BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 24362368)

  • 1. Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population.
    Venkatesh SK; Siddaiah A; Padakannaya P; Ramachandra NB
    Psychiatr Genet; 2014 Feb; 24(1):10-20. PubMed ID: 24362368
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with developmental dyslexia.
    Venkatesh SK; Siddaiah A; Padakannaya P; Ramachandra NB
    Gene; 2013 Oct; 529(2):215-9. PubMed ID: 23954868
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia.
    Tapia-Páez I; Tammimies K; Massinen S; Roy AL; Kere J
    FASEB J; 2008 Aug; 22(8):3001-9. PubMed ID: 18445785
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Association of short-term memory with a variant within DYX1C1 in developmental dyslexia.
    Marino C; Citterio A; Giorda R; Facoetti A; Menozzi G; Vanzin L; Lorusso ML; Nobile M; Molteni M
    Genes Brain Behav; 2007 Oct; 6(7):640-6. PubMed ID: 17309662
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia.
    Marino C; Giorda R; Luisa Lorusso M; Vanzin L; Salandi N; Nobile M; Citterio A; Beri S; Crespi V; Battaglia M; Molteni M
    Eur J Hum Genet; 2005 Apr; 13(4):491-9. PubMed ID: 15702132
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation.
    Bates TC; Lind PA; Luciano M; Montgomery GW; Martin NG; Wright MJ
    Mol Psychiatry; 2010 Dec; 15(12):1190-6. PubMed ID: 19901951
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children.
    Lim CK; Ho CS; Chou CH; Waye MM
    Behav Brain Funct; 2011 May; 7():16. PubMed ID: 21599957
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An examination of candidate gene SNPs for dyslexia in an Indian sample.
    Venkatesh SK; Siddaiah A; Padakannaya P; Ramachandra NB
    Behav Genet; 2011 Jan; 41(1):105-9. PubMed ID: 21203818
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.
    Tran C; Gagnon F; Wigg KG; Feng Y; Gomez L; Cate-Carter TD; Kerr EN; Field LL; Kaplan BJ; Lovett MW; Barr CL
    Am J Med Genet B Neuropsychiatr Genet; 2013 Mar; 162B(2):146-56. PubMed ID: 23341075
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population.
    Sun Y; Gao Y; Zhou Y; Chen H; Wang G; Xu J; Xia J; Huen MS; Siok WT; Jiang Y; Tan LH
    Am J Med Genet B Neuropsychiatr Genet; 2014 Dec; 165B(8):627-34. PubMed ID: 25230923
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Further evidence for DYX1C1 as a susceptibility factor for dyslexia.
    Dahdouh F; Anthoni H; Tapia-Páez I; Peyrard-Janvid M; Schulte-Körne G; Warnke A; Remschmidt H; Ziegler A; Kere J; Müller-Myhsok B; Nöthen MM; Schumacher J; Zucchelli M
    Psychiatr Genet; 2009 Apr; 19(2):59-63. PubMed ID: 19240663
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association analysis of dyslexia candidate genes in a Dutch longitudinal sample.
    Carrion-Castillo A; Maassen B; Franke B; Heister A; Naber M; van der Leij A; Francks C; Fisher SE
    Eur J Hum Genet; 2017 Apr; 25(4):452-460. PubMed ID: 28074887
    [TBL] [Abstract][Full Text] [Related]  

  • 13. No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy.
    Bellini G; Bravaccio C; Calamoneri F; Donatella Cocuzza M; Fiorillo P; Gagliano A; Mazzone D; del Giudice EM; Scuccimarra G; Militerni R; Pascotto A
    J Mol Neurosci; 2005; 27(3):311-4. PubMed ID: 16280601
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.
    Paracchini S; Ang QW; Stanley FJ; Monaco AP; Pennell CE; Whitehouse AJ
    Genes Brain Behav; 2011 Mar; 10(2):158-65. PubMed ID: 20846247
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis.
    Zou L; Chen W; Shao S; Sun Z; Zhong R; Shi J; Miao X; Song R
    Am J Med Genet B Neuropsychiatr Genet; 2012 Dec; 159B(8):970-6. PubMed ID: 23065966
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes.
    Mascheretti S; Bureau A; Battaglia M; Simone D; Quadrelli E; Croteau J; Cellino MR; Giorda R; Beri S; Maziade M; Marino C
    Genes Brain Behav; 2013 Feb; 12(1):47-55. PubMed ID: 23176554
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population.
    Venkatesh SK; Siddaiah A; Padakannaya P; Ramachandra NB
    J Hum Genet; 2013 Aug; 58(8):531-8. PubMed ID: 23677054
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Genome-wide association studies on the developmental dyslexia children].
    Wang Z; Cui G; Zhao A; Li P; Liu D; Shen L; Li D
    Wei Sheng Yan Jiu; 2015 Sep; 44(5):767-70, 779. PubMed ID: 26591772
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deficits in learning and memory in mice with a mutation of the candidate dyslexia susceptibility gene Dyx1c1.
    Rendall AR; Tarkar A; Contreras-Mora HM; LoTurco JJ; Fitch RH
    Brain Lang; 2017 Sep; 172():30-38. PubMed ID: 25989970
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    Müller B; Schaadt G; Boltze J; Emmrich F; ; Skeide MA; Neef NE; Kraft I; Brauer J; Friederici AD; Kirsten H; Wilcke A
    Brain Behav; 2017 Nov; 7(11):e00851. PubMed ID: 29201552
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.