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Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability.

Cope N, Eicher JD, Meng H, Gibson CJ, Hager K, Lacadie C, Fulbright RK, Constable RT, Page GP, Gruen JR.

Neuroimage. 2012 Oct 15;63(1):148-56. doi: 10.1016/j.neuroimage.2012.06.037. Epub 2012 Jun 27.


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. doi: 10.1097/YPG.0b013e32834acdb2.


A dyslexia-associated variant in DCDC2 changes gene expression.

Meng H, Powers NR, Tang L, Cope NA, Zhang PX, Fuleihan R, Gibson C, Page GP, Gruen JR.

Behav Genet. 2011 Jan;41(1):58-66. doi: 10.1007/s10519-010-9408-3. Epub 2010 Nov 2.


Polymorphism of DCDC2 Reveals Differences in Cortical Morphology of Healthy Individuals-A Preliminary Voxel Based Morphometry Study.

Meda SA, Gelernter J, Gruen JR, Calhoun VD, Meng H, Cope NA, Pearlson GD.

Brain Imaging Behav. 2008 Mar;2(1):21-26.


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.

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