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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.
Genome Research|October 1, 1996
An integrated YAC map of the human X chromosomeH Roest Crollius, M T Ross, A Grigoriev, et al.
Nature Genetics|October 20, 2022
Discovery of 42 genome-wide significant loci associated with dyslexiaCatherine Doust, Pierre Fontanillas, Else Eising, 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.
American Journal of Human Genetics|August 4, 2009
CMIP and ATP2C2 modulate phonological short-term memory in language impairmentDianne F Newbury, Laura Winchester, Laura Addis, et al.
European Journal of Human Genetics : EJHG|November 4, 2004
Mutation screening and association analysis of six candidate genes for autism on chromosome 7qElena Bonora, Janine A Lamb, Gabrielle Barnby, et al.
European Journal of Human Genetics : EJHG|September 12, 2013
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohortJessica Becker, Darina Czamara, Tom S Scerri, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosisC Dobson-Stone, A Danek, L Rampoldi, et al.
Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.
Translational Psychiatry|February 12, 2019
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexiaAlessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
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