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Items: 1 to 20 of 70

1.

Absence of de novo point mutations in exons of GRIN2B in a large schizophrenia trio sample.

Williams HJ, Georgieva L, Dwyer S, Kirov G, Owen MJ, O'Donovan MC.

Schizophr Res. 2012 Nov;141(2-3):274-6. doi: 10.1016/j.schres.2012.08.024. Epub 2012 Sep 15. No abstract available.

PMID:
22986046
2.

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.

3.

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.

4.

Systematic screening for mutations in the human N-methyl-D-aspartate receptor 1 gene in schizophrenic patients from the German population.

Paus S, Rietschel M, Schulze TG, Ohlraun S, Diaconu CC, Van Den Bogaert A, Maier W, Propping P, Cichon S, Nöthen MM.

Psychiatr Genet. 2004 Dec;14(4):233-4.

PMID:
15564900
5.
6.

N-methyl-D-aspartate receptor NR2B subunit gene GRIN2B in schizophrenia and bipolar disorder: Polymorphisms and mRNA levels.

Martucci L, Wong AH, De Luca V, Likhodi O, Wong GW, King N, Kennedy JL.

Schizophr Res. 2006 Jun;84(2-3):214-21. Epub 2006 Mar 20.

PMID:
16549338
7.
8.

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.

9.
10.

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
11.

Molecular genetics of schizophrenia: a critical review.

Berry N, Jobanputra V, Pal H.

J Psychiatry Neurosci. 2003 Nov;28(6):415-29. Review.

12.

Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex families.

Timms AE, Dorschner MO, Wechsler J, Choi KY, Kirkwood R, Girirajan S, Baker C, Eichler EE, Korvatska O, Roche KW, Horwitz MS, Tsuang DW.

JAMA Psychiatry. 2013 Jun;70(6):582-90. doi: 10.1001/jamapsychiatry.2013.1195.

PMID:
23553203
13.

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
14.

Exomic sequencing of the ionotropic glutamate receptor N-methyl-D-aspartate 3A gene (GRIN3A) reveals no association with schizophrenia.

Shen YC, Liao DL, Chen JY, Wang YC, Lai IC, Liou YJ, Chen YJ, Luu SU, Chen CH.

Schizophr Res. 2009 Oct;114(1-3):25-32. doi: 10.1016/j.schres.2009.07.005. Epub 2009 Aug 7.

PMID:
19665356
15.
16.

Association analysis of polymorphisms in the N-methyl-D-aspartate (NMDA) receptor subunit 2B (GRIN2B) gene and tardive dyskinesia in schizophrenia.

Liou YJ, Wang YC, Chen JY, Bai YM, Lin CC, Liao DL, Chen TT, Chen ML, Mo GH, Lai IC.

Psychiatry Res. 2007 Dec 3;153(3):271-5. Epub 2007 Jul 31.

PMID:
17669510
17.

Association study of N-methyl-D-aspartate glutamate receptor subunit genes and childhood-onset mood disorders.

Dorval KM, Burcescu I, Adams J, Wigg KG, King N, Kiss E, Kapornai K, Gádoros J, Tamás Z, Daróczi G, Baji I, Mayer L, Kennedy JL, Vetró A, Kovacs M, Barr CL.

Psychiatr Genet. 2009 Jun;19(3):156-7. doi: 10.1097/YPG.0b013e32832a5097. No abstract available.

PMID:
19352217
18.

Mutation analysis of the N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) in schizophrenia.

Sakurai K, Toru M, Yamakawa-Kobayashi K, Arinami T.

Neurosci Lett. 2000 Dec 22;296(2-3):168-70.

PMID:
11109007
19.

A recently-discovered NMDA receptor gene, GRIN3B, is associated with duration mismatch negativity.

Lin YT, Hsieh MH, Liu CC, Hwang TJ, Chien YL, Hwu HG, Liu CM.

Psychiatry Res. 2014 Aug 30;218(3):356-8. doi: 10.1016/j.psychres.2014.04.032. Epub 2014 Apr 28.

PMID:
24814139
20.

Mutation in the beta amyloid precursor protein gene and schizophrenia.

Nöthen MM, Erdmann J, Propping P, Lanczik M, Rietschel M, Körner J, Maier W, Albus M, Ertl MA, Wildenauer DB.

Biol Psychiatry. 1993 Oct 1;34(7):502. No abstract available.

PMID:
8268336

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