229 related articles for article (PubMed ID: 27071546)
1. Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia.
Zhou Z; Hu Z; Zhang L; Hu Z; Liu H; Liu Z; Du J; Zhao J; Zhou L; Xia K; Tang B; Shen L
Sci Rep; 2016 Apr; 6():24327. PubMed ID: 27071546
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 17684500
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 23277132
[No Abstract] [Full Text] [Related]
4. 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. PubMed ID: 21745129
[TBL] [Abstract][Full Text] [Related]
5. Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.
Dazzo E; Fanciulli M; Serioli E; Minervini G; Pulitano P; Binelli S; Di Bonaventura C; Luisi C; Pasini E; Striano S; Striano P; Coppola G; Chiavegato A; Radovic S; Spadotto A; Uzzau S; La Neve A; Giallonardo AT; Mecarelli O; Tosatto SC; Ottman R; Michelucci R; Nobile C
Am J Hum Genet; 2015 Jun; 96(6):992-1000. PubMed ID: 26046367
[TBL] [Abstract][Full Text] [Related]
6. Identification of RELN variant p.(Ser2486Gly) in an Iranian family with ankylosing spondylitis; the first association of RELN and AS.
Garshasbi M; Mahmoudi M; Razmara E; Vojdanian M; Aslani S; Farhadi E; Jensen LR; Arzaghi SM; Poursani S; Bitaraf A; Eidi M; Gharehdaghi EE; Kuss AW; Jamshidi A
Eur J Hum Genet; 2020 Jun; 28(6):754-762. PubMed ID: 32001840
[TBL] [Abstract][Full Text] [Related]
7. RELN rare variants in myoclonus-dystonia.
Groen JL; Ritz K; Jalalzadeh H; van der Salm SM; Jongejan A; Mook OR; Haagmans MA; Zwinderman AH; Motazacker MM; Hennekam RC; Baas F; Tijssen MA
Mov Disord; 2015 Mar; 30(3):415-9. PubMed ID: 25648840
[TBL] [Abstract][Full Text] [Related]
8. Female gender specific association of the Reelin (RELN) gene rs7341475 variant with schizophrenia.
Sozuguzel MD; Sazci A; Yildiz M
Mol Biol Rep; 2019 Jun; 46(3):3411-3416. PubMed ID: 30980267
[TBL] [Abstract][Full Text] [Related]
9. Exploring the mRNA expression level of RELN in peripheral blood of schizophrenia patients before and after antipsychotic treatment.
Yin J; Lu Y; Yu S; Dai Z; Zhang F; Yuan J
Hereditas; 2020 Nov; 157(1):43. PubMed ID: 33158463
[TBL] [Abstract][Full Text] [Related]
10. [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. PubMed ID: 22006801
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 22006802
[TBL] [Abstract][Full Text] [Related]
12. Association Between REELIN Gene Polymorphisms (rs7341475 and rs262355) and Risk of Schizophrenia: an Updated Meta-analysis.
Marzan S; Aziz MA; Islam MS
J Mol Neurosci; 2021 Apr; 71(4):675-690. PubMed ID: 32889693
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 23553203
[TBL] [Abstract][Full Text] [Related]
14. No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population.
He Y; Xun G; Xia K; Hu Z; Lv L; Deng Z; Zhao J
Psychiatry Res; 2011 May; 187(3):462-4. PubMed ID: 20554015
[TBL] [Abstract][Full Text] [Related]
15. The genetic variation of RELN expression in schizophrenia and bipolar disorder.
Ovadia G; Shifman S
PLoS One; 2011; 6(5):e19955. PubMed ID: 21603580
[TBL] [Abstract][Full Text] [Related]
16. 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; 441(1):56-60. PubMed ID: 18597938
[TBL] [Abstract][Full Text] [Related]
17. 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; 67(10):983-91. PubMed ID: 19922905
[TBL] [Abstract][Full Text] [Related]
18. Towards the identification of a genetic basis for Landau-Kleffner syndrome.
Conroy J; McGettigan PA; McCreary D; Shah N; Collins K; Parry-Fielder B; Moran M; Hanrahan D; Deonna TW; Korff CM; Webb D; Ennis S; Lynch SA; King MD
Epilepsia; 2014 Jun; 55(6):858-65. PubMed ID: 24828792
[TBL] [Abstract][Full Text] [Related]
19. Single-cell trajectory analysis of human homogenous neurons carrying a rare RELN variant.
Arioka Y; Shishido E; Kubo H; Kushima I; Yoshimi A; Kimura H; Ishizuka K; Aleksic B; Maeda T; Ishikawa M; Kuzumaki N; Okano H; Mori D; Ozaki N
Transl Psychiatry; 2018 Jul; 8(1):129. PubMed ID: 30022058
[TBL] [Abstract][Full Text] [Related]
20. Association between RELN polymorphisms and schizophrenia in a Han population from Northeast China.
Bai W; Fu Y; Yu X; Zhu B; Duan R; Yu Y; Kou C
Psychiatr Genet; 2019 Dec; 29(6):232-236. PubMed ID: 31469785
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
