Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment-Reference-Cited by-同舟云学术

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Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment

Published:2017-04-25 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Chen Xiaowei Sylvia,Reader Rose H.,Hoischen Alexander,Veltman Joris A.,Simpson Nuala H.,Francks Clyde,Newbury Dianne F.,Fisher Simon E.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep46105.pdf

Reference102 articles.

1. Norbury, C. F. et al. The impact of nonverbal ability on prevalence and clinical presentation of language disorder: evidence from a population study. J Child Psychol Psychiatry 57, 1247–1257, doi: 10.1111/jcpp.12573 (2016).

2. Tomblin, J. B., Records, N. L. & Zhang, X. A system for the diagnosis of specific language impairment in kindergarten children. J Speech Hear Res 39, 1284–1294 (1996).

3. Bishop, D. V., North, T. & Donlan, C. Genetic basis of specific language impairment: evidence from a twin study. Dev Med Child Neurol 37, 56–71 (1995).

4. Newbury, D. F., Fisher, S. E. & Monaco, A. P. Recent advances in the genetics of language impairment. Genome Med 2, 6, doi: 10.1186/gm127 (2010).

5. Evans, P. D., Mueller, K. L., Gamazon, E. R., Cox, N. J. & Tomblin, J. B. A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13. Genes Brain Behav 14, 387–397, doi: 10.1111/gbb.12223 (2015).

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