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Items: 1 to 20 of 159

1.

Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk.

Demontis D, Nyegaard M, Buttenschøn HN, Hedemand A, Pedersen CB, Grove J, Flint TJ, Nordentoft M, Werge T, Hougaard DM, Sørensen KM, Yolken RH, Mors O, Børglum AD, Mortensen PB.

Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(8):913-22. doi: 10.1002/ajmg.b.31234. Epub 2011 Sep 14.

PMID:
21919190
2.

Significant association between the genetic variations in the 5' end of the N-methyl-D-aspartate receptor subunit gene GRIN1 and schizophrenia.

Zhao X, Li H, Shi Y, Tang R, Chen W, Liu J, Feng G, Shi J, Yan L, Liu H, He L.

Biol Psychiatry. 2006 Apr 15;59(8):747-53. Epub 2006 Feb 14.

PMID:
16476413
3.
4.

Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia.

Tarabeux J, Kebir O, Gauthier J, Hamdan FF, Xiong L, Piton A, Spiegelman D, Henrion É, Millet B; S2D team, Fathalli F, Joober R, Rapoport JL, DeLisi LE, Fombonne É, Mottron L, Forget-Dubois N, Boivin M, Michaud JL, Drapeau P, Lafrenière RG, Rouleau GA, Krebs MO.

Transl Psychiatry. 2011 Nov 15;1:e55. doi: 10.1038/tp.2011.52.

5.

Association analysis of GRIN1 and GRIN2B polymorphisms and Parkinson's disease in a hospital-based case-control study.

Wu SL, Wang WF, Shyu HY, Ho YJ, Shieh JC, Fu YP, Wu ST, Cheng CW.

Neurosci Lett. 2010 Jul 5;478(2):61-5. doi: 10.1016/j.neulet.2010.04.063. Epub 2010 May 10.

PMID:
20438806
6.

Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: a case-control study.

Di Maria E, Gulli R, Begni S, De Luca A, Bignotti S, Pasini A, Bellone E, Pizzuti A, Dallapiccola B, Novelli G, Ajmar F, Gennarelli M, Mandich P.

Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):27-9.

PMID:
15211626
7.

Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample.

Georgi A, Jamra RA, Klein K, Villela AW, Schumacher J, Becker T, Paul T, Schmael C, Höfels S, Klopp N, Illig T, Propping P, Cichon S, Nöthen MM, Schulze TG, Rietschel M.

Psychiatr Genet. 2007 Oct;17(5):308-10.

PMID:
17728671
8.
9.

Genetic variants of the NMDA receptor influence cortical excitability and plasticity in humans.

Mori F, Ribolsi M, Kusayanagi H, Siracusano A, Mantovani V, Marasco E, Bernardi G, Centonze D.

J Neurophysiol. 2011 Oct;106(4):1637-43. doi: 10.1152/jn.00318.2011. Epub 2011 Jul 13.

10.

Schizophrenia susceptibility and NMDA-receptor mediated signalling: an association study involving 32 tagSNPs of DAO, DAOA, PPP3CC, and DTNBP1 genes.

Sacchetti E, Scassellati C, Minelli A, Valsecchi P, Bonvicini C, Pasqualetti P, Galluzzo A, Pioli R, Gennarelli M.

BMC Med Genet. 2013 Mar 9;14:33. doi: 10.1186/1471-2350-14-33.

11.

A microsatellite repeat in the promoter of the N-methyl-D-aspartate receptor 2A subunit (GRIN2A) gene suppresses transcriptional activity and correlates with chronic outcome in schizophrenia.

Itokawa M, Yamada K, Yoshitsugu K, Toyota T, Suga T, Ohba H, Watanabe A, Hattori E, Shimizu H, Kumakura T, Ebihara M, Meerabux JM, Toru M, Yoshikawa T.

Pharmacogenetics. 2003 May;13(5):271-8.

PMID:
12724619
12.

N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) in schizophrenia: TDT and case-control analyses.

Martucci L, Wong AH, Trakalo J, Cate-Carter T, Wong GW, Macciardi FM, Kennedy JL.

Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):24-7.

PMID:
12707933
13.

Analysis of correlation between serum D-serine levels and functional promoter polymorphisms of GRIN2A and GRIN2B genes.

Iwayama Y, Hashimoto K, Nakajima M, Toyota T, Yamada K, Shimizu E, Itokawa M, Hoshika A, Iyo M, Yoshikawa T.

Neurosci Lett. 2006 Feb 13;394(2):101-4. Epub 2005 Nov 2.

PMID:
16266783
14.

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.

15.

No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample.

Georgi A, Jamra RA, Schumacher J, Becker T, Schmael C, Deschner M, Höfels S, Wulff M, Schwarz M, Klopp N, Illig T, Propping P, Cichon S, Nöthen MM, Rietschel M, Schulze TG.

Psychiatr Genet. 2006 Oct;16(5):183-4.

PMID:
16969270
16.
17.

Psychosis and relapse in bipolar disorder are related to GRM3, DAOA, and GRIN2B genotype.

Dalvie S, Horn N, Nossek C, van der Merwe L, Stein DJ, Ramesar R.

Afr J Psychiatry (Johannesbg). 2010 Sep;13(4):297-301.

PMID:
20957330
18.

Mutation analysis of the NMDAR2B (GRIN2B) gene in schizophrenia.

Ohtsuki T, Sakurai K, Dou H, Toru M, Yamakawa-Kobayashi K, Arinami T.

Mol Psychiatry. 2001 Mar;6(2):211-6.

19.

Association analysis of ANK3 gene variants in nordic bipolar disorder and schizophrenia case-control samples.

Tesli M, Koefoed P, Athanasiu L, Mattingsdal M, Gustafsson O, Agartz I, Rimol LM, Brown A, Wirgenes KV, Smorr LL, Kähler AK, Werge T, Mors O, Mellerup E, Jönsson EG, Melle I, Morken G, Djurovic S, Andreassen OA.

Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(8):969-74. doi: 10.1002/ajmg.b.31244. Epub 2011 Oct 3.

PMID:
21972176
20.

Association between the G1001C polymorphism in the GRIN1 gene promoter region and schizophrenia.

Begni S, Moraschi S, Bignotti S, Fumagalli F, Rillosi L, Perez J, Gennarelli M.

Biol Psychiatry. 2003 Apr 1;53(7):617-9.

PMID:
12679240

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