Vorstman
Vorstman
Onderzoeker psychiatrie en genetica
Geverifieerd e-mailadres voor umcutrecht.nl
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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
6202014
22q11. 2 deletion syndrome
DM McDonald-McGinn, KE Sullivan, B Marino, N Philip, A Swillen, ...
Nature Reviews Disease Primers 1 (1), 1-19, 2015
4762015
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
4252011
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
4142006
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), eaap8757, 2018
3892018
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
3842014
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
3392006
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
3252012
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, 2017
2812017
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
1832017
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
1732017
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
1612012
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
1232015
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
1202011
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
1172006
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), 2009
1092009
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
1082008
Proline affects brain function in 22q11DS children with the low activity COMT 158 allele
JAS Vorstman, BI Turetsky, MEJ Sijmens-Morcus, MG De Sain, B Dorland, ...
Neuropsychopharmacology 34 (3), 739-746, 2009
772009
International Consortium on Brain and Behavior in 22q11. 2 Deletion Syndrome. Psychiatric disorders from childhood to adulthood in 22q11. 2 deletion syndrome: results from the …
M Schneider, M Debbané, AS Bassett, EW Chow, WL Fung, ...
Am J Psychiatry 171 (6), 627-639, 2014
742014
Cognitive development in children with 22q11. 2 deletion syndrome
SN Duijff, PWJ Klaassen, HFNS de Veye, FA Beemer, G Sinnema, ...
The British Journal of Psychiatry 200 (6), 462-468, 2012
732012
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Artikelen 1–20