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Jacob A.S. Vorstman
Jacob A.S. Vorstman
Professor Psychiatry, Senior Scientist SickKids Research Institute, University of Toronto, Canada
Geverifieerd e-mailadres voor sickkids.ca
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Jaar
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13512018
22q11. 2 deletion syndrome
DM McDonald-McGinn, KE Sullivan, B Marino, N Philip, A Swillen, ...
Nature reviews Disease primers 1 (1), 1-19, 2015
12382015
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
10582014
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
RK C Yuen, D Merico, M Bookman, J L Howe, B Thiruvahindrapuram, ...
Nature neuroscience 20 (4), 602-611, 2017
7512017
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
7162014
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
6742011
Preventive strategies for mental health
C Arango, CM Díaz-Caneja, PD McGorry, J Rapoport, IE Sommer, ...
The Lancet Psychiatry 5 (7), 591-604, 2018
5762018
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
4712006
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), 362-376, 2017
4642017
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
4552017
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
4452006
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
4422012
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
3272017
Social brain, social dysfunction and social withdrawal
S Porcelli, N Van Der Wee, S van der Werff, M Aghajani, JC Glennon, ...
Neuroscience & Biobehavioral Reviews 97, 10-33, 2019
3052019
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, 565-579, 2012
2282012
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
2262015
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
1732014
Large-scale mapping of cortical alterations in 22q11. 2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size
D Sun, CRK Ching, A Lin, JK Forsyth, L Kushan, A Vajdi, M Jalbrzikowski, ...
Molecular psychiatry 25 (8), 1822-1834, 2020
1572020
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
1472006
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
1462009
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Artikelen 1–20