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Items: 1 to 20 of 109

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. doi: 10.1097/YPG.0000000000000009.

PMID:
24362368
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 25;529(2):215-9. doi: 10.1016/j.gene.2013.08.017. Epub 2013 Aug 14.

PMID:
23954868
3.

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.

4.

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.

5.

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.

6.

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.

7.

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.

PMID:
19901951
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. doi: 10.1007/s10519-010-9441-2. Epub 2011 Jan 4.

PMID:
21203818
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. doi: 10.1002/ajmg.b.32267. Epub 2014 Sep 17.

PMID:
25230923
10.

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.

PMID:
19240663
11.

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

Cope N, Harold D, Hill G, Moskvina V, Stevenson J, Holmans P, Owen MJ, O'Donovan MC, Williams J.

Am J Hum Genet. 2005 Apr;76(4):581-91. Epub 2005 Feb 16. Erratum in: Am J Hum Genet. 2005 Nov;77(5):898.

12.

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.

PMID:
16280601
13.

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.

14.

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. doi: 10.1038/jhg.2013.46. Epub 2013 May 16.

PMID:
23677054
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. doi: 10.1002/ajmg.b.32102. Epub 2012 Oct 12.

PMID:
23065966
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. doi: 10.1111/gbb.12000. Epub 2012 Nov 24.

17.

[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.

PMID:
26591772
18.

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. doi: 10.1111/j.1601-183X.2010.00651.x. Epub 2010 Oct 19.

19.

Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits.

Bates TC, Luciano M, Medland SE, Montgomery GW, Wright MJ, Martin NG.

Behav Genet. 2011 Jan;41(1):50-7. doi: 10.1007/s10519-010-9402-9. Epub 2010 Oct 15.

PMID:
20949370
20.

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.

PMID:
22383464

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