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Items: 1 to 20 of 28

1.

Lack of association between COMT Val158Met and ZDHHC8 rs175174 polymorphisms and susceptibility to schizophrenia in a Brazilian population.

Moraes LS, Santos ACC, Ferreira-Fernandes H, Yoshioka FKN, Teixeira SS, Guimarães AC, da Rocha CAM, Rey JA, Pinto GR, Burbano RR.

Psychiatr Genet. 2017 Oct;27(5):197-198. doi: 10.1097/YPG.0000000000000179. No abstract available.

PMID:
28562378
2.

Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome.

Thompson CA, Karelis J, Middleton FA, Gentile K, Coman IL, Radoeva PD, Mehta R, Fremont WP, Antshel KM, Faraone SV, Kates WR.

Am J Med Genet B Neuropsychiatr Genet. 2017 Apr;174(3):295-314. doi: 10.1002/ajmg.b.32515. Epub 2017 Jan 31.

PMID:
28139055
3.

Linkage and Association Analyses of Schizophrenia with Genetic Variations on Chromosome 22q11 in Koreans.

Yoon SC, Jang YL, Kim JW, Cho EY, Park DY, Hong KS, Lee YS.

Psychiatry Investig. 2016 Nov;13(6):630-636. Epub 2016 Nov 24.

4.

Palmitoylation of cdc42 Promotes Spine Stabilization and Rescues Spine Density Deficit in a Mouse Model of 22q11.2 Deletion Syndrome.

Moutin E, Nikonenko I, Stefanelli T, Wirth A, Ponimaskin E, De Roo M, Muller D.

Cereb Cortex. 2017 Jul 1;27(7):3618-3629. doi: 10.1093/cercor/bhw183.

PMID:
27365300
5.

Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome.

Napoli E, Tassone F, Wong S, Angkustsiri K, Simon TJ, Song G, Giulivi C.

J Biol Chem. 2015 Sep 18;290(38):23240-53. doi: 10.1074/jbc.M115.672360. Epub 2015 Jul 28.

6.

Molecular substrates of altered axonal growth and brain connectivity in a mouse model of schizophrenia.

Mukai J, Tamura M, Fénelon K, Rosen AM, Spellman TJ, Kang R, MacDermott AB, Karayiorgou M, Gordon JA, Gogos JA.

Neuron. 2015 May 6;86(3):680-95. doi: 10.1016/j.neuron.2015.04.003. Epub 2015 Apr 23.

7.

Association between variants of zinc finger genes and psychiatric disorders: systematic review and meta-analysis.

Sun Y, Hu D, Liang J, Bao YP, Meng SQ, Lu L, Shi J.

Schizophr Res. 2015 Mar;162(1-3):124-37. doi: 10.1016/j.schres.2015.01.036. Epub 2015 Feb 7. Review.

PMID:
25667193
8.

ZDHHC8 gene may play a role in cortical volumes of patients with schizophrenia.

Ota VK, Gadelha A, Assunção IB, Santoro ML, Christofolini DM, Bellucco FT, Santos-Filho AF, Ottoni GL, Lara DR, Mari JJ, Melaragno MI, Smith MA, Bressan RA, Belangero SI, Jackowski AP.

Schizophr Res. 2013 Apr;145(1-3):33-5. doi: 10.1016/j.schres.2013.01.011. Epub 2013 Feb 8.

PMID:
23403413
9.

Putting proteins in their place: palmitoylation in Huntington disease and other neuropsychiatric diseases.

Young FB, Butland SL, Sanders SS, Sutton LM, Hayden MR.

Prog Neurobiol. 2012 May;97(2):220-38. doi: 10.1016/j.pneurobio.2011.11.002. Epub 2011 Dec 7. Review.

PMID:
22155432
10.

Testing for genetic association between the ZDHHC8 gene locus and susceptibility to schizophrenia: An integrated analysis of multiple datasets.

Xu M, St Clair D, He L.

Am J Med Genet B Neuropsychiatr Genet. 2010 Oct 5;153B(7):1266-75. doi: 10.1002/ajmg.b.31096.

PMID:
20661937
11.

Association of ZDHHC8 polymorphisms with smooth pursuit eye movement abnormality.

Shin HD, Park BL, Bae JS, Park TJ, Chun JY, Park CS, Sohn JW, Kim BJ, Kang YH, Kim JW, Kim KH, Shin TM, Woo SI.

Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1167-72. doi: 10.1002/ajmg.b.31083.

PMID:
20468065
12.

Schizophrenia pathophysiology: are we any closer to a complete model?

Lakhan SE, Vieira KF.

Ann Gen Psychiatry. 2009 May 15;8:12. doi: 10.1186/1744-859X-8-12.

13.

Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion.

Mukai J, Dhilla A, Drew LJ, Stark KL, Cao L, MacDermott AB, Karayiorgou M, Gogos JA.

Nat Neurosci. 2008 Nov;11(11):1302-10. doi: 10.1038/nn.2204. Epub 2008 Oct 5.

14.

Gene expression in the etiology of schizophrenia.

Bray NJ.

Schizophr Bull. 2008 May;34(3):412-8. doi: 10.1093/schbul/sbn013. Epub 2008 Mar 11. Review.

15.

HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention.

Liu YL, Fann CS, Liu CM, Chang CC, Yang WC, Wu JY, Hung SI, Chan HY, Chen JJ, Hsieh MH, Hwang TJ, Faraone SV, Tsuang MT, Chen WJ, Hwu HG.

Psychiatr Genet. 2007 Dec;17(6):333-8.

PMID:
18075473
16.

Molecular mechanisms of schizophrenia.

Lang UE, Puls I, Muller DJ, Strutz-Seebohm N, Gallinat J.

Cell Physiol Biochem. 2007;20(6):687-702. Review.

17.

ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophrenia.

Demily C, Legallic S, Bou J, Houy-Durand E, Van Amelsvoort T, Zinkstok J, Manouvrier-Hanue S, Vogels A, Drouin-Garraud V, Philip N, Philippe A, Héron D, Sarda P, Petit M, Thibaut F, Frébourg T, Campion D.

Psychiatr Genet. 2007 Oct;17(5):311-2. No abstract available.

PMID:
17728672
18.

Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility.

Glaser B, Moskvina V, Kirov G, Murphy KC, Williams H, Williams N, Owen MJ, O'Donovan MC.

Schizophr Res. 2006 Oct;87(1-3):21-7. Epub 2006 Jul 21.

PMID:
16860541
19.

Nonlinear tests for genomewide association studies.

Zhao J, Jin L, Xiong M.

Genetics. 2006 Nov;174(3):1529-38. Epub 2006 Jul 2.

20.

Molecular genetic studies of schizophrenia.

Riley B, Kendler KS.

Eur J Hum Genet. 2006 Jun;14(6):669-80. Review.

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