179 related articles for article (PubMed ID: 23028439)
1. Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population.
Zhang Y; Li J; Tardif T; Burmeister M; Villafuerte SM; McBride-Chang C; Li H; Shi B; Liang W; Zhang Z; Shu H
PLoS One; 2012; 7(9):e42969. PubMed ID: 23028439
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [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]
4. 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]
5. Association of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese Population.
Zhang Y; Li J; Song S; Tardif T; Burmeister M; Villafuerte SM; Su M; McBride C; Shu H
PLoS One; 2016; 11(4):e0153603. PubMed ID: 27100778
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. The rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation.
Tammimies K; Tapia-Páez I; Rüegg J; Rosin G; Kere J; Gustafsson JÅ; Nalvarte I
Mol Endocrinol; 2012 Apr; 26(4):619-29. PubMed ID: 22383464
[TBL] [Abstract][Full Text] [Related]
8.
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]
9. 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]
10. 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]
11. Visual statistical learning and orthographic awareness in Chinese children with and without developmental dyslexia.
Tong X; Leung WWS; Tong X
Res Dev Disabil; 2019 Sep; 92():103443. PubMed ID: 31374382
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.
Wigg KG; Feng Y; Crosbie J; Tannock R; Kennedy JL; Ickowicz A; Malone M; Schachar R; Barr CL
Genes Brain Behav; 2008 Nov; 7(8):877-86. PubMed ID: 19076634
[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. 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]
[Next] [New Search]