Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia

This publication has 27 references indexed in Scilit:

• On Confidence Intervals for Genotype Relative Risks and Attributable Risks from Case Parent Trio Designs for Candidate-Gene Studies
  Human Heredity, 2005
• Linkage analyses of chromosomal region 18p11-q12 in dyslexia
  Journal Of Neural Transmission-Parkinsons Disease and Dementia Section, 2005
• Developmental dyslexia
  The Lancet, 2004
• Sex Differences in Developmental Reading Disability
  JAMA, 2004
• Pedigree disequilibrium tests for multilocus haplotypes
  Genetic Epidemiology, 2003
• Continuing the search for dyslexia genes on 6p
  American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 2002
• Evidence for Linkage and Association with Reading Disability, on 6p21.3-22
  American Journal of Human Genetics, 2002
• Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention‐deficit/hyperactivity disorder
  American Journal of Medical Genetics, 2002
• Confidence Intervals for Genotype Relative Risks and Allele Frequencies from the Case Parent Trio Design for Candidate-Gene Studies
  Human Heredity, 2002
• Incidence of Reading Disability in a Population-Based Birth Cohort, 1976–1982, Rochester, Minn
  Mayo Clinic Proceedings, 2001