A S. Vorstman

Utrecht, UT, Netherlands

Last Updated: 09/26/2026

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Found 11 publications

Smartphone-based Monitoring and cognition Modification Against Recurrence of Depression (SMARD): An RCT of Memory Bias Modification Training vs. Cognitive Control Training vs. Attention Bias Modification Training in remitted recurrently depressed patients with 1.5 year follow-up.

Smartphone-based Monitoring and cognition Modification Against Recurrence of Depression (SMARD): An RCT of Memory Bias Modification Training vs. Cognitive Control Training vs. Attention Bias Modification Training in remitted recurrently depressed patients with 1.5 year follow-up.

Journal: BMC psychiatry

Published: March 27, 2025

A comprehensive overview of neuropsychiatric symptoms in adolescents with 22q11.2 deletion syndrome.

A comprehensive overview of neuropsychiatric symptoms in adolescents with 22q11.2 deletion syndrome.

Journal: Journal of intellectual disability research : JIDR

Published: February 12, 2024

Guidelines on genetic testing in psychiatry: an overview

Guidelines on genetic testing in psychiatry: an overview

Journal: Tijdschrift voor psychiatrie

Published: June 23, 2022

Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia.

Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia.

Journal: Psychological medicine

Published: August 02, 2018

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium.

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium.

Journal: Molecular psychiatry

Published: February 23, 2017

Autism Spectrum and psychosis risk in the 22q11.2 deletion syndrome. Findings from a prospective longitudinal study.

Autism Spectrum and psychosis risk in the 22q11.2 deletion syndrome. Findings from a prospective longitudinal study.

Journal: Schizophrenia research

Published: October 10, 2016

The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome.

The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome.

Journal: Clinical genetics

Published: December 08, 2015

Pharmacological treatment of 22q11.2 deletion syndrome-related psychoses.

Pharmacological treatment of 22q11.2 deletion syndrome-related psychoses.

Journal: Pharmacopsychiatry

Published: June 20, 2015

Intellectual functioning in relation to autism and ADHD symptomatology in children and adolescents with 22q11.2 deletion syndrome.

Intellectual functioning in relation to autism and ADHD symptomatology in children and adolescents with 22q11.2 deletion syndrome.

Journal: Journal of intellectual disability research : JIDR

Published: December 19, 2014

Individual common variants exert weak effects on the risk for autism spectrum disorders.

Individual common variants exert weak effects on the risk for autism spectrum disorders.

Journal: Human molecular genetics

Published: July 31, 2012

Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.

Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.

Journal: Cytogenetic and genome research

Published: November 08, 2011

Showing 1-11 of 11

Last Updated: 09/26/2026