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.
254 related articles for article (PubMed ID: 21046216)
21. Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment. Powers NR; Eicher JD; Butter F; Kong Y; Miller LL; Ring SM; Mann M; Gruen JR Am J Hum Genet; 2013 Jul; 93(1):19-28. PubMed ID: 23746548 [TBL] [Abstract][Full Text] [Related]
22. Position of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes. Adler WT; Platt MP; Mehlhorn AJ; Haight JL; Currier TA; Etchegaray MA; Galaburda AM; Rosen GD PLoS One; 2013; 8(5):e65179. PubMed ID: 23724130 [TBL] [Abstract][Full Text] [Related]
23. 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]
24. The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems. Riva V; Marino C; Giorda R; Molteni M; Nobile M Eur Child Adolesc Psychiatry; 2015 Mar; 24(3):309-18. PubMed ID: 25012462 [TBL] [Abstract][Full Text] [Related]
25. Family-based association study of DYX1C1 variants in autism. Ylisaukko-Oja T; Peyrard-Janvid M; Lindgren CM; Rehnström K; Vanhala R; Peltonen L; Järvelä I; Kere J Eur J Hum Genet; 2005 Jan; 13(1):127-30. PubMed ID: 15470369 [TBL] [Abstract][Full Text] [Related]
26. Polymorphisms in DCDC2 and S100B associate with developmental dyslexia. Matsson H; Huss M; Persson H; Einarsdottir E; Tiraboschi E; Nopola-Hemmi J; Schumacher J; Neuhoff N; Warnke A; Lyytinen H; Schulte-Körne G; Nöthen MM; Leppänen PH; Peyrard-Janvid M; Kere J J Hum Genet; 2015 Jul; 60(7):399-401. PubMed ID: 25877001 [TBL] [Abstract][Full Text] [Related]
27. [Genetics of dyslexia]. Schulte-Körne G; Warnke A; Remschmidt H Z Kinder Jugendpsychiatr Psychother; 2006 Nov; 34(6):435-44. PubMed ID: 17094062 [TBL] [Abstract][Full Text] [Related]
28. Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs. Tammimies K; Bieder A; Lauter G; Sugiaman-Trapman D; Torchet R; Hokkanen ME; Burghoorn J; Castrén E; Kere J; Tapia-Páez I; Swoboda P FASEB J; 2016 Oct; 30(10):3578-3587. PubMed ID: 27451412 [TBL] [Abstract][Full Text] [Related]
29. Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Schumacher J; Anthoni H; Dahdouh F; König IR; Hillmer AM; Kluck N; Manthey M; Plume E; Warnke A; Remschmidt H; Hülsmann J; Cichon S; Lindgren CM; Propping P; Zucchelli M; Ziegler A; Peyrard-Janvid M; Schulte-Körne G; Nöthen MM; Kere J Am J Hum Genet; 2006 Jan; 78(1):52-62. PubMed ID: 16385449 [TBL] [Abstract][Full Text] [Related]
30. 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]
31. Association of polymorphisms in the DCDC2 gene with developmental dyslexia in the Han Chinese. Zuo PX; Wu HR; Li ZC; Cao XD; Pang LJ; Yang L; Liu F; Zhao F Chin Med J (Engl); 2012 Feb; 125(4):622-5. PubMed ID: 22490485 [TBL] [Abstract][Full Text] [Related]
32. 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]
33. Genotype-environment correlations for language-related abilities: implications for typical and atypical learners. Gilger JW; Ho HZ; Whipple AD; Spitz R J Learn Disabil; 2001; 34(6):492-502. PubMed ID: 15503564 [TBL] [Abstract][Full Text] [Related]
34. Moving closer to a public health model of language and learning disabilities: the role of genetics and the search for etiologies. Miller B; McCardle P Behav Genet; 2011 Jan; 41(1):1-5. PubMed ID: 21229298 [TBL] [Abstract][Full Text] [Related]
35. Genetic variant in DIP2A gene is associated with developmental dyslexia in Chinese population. Kong R; Shao S; Wang J; Zhang X; Guo S; Zou L; Zhong R; Lou J; Zhou J; Zhang J; Song R Am J Med Genet B Neuropsychiatr Genet; 2016 Mar; 171B(2):203-8. PubMed ID: 26452339 [TBL] [Abstract][Full Text] [Related]
36. 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]
37. Meta-analysis of the association between DCDC2 polymorphisms and risk of dyslexia. Zhong R; Yang B; Tang H; Zou L; Song R; Zhu LQ; Miao X Mol Neurobiol; 2013 Feb; 47(1):435-42. PubMed ID: 23229871 [TBL] [Abstract][Full Text] [Related]
38. Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment. SLI Consortium (SLIC) Am J Hum Genet; 2004 Jun; 74(6):1225-38. PubMed ID: 15133743 [TBL] [Abstract][Full Text] [Related]
39. Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. Lind PA; Luciano M; Wright MJ; Montgomery GW; Martin NG; Bates TC Eur J Hum Genet; 2010 Jun; 18(6):668-73. PubMed ID: 20068590 [TBL] [Abstract][Full Text] [Related]
40. Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q. Chapman NH; Igo RP; Thomson JB; Matsushita M; Brkanac Z; Holzman T; Berninger VW; Wijsman EM; Raskind WH Am J Med Genet B Neuropsychiatr Genet; 2004 Nov; 131B(1):67-75. PubMed ID: 15389770 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]