메뉴 건너뛰기




Volumn 125, Issue 4, 2012, Pages 622-625

Association of polymorphisms in the DCDC2 gene with developmental dyslexia in the Han Chinese

Author keywords

Case control; DCDC2; Genetic association study

Indexed keywords

ARTICLE; CHILD; CHINESE; CONTROLLED STUDY; DCDC2 GENE; DNA ISOLATION; DNA POLYMORPHISM; DYSLEXIA; FEMALE; GENE; GENE AMPLIFICATION; GENE FREQUENCY; GENE LOCUS; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENOTYPE; HAPLOTYPE; HEREDITY; HUMAN; INTELLIGENCE QUOTIENT; MAJOR CLINICAL STUDY; MALE; MOUTH MUCOSA; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84863160070     PISSN: 03666999     EISSN: None     Source Type: Journal    
DOI: 10.3760/cma.j.issn.0366-6999.2012.04.012     Document Type: Article
Times cited : (8)

References (29)
  • 1
    • 78650945727 scopus 로고    scopus 로고
    • The prevention, diagnosis, and treatment ofdyslexia
    • Schulte-Körne G. The prevention, diagnosis, and treatment ofdyslexia. Dtsch Arztebl Int 2010; 107: 718-726.
    • (2010) Dtsch Arztebl Int , vol.107 , pp. 718-726
    • Schulte-Körne, G.1
  • 3
    • 77951174989 scopus 로고    scopus 로고
    • Recent advances in thegenetics of language impairment
    • Newbury DF, Fisher SE, Monaco AP. Recent advances in thegenetics of language impairment. Genome Med 2010; 2: 6
    • (2010) Genome Med , vol.2 , pp. 6
    • Newbury, D.F.1    Fisher, S.E.2    Monaco, A.P.3
  • 5
    • 33846693674 scopus 로고    scopus 로고
    • Further evidence of pleiotropy influencing speech and language: Analysis of the DYX8 region
    • Miscimarra L, Stein C, Millard C, Kluge A, Cartier K, Freebairn L, et al. Further evidence of pleiotropy influencing speech and language: analysis of the DYX8 region. Hum Hered 2007; 63: 47-58.
    • (2007) Hum Hered , vol.63 , pp. 47-58
    • Miscimarra, L.1    Stein, C.2    Millard, C.3    Kluge, A.4    Cartier, K.5    Freebairn, L.6
  • 7
    • 0036168959 scopus 로고    scopus 로고
    • Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families
    • Petryshen TL, Kaplan BJ, Hughes ML, Tzenova J, Field LL. Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families. J Med Genet 2002; 39: 125-126
    • (2002) J Med Genet , vol.39 , pp. 125-126
    • Petryshen, T.L.1    Kaplan, B.J.2    Hughes, M.L.3    Tzenova, J.4    Field, L.L.5
  • 10
    • 0033928210 scopus 로고    scopus 로고
    • Chromosome 6p influences on different dyslexia-related cognitive processes: Further confirmation
    • Grigorenko EL, Wood FB, Meyer MS, Pauls DL. Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation. Am J Hum Genet 2000; 66: 715-723.
    • (2000) Am J Hum Genet , vol.66 , pp. 715-723
    • Grigorenko, E.L.1    Wood, F.B.2    Meyer, M.S.3    Pauls, D.L.4
  • 11
    • 0031027824 scopus 로고    scopus 로고
    • Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
    • Grigorenko EL, Wood FB, Meyer MS, Hart LA, Speed WC, Shuster A, et al. Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15. Am J Hum Genet 1997; 60: 27-39.
    • (1997) Am J Hum Genet , vol.60 , pp. 27-39
    • Grigorenko, E.L.1    Wood, F.B.2    Meyer, M.S.3    Hart, L.A.4    Speed, W.C.5    Shuster, A.6
  • 12
    • 0038577166 scopus 로고    scopus 로고
    • A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32
    • Kaminen N, Hannula-Jouppi K, Kestilä M, Lahermo P, Muller K, Kaaranen M, et al. A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32. J Med Genet 2003; 40: 340-345.
    • (2003) J Med Genet , vol.40 , pp. 340-345
    • Kaminen, N.1    Hannula-Jouppi, K.2    Kestilä, M.3    Lahermo, P.4    Muller, K.5    Kaaranen, M.6
  • 13
    • 0034701254 scopus 로고    scopus 로고
    • Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q
    • Morris DW, Robinson L, Turic D, Duke M, Webb V, Milham C, et al. Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q. Hum Mol Genet 2000; 9: 843-848.
    • (2000) Hum Mol Genet , vol.9 , pp. 843-848
    • Morris, D.W.1    Robinson, L.2    Turic, D.3    Duke, M.4    Webb, V.5    Milham, C.6
  • 16
    • 18544365699 scopus 로고    scopus 로고
    • Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
    • Fisher SE, Francks C, Marlow AJ, MacPhie IL, Newbury DF, Cardon LR, et al. Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nat Genet 2002; 30: 86-91.
    • (2002) Nat Genet , vol.30 , pp. 86-91
    • Fisher, S.E.1    Francks, C.2    Marlow, A.J.3    Macphie, I.L.4    Newbury, D.F.5    Cardon, L.R.6
  • 17
    • 4444356020 scopus 로고    scopus 로고
    • Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family
    • de Kovel CG, Hol FA, Heister JG, Willemen JJ, Sandkuijl LA, Franke B, et al. Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family. J Med Genet 2004; 41: 652-657.
    • (2004) J Med Genet , vol.41 , pp. 652-657
    • de Kovel, C.G.1    Hol, F.A.2    Heister, J.G.3    Willemen, J.J.4    Sandkuijl, L.A.5    Franke, B.6
  • 19
    • 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 2005; 102: 17053-17058.
    • (2005) Proc Natl Acad Sci U S A , vol.102 , pp. 17053-17058
    • Meng, H.1    Smith, S.D.2    Hager, K.3    Held, M.4    Liu, J.5    Olson, R.K.6
  • 20
    • 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 2005; 76: 581-591
    • (2005) Am J Hum Genet , vol.76 , pp. 581-591
    • Cope, N.1    Harold, D.2    Hill, G.3    Moskvina, V.4    Stevenson, J.5    Holmans, P.6
  • 21
    • 33845246158 scopus 로고    scopus 로고
    • Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia
    • 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: 1085-1091.
    • (2006) Mol Psychiatry , vol.11 , pp. 1085-1091
    • Harold, D.1    Paracchini, S.2    Scerri, T.3    Dennis, M.4    Cope, N.5    Hill, G.6
  • 25
    • 20244377078 scopus 로고    scopus 로고
    • A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia
    • Marino C, Giorda R, Lorusso ML, Vanzin L, Salandi N, Nobile M, et al. A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia. Eur J Hum Genet 2005; 13: 491-499.
    • (2005) Eur J Hum Genet , vol.13 , pp. 491-499
    • Marino, C.1    Giorda, R.2    Lorusso, M.L.3    Vanzin, L.4    Salandi, N.5    Nobile, M.6
  • 26
    • 52949101814 scopus 로고
    • The pupil rating scale revised-screening for learning disabilities revision and application in elementary school
    • Jing J, Yu M, Deng GF. The pupil rating scale revised-screening for learning disabilities revision and application in elementary school. Psych Dev Educ (Chin) 1995; 1: 24-29.
    • (1995) Psych Dev Educ (Chin) , vol.1 , pp. 24-29
    • Jing, J.1    Yu, M.2    Deng, G.F.3
  • 27
    • 79952764665 scopus 로고    scopus 로고
    • Study on the reliability and validity of the dyslexia checklist for Chinese children
    • Wu HR, Song RR, Yao B. Study on the reliability and validity of the dyslexia checklist for Chinese children. Chin J School Health (Chin) 2006; 27: 468-469.
    • (2006) Chin J School Health (Chin) , vol.27 , pp. 468-469
    • Wu, H.R.1    Song, R.R.2    Yao, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.