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Items: 16

1.

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
2.

A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility.

Kimura H, Fujita Y, Kawabata T, Ishizuka K, Wang C, Iwayama Y, Okahisa Y, Kushima I, Morikawa M, Uno Y, Okada T, Ikeda M, Inada T, Branko A, Mori D, Yoshikawa T, Iwata N, Nakamura H, Yamashita T, Ozaki N.

Transl Psychiatry. 2017 Aug 22;7(8):e1214. doi: 10.1038/tp.2017.170.

3.

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
4.

Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1-LGI1 signaling.

Thomas RA, Ambalavanan A, Rouleau GA, Barker PA.

Mol Genet Genomic Med. 2016 Mar 11;4(4):447-56. doi: 10.1002/mgg3.215. eCollection 2016 Jul.

5.

Polymorphism within a Neuronal Activity-Dependent Enhancer of NgR1 Is Associated with Corpus Callosum Morphology in Humans.

Isobe M, Tanigaki K, Muraki K, Miyata J, Takemura A, Sugihara G, Takahashi H, Aso T, Fukuyama H, Hazama M, Murai T.

Mol Neuropsychiatry. 2015 Jul;1(2):105-15. doi: 10.1159/000430463. Epub 2015 Jun 24.

6.

Amygdala NRG1-ErbB4 is critical for the modulation of anxiety-like behaviors.

Bi LL, Sun XD, Zhang J, Lu YS, Chen YH, Wang J, Geng F, Liu F, Zhang M, Liu JH, Li XW, Mei L, Gao TM.

Neuropsychopharmacology. 2015 Mar;40(4):974-86. doi: 10.1038/npp.2014.274. Epub 2014 Oct 13.

7.

White matter abnormalities in 22q11.2 deletion syndrome: preliminary associations with the Nogo-66 receptor gene and symptoms of psychosis.

Perlstein MD, Chohan MR, Coman IL, Antshel KM, Fremont WP, Gnirke MH, Kikinis Z, Middleton FA, Radoeva PD, Shenton ME, Kates WR.

Schizophr Res. 2014 Jan;152(1):117-23. doi: 10.1016/j.schres.2013.11.015. Epub 2013 Dec 8.

8.

Nogo and Nogo receptor: relevance to schizophrenia?

Willi R, Schwab ME.

Neurobiol Dis. 2013 Jun;54:150-7. doi: 10.1016/j.nbd.2013.01.011. Epub 2013 Jan 28. Review.

PMID:
23369871
9.

Missense mutation of the reticulon-4 receptor alters spatial memory and social interaction in mice.

Lazar NL, Singh S, Paton T, Clapcote SJ, Gondo Y, Fukumura R, Roder JC, Cain DP.

Behav Brain Res. 2011 Oct 10;224(1):73-9. doi: 10.1016/j.bbr.2011.05.020. Epub 2011 May 27.

PMID:
21645550
10.

Association study of Nogo-related genes with schizophrenia in a Japanese case-control sample.

Jitoku D, Hattori E, Iwayama Y, Yamada K, Toyota T, Kikuchi M, Maekawa M, Nishikawa T, Yoshikawa T.

Am J Med Genet B Neuropsychiatr Genet. 2011 Jul;156B(5):581-92. doi: 10.1002/ajmg.b.31199. Epub 2011 May 11.

PMID:
21563301
11.

Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population.

Pasaje CF, Bae JS, Park BL, Park CS, Kim BJ, Lee CS, Kim JW, Choi WH, Shin TM, Koh IS, Choi IG, Woo SL, Shin HD.

Psychiatry Res. 2011 Sep 30;189(2):312-4. doi: 10.1016/j.psychres.2011.02.006. Epub 2011 Mar 5.

PMID:
21377214
12.

Converging evidence for the Nogo-66 receptor gene in schizophrenia.

Voineskos AN.

J Neurosci. 2009 Apr 22;29(16):5045-7. doi: 10.1523/JNEUROSCI.0477-09.2009. Review. No abstract available.

13.

Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.

Budel S, Padukkavidana T, Liu BP, Feng Z, Hu F, Johnson S, Lauren J, Park JH, McGee AW, Liao J, Stillman A, Kim JE, Yang BZ, Sodi S, Gelernter J, Zhao H, Hisama F, Arnsten AF, Strittmatter SM.

J Neurosci. 2008 Dec 3;28(49):13161-72. doi: 10.1523/JNEUROSCI.3828-08.2008.

14.

Nogo Receptor 1 (RTN4R) as a candidate gene for schizophrenia: analysis using human and mouse genetic approaches.

Hsu R, Woodroffe A, Lai WS, Cook MN, Mukai J, Dunning JP, Swanson DJ, Roos JL, Abecasis GR, Karayiorgou M, Gogos JA.

PLoS One. 2007 Nov 28;2(11):e1234.

15.

No association between the genetic polymorphisms in the RTN4R gene and schizophrenia in the Chinese population.

Meng J, Shi Y, Zhao X, Guo S, Wang H, Zheng Y, Tang R, Feng G, Gu N, Liu H, Zhu S, He L.

J Neural Transm (Vienna). 2007 Feb;114(2):249-54. Epub 2006 Aug 10.

PMID:
16897606
16.

Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia.

Sinibaldi L, De Luca A, Bellacchio E, Conti E, Pasini A, Paloscia C, Spalletta G, Caltagirone C, Pizzuti A, Dallapiccola B.

Hum Mutat. 2004 Dec;24(6):534-5.

PMID:
15532024

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