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Items: 1 to 20 of 115

1.

Replication of an association of a common variant in the Reelin gene (RELN) with schizophrenia in Ashkenazi Jewish women.

Liu Y, Chen PL, McGrath J, Wolyniec P, Fallin D, Nestadt G, Liang KY, Pulver A, Valle D, Avramopoulos D.

Psychiatr Genet. 2010 Aug;20(4):184-6. doi: 10.1097/YPG.0b013e32833a220b.

2.

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women.

Shifman S, Johannesson M, Bronstein M, Chen SX, Collier DA, Craddock NJ, Kendler KS, Li T, O'Donovan M, O'Neill FA, Owen MJ, Walsh D, Weinberger DR, Sun C, Flint J, Darvasi A.

PLoS Genet. 2008 Feb;4(2):e28. doi: 10.1371/journal.pgen.0040028.

3.

Association of reelin (RELN) single nucleotide polymorphism rs7341475 with prepulse inhibition in the Jewish Israeli population.

Greenbaum L, Levin R, Lerer E, Alkelai A, Kohn Y, Heresco-Levy U, Ebstein RP, Lerer B.

Biol Psychiatry. 2011 Mar 1;69(5):e17-8; author reply e19. doi: 10.1016/j.biopsych.2010.09.059. Epub 2010 Dec 31. No abstract available.

PMID:
21195391
4.

Association study of RELN polymorphisms with schizophrenia in Han Chinese population.

Li W, Song X, Zhang H, Yang Y, Jiang C, Xiao B, Li W, Yang G, Zhao J, Guo W, Lv L.

Prog Neuropsychopharmacol Biol Psychiatry. 2011 Aug 1;35(6):1505-11. doi: 10.1016/j.pnpbp.2011.04.007. Epub 2011 Apr 23.

PMID:
21549172
5.

Evaluating the relationship between reelin gene variants (rs7341475 and rs262355) and schizophrenia: A meta-analysis.

Li W, Guo X, Xiao S.

Neurosci Lett. 2015 Nov 16;609:42-7. doi: 10.1016/j.neulet.2015.10.014. Epub 2015 Oct 9.

PMID:
26455866
6.

[Association of RELN SNP rs7341475 with schizophrenia in the Chinese population].

Liu XY, Li M, Yang SY, Su B, Yin LD.

Dongwuxue Yanjiu. 2011 Oct;32(5):499-503. doi: 10.3724/SP.J.1141.2011.05499. Chinese.

7.

Further investigation of the association between rs7341475 and rs17746501 and schizophrenia.

Ben-David E, Shifman S; International Schizophrenia Consortium.

Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1244-7. doi: 10.1002/ajmg.b.31093.

PMID:
20468075
8.

The genetic variation of RELN expression in schizophrenia and bipolar disorder.

Ovadia G, Shifman S.

PLoS One. 2011;6(5):e19955. doi: 10.1371/journal.pone.0019955. Epub 2011 May 16.

9.

A new single-nucleotide mutation (rs362719) of the reelin (RELN) gene associated with schizophrenia in female Chinese Han.

Kuang WJ, Sun RF, Zhu YS, Li SB.

Genet Mol Res. 2011;10(3):1650-8. doi: 10.4238/vol10-3gmr1343.

10.

A variant in the reelin gene increases the risk of schizophrenia and schizoaffective disorder but not bipolar disorder.

Pisanté A, Bronstein M, Yakir B, Darvasi A.

Psychiatr Genet. 2009 Aug;19(4):212. doi: 10.1097/YPG.0b013e32832cebe6. No abstract available.

PMID:
19436241
11.

Analysis of common genetic variants identifies RELN as a risk gene for schizophrenia in Chinese population.

Li M, Luo XJ, Xiao X, Shi L, Liu XY, Yin LD, Ma XY, Yang SY, Pu XF, Yu J, Diao HB, Shi H, Su B.

World J Biol Psychiatry. 2013 Mar;14(2):91-9. doi: 10.3109/15622975.2011.587891. Epub 2011 Jul 11.

PMID:
21745129
12.

No effect of a common allelic variant in the reelin gene on intermediate phenotype measures of brain structure, brain function, and gene expression.

Tost H, Lipska BK, Vakkalanka R, Lemaitre H, Callicott JH, Mattay VS, Kleinman JE, Marenco S, Weinberger DR.

Biol Psychiatry. 2010 Jul 1;68(1):105-7. doi: 10.1016/j.biopsych.2010.02.023.

13.

Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.

Dutta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Usha R.

Neurosci Lett. 2008 Aug 15;441(1):56-60. doi: 10.1016/j.neulet.2008.06.022. Epub 2008 Jun 13.

PMID:
18597938
14.

Association of RELN promoter SNPs with schizophrenia in the Chinese population.

Chang LH, Li M, Luo XJ, Liu XY, Yin LD, Yang SY, Diao HB, Su B, Pu XF.

Dongwuxue Yanjiu. 2011 Oct;32(5):504-8. doi: 10.3724/SP.J.1141.2011.05504.

15.

Association study of the reelin (RELN) gene with Chinese Va schizophrenia.

Yang XB, Kang C, Liu H, Yang J.

Psychiatr Genet. 2013 Jun;23(3):138. doi: 10.1097/YPG.0b013e32835d705c. No abstract available.

PMID:
23277132
16.

Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia.

Wedenoja J, Tuulio-Henriksson A, Suvisaari J, Loukola A, Paunio T, Partonen T, Varilo T, Lönnqvist J, Peltonen L.

Biol Psychiatry. 2010 May 15;67(10):983-91. doi: 10.1016/j.biopsych.2009.09.026. Epub 2009 Nov 17.

17.

Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families.

Wedenoja J, Loukola A, Tuulio-Henriksson A, Paunio T, Ekelund J, Silander K, Varilo T, Heikkilä K, Suvisaari J, Partonen T, Lönnqvist J, Peltonen L.

Mol Psychiatry. 2008 Jul;13(7):673-84. Epub 2007 Aug 7.

PMID:
17684500
18.

[The association of polymorphisms in SLC18A1, TPH1 and RELN genes with risk of paranoid schizophrenia].

Galaktionova DIu, Gareeva AE, Khusnutdinova EK, Nasedkina TV.

Mol Biol (Mosk). 2014 Jul-Aug;48(4):629-39. Russian.

19.

Reelin and glutamic acid decarboxylase67 promoter remodeling in an epigenetic methionine-induced mouse model of schizophrenia.

Dong E, Agis-Balboa RC, Simonini MV, Grayson DR, Costa E, Guidotti A.

Proc Natl Acad Sci U S A. 2005 Aug 30;102(35):12578-83. Epub 2005 Aug 19.

20.

Contribution of Common Variants in GABRG2, RELN and NRG3 and Interaction Networks to the Risk of Hirschsprung Disease.

Wang Y, Wang J, Zhou Y, Wei Z, Xiao Y, Zhou K, Wen J, Yan J, Cai W.

Cell Physiol Biochem. 2016;40(3-4):509-526. Epub 2016 Nov 25.

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