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Journal Abstract Search

270 related items for PubMed ID: 21549172

  • 1. 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 01; 35(6):1505-11. PubMed ID: 21549172
    [Abstract] [Full Text] [Related]

  • 2. 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 01; 29(6):232-236. PubMed ID: 31469785
    [Abstract] [Full Text] [Related]

  • 3. 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 Dec 01; 10(3):1650-8. PubMed ID: 21863557
    [Abstract] [Full Text] [Related]

  • 4. Female gender specific association of the Reelin (RELN) gene rs7341475 variant with schizophrenia.
    Sozuguzel MD, Sazci A, Yildiz M.
    Mol Biol Rep; 2019 Jun 01; 46(3):3411-3416. PubMed ID: 30980267
    [Abstract] [Full Text] [Related]

  • 5. 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 01; 32(5):504-8. PubMed ID: 22006802
    [Abstract] [Full Text] [Related]

  • 6. RELN gene polymorphisms and susceptibility to autism in Chinese Han population.
    Tian P.
    Neurol India; 2012 Oct 01; 60(6):581-4. PubMed ID: 23287318
    [Abstract] [Full Text] [Related]

  • 7. Association study between genes in Reelin signaling pathway and autism identifies DAB1 as a susceptibility gene in a Chinese Han population.
    Li J, Liu J, Zhao L, Ma Y, Jia M, Lu T, Ruan Y, Li Q, Yue W, Zhang D, Wang L.
    Prog Neuropsychopharmacol Biol Psychiatry; 2013 Jul 01; 44():226-32. PubMed ID: 23333377
    [Abstract] [Full Text] [Related]

  • 8. [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 01; 32(5):499-503. PubMed ID: 22006801
    [Abstract] [Full Text] [Related]

  • 9. Two single-nucleotide polymorphisms of the RELN gene and symptom-based and developmental deficits among children and adolescents with autistic spectrum disorders in the Tianjin, China.
    Wang GF, Ye S, Gao L, Han Y, Guo X, Dong XP, Su YY, Zhang X.
    Behav Brain Res; 2018 Sep 17; 350():1-5. PubMed ID: 29753726
    [Abstract] [Full Text] [Related]

  • 10. Analysis of the RELN gene as a genetic risk factor for autism.
    Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, DeLong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA.
    Mol Psychiatry; 2005 Jun 17; 10(6):563-71. PubMed ID: 15558079
    [Abstract] [Full Text] [Related]

  • 11. Absence of association of a polymorphic GGC repeat at the 5' untranslated region of the reelin gene with schizophrenia.
    Huang CH, Chen CH.
    Psychiatry Res; 2006 May 30; 142(1):89-92. PubMed ID: 16556465
    [Abstract] [Full Text] [Related]

  • 12. Association and gene-gene interactions study of reelin signaling pathway related genes with autism in the Han Chinese population.
    Shen Y, Xun G, Guo H, He Y, Ou J, Dong H, Xia K, Zhao J.
    Autism Res; 2016 Apr 30; 9(4):436-42. PubMed ID: 26285919
    [Abstract] [Full Text] [Related]

  • 13. 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. PubMed ID: 26455866
    [Abstract] [Full Text] [Related]

  • 14. 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 16; 4(2):e28. PubMed ID: 18282107
    [Abstract] [Full Text] [Related]

  • 15. Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.
    Sharma JR, Arieff Z, Gameeldien H, Davids M, Kaur M, van der Merwe L.
    Genet Test Mol Biomarkers; 2013 Feb 16; 17(2):93-8. PubMed ID: 23216241
    [Abstract] [Full Text] [Related]

  • 16. 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 16; 20(4):184-6. PubMed ID: 20431428
    [Abstract] [Full Text] [Related]

  • 17. 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. PubMed ID: 18597938
    [Abstract] [Full Text] [Related]

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  • 19. Correlation of Four Single Nucleotide Polymorphisms of the RELN Gene With Schizophrenia.
    Ping J, Zhang J, Wan J, Banerjee A, Huang C, Yu J, Jiang T, Du B.
    East Asian Arch Psychiatry; 2021 Dec 15; 31(4):112-118. PubMed ID: 34987122
    [Abstract] [Full Text] [Related]

  • 20. 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 15; 14(2):91-9. PubMed ID: 21745129
    [Abstract] [Full Text] [Related]

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