BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 23216241)

  • 21. 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]  

  • 22. The role of reelin gene polymorphisms in the pathogenesis of Alzheimer's disease in a Greek population.
    Antoniades D; Katopodi T; Pappa S; Lampropoulos A; Konsta V; Frydas E; Mpalogiannis S; Hatzistilianou M
    J Biol Regul Homeost Agents; 2011; 25(3):351-8. PubMed ID: 22023759
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A pilot Indian family-based association study between dyslexia and Reelin pathway genes, DCDC2 and ROBO1, identifies modest association with a triallelic unit TAT in the gene RELN.
    Devasenapathy S; Midha R; Naskar T; Mehta A; Prajapati B; Ummekulsum M; Sagar R; Singh NC; Sinha S
    Asian J Psychiatr; 2018 Oct; 37():121-129. PubMed ID: 30199849
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Relationship between RELN signaling pathway genes and language development of autism based on a cluster model.
    Shen Y; Dong H; Zhao J; Xia K; Ou J
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2022 Jul; 47(7):858-864. PubMed ID: 36039581
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Analysis of reelin as a candidate gene for autism.
    Bonora E; Beyer KS; Lamb JA; Parr JR; Klauck SM; Benner A; Paolucci M; Abbott A; Ragoussis I; Poustka A; Bailey AJ; Monaco AP;
    Mol Psychiatry; 2003 Oct; 8(10):885-92. PubMed ID: 14515139
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Reelin gene alleles and susceptibility to autism spectrum disorders.
    Zhang H; Liu X; Zhang C; Mundo E; Macciardi F; Grayson DR; Guidotti AR; Holden JJ
    Mol Psychiatry; 2002; 7(9):1012-7. PubMed ID: 12399956
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Polymorphisms of candidate genes in Slovak autistic patients.
    Kelemenova S; Schmidtova E; Ficek A; Celec P; Kubranska A; Ostatnikova D
    Psychiatr Genet; 2010 Aug; 20(4):137-9. PubMed ID: 20436377
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.
    Persico AM; D'Agruma L; Maiorano N; Totaro A; Militerni R; Bravaccio C; Wassink TH; Schneider C; Melmed R; Trillo S; Montecchi F; Palermo M; Pascucci T; Puglisi-Allegra S; Reichelt KL; Conciatori M; Marino R; Quattrocchi CC; Baldi A; Zelante L; Gasparini P; Keller F;
    Mol Psychiatry; 2001 Mar; 6(2):150-9. PubMed ID: 11317216
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Reelin signaling is impaired in autism.
    Fatemi SH; Snow AV; Stary JM; Araghi-Niknam M; Reutiman TJ; Lee S; Brooks AI; Pearce DA
    Biol Psychiatry; 2005 Apr; 57(7):777-87. PubMed ID: 15820235
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [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]  

  • 31. Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population.
    Mowat AJ; Crompton M; Ziff JL; Aldren CP; Lavy JA; Saeed SR; Dawson SJ
    Hum Genet; 2018 May; 137(5):357-363. PubMed ID: 29728750
    [TBL] [Abstract][Full Text] [Related]  

  • 32. An association analysis of reelin gene (RELN) polymorphisms with childhood epilepsy in eastern Indian population from West Bengal.
    Dutta S; Gangopadhyay PK; Sinha S; Chatterjee A; Ghosh S; Rajamma U
    Cell Mol Neurobiol; 2011 Jan; 31(1):45-56. PubMed ID: 20697953
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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. PubMed ID: 21863557
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Controversies in RELN/reelin expression in otosclerosis.
    Csomor P; Sziklai I; Karosi T
    Eur Arch Otorhinolaryngol; 2012 Feb; 269(2):431-40. PubMed ID: 21630058
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. 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. PubMed ID: 27889765
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The involvement of Reelin in neurodevelopmental disorders.
    Folsom TD; Fatemi SH
    Neuropharmacology; 2013 May; 68():122-35. PubMed ID: 22981949
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Completed suicide, depression, and RELN polymorphisms.
    Bučić M; Pregelj P; Zupanc T; Videtič Paska A
    Psychiatr Genet; 2016 Oct; 26(5):218-22. PubMed ID: 27537376
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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. PubMed ID: 18282107
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.