Hande S. Caglayan
Istanbul, Turkey
Last Updated: 09/26/2026
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Found 20 publications
Exome data of developmental and epileptic encephalopathy patients reveals de novo and inherited pathologic variants in epilepsy-associated genes.
Journal: Seizure
Published: February 24, 2023
Current practice in diagnostic genetic testing of the epilepsies
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: July 13, 2022
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
Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies.
Journal: EBioMedicine
Published: October 21, 2021
De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies.
Journal: Brain : a journal of neurology
Published: June 14, 2021
Possible role of SCN4A skeletal muscle mutation in apnea during seizure.
Journal: Epilepsia open
Published: November 20, 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 variants in neurodevelopmental disorders with epilepsy.
Journal: Nature genetics
Published: March 20, 2017
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
Journal: Brain : a journal of neurology
Published: December 08, 2016
Pitfalls in genetic testing: the story of missed SCN1A mutations.
Journal: Molecular genetics & genomic medicine
Published: November 25, 2015
Last Updated: 09/26/2026