATIONS
75CO-AUTHORS
Medical infection agents (incl. prions)Epigenetics (incl. genome methylation and epigenomics)Other European languagesGene expression (incl. microarray and other genome-wide approaches)Cellular nervous system
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Publications (13)

|Nov 07, 2026
Repetitive clustered low-voltage fast activity on intracranial electroencephalogram in mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy: A candidate electroencephalographic biomarker study.

|Oct 08, 2026
Deep whole genome sequencing of epileptogenic brain lesions.

|Aug 01, 2026
Astrocyte subtype-specific alterations in the dentate gyrus of individuals with mesial temporal lobe epilepsy.

|May 30, 2026
High incidence of Y-chromosome mosaicism in male and female individuals with mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy.

|Mar 05, 2025
Human brain tissue with MOGHE carrying somatic SLC35A2 variants reveal aberrant protein expression and protein loss in the white matter.

Erica Cecchini, Simon Geffers, Roland Coras

|Aug 09, 2023
The specific DNA methylation landscape in focal cortical dysplasia ILAE type 3D.

Dan-Dan Wang, Mitali Katoch, Samir Jabari

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Frequent Collaborators

8 joint publications

Ingmar Blümcke

6 joint publications

Katja Kobow

4 joint publications

Lucas Hoffmann

4 joint publications

Till Hartlieb