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Items: 1 to 20 of 637

1.

Association between function and structure of the triple network and catechol-O-methyltransferase val158met polymorphism in the first episode schizophrenia.

Kang Y, Huang K, Cai S, Wang H, Liu J, Wang Y, Lv Y, Zhang W, Wang Q, Huang L, Wang J, Tian J.

Neurosci Lett. 2018 Sep 18. pii: S0304-3940(18)30639-6. doi: 10.1016/j.neulet.2018.09.033. [Epub ahead of print]

PMID:
30240822
2.

Catechol-O-methyltransferase (COMT) genotypes are associated with varying soluble, but not membrane-bound COMT protein in the human prefrontal cortex.

Parkin GM, Udawela M, Gibbons A, Scarr E, Dean B.

J Hum Genet. 2018 Sep 14. doi: 10.1038/s10038-018-0511-2. [Epub ahead of print]

PMID:
30218069
3.

Association between COMT gene rs165599 SNP and schizophrenia: A meta-analysis of case-control studies.

Gozukara Bag HG.

Mol Genet Genomic Med. 2018 Aug 30. doi: 10.1002/mgg3.468. [Epub ahead of print]

4.

Interrogating the Relationship Between Schizotypy, the Catechol-O-Methyltransferase (COMT) Val158Met Polymorphism, and Neuronal Oscillatory Activity.

Steiner GZ, Fernandez FM, Coles M, Karamacoska D, Barkus E, Broyd SJ, Solowij N, Watson OT, Chiu CL, Lind JM, Barry RJ.

Cereb Cortex. 2018 Jul 31. doi: 10.1093/cercor/bhy171. [Epub ahead of print]

PMID:
30084963
5.

Haplotypic and Genotypic Association of Catechol-O-Methyltransferase rs4680 and rs4818 Polymorphisms and Treatment Resistance in Schizophrenia.

Sagud M, Tudor L, Uzun S, Perkovic MN, Zivkovic M, Konjevod M, Kozumplik O, Vuksan Cusa B, Svob Strac D, Rados I, Mimica N, Mihaljevic Peles A, Nedic Erjavec G, Pivac N.

Front Pharmacol. 2018 Jul 3;9:705. doi: 10.3389/fphar.2018.00705. eCollection 2018.

6.

Genetic and clinical features of social cognition in 22q11.2 deletion syndrome.

Lattanzi GM, Buzzanca A, Frascarelli M, Di Fabio F.

J Neurosci Res. 2018 Oct;96(10):1631-1640. doi: 10.1002/jnr.24265. Epub 2018 Jul 13. Review.

PMID:
30004142
7.

COMT Val 108/158 Met polymorphism and treatment response to aripiprazole in patients with acute schizophrenia.

Kaneko H, Miura I, Kanno-Nozaki K, Horikoshi S, Hino M, Yabe H.

Neuropsychiatr Dis Treat. 2018 Jun 22;14:1657-1663. doi: 10.2147/NDT.S164647. eCollection 2018.

8.

Association between catechol-O-methyltransferase genetic variation and functional connectivity in patients with first-episode schizophrenia.

Wang H, Zhang B, Zeng B, Tang Y, Zhang T, Zhao S, Li C, Wang J, Goff DC.

Schizophr Res. 2018 Sep;199:214-220. doi: 10.1016/j.schres.2018.04.023. Epub 2018 May 3.

PMID:
29730044
9.

Brain, blood, cerebrospinal fluid, and serum biomarkers in schizophrenia.

Mohammadi A, Rashidi E, Amooeian VG.

Psychiatry Res. 2018 Jul;265:25-38. doi: 10.1016/j.psychres.2018.04.036. Epub 2018 Apr 13. Review.

PMID:
29680514
10.

Interaction between childhood adversity and functional polymorphisms in the dopamine pathway on first-episode psychosis.

Trotta A, Iyegbe C, Yiend J, Dazzan P, David AS, Pariante C, Mondelli V, Colizzi M, Murray RM, Di Forti M, Fisher HL.

Schizophr Res. 2018 Apr 10. pii: S0920-9964(18)30199-3. doi: 10.1016/j.schres.2018.04.010. [Epub ahead of print]

PMID:
29653893
11.

Association between COMT gene polymorphisms, clinical symptoms, and cognitive functions in Han Chinese patients with schizophrenia.

Sun Z, Zhang Z, Mao P, Ma Y, Li W, Li J, Yang X, Ling S, Tang Y.

Psychiatr Genet. 2018 Jun;28(3):47-54. doi: 10.1097/YPG.0000000000000194.

PMID:
29634613
12.

Genetic Polymorphisms Associated With Constipation and Anticholinergic Symptoms in Patients Receiving Clozapine.

Solismaa A, Kampman O, Lyytikäinen LP, Seppälä N, Viikki M, Mononen N, Lehtimäki T, Leinonen E.

J Clin Psychopharmacol. 2018 Jun;38(3):193-199. doi: 10.1097/JCP.0000000000000885.

PMID:
29620694
13.

Maternal deprivation induces alterations in cognitive and cortical function in adulthood.

Janetsian-Fritz SS, Timme NM, Timm MM, McCane AM, Baucum Ii AJ, O'Donnell BF, Lapish CC.

Transl Psychiatry. 2018 Mar 27;8(1):71. doi: 10.1038/s41398-018-0119-5. Erratum in: Transl Psychiatry. 2018 Jul 31;8(1):137.

14.

Gene polymorphisms and response to transcranial direct current stimulation for auditory verbal hallucinations in schizophrenia.

Chhabra H, Shivakumar V, Subbanna M, Kalmady SV, Bose A, Agarwal SM, Sreeraj VS, Dinakaran D, Narayanaswamy JC, Debnath M, Venkatasubramanian G.

Acta Neuropsychiatr. 2018 Aug;30(4):218-225. doi: 10.1017/neu.2018.4. Epub 2018 Mar 21.

PMID:
29559020
16.

Analysis of COMT Val158Met polymorphisms and methylation in Chinese male schizophrenia patients with homicidal behavior.

Hu Y, Li C, Wang Y, Li Q, Liu Y, Liao S, Cao P, Xu H.

Int J Legal Med. 2018 Feb 17. doi: 10.1007/s00414-018-1773-0. [Epub ahead of print]

PMID:
29455339
17.

COMT and GAD1 gene polymorphisms are associated with impaired antisaccade task performance in schizophrenic patients.

Kirenskaya AV, Storozheva ZI, Gruden MA, Sewell RDE.

Eur Arch Psychiatry Clin Neurosci. 2018 Sep;268(6):571-584. doi: 10.1007/s00406-018-0881-7. Epub 2018 Feb 10.

18.

The Influence of DAT1, COMT, and BDNF Genetic Polymorphisms on Total and Subregional Hippocampal Volumes in Early Onset Heavy Cannabis Users.

Batalla A, Lorenzetti V, Chye Y, Yücel M, Soriano-Mas C, Bhattacharyya S, Torrens M, Crippa JAS, Martín-Santos R.

Cannabis Cannabinoid Res. 2018 Feb 1;3(1):1-10. doi: 10.1089/can.2017.0021. eCollection 2018.

19.

Fast sleep spindle density is associated with rs4680 (Val108/158Met) genotype of catechol-O-methyltransferase (COMT).

Schilling C, Gappa L, Schredl M, Streit F, Treutlein J, Frank J, Deuschle M, Meyer-Lindenberg A, Rietschel M, Witt SH.

Sleep. 2018 Mar 1;41(3). doi: 10.1093/sleep/zsy007.

PMID:
29325115
20.

Meta-analysis on the association between genetic polymorphisms and prepulse inhibition of the acoustic startle response.

Quednow BB, Ejebe K, Wagner M, Giakoumaki SG, Bitsios P, Kumari V, Roussos P.

Schizophr Res. 2018 Aug;198:52-59. doi: 10.1016/j.schres.2017.12.011. Epub 2017 Dec 26.

PMID:
29287625

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