Beemer FA - Search Results

1

[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. Among authors: beemer fa. Ned Tijdschr Geneeskd. 2002 Oct 26;146(43):2033-6. Ned Tijdschr Geneeskd. 2002. PMID: 12428463 Dutch.

2

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. Among authors: beemer fa. 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.

3

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. Among authors: beemer fa. Br J Psychiatry. 2012 Jun;200(6):462-8. doi: 10.1192/bjp.bp.111.097139. Br J Psychiatry. 2012. PMID: 22661678

4

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. Among authors: beemer fa. 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

5

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. Among authors: beemer fa. 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

6

Behavior in preschool children with the 22q11.2 deletion syndrome.

Klaassen P, Duijff S, Swanenburg de Veye H, Vorstman J, Beemer F, Sinnema G. Klaassen P, et al. Am J Med Genet A. 2013 Jan;161A(1):94-101. doi: 10.1002/ajmg.a.35685. Epub 2012 Dec 13. Am J Med Genet A. 2013. PMID: 23239609

7

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. Among authors: beemer fa. Neuropsychopharmacology. 2009 Feb;34(3):739-46. doi: 10.1038/npp.2008.132. Epub 2008 Sep 3. Neuropsychopharmacology. 2009. PMID: 18769474 Free PMC article.

8

Intelligence and visual motor integration in 5-year-old children with 22q11-deletion syndrome.

Duijff S, Klaassen P, Beemer F, Swanenburg de Veye H, Vorstman J, Sinnema G. Duijff S, et al. Res Dev Disabil. 2012 Mar-Apr;33(2):334-40. doi: 10.1016/j.ridd.2011.10.004. Epub 2011 Nov 24. Res Dev Disabil. 2012. PMID: 22119678

9

Cognitive and behavioral trajectories in 22q11DS from childhood into adolescence: a prospective 6-year follow-up study.

Duijff SN, Klaassen PW, Swanenburg de Veye HF, Beemer FA, Sinnema G, Vorstman JA. Duijff SN, et al. Among authors: beemer fa. Res Dev Disabil. 2013 Sep;34(9):2937-45. doi: 10.1016/j.ridd.2013.06.001. Epub 2013 Jun 29. Res Dev Disabil. 2013. PMID: 23816629

10

Explaining the variable penetrance of CNVs: Parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion.

Klaassen P, Duijff S, Swanenburg de Veye H, Beemer F, Sinnema G, Breetvelt E, Schappin R, Vorstman J. Klaassen P, et al. Am J Med Genet B Neuropsychiatr Genet. 2016 Sep;171(6):790-6. doi: 10.1002/ajmg.b.32441. Epub 2016 Mar 8. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 26953189

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