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Volumn 41, Issue 1, 2011, Pages 105-109

An examination of candidate gene SNPs for dyslexia in an Indian sample

Author keywords

DCDC2; Developmental dyslexia; DYX1C1; KIAA0319; MassARRAY; SNPs

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHILD; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; CONTROLLED STUDY; DCDC2 GENE; DEVELOPMENTAL DYSLEXIA; DYSLEXIA; DYX1C1 GENE; GENE; GENE LOCATION; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC VARIABILITY; HUMAN; INDIA; INDIAN; KIAA0319 GENE; PRESCHOOL CHILD; RISK ASSESSMENT; RISK FACTOR; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 79952442026     PISSN: 00018244     EISSN: 15733297     Source Type: Journal    
DOI: 10.1007/s10519-010-9441-2     Document Type: Article
Times cited : (19)

References (23)
  • 3
    • 3543029197 scopus 로고    scopus 로고
    • Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: Linkage and association analyses
    • KE Deffenbacher JB Kenyon DM Hoover RK Olson BF Pennington JC DeFries SD Smith 2004 Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses Hum Genet 115 2 128 138 10.1007/s00439-004-1126-6 15138886 (Pubitemid 39010927)
    • (2004) Human Genetics , 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    Smith, S.D.7
  • 6
    • 0033928210 scopus 로고    scopus 로고
    • Chromosome 6p influences on different dyslexia-related cognitive processes: Further confirmation
    • DOI 10.1086/302755
    • EL Grigorenko FB Wood MS Meyer DL Pauls 2000 Chromosome 6p influences on different dyslexia-related cognitive processes: Further confirmation Am J Hum Genet 66 715 723 10.1086/302755 10677331 (Pubitemid 30468849)
    • (2000) American Journal of Human Genetics , vol.66 , Issue.2 , pp. 715-723
    • Grigorenko, E.L.1    Wood, F.B.2    Meyer, M.S.3    Pauls, D.L.4
  • 9
    • 0034758491 scopus 로고    scopus 로고
    • Incidence of reading disability in a population-based birth cohort, 1976-1982, Rochester, Minn
    • SK Katusic RC Colligan WJ Barbaresi DJ Schaid SJ Jacobsen 2001 Incidence of reading disability in a population-based birth cohort, 1976-1982, Rochester, Minn Mayo Clin Proc 76 1081 1092 10.4065/76.11.1081 11702896 (Pubitemid 33032385)
    • (2001) Mayo Clinic Proceedings , vol.76 , Issue.11 , pp. 1081-1092
    • Katusic, S.K.1    Colligan, R.C.2    Barbaresi, W.J.3    Schaid, D.J.4    Jacobsen, S.J.5
  • 15
    • 31044437285 scopus 로고    scopus 로고
    • Modes of genetic transmission of dyslexia in South Indian families
    • P Saviour NB Ramachandra 2005 Modes of genetic transmission of dyslexia in South Indian families Ind J Hum Gen 11 3 135 139 10.4103/0971-6866.19532 (Pubitemid 43120856)
    • (2005) Indian Journal of Human Genetics , vol.11 , Issue.3 , pp. 135-139
    • Saviour, P.1    Ramachandra, N.B.2
  • 17
    • 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
    • DOI 10.1136/jmg.2004.018341
    • TS Scerri SE Fisher C Francks IL MacPhie S Paracchini AJ Richardson JF Stein AP Monaco 2004 Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK J Med Genet 41 853 857 10.1136/jmg.2004.018341 15520411 (Pubitemid 39524313)
    • (2004) Journal of Medical Genetics , 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    Stein, J.F.7    Monaco, A.P.8
  • 22
    • 70649088948 scopus 로고    scopus 로고
    • Genetic variation in CYP27B1 is associated with congestive heart failure in patient with hypertension
    • 10.2217/pgs.09.101
    • RA Wilke RU Simpson BN Mukesh SV Bhupathi RA Dart NR Ghebranious CA McCarty 2009 Genetic variation in CYP27B1 is associated with congestive heart failure in patient with hypertension Pharmaco 10 1789 1797 10.2217/pgs.09.101
    • (2009) Pharmaco , vol.10 , pp. 1789-1797
    • Wilke, R.A.1    Simpson, R.U.2    Mukesh, B.N.3    Bhupathi, S.V.4    Dart, R.A.5    Ghebranious, N.R.6    McCarty, C.A.7
  • 23
    • 33744455435 scopus 로고    scopus 로고
    • The genetics of developmental dyslexia
    • DOI 10.1038/sj.ejhg.5201575, PII 5201575
    • J Williams MC O'Donovan 2006 The genetics of developmental dyslexia Eur J Hum Genet 14 681 689 10.1038/sj.ejhg.5201575 16721404 (Pubitemid 43797265)
    • (2006) European Journal of Human Genetics , vol.14 , Issue.6 , pp. 681-689
    • Williams, J.1    O'Donovan, M.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.