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Volumn 3, Issue 4, 2011, Pages 365-373

Dissection of genetic associations with language-related traits in population-based cohorts

Author keywords

Association studies; Cognition; Dyslexia; Epidemiology; Language; Neurodevelopmental disorders; Quantitative genetics

Indexed keywords


EID: 82755197778     PISSN: 18661947     EISSN: 18661955     Source Type: Journal    
DOI: 10.1007/s11689-011-9091-6     Document Type: Article
Times cited : (25)

References (82)
  • 1
    • 38749140677 scopus 로고    scopus 로고
    • Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
    • Alarcon M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, et al. Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am J Hum Genet. 2008; 82(1): 150-9.
    • (2008) Am J Hum Genet. , vol.82 , Issue.1 , pp. 150-159
    • Alarcon, M.1    Abrahams, B.S.2    Stone, J.L.3    Duvall, J.A.4    Perederiy, J.V.5    Bomar, J.M.6
  • 4
  • 5
    • 38749096303 scopus 로고    scopus 로고
    • A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
    • Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, et al. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am J Hum Genet. 2008; 82(1): 160-4.
    • (2008) Am J Hum Genet. , vol.82 , Issue.1 , pp. 160-164
    • Arking, D.E.1    Cutler, D.J.2    Brune, C.W.3    Teslovich, T.M.4    West, K.5    Ikeda, M.6
  • 6
    • 38749099110 scopus 로고    scopus 로고
    • Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders
    • Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, et al. Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. Am J Hum Genet. 2008; 82(1): 165-73.
    • (2008) Am J Hum Genet. , vol.82 , Issue.1 , pp. 165-173
    • Bakkaloglu, B.1    O'Roak, B.J.2    Louvi, A.3    Gupta, A.R.4    Abelson, J.F.5    Morgan, T.M.6
  • 7
    • 67649945780 scopus 로고    scopus 로고
    • Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient
    • Ballarati L, Recalcati MP, Bedeschi MF, Lalatta F, Valtorta C, Bellini M, et al. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient. Eur J Med Genet. 2009; 52(4): 218-23.
    • (2009) Eur J Med Genet. , vol.52 , Issue.4 , pp. 218-223
    • Ballarati, L.1    Recalcati, M.P.2    Bedeschi, M.F.3    Lalatta, F.4    Valtorta, C.5    Bellini, M.6
  • 8
    • 33846139314 scopus 로고    scopus 로고
    • Heritable risk factors associated with language impairments
    • Barry JG, Yasin I, Bishop DV. Heritable risk factors associated with language impairments. Genes Brain Behav. 2007; 6(1): 66-76.
    • (2007) Genes Brain Behav. , vol.6 , Issue.1 , pp. 66-76
    • Barry, J.G.1    Yasin, I.2    Bishop, D.V.3
  • 9
    • 78650241792 scopus 로고    scopus 로고
    • Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation
    • Bates TC, Lind PA, Luciano M, Montgomery GW, Martin NG, Wright MJ. Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation. Mol Psychiatry; 2010; 15(12): 1190-6.
    • (2010) Mol Psychiatry , vol.15 , Issue.12 , pp. 1190-1196
    • Bates, T.C.1    Lind, P.A.2    Luciano, M.3    Montgomery, G.W.4    Martin, N.G.5    Wright, M.J.6
  • 10
    • 79952443930 scopus 로고    scopus 로고
    • Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits
    • Bates TC, Luciano M, Medland SE, Montgomery GW, Wright MJ, Martin NG. Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. Behav Genet. 2011; 41(1): 50-7.
    • (2011) Behav Genet. , vol.41 , Issue.1 , pp. 50-57
    • Bates, T.C.1    Luciano, M.2    Medland, S.E.3    Montgomery, G.W.4    Wright, M.J.5    Martin, N.G.6
  • 12
    • 0029865799 scopus 로고    scopus 로고
    • Nonword repetition as a behavioural marker for inherited language impairment: evidence from a twin study
    • Bishop DV, North T, Donlan C. Nonword repetition as a behavioural marker for inherited language impairment: evidence from a twin study. J Child Psychol Psychiatry. 1996; 37(4): 391-403.
    • (1996) J Child Psychol Psychiatry. , vol.37 , Issue.4 , pp. 391-403
    • Bishop, D.V.1    North, T.2    Donlan, C.3
  • 14
    • 0000841833 scopus 로고
    • Remarques sur le siége de la faculté du language articulé, suivies d'une observation d'aphémie (perte de la parole)
    • Broca P. Remarques sur le siége de la faculté du language articulé, suivies d'une observation d'aphémie (perte de la parole). Bull Soc Anat. 1861; 6: 330-57.
    • (1861) Bull Soc Anat. , vol.6 , pp. 330-357
    • Broca, P.1
  • 15
    • 15944363095 scopus 로고    scopus 로고
    • No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia
    • Cope NA, Hill G, van den Bree M, Harold D, Moskvina V, Green EK, et al. No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia. Mol Psychiatry. 2005a; 10(3): 237-8.
    • (2005) Mol Psychiatry , vol.10 , Issue.3 , pp. 237-238
    • Cope, N.A.1    Hill, G.2    van den Bree, M.3    Harold, D.4    Moskvina, V.5    Green, E.K.6
  • 16
    • 15944372645 scopus 로고    scopus 로고
    • Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia
    • Cope N, Harold D, Hill G, Moskvina V, Stevenson J, Holmans P, et al. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am J Hum Genet. 2005b; 76(4): 581-91.
    • (2005) Am J Hum Genet. , vol.76 , Issue.4 , pp. 581-591
    • Cope, N.1    Harold, D.2    Hill, G.3    Moskvina, V.4    Stevenson, J.5    Holmans, P.6
  • 18
    • 67651048992 scopus 로고    scopus 로고
    • Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p
    • Couto JM, Gomez L, Wigg K, Ickowicz A, Pathare T, Malone M, et al. Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p. Biol Psychiatry. 2009; 66(4): 368-75.
    • (2009) Biol Psychiatry. , vol.66 , Issue.4 , pp. 368-375
    • Couto, J.M.1    Gomez, L.2    Wigg, K.3    Ickowicz, A.4    Pathare, T.5    Malone, M.6
  • 19
    • 79952437992 scopus 로고    scopus 로고
    • Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia
    • Czamara D, Bruder J, Becker J, Bartling J, Hoffmann P, Ludwig KU, et al. Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia. Behav Genet. 2011; 41(1): 110-9.
    • (2011) Behav Genet , vol.41 , Issue.1 , pp. 110-119
    • Czamara, D.1    Bruder, J.2    Becker, J.3    Bartling, J.4    Hoffmann, P.5    Ludwig, K.U.6
  • 21
    • 3543029197 scopus 로고    scopus 로고
    • Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses
    • Deffenbacher KE, Kenyon JB, Hoover DM, Olson RK, Pennington BF, DeFries JC, et al. Refinement of the 6p21. 3 quantitative trait locus influencing dyslexia: linkage and association analyses. Hum Genet. 2004; 115(2): 128-38.
    • (2004) Hum Genet. , vol.115 , Issue.2 , pp. 128-138
    • Deffenbacher, K.E.1    Kenyon, J.B.2    Hoover, D.M.3    Olson, R.K.4    Pennington, B.F.5    Defries, J.C.6
  • 23
    • 57649136554 scopus 로고    scopus 로고
    • Progress and challenges in genome-wide association studies in humans
    • Donnelly P. Progress and challenges in genome-wide association studies in humans. Nature. 2008; 456(7223): 728-31.
    • (2008) Nature. , vol.456 , Issue.7223 , pp. 728-731
    • Donnelly, P.1
  • 24
    • 77952887857 scopus 로고    scopus 로고
    • Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
    • Elia J, Gai X, Xie HM, Perin JC, Geiger E, Glessner JT, et al. Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes. Mol Psychiatry. 2010; 15(6): 637-46.
    • (2010) Mol Psychiatry , vol.15 , Issue.6 , pp. 637-646
    • Elia, J.1    Gai, X.2    Xie, H.M.3    Perin, J.C.4    Geiger, E.5    Glessner, J.T.6
  • 25
    • 0036779497 scopus 로고    scopus 로고
    • Developmental dyslexia: genetic dissection of a complex cognitive trait
    • Fisher SE, DeFries JC. Developmental dyslexia: genetic dissection of a complex cognitive trait. Nat Rev Neurosci. 2002; 3(10): 767-80.
    • (2002) Nat Rev Neurosci. , vol.3 , Issue.10 , pp. 767-780
    • Fisher, S.E.1    Defries, J.C.2
  • 26
  • 27
    • 8844258018 scopus 로고    scopus 로고
    • A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States
    • Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, et al. A 77-kilobase region of chromosome 6p22. 2 is associated with dyslexia in families from the United Kingdom and from the United States. Am J Hum Genet. 2004; 75(6): 1046-58.
    • (2004) Am J Hum Genet. , vol.75 , Issue.6 , pp. 1046-1058
    • Francks, C.1    Paracchini, S.2    Smith, S.D.3    Richardson, A.J.4    Scerri, T.S.5    Cardon, L.R.6
  • 30
    • 0035130957 scopus 로고    scopus 로고
    • ALSPAC-the Avon Longitudinal Study of Parents and Children: I. Study methodology
    • Golding J, Pembrey M, Jones R. ALSPAC-the Avon Longitudinal Study of Parents and Children: I. Study methodology. Paediatr Perinat Epidemiol. 2001; 15(1): 74-87.
    • (2001) Paediatr Perinat Epidemiol. , vol.15 , Issue.1 , pp. 74-87
    • Golding, J.1    Pembrey, M.2    Jones, R.3
  • 32
    • 33845246158 scopus 로고    scopus 로고
    • Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia
    • 61
    • Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, et al. Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Mol Psychiatry. 2006; 11(12): 1085-91.
    • (2006) Mol Psychiatry , vol.11 , Issue.12 , pp. 1085-1091
    • Harold, D.1    Paracchini, S.2    Scerri, T.3    Dennis, M.4    Cope, N.5    Hill, G.6
  • 33
    • 62149099978 scopus 로고    scopus 로고
    • Gene associated with seizures, autism, and hepatomegaly in an Amish girl
    • Jackman C, Horn ND, Molleston JP, Sokol DK. Gene associated with seizures, autism, and hepatomegaly in an Amish girl. Pediatr Neurol. 2009; 40(4): 310-3.
    • (2009) Pediatr Neurol. , vol.40 , Issue.4 , pp. 310-313
    • Jackman, C.1    Horn, N.D.2    Molleston, J.P.3    Sokol, D.K.4
  • 34
    • 0035807360 scopus 로고    scopus 로고
    • A forkhead-domain gene is mutated in a severe speech and language disorder
    • Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature. 2001; 413(6855): 519-23.
    • (2001) Nature. , vol.413 , Issue.6855 , pp. 519-523
    • Lai, C.S.1    Fisher, S.E.2    Hurst, J.A.3    Vargha-Khadem, F.4    Monaco, A.P.5
  • 36
    • 55349128167 scopus 로고    scopus 로고
    • Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies
    • Lesch KP, Timmesfeld N, Renner TJ, Halperin R, Roser C, Nguyen TT, et al. Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. J Neural Transm. 2008; 115(11): 1573-85.
    • (2008) J Neural Transm. , vol.115 , Issue.11 , pp. 1573-1585
    • Lesch, K.P.1    Timmesfeld, N.2    Renner, T.J.3    Halperin, R.4    Roser, C.5    Nguyen, T.T.6
  • 37
    • 77952673657 scopus 로고    scopus 로고
    • Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample
    • Lind PA, Luciano M, Wright MJ, Montgomery GW, Martin NG, Bates TC. Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. Eur J Hum Genet. 2010; 18(6): 668-73.
    • (2010) Eur J Hum Genet. , vol.18 , Issue.6 , pp. 668-673
    • Lind, P.A.1    Luciano, M.2    Wright, M.J.3    Montgomery, G.W.4    Martin, N.G.5    Bates, T.C.6
  • 38
    • 34548473808 scopus 로고    scopus 로고
    • A Haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability
    • Luciano M, Lind PA, Duffy DL, Castles A, Wright MJ, Montgomery GW, et al. A Haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biol Psychiatry. 2007; 62(7): 811-7.
    • (2007) Biol Psychiatry , vol.62 , Issue.7 , pp. 811-817
    • Luciano, M.1    Lind, P.A.2    Duffy, D.L.3    Castles, A.4    Wright, M.J.5    Montgomery, G.W.6
  • 39
    • 57149129848 scopus 로고    scopus 로고
    • Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample
    • Ludwig KU, Schumacher J, Schulte-Korne G, Konig IR, Warnke A, Plume E, et al. Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample. Psychiatr Genet. 2008; 18(6): 310-2.
    • (2008) Psychiatr Genet. , vol.18 , Issue.6 , pp. 310-312
    • Ludwig, K.U.1    Schumacher, J.2    Schulte-Korne, G.3    Konig, I.R.4    Warnke, A.5    Plume, E.6
  • 40
    • 34748875368 scopus 로고    scopus 로고
    • Association of short-term memory with a variant within DYX1C1 in developmental dyslexia
    • Marino C, Citterio A, Giorda R, Facoetti A, Menozzi G, Vanzin L, et al. Association of short-term memory with a variant within DYX1C1 in developmental dyslexia. Genes Brain Behav. 2007; 6(7): 640-6.
    • (2007) Genes Brain Behav. , vol.6 , Issue.7 , pp. 640-646
    • Marino, C.1    Citterio, A.2    Giorda, R.3    Facoetti, A.4    Menozzi, G.5    Vanzin, L.6
  • 42
    • 0032900220 scopus 로고    scopus 로고
    • Genetic and environmental contributions to size, color, shape, and other characteristics of melanocytic naevi in a sample of adolescent twins
    • McGregor B, Pfitzner J, Zhu G, Grace M, Eldridge A, Pearson J, et al. Genetic and environmental contributions to size, color, shape, and other characteristics of melanocytic naevi in a sample of adolescent twins. Genet Epidemiol. 1999; 16(1): 40-53.
    • (1999) Genet Epidemiol. , vol.16 , Issue.1 , pp. 40-53
    • McGregor, B.1    Pfitzner, J.2    Zhu, G.3    Grace, M.4    Eldridge, A.5    Pearson, J.6
  • 43
    • 33744733429 scopus 로고    scopus 로고
    • TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort
    • Meng H, Hager K, Held M, Page GP, Olson RK, Pennington BF, et al. TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort. Hum Genet. 2005a; 118(1): 87-90.
    • (2005) Hum Genet. , vol.118 , Issue.1 , pp. 87-90
    • Meng, H.1    Hager, K.2    Held, M.3    Page, G.P.4    Olson, R.K.5    Pennington, B.F.6
  • 44
    • 28044465597 scopus 로고    scopus 로고
    • DCDC2 is associated with reading disability and modulates neuronal development in the brain
    • Meng H, Smith SD, Hager K, Held M, Liu J, Olson RK, et al. DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci U S A. 2005b; 102(47): 17053-8.
    • (2005) Proc Natl Acad Sci U S A. , vol.102 , Issue.47 , pp. 17053-17058
    • Meng, H.1    Smith, S.D.2    Hager, K.3    Held, M.4    Liu, J.5    Olson, R.K.6
  • 45
    • 77957904400 scopus 로고    scopus 로고
    • Genetic advances in the study of speech and language disorders
    • Newbury DF, Monaco AP. Genetic advances in the study of speech and language disorders. Neuron. 2010; 68(2): 309-20.
    • (2010) Neuron. , vol.68 , Issue.2 , pp. 309-320
    • Newbury, D.F.1    Monaco, A.P.2
  • 46
    • 27544444173 scopus 로고    scopus 로고
    • Genetic influences on language impairment and phonological short-term memory
    • Newbury DF, Bishop DV, Monaco AP. Genetic influences on language impairment and phonological short-term memory. Trends Cogn Sci. 2005; 9(11): 528-34.
    • (2005) Trends Cogn Sci. , vol.9 , Issue.11 , pp. 528-534
    • Newbury, D.F.1    Bishop, D.V.2    Monaco, A.P.3
  • 48
    • 79952443636 scopus 로고    scopus 로고
    • Investigation of dyslexia and SLI risk variants in reading and language-impaired subjects
    • Newbury DF, Paracchini S, Scerri TS, Winchester L, Addis L, Walter J, et al. Investigation of dyslexia and SLI risk variants in reading and language-impaired subjects. Behav Genet. 2011; 41(1): 90-104.
    • (2011) Behav Genet. , vol.41 , Issue.1 , pp. 90-104
    • Newbury, D.F.1    Paracchini, S.2    Scerri, T.S.3    Winchester, L.4    Addis, L.5    Walter, J.6
  • 49
    • 0027379214 scopus 로고
    • Effects of frequent ultrasound during pregnancy: a randomised controlled trial
    • Newnham JP, Evans SF, Michael CA, Stanley FJ, Landau LI. Effects of frequent ultrasound during pregnancy: a randomised controlled trial. Lancet. 1993; 342(8876): 887-91.
    • (1993) Lancet. , vol.342 , Issue.8876 , pp. 887-891
    • Newnham, J.P.1    Evans, S.F.2    Michael, C.A.3    Stanley, F.J.4    Landau, L.I.5
  • 51
    • 33744920683 scopus 로고    scopus 로고
    • The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
    • Paracchini S, Thomas A, Castro S, Lai C, Paramasivam M, Wang Y, et al. The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum Mol Genet. 2006; 15(10): 1659-66.
    • (2006) Hum Mol Genet. , vol.15 , Issue.10 , pp. 1659-1666
    • Paracchini, S.1    Thomas, A.2    Castro, S.3    Lai, C.4    Paramasivam, M.5    Wang, Y.6
  • 53
    • 57349157021 scopus 로고    scopus 로고
    • Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population
    • Paracchini S, Steer CD, Buckingham LL, Morris AP, Ring S, Scerri T, et al. Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. Am J Psychiatry. 2008; 165(12): 1576-84.
    • (2008) Am J Psychiatry. , vol.165 , Issue.12 , pp. 1576-1584
    • Paracchini, S.1    Steer, C.D.2    Buckingham, L.L.3    Morris, A.P.4    Ring, S.5    Scerri, T.6
  • 54
  • 55
    • 60549109887 scopus 로고    scopus 로고
    • Relations among speech, language, and reading disorders
    • Pennington BF, Bishop DV. Relations among speech, language, and reading disorders. Annu Rev Psychol. 2009; 60: 283-306.
    • (2009) Annu Rev Psychol. , vol.60 , pp. 283-306
    • Pennington, B.F.1    Bishop, D.V.2
  • 56
    • 23844450016 scopus 로고    scopus 로고
    • Generalist genes and learning disabilities
    • Plomin R, Kovas Y. Generalist genes and learning disabilities. Psychol Bull. 2005; 131(4): 592-617.
    • (2005) Psychol Bull. , vol.131 , Issue.4 , pp. 592-617
    • Plomin, R.1    Kovas, Y.2
  • 57
    • 76549104658 scopus 로고    scopus 로고
    • Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder
    • Poot M, Beyer V, Schwaab I, Damatova N, Van't Slot R, Prothero J, et al. Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder. Neurogenetics. 2010; 11(1): 81-9.
    • (2010) Neurogenetics. , vol.11 , Issue.1 , pp. 81-89
    • Poot, M.1    Beyer, V.2    Schwaab, I.3    Damatova, N.4    van't Slot, R.5    Prothero, J.6
  • 58
    • 12244264435 scopus 로고    scopus 로고
    • Genetic power calculator: design of linkage and association genetic mapping studies of complex traits
    • Purcell S, Cherny SS, Sham PC. Genetic power calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics. 2003; 19(1): 149-50.
    • (2003) Bioinformatics. , vol.19 , Issue.1 , pp. 149-150
    • Purcell, S.1    Cherny, S.S.2    Sham, P.C.3
  • 59
    • 77950852556 scopus 로고    scopus 로고
    • Convergent genetic linkage and associations to language, speech and reading measures in families of probands with specific language impairment
    • Rice ML, Smith SD, Gayan J. Convergent genetic linkage and associations to language, speech and reading measures in families of probands with specific language impairment. J Neurodev Disord. 2009; 1(4): 264-82.
    • (2009) J Neurodev Disord. , vol.1 , Issue.4 , pp. 264-282
    • Rice, M.L.1    Smith, S.D.2    Gayan, J.3
  • 60
    • 56649085194 scopus 로고    scopus 로고
    • A 12 Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea
    • Rossi E, Verri AP, Patricelli MG, Destefani V, Ricca I, Vetro A, et al. A 12 Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea. Eur J Med Genet. 2008; 51(6): 631-8.
    • (2008) Eur J Med Genet. , vol.51 , Issue.6 , pp. 631-638
    • Rossi, E.1    Verri, A.P.2    Patricelli, M.G.3    Destefani, V.4    Ricca, I.5    Vetro, A.6
  • 62
    • 8744255235 scopus 로고    scopus 로고
    • Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK
    • Scerri TS, Fisher SE, Francks C, MacPhie IL, Paracchini S, Richardson AJ, et al. Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. J Med Genet. 2004; 41(11): 853-7.
    • (2004) J Med Genet. , vol.41 , Issue.11 , pp. 853-857
    • Scerri, T.S.1    Fisher, S.E.2    Francks, C.3    Macphie, I.L.4    Paracchini, S.5    Richardson, A.J.6
  • 67
    • 16944366964 scopus 로고    scopus 로고
    • Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
    • Skuse DH, James RS, Bishop DV, Coppin B, Dalton P, Aamodt-Leeper G, et al. Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature. 1997; 387(6634): 705-8.
    • (1997) Nature. , vol.387 , Issue.6634 , pp. 705-708
    • Skuse, D.H.1    James, R.S.2    Bishop, D.V.3    Coppin, B.4    Dalton, P.5    Aamodt-Leeper, G.6
  • 68
    • 18244408330 scopus 로고    scopus 로고
    • A genomewide scan identifies two novel loci involved in specific language impairment
    • SLI Consortium
    • SLI Consortium. A genomewide scan identifies two novel loci involved in specific language impairment. Am J Hum Genet. 2002; 70(2): 384-398.
    • (2002) Am J Hum Genet , vol.70 , Issue.2 , pp. 384-398
  • 69
    • 33947106510 scopus 로고    scopus 로고
    • Genes, language development, and language disorders
    • Smith SD. Genes, language development, and language disorders. Ment Retard Dev Disabil Res Rev. 2007; 13(1): 96-105.
    • (2007) Ment Retard Dev Disabil Res Rev. , vol.13 , Issue.1 , pp. 96-105
    • Smith, S.D.1
  • 71
    • 0033943099 scopus 로고    scopus 로고
    • Is preschool language impairment a risk factor for dyslexia in adolescence?
    • Snowling M, Bishop DV, Stothard SE. Is preschool language impairment a risk factor for dyslexia in adolescence? J Child Psychol Psychiatry. 2000; 41(5): 587-600.
    • (2000) J Child Psychol Psychiatry. , vol.41 , Issue.5 , pp. 587-600
    • Snowling, M.1    Bishop, D.V.2    Stothard, S.E.3
  • 72
    • 79954605497 scopus 로고    scopus 로고
    • A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits
    • Stein MB, Yang BZ, Chavira DA, Hitchcock CA, Sung SC, Shipon-Blum E, et al. A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits. Biol Psychiatry. 2011; 69(9): 825-31.
    • (2011) Biol Psychiatry. , vol.69 , Issue.9 , pp. 825-831
    • Stein, M.B.1    Yang, B.Z.2    Chavira, D.A.3    Hitchcock, C.A.4    Sung, S.C.5    Shipon-Blum, E.6
  • 74
    • 0141482054 scopus 로고    scopus 로고
    • A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain
    • Taipale M, Kaminen N, Nopola-Hemmi J, Haltia T, Myllyluoma B, Lyytinen H, et al. A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proc Natl Acad Sci U S A. 2003; 100(20): 11553-8.
    • (2003) Proc Natl Acad Sci U S A. , vol.100 , Issue.20 , pp. 11553-11558
    • Taipale, M.1    Kaminen, N.2    Nopola-Hemmi, J.3    Haltia, T.4    Myllyluoma, B.5    Lyytinen, H.6
  • 76
    • 0038278610 scopus 로고    scopus 로고
    • CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder
    • Verkerk AJ, Mathews CA, Joosse M, Eussen BH, Heutink P, Oostra BA. CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder. Genomics. 2003; 82(1): 1-9.
    • (2003) Genomics. , vol.82 , Issue.1 , pp. 1-9
    • Verkerk, A.J.1    Mathews, C.A.2    Joosse, M.3    Eussen, B.H.4    Heutink, P.5    Oostra, B.A.6
  • 80
    • 23844555333 scopus 로고    scopus 로고
    • Investigation of the relationship of attention deficit hyperactivity disorder to the EKN1 gene on chromosome 15q21
    • Wigg KG, Couto JM, Feng Y, Crosbie J, Anderson B, Cate-Carter T, et al. Investigation of the relationship of attention deficit hyperactivity disorder to the EKN1 gene on chromosome 15q21. Sci Stud Reading. 2005; 9(3): 261-83.
    • (2005) Sci Stud Reading. , vol.9 , Issue.3 , pp. 261-283
    • Wigg, K.G.1    Couto, J.M.2    Feng, Y.3    Crosbie, J.4    Anderson, B.5    Cate-Carter, T.6
  • 81
    • 33744455435 scopus 로고    scopus 로고
    • The genetics of developmental dyslexia
    • Williams J, O'Donovan MC. The genetics of developmental dyslexia. Eur J Hum Genet. 2006; 14(6): 681-9.
    • (2006) Eur J Hum Genet. , vol.14 , Issue.6 , pp. 681-689
    • Williams, J.1    O'Donovan, M.C.2
  • 82
    • 72149095158 scopus 로고    scopus 로고
    • CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila
    • Zweier C, de Jong EK, Zweier M, Orrico A, Ousager LB, Collins AL, et al. CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila. Am J Hum Genet. 2009; 85(5): 655-66.
    • (2009) Am J Hum Genet. , vol.85 , Issue.5 , pp. 655-666
    • Zweier, C.1    de Jong, E.K.2    Zweier, M.3    Orrico, A.4    Ousager, L.B.5    Collins, A.L.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.