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Human Molecular Genetics|April 8, 2006
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migrationSilvia Paracchini, Ankur Thomas, Sandra Castro, et al.American Journal of Human Genetics|October 23, 1997
Chorea-acanthocytosis: genetic linkage to chromosome 9q21J P Rubio, A Danek, C Stone, et al.American Journal of Human Genetics|June 13, 1998
Refined genetic mapping of the darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical regionS Monk, A Sakuntabhai, S A Carter, et al.American Journal of Human Genetics|April 2, 2002
A genomewide scan for loci involved in attention-deficit/hyperactivity disorderSimon E Fisher, Clyde Francks, James T McCracken, et al.Nature Genetics|May 31, 2001
A conserved sorting-associated protein is mutant in chorea-acanthocytosisL Rampoldi, C Dobson-Stone, J P Rubio, et al.Nature Genetics|December 18, 2001
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexiaSimon E Fisher, Clyde Francks, Angela J Marlow, et al.Journal of Medical Genetics|October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityAlistair T Pagnamenta, Hameed Khan, Susan Walker, et al.Annals of Neurology|January 5, 2002
McLeod neuroacanthocytosis: genotype and phenotypeA Danek, J P Rubio, L Rampoldi, 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.Human Mutation|September 18, 2010
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficitsDenise Horn, Johannes Kapeller, Núria Rivera-Brugués, et al.Pageof 59