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Two translocations of chromosome 15q associated with dyslexia

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References

1994Quantitative Trait Locus for Reading Disability on Chromosome 6532 cited
1995Toward a definition of dyslexia476 cited
1997Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15.445 cited
1983Specific Reading Disability: Identification of an Inherited Form Through Linkage Analysis328 cited
1987Evidence for a genetic aetiology in reading disability of twins312 cited
1999Quantitative-Trait Locus for Specific Language and Reading Deficits on Chromosome 6p249 cited
1999A new gene (DYX3) for dyslexia is located on chromosome 2192 cited
1998Evidence for Linkage of Spelling Disability to Chromosome 15171 cited
1993Suggestive linkage of developmental dyslexia to chromosome 1p34-p36148 cited
2000Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q112 cited
1987Neuropsychological Assessment of Children101 cited

Cited by

2004Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK102 cited
2005Bivariate linkage scan for reading disability and attention‐deficit/hyperactivity disorder localizes pleiotropic loci102 cited
2002The genetic basis of dyslexia

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99 cited

2004Linkage analyses of four regions previously implicated in dyslexia: Confirmation of a locus on chromosome 15q91 cited

2014The molecular genetics and neurobiology of developmental dyslexia as model of a complex phenotype89 cited

2005A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia89 cited

2011Genetics of Speech and Language Disorders88 cited

2006Association of short‐term memory with a variant within DYX1C1 in developmental dyslexia82 cited

2006Breakthroughs in the search for dyslexia candidate genes82 cited

2006The genetics of developmental dyslexia79 cited

2005TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort76 cited

2008Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion75 cited

2012The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language71 cited

2013The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes71 cited

2008The complex of TFII‐I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia71 cited

2007Genes, language development, and language disorders65 cited