Esther A. Van Duin
Maastricht, LI, Netherlands
Last Updated: 09/26/2026
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Found 17 publications
Psychotic-like experiences and multimorbid psychopathology: The relationship between the 16-item prodromal questionnaire and DSM-IV classifications in a help-seeking population.
Journal: Early intervention in psychiatry
Published: November 28, 2022
Glutamatergic and GABAergic reactivity and cognition in 22q11.2 deletion syndrome and healthy volunteers: A randomized double-blind 7-Tesla pharmacological MRS study.
Journal: Journal of psychopharmacology (Oxford, England)
Published: May 26, 2020
Affective and psychotic reactivity to daily-life stress in adults with 22q11DS: a study using the experience sampling method.
Journal: Journal of neurodevelopmental disorders
Published: March 09, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
Journal: Molecular psychiatry
Published: June 05, 2019
Lower [18F]fallypride binding to dopamine D2/3 receptors in frontal brain areas in adults with 22q11.2 deletion syndrome: a positron emission tomography study.
Journal: Psychological medicine
Published: April 03, 2019
Low prevalence of substance use in people with 22q11.2 deletion syndrome.
Journal: The British journal of psychiatry : the journal of mental science
Published: January 04, 2019
Lower cortisol levels and attenuated cortisol reactivity to daily-life stressors in adults with 22q11.2 deletion syndrome.
Journal: Psychoneuroendocrinology
Published: October 09, 2018
Intact striatal dopaminergic modulation of reward learning and daily-life reward-oriented behavior in first-degree relatives of individuals with psychotic disorder.
Journal: Psychological medicine
Published: December 14, 2017
Striatal dopamine release and impaired reinforcement learning in adults with 22q11.2 deletion syndrome.
Journal: European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology
Published: August 06, 2017
Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Journal: The American journal of psychiatry
Published: July 29, 2017
Female-specific association of NOS1 genotype with white matter microstructure in ADHD patients and controls.
Journal: Journal of child psychology and psychiatry, and allied disciplines
Published: March 17, 2017
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3.
Journal: Circulation. Cardiovascular genetics
Published: December 16, 2016
Last Updated: 09/26/2026