Similar articles for PMID: 19617637

Year	Number of Results
1992	1
2001	1
2003	1
2004	6
2005	10
2006	4
2007	8
2008	9
2009	9
2010	3
2011	4
2012	4
2013	1
2014	5
2015	4
2016	6
2017	8
2018	6
2019	6
2020	3
2021	2
2022	1
2024	0

1

Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice.

Suzuki G, Harper KM, Hiramoto T, Funke B, Lee M, Kang G, Buell M, Geyer MA, Kucherlapati R, Morrow B, Männistö PT, Agatsuma S, Hiroi N. Suzuki G, et al. Hum Mol Genet. 2009 Oct 15;18(20):3914-25. doi: 10.1093/hmg/ddp334. Epub 2009 Jul 19. Hum Mol Genet. 2009. PMID: 19617637 Free PMC article.

2

Human COMT over-expression confers a heightened susceptibility to dyskinesia in mice.

Solís O, García-Montes JR, Garcia-Sanz P, Herranz AS, Asensio MJ, Kang G, Hiroi N, Moratalla R. Solís O, et al. Neurobiol Dis. 2017 Jun;102:133-139. doi: 10.1016/j.nbd.2017.03.006. Epub 2017 Mar 16. Neurobiol Dis. 2017. PMID: 28315782 Free PMC article.

3

Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.

Sanders AR, Rusu I, Duan J, Vander Molen JE, Hou C, Schwab SG, Wildenauer DB, Martinez M, Gejman PV. Sanders AR, et al. Mol Psychiatry. 2005 Apr;10(4):353-65. doi: 10.1038/sj.mp.4001586. Mol Psychiatry. 2005. PMID: 15340358 Clinical Trial.

4

Copy number elevation of 22q11.2 genes arrests the developmental maturation of working memory capacity and adult hippocampal neurogenesis.

Boku S, Izumi T, Abe S, Takahashi T, Nishi A, Nomaru H, Naka Y, Kang G, Nagashima M, Hishimoto A, Enomoto S, Duran-Torres G, Tanigaki K, Zhang J, Ye K, Kato S, Männistö PT, Kobayashi K, Hiroi N. Boku S, et al. Mol Psychiatry. 2018 Apr;23(4):985-992. doi: 10.1038/mp.2017.158. Epub 2017 Aug 22. Mol Psychiatry. 2018. PMID: 28827761 Free PMC article.

5

Mutation analysis of ARVCF gene on chromosome 22q11 as a candidate for a schizophrenia gene.

Chen HY, Yeh JI, Hong CJ, Chen CH. Chen HY, et al. Schizophr Res. 2005 Jan 1;72(2-3):275-7. doi: 10.1016/j.schres.2004.03.004. Schizophr Res. 2005. PMID: 15560973 No abstract available.

6

ARVCF depletion cooperates with Tbx1 deficiency in the development of 22q11.2DS-like phenotypes in Xenopus.

Tran HT, Delvaeye M, Verschuere V, Descamps E, Crabbe E, Van Hoorebeke L, McCrea P, Adriaens D, Van Roy F, Vleminckx K. Tran HT, et al. Dev Dyn. 2011 Dec;240(12):2680-7. doi: 10.1002/dvdy.22765. Epub 2011 Oct 25. Dev Dyn. 2011. PMID: 22028109 Free article.

7

ARVCF single marker and haplotypic association with schizophrenia.

Mas S, Bernardo M, Parellada E, Garcia-Rizo C, Gassó P, Alvarez S, Lafuente A. Mas S, et al. Prog Neuropsychopharmacol Biol Psychiatry. 2009 Aug 31;33(6):1064-9. doi: 10.1016/j.pnpbp.2009.06.001. Epub 2009 Jun 7. Prog Neuropsychopharmacol Biol Psychiatry. 2009. PMID: 19508883

8

Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome.

Jurata LW, Gallagher P, Lemire AL, Charles V, Brockman JA, Illingworth EL, Altar CA. Jurata LW, et al. Schizophr Res. 2006 Dec;88(1-3):251-9. doi: 10.1016/j.schres.2006.07.017. Epub 2006 Sep 26. Schizophr Res. 2006. PMID: 17008057

9

Haplotype analysis of the COMT-ARVCF gene region in Israeli anorexia nervosa family trios.

Michaelovsky E, Frisch A, Leor S, Stein D, Danziger Y, Carel C, Fennig S, Mimouni M, Klauck SM, Benner A, Poustka A, Apter A, Weizman A. Michaelovsky E, et al. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):45-50. doi: 10.1002/ajmg.b.30230. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16118784

10

Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model.

Hiramoto T, Kang G, Suzuki G, Satoh Y, Kucherlapati R, Watanabe Y, Hiroi N. Hiramoto T, et al. Hum Mol Genet. 2011 Dec 15;20(24):4775-85. doi: 10.1093/hmg/ddr404. Epub 2011 Sep 9. Hum Mol Genet. 2011. PMID: 21908517 Free PMC article.

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