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References

  • Annilo, T. & Dean, M. (2004) Degeneration of an ATP-binding cassette transporter gene, ABCC13, in different mammalian lineages. Genomics 84, 3446.
  • Bates, T.C., Castles, A., Coltheart, M., Gillespie, N., Wright, M.J. & Martin, N.G. (2004) Behaviour genetic analyses of reading and spelling: a component processes approach. Aust J Psychol 56, 115126.
  • Bates, T.C., Lind, P.A., Luciano, M., Montgomery, G.W., Martin, N.G. & Wright, M.J. (2010) Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation. Mol Psychiatry 15, 11901196.
  • Bates, T.C., Luciano, M., Medland, S.E., Montgomery, G.W., Wright, M.J. & Martin, N.G. (2011) Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. Behav Genet 41, 5057.
  • Bishop, D.V. (2001) Genetic influences on language impairment and literacy problems in children: same or different? J Child Psychol Psychiatry 42, 189198.
  • Bishop, D.V.M. & Hayiou-Thomas, M.E. (2008) Heritability of specific language impairment depends on diagnostic criteria. Genes Brain Behav 7, 365372.
  • Bishop, D.V., Laws, G., Adams, C. & Norbury, C.F. (2006) High heritability of speech and language impairments in 6-year-old twins demonstrated using parent and teacher report. Behav Genet 36, 173184.
  • Castles, A. & Coltheart, M. (1993) Varieties of developmental dyslexia. Cognition 47, 149180.
  • Chen, W.M. & Abecasis, G.R. (2007) Family-based association tests for genomewide association scans. Am J Hum Genet 81, 913926.
  • Cope, N., Harold, D., Hill, G., Moskvina, V., Stevenson, J., Holmans, P., Owen, M.J., O'Donovan, M.C. & Williams, J. (2005) Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am J Hum Genet 76, 581591.
  • Dollaghan, C. & Campbell, T.F. (1998) Nonword repetition and child language impairment. J Speech Lang Hear Res 41, 11361146.
  • Dudbridge, F. & Gusnanto, A. (2008) Estimation of significance thresholds for genomewide association scans. Genet Epidemiol 32, 227234.
  • Duggal, P., Gillanders, E.M., Holmes, T.N. & Bailey-Wilson, J.E. (2008) Establishing an adjusted p-value threshold to control the family-wide type 1 error in genome wide association studies. BMC Genomics 9, 516.
  • Field, L.L., Shumansky, K., Ryan, J., Truong, D., Swiergala, E. & Kaplan, B.J. (2013) Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36. Genes Brain Behav 12, 5669.
  • Gathercole, S.E. (1994) Neuropsychology and working memory: a review. Neuropsychology 8, 494505.
  • Golding, J., Pembrey, M. & Jones, R. (2001) ALSPAC--the Avon Longitudinal Study of Parents and Children. I. Study methodology. Paediatr Perinat Epidemiol 15, 7487.
  • Hannula-Jouppi, K., Kaminen-Ahola, N., Taipale, M., Eklund, R., Nopola-Hemmi, J., Kaariainen, H. & Kere, J. (2005) The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS Genet 1, e50.
  • Harlaar, N., Spinath, F.M., Dale, P.S. & Plomin, R. (2005) Genetic influences on early word recognition abilities and disabilities: a study of 7-year-old twins. J Child Psychol Psychiatry 46, 373384.
  • Harlaar, N., Dale, P.S. & Plomin, R. (2007) From learning to read to reading to learn: substantial and stable genetic influence. Child Dev 78, 116131.
  • Hawke, J.L., Wadsworth, S.J. & DeFries, J.C. (2006) Genetic influences on reading difficulties in boys and girls: the Colorado twin study. Dyslexia 12, 2129.
  • Jackson, D.N. (1984) Manual for the Multidimensional Aptitude Battery. Research Psychologists Press, Port Huron, MI.
  • Li, Y., Willer, C., Sanna, S. & Abecasis, G. (2009) Genotype imputation. Annu Rev Genomics Hum Genet 10, 387406.
  • Li, Y., Willer, C.J., Ding, J., Scheet, P. & Abecasis, G.R. (2010) MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet Epidemiol 34, 816834.
  • Lind, P.A., Luciano, M., Wright, M.J., Montgomery, G.W., Martin, N.G. & Bates, T.C. (2010) Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. Eur J Hum Genet 18, 668673.
  • Liu, J.Z., McRae, A.F., Nyholt, D.R., Medland, S.E., Wray, N.R., Brown, K.M., Hayward, N.K., Montgomery, G.W., Visscher, P.M., Martin, N.G. & Macgregor, S. (2010) A versatile gene-based test for genome-wide association studies. Am J Hum Genet 87, 139145.
  • Luciano, M., Lind, P.A., Duffy, D.L., Castles, A., Wright, M.J., Montgomery, G.W., Martin, N.G. & Bates, T.C. (2007) A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biol Psychiatry 62, 811817.
  • Luciano, M., Montgomery, G.W., Martin, N.G., Wright, M.J. & Bates, T.C. (2011) SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample. Twin Res Hum Genet 14, 228232.
  • Meaburn, E.L., Harlaar, N., Craig, I.W., Schalkwyk, L.C. & Plomin, R. (2008) Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children. Mol Psychiatry 13, 729740.
  • Medland, S.E., Nyholt, D.R., Painter, J.N., McEvoy, B.P., McRae, A.F., Zhu, G., Gordon, S.D., Ferreira, M.A., Wright, M.J., Henders, A.K., Campbell, M.J., Duffy, D.L., Hansell, N.K., Macgregor, S., Slutske, W.S., Heath, A.C., Montgomery, G.W. & Martin, N.G. (2009) Common variants in the trichohyalin gene are associated with straight hair in Europeans. Am J Hum Genet 85, 750755.
  • Meng, H., Smith, S.D., Hager, K., Held, M., Liu, J., Olson, R.K., Pennington, B.F., Defries, J.C., Gelernter, J., O'Reilly-Pol, T., Somlo, S., Skudlarski, P., Shaywitz, S.E., Shaywitz, B.A., Marchione, K., Wang, Y., Paramasivam, M., Loturco, J.J., Page, G.P. & Gruen, J.R. (2005) DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci U S A 102, 1705317058.
  • Miller, M.B. (1998) Monozygotic twins increase the power of genetic association studies of complex phenotypes. Behav Genet 28, 476.
  • Newbury, D.F., Winchester, L., Addis, L. et al (2009) CMIP and ATP2C2 modulate phonological short-term memory in language impairment. Am J Hum Genet 85, 264272.
  • Newbury, D.F., Paracchini, S., Scerri, T.S., Winchester, L., Addis, L., Richardson, A.J., Walter, J., Stein, J.F., Talcott, J.B. & Monaco, A.P. (2011) Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behav Genet 41, 90104.
  • Nunes, T., Bryant, P. & Olsson, J. (2003) Learning morphological and phonological spelling rules: an intervention study. Sci Stud Read 7, 289307.
  • O'Reilly, P.F., Hoggart, C.J., Pomyen, Y., Calboli, F.C., Elliott, P., Jarvelin, M.R. & Coin, L.J. (2012) MultiPhen: joint model of multiple phenotypes can increase discovery in GWAS. PLoS One 7, e34861.
  • Panagiotou, O.A. & Ioannidis, J.P. (2012) What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations. Int J Epidemiol 41, 273286.
  • Paracchini, S., Steer, C.D., Buckingham, L.L., Morris, A.P., Ring, S., Scerri, T., Stein, J., Pembrey, M.E., Ragoussis, J., Golding, J. & Monaco, A.P. (2008) Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. Am J Psychiatry 165, 15761584.
  • Rice, M.L., Smith, S.D. & Gayan, J. (2009) Convergent genetic linkage and associations to language, speech and reading measures in families of probands with specific language impairment. J Neurodev Disord 1, 264282.
  • Roeske, D., Ludwig, K.U., Neuhoff, N., Becker, J., Bartling, J., Bruder, J., Brockschmidt, F.F., Warnke, A., Remschmidt, H., Hoffmann, P., Muller-Myhsok, B., Nothen, M.M. & Schulte-Korne, G. (2011) First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. Mol Psychiatry 16, 97107.
  • Scerri, T.S., Morris, A.P., Buckingham, L.L., Newbury, D.F., Miller, L.L., Monaco, A.P., Bishop, D.V. & Paracchini, S. (2011) DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Biol Psychiatry 70, 237245.
  • Schonell, F.J. & Schonell, P.E. (1960) Diagnostic and Attainment Testing. Oliver & Boyd, Edinburgh.
  • Skiba, T., Landi, N., Wagner, R. & Grigorenko, E.L. (2011) In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes. Behav Genet 41, 630.
  • SLI Consortium (2002) A genomewide scan identifies two novel loci involved in specific language impairment. Am J Hum Genet 70, 384398.
  • Taipale, M., Kaminen, N., Nopola-Hemmi, J., Haltia, T., Myllyluoma, B., Lyytinen, H., Muller, K., Kaaranen, M., Lindsberg, P.J., Hannula-Jouppi, K. & Kere, J. (2003) A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proc Natl Acad Sci U S A 100, 1155311558.
  • Tran, C., Gagnon, F., Wigg, K.G., Feng, Y., Gomez, L., Cate-Carter, T.D., Kerr, E.N., Field, L.L., Kaplan, B.J., Lovett, M.W. & Barr, C.L. (2013) A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1. Am J Med Genet B Neuropsychiatr Genet 162, 146156.
  • Vernes, S.C., Newbury, D.F., Abrahams, B.S., Winchester, L., Nicod, J., Groszer, M., Alarcon, M., Oliver, P.L., Davies, K.E., Geschwind, D.H., Monaco, A.P. & Fisher, S.E. (2008) A functional genetic link between distinct developmental language disorders. N Engl J Med 359, 23372345.
  • Villanueva, P., Newbury, D.F., Jara, L., De Barbieri, Z., Mirza, G., Palomino, H.M., Fernandez, M.A., Cazier, J.B., Monaco, A.P. & Palomino, H. (2011) Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population. Eur J Hum Genet 19, 687695.
  • Wadsworth, S.J., Corley, R.P., Hewitt, J.K. & Defries, J.C. (2001) Stability of genetic and environmental influences on reading performance at 7, 12, and 16 years of age in the Colorado Adoption Project. Behav Genet 31, 353359.
  • Wechsler, D., Golombok, S. & Rust, J. (1992) WISC-IIIUK Wechsler Intelligence Scale for Children: UK Manual, 3rd edn. Psychological Corporation, Sidcup.
  • Whitehouse, A.J., Bishop, D.V., Ang, Q.W., Pennell, C.E. & Fisher, S.E. (2011) CNTNAP2 variants affect early language development in the general population. Genes Brain Behav 10, 451456.
  • Willer, C.J., Li, Y. & Abecasis, G.R. (2010) METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 26, 21902191.
  • Wright, M., De Geus, E., Ando, J., Luciano, M., Posthuma, D., Ono, Y., Hansell, N., Van Baal, C., Hiraishi, K., Hasegawa, T., Smith, G., Geffen, G., Geffen, L., Kanba, S., Miyake, A., Martin, N. & Boomsma, D. (2001) Genetics of cognition: outline of a collaborative twin study. Twin Res 4, 4856.
  • Zhong, R., Yang, B., Tang, H., Zou, L., Song, R., Zhu, L.Q. & Miao, X. (2013) Meta-analysis of the association between DCDC2 polymorphisms and risk of dyslexia. Mol Neurobiol 47, 435442.
  • Zhou, S.F., Wang, L.L., Di, Y.M., Xue, C.C., Duan, W., Li, C.G. & Li, Y. (2008) Substrates and inhibitors of human multidrug resistance associated proteins and the implications in drug development. Curr Med Chem 15, 19812039.
  • Zou, L., Chen, W., Shao, S., Sun, Z., Zhong, R., Shi, J., Miao, X. & Song, R. (2012) Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis. Am J Med Genet B Neuropsychiatr Genet 159B, 970976.