Genome-wide association study of shared components of reading disability and language impairment
Article first published online: 9 OCT 2013
© 2013 The Authors. Genes, Brain and Behavior published by International Behavioural and Neural Genetics Society and John Wiley & Sons Ltd.
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Genes, Brain and Behavior
Volume 12, Issue 8, pages 792–801, November 2013
How to Cite
Eicher, J. D., Powers, N. R., Miller, L. L., Akshoomoff, N., Amaral, D. G., Bloss, C. S., Libiger, O., Schork, N. J., Darst, B. F., Casey, B. J., Chang, L., Ernst, T., Frazier, J., Kaufmann, W. E., Keating, B., Kenet, T., Kennedy, D., Mostofsky, S., Murray, S. S., Sowell, E. R., Bartsch, H., Kuperman, J. M., Brown, T. T., Hagler, D. J., Dale, A. M., Jernigan, T. L., St. Pourcain, B., Davey Smith, G., Ring, S. M., Gruen, J. R. and for the Pediatric Imaging, Neurocognition, and Genetics Study (2013), Genome-wide association study of shared components of reading disability and language impairment. Genes, Brain and Behavior, 12: 792–801. doi: 10.1111/gbb.12085
- Issue published online: 30 OCT 2013
- Article first published online: 9 OCT 2013
- Accepted manuscript online: 11 SEP 2013 12:51PM EST
- Manuscript Accepted: 9 SEP 2013
- Manuscript Revised: 6 SEP 2013
- Manuscript Revised: 16 AUG 2013
- Manuscript Received: 21 JUN 2013
- UK medical research council
- Wellcome Trust. Grant Number: 092731
- National Institutes of Health. Grant Numbers: RC2DA029475, R01 NS043530, F31 DC012270
- National Institute on Drug Abuse
- Eunice Kennedy Shriver National Institute of Child Health & Human Development
|gbb12085-sup-0001-TableS1.doc||Word document||58K||Table S1: Associations of markers within genes previously implicated in RD and/or LI with (a) Comorbid RD and LI, (b) LI individually and (c) RD individually.|
|gbb12085-sup-0002-TableS2.doc||Word document||64K||Table S2: Gene-based analyses of comorbid RD and LI, LI individually and RD individually. The top 10 gene-based associations for each are shown.|
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