Vorstman
Vorstman
Onderzoeker psychiatrie en genetica
Geverifieerd e-mailadres voor umcutrecht.nl
TitelGeciteerd doorJaar
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
5992014
22q11. 2 deletion syndrome
DM McDonald-McGinn, KE Sullivan, B Marino, N Philip, A Swillen, ...
Nature Reviews Disease Primers 1 (1), 1-19, 2015
4402015
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
4082011
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
4072006
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
3692014
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
3472018
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
3362006
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
3112012
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
2582017
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
1712017
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
1562012
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
1532017
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
1192011
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
1182015
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
1152006
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
1072009
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
1062008
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
Dissecting the clinical heterogeneity of autism spectrum disorders through defined genotypes
H Bruining, L De Sonneville, H Swaab, M De Jonge, M Kas, ...
PloS one 5 (5), 2010
732010
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Artikelen 1–20