Vorstman JAS - Search Results

1

Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia.

Fiksinski AM, Breetvelt EJ, Lee YJ, Boot E, Butcher N, Palmer L, Chow EWC, Kahn RS, Vorstman JAS, Bassett AS. Fiksinski AM, et al. Among authors: vorstman jas. Psychol Med. 2019 Apr;49(6):1047-1054. doi: 10.1017/S0033291718001824. Epub 2018 Aug 1. Psychol Med. 2019. PMID: 30064532

2

[A bifid uvula in a patient with schizophrenia as a sign of 22q11 deletion syndrome].

Vorstman JA, de Ranitz AG, Udink ten Cate FE, Beemer FA, Kahn RS. Vorstman JA, et al. Ned Tijdschr Geneeskd. 2002 Oct 26;146(43):2033-6. Ned Tijdschr Geneeskd. 2002. PMID: 12428463 Dutch.

3

The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.

Vorstman JAS, Morcus MEJ, Duijff SN, Klaassen PWJ, Heineman-de Boer JA, Beemer FA, Swaab H, Kahn RS, van Engeland H. Vorstman JAS, et al. J Am Acad Child Adolesc Psychiatry. 2006 Sep;45(9):1104-1113. doi: 10.1097/01.chi.0000228131.56956.c1. J Am Acad Child Adolesc Psychiatry. 2006. PMID: 16926618

4

Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia.

Hoogendoorn ML, Vorstman JA, Jalali GR, Selten JP, Sinke RJ, Emanuel BS, Kahn RS. Hoogendoorn ML, et al. Schizophr Res. 2008 Jan;98(1-3):84-8. doi: 10.1016/j.schres.2007.09.025. Epub 2007 Oct 26. Schizophr Res. 2008. PMID: 17964762 Free PMC article.

5

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.

6

Proline affects brain function in 22q11DS children with the low activity COMT 158 allele.

Vorstman JA, Turetsky BI, Sijmens-Morcus ME, de Sain MG, Dorland B, Sprong M, Rappaport EF, Beemer FA, Emanuel BS, Kahn RS, van Engeland H, Kemner C. Vorstman JA, et al. Neuropsychopharmacology. 2009 Feb;34(3):739-46. doi: 10.1038/npp.2008.132. Epub 2008 Sep 3. Neuropsychopharmacology. 2009. PMID: 18769474 Free PMC article.

7

A double hit implicates DIAPH3 as an autism risk gene.

Vorstman JA, van Daalen E, Jalali GR, Schmidt ER, Pasterkamp RJ, de Jonge M, Hennekam EA, Janson E, Staal WG, van der Zwaag B, Burbach JP, Kahn RS, Emanuel BS, van Engeland H, Ophoff RA. Vorstman JA, et al. Mol Psychiatry. 2011 Apr;16(4):442-51. doi: 10.1038/mp.2010.26. Epub 2010 Mar 23. Mol Psychiatry. 2011. PMID: 20308993 Free PMC article.

8

Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.

Buizer-Voskamp JE, Muntjewerff JW; Genetic Risk and Outcome in Psychosis (GROUP) Consortium Members; Strengman E, Sabatti C, Stefansson H, Vorstman JA, Ophoff RA. Buizer-Voskamp JE, et al. Biol Psychiatry. 2011 Oct 1;70(7):655-62. doi: 10.1016/j.biopsych.2011.02.015. Epub 2011 Apr 13. Biol Psychiatry. 2011. PMID: 21489405 Free PMC article.

9

Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis.

Derks EM, Vorstman JA, Ripke S, Kahn RS; Schizophrenia Psychiatric Genomic Consortium; Ophoff RA. Derks EM, et al. PLoS One. 2012;7(6):e37852. doi: 10.1371/journal.pone.0037852. Epub 2012 Jun 22. PLoS One. 2012. PMID: 22761660 Free PMC article.

10

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

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