[1] Gillis JJ, Gilger JW, Pennington BF, et al. Attention deficit disorder in reading-disabled twins: evidence for a genetic aetiology[J]. Journal of Abnormal Child Psychology,1992,20,303-315.
[2] Alarcon M, Plomin R, Fulker DW, et al. Multivariate path analysis of specific cognitive abilities data at 12 years of age in the Colorado adoption project[J]. Behavior Genetics,1998,28:255-264.
[3] Hallgren B. Specific dyslexia('congenital word-blindness'): a clinical and genetic study[J]. Acta Psychiat Neurol Scand,1950,65(S):1-287.
[4] Zahalkova M,Vrzal V,Kloboukova E, et al. Genetical investigations in dyslexia[J]. J Med Genet,1972,9:48-52.
[5] Finucci JM,Guthrie JT, Childs AL, et al. The genetics of specific reading disability[J]. Ann Hum Genet,1976,40:1-23.
[6] DeFries JC, Fulker DW, LaBuda MC. Evidence for a genetic aetiology in reading disability of twins[J]. Nature,1987,329(6139):537-539.
[7] Sullivan PF, Kendler KS, Neale MC. Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies[J]. Archives of General Psychiatry,2003,60(12):1187-1192.
[8] Bishop DV, North T, Donlan C. Genetic basis of specific language impairment: Evidence from a twin study[J]. Developmental Medicine and Child Neurology,1995,37(1):56–71.
[9] Gregory S, Gilbert J. Strategies for genotype generation[M]∥ Haines JL,Korf BR,Morton CC, et al. Current Protocols in Human Genetics. NY: Wiley and Sons,2005:1.3.1-1.3.16.
[10] Smith SD, Kimberling WJ, Pennington BF, et al.Specific reading disability: identification of an inherited form through linkage analysis[J]. Science,1983,219(4590):1345-1347.
[11] Wigg KG, Couto JM, Feng Y, et al. Support for EKN1 as the susceptibility locus for dyslexia on 15q21[J]. Molecular Psychiatry,2004,9(12):1111-1121.
[12] Fisher SE, Marlow AJ, Lamb J, et al. A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia[J]. American Journal of Human Genetics,1999,64(1):146–156.
[13] Nopola-Hemmi J, Taipale M, Haltia T, et al. Two translocations of chromosome 15q associated with dyslexia[J]. Journal of Medical Genetics,2000,37(10):771-775.
[14] Fisher SE, Francks C, Marlow AJ, et al. Independent genomewide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia[J]. Nature Genetics,2002,30:86-91.
[15] Cope N, Harold D, Hill G, et al. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia[J]. American Journal of Human Genetics,2005,76(4):581-591.
[16] Meng H, Smith SD, Hager K, et al. DCDC2 is associated with reading disability and modulates neuronal development in the brain[J]. Proceedings of the National Academy of Sciences of the United States of America,2005,102(47):17053-17058.
[17] Schumacher J, Anthoni H, Dahdouh F, et al. Strong evidence of DCDC2 as a susceptibility gene for dyslexia[J]. American Journal of Human Genetics,2006,78(1):52-62.
[18] Harold D, Paracchini S, Scerri T, et al. Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia[J]. Molecular Psychiatry,2006,11(12):1085-1091.
[19] Luciano M, Lind PA, Duffy DL, et al. A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability[J]. Biological Psychiatry,2007,62(7):811-817.
[20] Taipale M, Kaminen N, Nopola-Hemmi J, et al. A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain[J]. Proceedings of the National Academy of Sciences of the United States of America,2003,100(20):11553-11558.
[21] Marino C, Giorda R, Lorusso ML, et al. A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia[J]. European Journal of Human Genetics,2005,13(4):491-499.
[22] Nopola-Hemmi J, Myllyluoma B, Haltia T, et al. A dominant gene for developmental dyslexia on chromosome 3[J]. Journal of Medical Genetics,2001;38(10):658-64.
[23] Christopher JG, Jeffrey RG, The human lexinome: Genes of language and reading[J]. J Commun Disord,2008,41(5):409-420.
[24] Paracchini S, Thomas A, Castro S, et al. The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration[J]. Human Molecular Genetics,2006,15(10):1659-1666.
[25] Velayos-Baeza A, Toma C, Paracchini S, et al. The dyslexia-associated gene Kiaa0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms[J]. Human Molecular Genetics,2007,21(S):581-591.
[26] Hannula-Jouppi K, Kaminen-Ahola N, Taipale M, et al. The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia[J]. PLOS Genetics,2005,1(4):e50-60.