Krenn, M.* et al. ADAM23 haploinsufficiency as a putative oligogenic contributor in an individual with focal epilepsy. Seizure 131, 454-457 (2025)
Krenn, M.* et al. Delineation of epileptic and neurodevelopmental phenotypes associated with variants in STX1B. Seizure 87, 25-29 (2021)