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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 20;7:16. doi: 10.1186/1744-9081-7-16.


[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. Chinese.


A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children.

Lim CK, Wong AM, Ho CS, Waye MM.

Behav Brain Funct. 2014 Jul 11;10:23. doi: 10.1186/1744-9081-10-23.


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. doi: 10.1371/journal.pone.0042969. Epub 2012 Sep 13.


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. doi: 10.1002/ajmg.b.32267. Epub 2014 Sep 17.


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. doi: 10.1096/fj.07-104455. Epub 2008 Apr 29.


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.


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. doi: 10.1038/mp.2009.120. Epub 2009 Nov 10.


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. doi: 10.1007/s10519-010-9441-2. Epub 2011 Jan 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. Epub 2007 Feb 13.


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. doi: 10.1097/YPG.0b013e32832080e1.


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. doi: 10.1097/YPG.0000000000000009.


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. doi: 10.1002/ajmg.b.32102. Epub 2012 Oct 12.


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.


A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.

Yu J, He X, Yao D, Li Z, Li H, Zhao Z.

Behav Brain Funct. 2011 May 14;7:13. doi: 10.1186/1744-9081-7-13.


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. doi: 10.1002/ajmg.b.32392. Epub 2015 Oct 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. doi: 10.1002/ajmg.b.32123. Epub 2013 Jan 22.


Support for EKN1 as the susceptibility locus for dyslexia on 15q21.

Wigg KG, Couto JM, Feng Y, Anderson B, Cate-Carter TD, Macciardi F, Tannock R, Lovett MW, Humphries TW, Barr CL.

Mol Psychiatry. 2004 Dec;9(12):1111-21.


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. doi: 10.1210/me.2011-1376. Epub 2012 Mar 1.


Stuttering candidate genes DRD2 but not SLC6A3 is associated with developmental dyslexia in Chinese population.

Chen H, Wang G, Xia J, Zhou Y, Gao Y, Xu J, Huen MS, Siok WT, Jiang Y, Tan LH, Sun Y.

Behav Brain Funct. 2014 Sep 1;10(1):29. doi: 10.1186/1744-9081-10-29.

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