Baas F - Search Results

1

Striatal dopamine transporter availability associated with polymorphisms in the dopamine transporter gene SLC6A3.

van de Giessen E, de Win MM, Tanck MW, van den Brink W, Baas F, Booij J. van de Giessen E, et al. Among authors: baas f. J Nucl Med. 2009 Jan;50(1):45-52. doi: 10.2967/jnumed.108.053652. Epub 2008 Dec 17. J Nucl Med. 2009. PMID: 19091889 Free article.

2

Association tests of striatal DAT availability and SNPs that impact a novel splice variant in the DAT gene.

van de Giessen E, Nimgaonkar VL, Watson AM, Kodavali C, Baas F, Tanck MW, de Win MM, van den Brink W, Booij J. van de Giessen E, et al. Among authors: baas f. J Nucl Med. 2012 May;53(5):839. doi: 10.2967/jnumed.111.100271. Epub 2012 Mar 16. J Nucl Med. 2012. PMID: 22427685 Free article. No abstract available.

3

Is TOR1A a risk factor in adult-onset primary torsion dystonia?

Groen JL, Ritz K, Tanck MW, van de Warrenburg BP, van Hilten JJ, Aramideh M, Baas F, Tijssen MA. Groen JL, et al. Among authors: baas f. Mov Disord. 2013 Jun;28(6):827-31. doi: 10.1002/mds.25381. Epub 2013 Mar 4. Mov Disord. 2013. PMID: 23460578

4

The COMT val158met polymorphism and brain morphometry in healthy young adults.

Zinkstok J, Schmitz N, van Amelsvoort T, de Win M, van den Brink W, Baas F, Linszen D. Zinkstok J, et al. Among authors: baas f. Neurosci Lett. 2006 Sep 11;405(1-2):34-9. doi: 10.1016/j.neulet.2006.06.034. Epub 2006 Jul 18. Neurosci Lett. 2006. PMID: 16857316

5

Serotonin transporter gene promoter polymorphisms modify the association between paroxetine serotonin transporter occupancy and clinical response in major depressive disorder.

Ruhé HG, Ooteman W, Booij J, Michel MC, Moeton M, Baas F, Schene AH. Ruhé HG, et al. Among authors: baas f. Pharmacogenet Genomics. 2009 Jan;19(1):67-76. doi: 10.1097/FPC.0b013e32831a6a3a. Pharmacogenet Genomics. 2009. PMID: 18987562

6

Polymorphisms in the catechol-o-methyltransferase gene and delirium in the elderly.

van Munster BC, Baas F, Tanck MW, de Rooij SE. van Munster BC, et al. Among authors: baas f. Dement Geriatr Cogn Disord. 2011;31(5):358-62. doi: 10.1159/000327353. Epub 2011 May 25. Dement Geriatr Cogn Disord. 2011. PMID: 21613790

7

Striatal D₂ receptor binding in 22q11 deletion syndrome: an [¹²³I]IBZM SPECT study.

Boot E, Booij J, Zinkstok JR, de Haan L, Linszen DH, Baas F, van Amelsvoort TA. Boot E, et al. Among authors: baas f. J Psychopharmacol. 2010 Oct;24(10):1525-31. doi: 10.1177/0269881109104854. Epub 2009 Apr 30. J Psychopharmacol. 2010. PMID: 19406852

8

Disrupted dopaminergic neurotransmission in 22q11 deletion syndrome.

Boot E, Booij J, Zinkstok J, Abeling N, de Haan L, Baas F, Linszen D, van Amelsvoort T. Boot E, et al. Among authors: baas f. Neuropsychopharmacology. 2008 May;33(6):1252-8. doi: 10.1038/sj.npp.1301508. Epub 2007 Jul 25. Neuropsychopharmacology. 2008. PMID: 17653112

9

COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome.

Boot E, Booij J, Zinkstok JR, Baas F, Swillen A, Owen MJ, Murphy DG, Murphy KC, Linszen DH, Van Amelsvoort TA. Boot E, et al. Among authors: baas f. Synapse. 2011 Sep;65(9):967-70. doi: 10.1002/syn.20932. Epub 2011 Apr 26. Synapse. 2011. PMID: 21465565

10

Association between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblings.

Zinkstok JR, de Wilde O, van Amelsvoort TA, Tanck MW, Baas F, Linszen DH. Zinkstok JR, et al. Among authors: baas f. Behav Brain Funct. 2007 Apr 20;3:19. doi: 10.1186/1744-9081-3-19. Behav Brain Funct. 2007. PMID: 17445278 Free PMC article.

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