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Brain : a Journal of Neurology|February 24, 2019
Dorsal language stream anomalies in an inherited speech disorderFrédérique J Liégeois, Samantha J Turner, Angela Mayes, et al.
Translational Psychiatry|July 26, 2017
The DCDC2 deletion is not a risk factor for dyslexiaT S Scerri, E Macpherson, A Martinelli, et al.
Molecular Psychiatry|February 22, 2018
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech developmentElse Eising, Amaia Carrion-Castillo, Arianna Vino, et al.
American Journal of Human Genetics|October 30, 2004
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United StatesClyde Francks, Silvia Paracchini, Shelley D Smith, et al.
Plos One|December 5, 2012
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structureThomas S Scerri, Fahimeh Darki, Dianne F Newbury, et al.
Plos Genetics|September 27, 2013
Common variants in left/right asymmetry genes and pathways are associated with relative hand skillWilliam M Brandler, Andrew P Morris, David M Evans, et al.
Developmental Medicine and Child Neurology|October 15, 2013
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexiaNuala H Simpson, Laura Addis, William M Brandler, et al.
Genes, Brain, and Behavior|July 29, 2014
Genome-wide screening for DNA variants associated with reading and language traitsA Gialluisi, D F Newbury, E G Wilcutt, et al.
Molecular Psychiatry|April 30, 2009
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibilityE Maestrini, A T Pagnamenta, J A Lamb, et al.
Biological Psychiatry|March 30, 2010
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexiaAlistair T Pagnamenta, Elena Bacchelli, Maretha V de Jonge, et al.
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