Onderzoeker psychiatrie en genetica
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Cited by
Cited by
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
D Pinto, E Delaby, D Merico, M Barbosa, A Merikangas, L Klei, ...
The American Journal of Human Genetics 94 (5), 677-694, 2014
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
22q11. 2 deletion syndrome
DM McDonald-McGinn, KE Sullivan, B Marino, N Philip, A Swillen, ...
Nature reviews Disease primers 1 (1), 1-19, 2015
Practical guidelines for managing patients with 22q11. 2 deletion syndrome
AS Bassett, DM McDonald-McGinn, K Devriendt, MC Digilio, ...
The Journal of pediatrics 159 (2), 332-339. e1, 2011
Psychiatric disorders from childhood to adulthood in 22q11. 2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11. 2 Deletion Syndrome
M Schneider, M Debbané, AS Bassett, EWC Chow, WLA Fung, ...
American Journal of Psychiatry 171 (6), 627-639, 2014
Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism
JAS Vorstman, WG Staal, E Van Daalen, H Van Engeland, ...
Molecular psychiatry 11 (1), 18-28, 2006
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
RKC Yuen, D Merico, M Bookman, JL Howe, B Thiruvahindrapuram, ...
Nature neuroscience 20 (4), 602-611, 2017
Individual common variants exert weak effects on the risk for autism spectrum disorders
R Anney, L Klei, D Pinto, J Almeida, E Bacchelli, G Baird, N Bolshakova, ...
Human molecular genetics 21 (21), 4781-4792, 2012
The 22q11. 2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms
JAS Vorstman, MEJ Morcus, SN Duijff, PWJ Klaassen, FA BEEMER, ...
Journal of the American Academy of Child & Adolescent Psychiatry 45 (9 …, 2006
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium
Science (New York, NY) 360 (6395), 2018
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ...
Nature genetics 49 (7), 978-985, 2017
Autism genetics: opportunities and challenges for clinical translation
JAS Vorstman, JR Parr, D Moreno-De-Luca, RJL Anney, JI Nurnberger Jr, ...
Nature Reviews Genetics 18 (6), 362, 2017
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
JP Casey, T Magalhaes, JM Conroy, R Regan, N Shah, R Anney, ...
Human genetics 131 (4), 565-579, 2012
Preventive strategies for mental health
C Arango, CM Díaz-Caneja, PD McGorry, J Rapoport, IE Sommer, ...
The Lancet Psychiatry 5 (7), 591-604, 2018
Cognitive decline preceding the onset of psychosis in patients with 22q11. 2 deletion syndrome
JAS Vorstman, EJ Breetvelt, SN Duijff, S Eliez, M Schneider, ...
JAMA psychiatry 72 (4), 377-385, 2015
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24. 32 and a significant overlap with schizophrenia
Molecular autism 8, 1-17, 2017
Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for …
R Hochstenbach, JE Buizer-Voskamp, JAS Vorstman, RA Ophoff
Cytogenetic and genome research 135 (3-4), 174-202, 2011
MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q
JAS Vorstman, GR Jalali, EF Rappaport, AM Hacker, C Scott, BS Emanuel
Human mutation 27 (8), 814-821, 2006
Gene-network analysis identifies susceptibility genes related to glycobiology in autism
B van der Zwaag, L Franke, M Poot, R Hochstenbach, HA Spierenburg, ...
PloS one 4 (5), e5324, 2009
Detailed analysis of 22q11. 2 with a high density MLPA probe set
GR Jalali, JAS Vorstman, AB Errami, R Vijzelaar, J Biegel, T Shaikh, ...
Human mutation 29 (3), 433-440, 2008
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