Helenius J. Schelhaas
Zwolle, OV, Netherlands
Last Updated: 09/26/2026
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Found 66 publications
Correction: GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy.
Journal: Molecular psychiatry
Published: January 07, 2026
GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy.
Journal: Molecular psychiatry
Published: November 15, 2024
Psychogenic non-epileptic (functional) seizures in adults with intellectual disability and epilepsy: A matched case-control study.
Journal: Epilepsia
Published: March 28, 2024
SCN1A-deficient excitatory neuronal networks display mutation-specific phenotypes.
Journal: Brain : a journal of neurology
Published: January 18, 2023
Human KCNQ5 de novo mutations underlie epilepsy and intellectual disability.
Journal: Journal of neurophysiology
Published: May 18, 2022
People with epilepsy and intellectual disability: More than a sum of two conditions.
Journal: Epilepsy & behavior : E&B
Published: August 08, 2021
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 08, 2020
Breath analysis in detecting epilepsy.
Journal: Journal of breath research
Published: January 24, 2020
Efficacy and tolerability of brivaracetam in patients with intellectual disability and epilepsy.
Journal: Acta neurologica Belgica
Published: January 02, 2020
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.
Journal: American journal of human genetics
Published: March 09, 2019
Last Updated: 09/26/2026