Thomas Sander
Koeln, NW, Germany
Last Updated: 09/26/2026
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Found 46 publications
mGlu3 Metabotropic Glutamate Receptors as a Target for the Treatment of Absence Epilepsy: Preclinical and Human Genetics Data.
Journal: Current neuropharmacology
Published: January 13, 2022
Distinct gene-set burden patterns underlie common generalized and focal epilepsies.
Journal: EBioMedicine
Published: May 24, 2021
Gene expression analysis in epileptic hippocampi reveals a promoter haplotype conferring reduced aldehyde dehydrogenase 5a1 expression and responsiveness.
Journal: Epilepsia
Published: October 14, 2020
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.
Journal: Pharmacogenomics
Published: April 21, 2020
ME2 association analysis in adolescent onset genetic generalized epilepsies.
Journal: Epilepsia
Published: February 18, 2019
Linkage Evidence for a Two-Locus Inheritance of LQT-Associated Seizures in a Multigenerational LQT Family With a Novel KCNQ1 Loss-of-Function Mutation.
Journal: Frontiers in neurology
Published: December 15, 2018
Rare gene deletions in genetic generalized and Rolandic epilepsies.
Journal: PloS one
Published: March 16, 2018
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study.
Journal: The Lancet. Neurology
Published: August 02, 2017
De novo 8p23.1 deletion in a patient with absence epilepsy.
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: May 24, 2017
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy.
Journal: European journal of human genetics : EJHG
Published: May 08, 2017
Last Updated: 09/26/2026