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Items: 1 to 20 of 62

1.

Weighted Burden Analysis of Exome-Sequenced Case-Control Sample Implicates Synaptic Genes in Schizophrenia Aetiology.

Curtis D, Coelewij L, Liu SH, Humphrey J, Mott R.

Behav Genet. 2018 May;48(3):198-208. doi: 10.1007/s10519-018-9893-3. Epub 2018 Mar 21.

3.

[A role of interactions between N-methyl-D-aspartate and dopamine receptors in facial emotion recognition impairment in schizophrenia].

Alfimova MV, Golimbet VE, Korovaitseva GI, Lezheiko TV, Tikhonov DV, Ganisheva TK, Berezin NB, Snegireva AA, Shemiakina TK.

Zh Nevrol Psikhiatr Im S S Korsakova. 2017;117(6):47-52. doi: 10.17116/jnevro20171176147-52. Russian.

PMID:
28745671
4.

Epigenetic mechanisms underlying NMDA receptor hypofunction in the prefrontal cortex of juvenile animals in the MAM model for schizophrenia.

Gulchina Y, Xu SJ, Snyder MA, Elefant F, Gao WJ.

J Neurochem. 2017 Nov;143(3):320-333. doi: 10.1111/jnc.14101. Epub 2017 Sep 5.

PMID:
28628228
5.

Chromosome 12p Deletion Spanning the GRIN2B Gene Presenting With a Neurodevelopmental Phenotype: A Case Report and Review of Literature.

Mishra N, Kouzmitcheva E, Orsino A, Minassian BA.

Child Neurol Open. 2016 Apr 4;3:2329048X16629980. doi: 10.1177/2329048X16629980. eCollection 2016 Jan-Dec.

6.

Pharmacogenetics of Ketamine-Induced Emergence Phenomena: A Pilot Study.

Aroke EN, Crawford SL, Dungan JR.

Nurs Res. 2017 Mar/Apr;66(2):105-114. doi: 10.1097/NNR.0000000000000197.

7.

Human GRIN2B variants in neurodevelopmental disorders.

Hu C, Chen W, Myers SJ, Yuan H, Traynelis SF.

J Pharmacol Sci. 2016 Oct;132(2):115-121. doi: 10.1016/j.jphs.2016.10.002. Epub 2016 Oct 19. Review.

8.

Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders.

Wolfe K, Strydom A, Morrogh D, Carter J, Cutajar P, Eyeoyibo M, Hassiotis A, McCarthy J, Mukherjee R, Paschos D, Perumal N, Read S, Shankar R, Sharif S, Thirulokachandran S, Thygesen JH, Patch C, Ogilvie C, Flinter F, McQuillin A, Bass N.

Eur J Hum Genet. 2016 Jan;25(1):66-72. doi: 10.1038/ejhg.2016.107. Epub 2016 Sep 21.

9.

Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population.

Takasaki Y, Koide T, Wang C, Kimura H, Xing J, Kushima I, Ishizuka K, Mori D, Sekiguchi M, Ikeda M, Aizawa M, Tsurumaru N, Iwayama Y, Yoshimi A, Arioka Y, Yoshida M, Noma H, Oya-Ito T, Nakamura Y, Kunimoto S, Aleksic B, Uno Y, Okada T, Ujike H, Egawa J, Kuwabara H, Someya T, Yoshikawa T, Iwata N, Ozaki N.

Sci Rep. 2016 Sep 12;6:33311. doi: 10.1038/srep33311.

10.

A study of single nucleotide polymorphisms of GRIN2B in schizophrenia from Chinese Han population.

Guo Z, Niu W, Bi Y, Zhang R, Ren D, Hu J, Huang X, Wu X, Cao Y, Yang F, Wang L, Li W, Li X, Xu Y, He L, Yu T, He G.

Neurosci Lett. 2016 Sep 6;630:132-135. doi: 10.1016/j.neulet.2016.07.038. Epub 2016 Jul 21.

PMID:
27453061
11.

[Polymorphism C366G of gene GRIN2B and verbal episodic memory: No association with schizophrenia].

Alfimova MV, Golimbet VE, Korovaitseva GI, Lezheiko TV, Abramova LI, Kaleda VG.

Genetika. 2016 Jun;52(6):713-7. Russian.

PMID:
29368832
12.

[The association between the GRIN2B gene and verbal fluency and impairment of abstract thinking in schizophrenia].

Alfimova MV, Golimbet VE, Korovaitseva GI, Abramova LI, Lezheiko TV, Aksenova EV.

Zh Nevrol Psikhiatr Im S S Korsakova. 2016;116(4):42-46. doi: 10.17116/jnevro20161164142-46. Russian.

PMID:
27240047
13.

Receptor Tyrosine Kinase MET Interactome and Neurodevelopmental Disorder Partners at the Developing Synapse.

Xie Z, Li J, Baker J, Eagleson KL, Coba MP, Levitt P.

Biol Psychiatry. 2016 Dec 15;80(12):933-942. doi: 10.1016/j.biopsych.2016.02.022. Epub 2016 Feb 26.

14.

Genetic association analysis of N-methyl-D-aspartate receptor subunit gene GRIN2B and clinical response to clozapine.

Taylor DL, Tiwari AK, Lieberman JA, Potkin SG, Meltzer HY, Knight J, Remington G, Müller DJ, Kennedy JL.

Hum Psychopharmacol. 2016 Mar;31(2):121-34. doi: 10.1002/hup.2519. Epub 2016 Feb 15.

PMID:
26876050
15.

Genetic assessment of additional endophenotypes from the Consortium on the Genetics of Schizophrenia Family Study.

Greenwood TA, Lazzeroni LC, Calkins ME, Freedman R, Green MF, Gur RE, Gur RC, Light GA, Nuechterlein KH, Olincy A, Radant AD, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Sugar CA, Swerdlow NR, Tsuang DW, Tsuang MT, Turetsky BI, Braff DL.

Schizophr Res. 2016 Jan;170(1):30-40. doi: 10.1016/j.schres.2015.11.008. Epub 2015 Nov 18. Review.

16.

Polymorphisms in MicroRNA Genes And Genes Involving in NMDAR Signaling and Schizophrenia: A Case-Control Study in Chinese Han Population.

Zhang Y, Fan M, Wang Q, He G, Fu Y, Li H, Yu S.

Sci Rep. 2015 Aug 10;5:12984. doi: 10.1038/srep12984.

17.

Association Study of N-Methyl-D-Aspartate Receptor Subunit 2B (GRIN2B) Polymorphisms and Schizophrenia Symptoms in the Han Chinese Population.

Yang Y, Li W, Zhang H, Yang G, Wang X, Ding M, Jiang T, Lv L.

PLoS One. 2015 May 28;10(5):e0125925. doi: 10.1371/journal.pone.0125925. eCollection 2015.

18.

Changes in cortical N-methyl-D-aspartate receptors and post-synaptic density protein 95 in schizophrenia, mood disorders and suicide.

Dean B, Gibbons AS, Boer S, Uezato A, Meador-Woodruff J, Scarr E, McCullumsmith RE.

Aust N Z J Psychiatry. 2016 Mar;50(3):275-83. doi: 10.1177/0004867415586601. Epub 2015 May 26.

PMID:
26013316
19.

LPA signaling initiates schizophrenia-like brain and behavioral changes in a mouse model of prenatal brain hemorrhage.

Mirendil H, Thomas EA, De Loera C, Okada K, Inomata Y, Chun J.

Transl Psychiatry. 2015 Apr 7;5:e541. doi: 10.1038/tp.2015.33.

20.

Conserved higher-order chromatin regulates NMDA receptor gene expression and cognition.

Bharadwaj R, Peter CJ, Jiang Y, Roussos P, Vogel-Ciernia A, Shen EY, Mitchell AC, Mao W, Whittle C, Dincer A, Jakovcevski M, Pothula V, Rasmussen TP, Giakoumaki SG, Bitsios P, Sherif A, Gardner PD, Ernst P, Ghose S, Sklar P, Haroutunian V, Tamminga C, Myers RH, Futai K, Wood MA, Akbarian S.

Neuron. 2014 Dec 3;84(5):997-1008. doi: 10.1016/j.neuron.2014.10.032. Epub 2014 Nov 13.

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