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Molecular Psychiatry|October 13, 2006
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexiaD Harold, S Paracchini, T Scerri, et al.American Journal of Human Genetics|March 15, 2002
FOXP2 is not a major susceptibility gene for autism or specific language impairmentD F Newbury, E Bonora, J A Lamb, et al.Genes, Brain, and Behavior|February 28, 2014
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairmentR Nudel, N H Simpson, G Baird, et al.Nature Genetics|March 18, 1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseA Sakuntabhai, V Ruiz-Perez, S Carter, 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.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.Nature Genetics|May 31, 2001
A conserved sorting-associated protein is mutant in chorea-acanthocytosisL Rampoldi, C Dobson-Stone, J P Rubio, 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.Pageof 29