These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

223 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]
    of 12.