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.
164 related articles for article (PubMed ID: 27100778)
1. 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]
2. 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]
3. 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]
4. The role of gene DCDC2 in German dyslexics. Wilcke A; Weissfuss J; Kirsten H; Wolfram G; Boltze J; Ahnert P Ann Dyslexia; 2009 Jun; 59(1):1-11. PubMed ID: 19238550 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. DCDC2 genetic variants and susceptibility to developmental dyslexia. Marino C; Meng H; Mascheretti S; Rusconi M; Cope N; Giorda R; Molteni M; Gruen JR Psychiatr Genet; 2012 Feb; 22(1):25-30. PubMed ID: 21881542 [TBL] [Abstract][Full Text] [Related]
9. The influence of DCDC2 risk genetic variants on reading: Testing main and haplotypic effects. Riva V; Mozzi A; Forni D; Trezzi V; Giorda R; Riva S; Villa M; Sironi M; Cagliani R; Mascheretti S Neuropsychologia; 2019 Jul; 130():52-58. PubMed ID: 29803723 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Scerri TS; Morris AP; Buckingham LL; Newbury DF; Miller LL; Monaco AP; Bishop DV; Paracchini S Biol Psychiatry; 2011 Aug; 70(3):237-45. PubMed ID: 21457949 [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. DCDC2 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children. Chen Y; Zhao H; Zhang YX; Zuo PX Neural Regen Res; 2017 Feb; 12(2):259-266. PubMed ID: 28400808 [TBL] [Abstract][Full Text] [Related]
14. The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effects. Trezzi V; Forni D; Giorda R; Villa M; Molteni M; Marino C; Mascheretti S J Hum Genet; 2017 Nov; 62(11):949-955. PubMed ID: 29066855 [TBL] [Abstract][Full Text] [Related]
15. The DCDC2 deletion is not a risk factor for dyslexia. Scerri TS; Macpherson E; Martinelli A; Wa WC; Monaco AP; Stein J; Zheng M; Suk-Han Ho C; McBride C; Snowling M; Hulme C; Hayiou-Thomas ME; Waye MMY; Talcott JB; Paracchini S Transl Psychiatry; 2017 Jul; 7(7):e1182. PubMed ID: 28742079 [TBL] [Abstract][Full Text] [Related]
16. Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. Paracchini S; Steer CD; Buckingham LL; Morris AP; Ring S; Scerri T; Stein J; Pembrey ME; Ragoussis J; Golding J; Monaco AP Am J Psychiatry; 2008 Dec; 165(12):1576-84. PubMed ID: 18829873 [TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 20949370 [TBL] [Abstract][Full Text] [Related]