Vorstman JAS - Search Results

1

Neurobiological perspective of 22q11.2 deletion syndrome.

Zinkstok JR, Boot E, Bassett AS, Hiroi N, Butcher NJ, Vingerhoets C, Vorstman JAS, van Amelsvoort TAMJ. Zinkstok JR, et al. Among authors: vorstman jas. Lancet Psychiatry. 2019 Nov;6(11):951-960. doi: 10.1016/S2215-0366(19)30076-8. Epub 2019 Aug 5. Lancet Psychiatry. 2019. PMID: 31395526 Free PMC article. Review.

2

Behavioral problems in relation to intelligence in children with 22q11.2 deletion syndrome: a matched control study.

Jansen PW, Duijff SN, Beemer FA, Vorstman JA, Klaassen PW, Morcus ME, Heineman-de Boer JA. Jansen PW, et al. Am J Med Genet A. 2007 Mar 15;143A(6):574-80. doi: 10.1002/ajmg.a.31623. Am J Med Genet A. 2007. PMID: 17318841

3

Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome.

Vorstman JA, Chow EW, Ophoff RA, van Engeland H, Beemer FA, Kahn RS, Sinke RJ, Bassett AS. Vorstman JA, et al. Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):430-3. doi: 10.1002/ajmg.b.30827. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18646052 Free PMC article.

4

Proline and COMT status affect visual connectivity in children with 22q11.2 deletion syndrome.

Magnée MJ, Lamme VA, de Sain-van der Velden MG, Vorstman JA, Kemner C. Magnée MJ, et al. PLoS One. 2011;6(10):e25882. doi: 10.1371/journal.pone.0025882. Epub 2011 Oct 5. PLoS One. 2011. PMID: 21998713 Free PMC article.

5

Cognitive development in children with 22q11.2 deletion syndrome.

Duijff SN, Klaassen PW, de Veye HF, Beemer FA, Sinnema G, Vorstman JA. Duijff SN, et al. Br J Psychiatry. 2012 Jun;200(6):462-8. doi: 10.1192/bjp.bp.111.097139. Br J Psychiatry. 2012. PMID: 22661678

6

Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion.

Vorstman JA, Breetvelt EJ, Thode KI, Chow EW, Bassett AS. Vorstman JA, et al. Schizophr Res. 2013 Jan;143(1):55-9. doi: 10.1016/j.schres.2012.10.010. Epub 2012 Nov 13. Schizophr Res. 2013. PMID: 23153825

7

Intellectual functioning in relation to autism and ADHD symptomatology in children and adolescents with 22q11.2 deletion syndrome.

Hidding E, Swaab H, de Sonneville LM, van Engeland H, Sijmens-Morcus ME, Klaassen PW, Duijff SN, Vorstman JA. Hidding E, et al. J Intellect Disabil Res. 2015 Sep;59(9):803-15. doi: 10.1111/jir.12187. Epub 2015 Feb 13. J Intellect Disabil Res. 2015. PMID: 25683771

8

Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.

Vorstman JA, Breetvelt EJ, Duijff SN, Eliez S, Schneider M, Jalbrzikowski M, Armando M, Vicari S, Shashi V, Hooper SR, Chow EW, Fung WL, Butcher NJ, Young DA, McDonald-McGinn DM, Vogels A, van Amelsvoort T, Gothelf D, Weinberger R, Weizman A, Klaassen PW, Koops S, Kates WR, Antshel KM, Simon TJ, Ousley OY, Swillen A, Gur RE, Bearden CE, Kahn RS, Bassett AS; International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. Vorstman JA, et al. JAMA Psychiatry. 2015 Apr;72(4):377-85. doi: 10.1001/jamapsychiatry.2014.2671. JAMA Psychiatry. 2015. PMID: 25715178 Free PMC article.

9

Pharmacological treatment of 22q11.2 deletion syndrome-related psychoses.

Boot E, Butcher NJ, Vorstman JA, van Amelsvoort TA, Fung WL, Bassett AS. Boot E, et al. Pharmacopsychiatry. 2015 Sep;48(6):219-20. doi: 10.1055/s-0035-1554645. Epub 2015 Jun 19. Pharmacopsychiatry. 2015. PMID: 26091278

10

The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome.

Hidding E, Swaab H, de Sonneville LM, van Engeland H, Vorstman JA. Hidding E, et al. Clin Genet. 2016 Nov;90(5):420-427. doi: 10.1111/cge.12766. Epub 2016 Apr 19. Clin Genet. 2016. PMID: 26919535

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