Danique M. Vlaskamp
Groningen, GR, Netherlands
Last Updated: 09/26/2026
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Found 15 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
Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome.
Journal: Epilepsia open
Published: February 22, 2023
Functional correlates of clinical phenotype and severity in recurrent SCN2A variants.
Journal: Communications biology
Published: October 29, 2021
Changes in empowerment and anxiety of patients and parents during genetic counselling for epilepsy.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: August 31, 2020
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
GRIN2A-related disorders: genotype and functional consequence predict phenotype.
Journal: Brain : a journal of neurology
Published: July 01, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detection.
Journal: Human mutation
Published: June 28, 2018
Schizophrenia is a later-onset feature of PCDH19 Girls Clustering Epilepsy.
Journal: Epilepsia
Published: June 25, 2018
PRRT2-related phenotypes in patients with a 16p11.2 deletion.
Journal: European journal of medical genetics
Published: April 17, 2018
Last Updated: 09/26/2026