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Volumn 9, Issue 5, 2000, Pages 843-848

Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

EID: 0034701254     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/9.5.843     Document Type: Article
Times cited : (107)

References (41)
  • 1
    • 0027014164 scopus 로고
    • Discrepancy compared to low achievement definitions of reading disability
    • Shaywitz, B.A., Fletcher, J.M., Holahan, J.M. and Shaywitz, S.E. (1992) Discrepancy compared to low achievement definitions of reading disability. J. Read. Disabil., 25, 639-648.
    • (1992) J. Read. Disabil. , vol.25 , pp. 639-648
    • Shaywitz, B.A.1    Fletcher, J.M.2    Holahan, J.M.3    Shaywitz, S.E.4
  • 2
    • 0000517679 scopus 로고    scopus 로고
    • Poor readers in adulthood: Psychosocial functioning
    • Maughan, B. and Hagell, A. (1996) Poor readers in adulthood: psychosocial functioning. Dev. Psychopathol., 8, 457-476.
    • (1996) Dev. Psychopathol. , vol.8 , pp. 457-476
    • Maughan, B.1    Hagell, A.2
  • 3
    • 0012260103 scopus 로고
    • Behavioural development and reading disabilities
    • Hulme, C. and Snowling, M. (eds). Whurr, London, UK
    • Maughan, B. (1994) Behavioural development and reading disabilities. In Hulme, C. and Snowling, M. (eds). Reading Development and Dyslexia. Whurr, London, UK, pp. 128-143.
    • (1994) Reading Development and Dyslexia , pp. 128-143
    • Maughan, B.1
  • 5
    • 0023299180 scopus 로고
    • A twin study of genetic influences on reading and spelling ability and disability
    • Stevenson, J., Graham, P., Fredman, G. and McLoughlin, V. (1987) A twin study of genetic influences on reading and spelling ability and disability. J. Child Psychol. Psych., 28, 229-247.
    • (1987) J. Child Psychol. Psych. , vol.28 , pp. 229-247
    • Stevenson, J.1    Graham, P.2    Fredman, G.3    McLoughlin, V.4
  • 6
    • 0002435026 scopus 로고
    • Genetics of reading disability
    • Plomin, R. and McClearn, G.F. (eds), APA Books, New York, NY
    • DeFries, J.C. and Gillis, J.J. (1993) Genetics of reading disability. In Plomin, R. and McClearn, G.F. (eds), Nature, Nurture and Psychology. APA Books, New York, NY, pp. 121-145.
    • (1993) Nature, Nurture and Psychology , pp. 121-145
    • DeFries, J.C.1    Gillis, J.J.2
  • 8
    • 0023179955 scopus 로고
    • Evidence for a genetic etiology in reading disability of twins
    • DeFries, J.C., Fulker, D.W. and Labuda, M.C. (1987) Evidence for a genetic etiology in reading disability of twins. Nature, 329, 537-539.
    • (1987) Nature , vol.329 , pp. 537-539
    • DeFries, J.C.1    Fulker, D.W.2    Labuda, M.C.3
  • 10
    • 0033087303 scopus 로고    scopus 로고
    • The structure of genetic influences on general cognitive, language, phonological and reading abilities
    • Hohnen, B. and Stevenson, J. (1999) The structure of genetic influences on general cognitive, language, phonological and reading abilities. Dev. Psychol., 35, 590-603.
    • (1999) Dev. Psychol. , vol.35 , pp. 590-603
    • Hohnen, B.1    Stevenson, J.2
  • 11
    • 0028046213 scopus 로고
    • Commingling and segregation analysis of reading performance families of normal reading probands
    • Gilger, J.W., Borecki, I.B., DeFries, J.C. and Pennington, B.F. (1994) Commingling and segregation analysis of reading performance families of normal reading probands. Behav. Genet., 24, 345-355.
    • (1994) Behav. Genet. , vol.24 , pp. 345-355
    • Gilger, J.W.1    Borecki, I.B.2    DeFries, J.C.3    Pennington, B.F.4
  • 12
    • 0000253671 scopus 로고
    • Which aspects of processing text mediate genetic effects
    • Stevenson, J. (1991) Which aspects of processing text mediate genetic effects. Reading Writing, 3, 249-269.
    • (1991) Reading Writing , vol.3 , pp. 249-269
    • Stevenson, J.1
  • 13
    • 0024689078 scopus 로고
    • Specific deficits in component reading and language skills - Genetic and environmental influences
    • Olson, R., Wise, B., Conners, F., Rack, J. and Fulker, D. (1989) Specific deficits in component reading and language skills - genetic and environmental influences. J. Learn. Disabil. 22, 339-348.
    • (1989) J. Learn. Disabil. , vol.22 , pp. 339-348
    • Olson, R.1    Wise, B.2    Conners, F.3    Rack, J.4    Fulker, D.5
  • 14
    • 0028872434 scopus 로고
    • Genetic basis of specific language impairment - Evidence from a twin study
    • Bishop, D.V.M., North, T. and Donlan, C. (1995) Genetic basis of specific language impairment - evidence from a twin study. Dev. Med. Child Neurol., 37, 56-71.
    • (1995) Dev. Med. Child Neurol. , vol.37 , pp. 56-71
    • Bishop, D.V.M.1    North, T.2    Donlan, C.3
  • 16
    • 0020622130 scopus 로고
    • Specific reading disability - Identification of an inherited form through linkage analysis
    • Smith, S.D., Kimberling, W.J., Pennington, B.F. and Lubs, H.A. (1983) Specific reading disability - identification of an inherited form through linkage analysis. Science, 219, 1345.
    • (1983) Science , vol.219 , pp. 1345
    • Smith, S.D.1    Kimberling, W.J.2    Pennington, B.F.3    Lubs, H.A.4
  • 22
    • 0027213075 scopus 로고
    • Suggestive linkage of developmental dyslexia to chromosome 1p34-p36
    • Rabin, M., Wen, X.L., Hepburn, M., Lubs, H.A., Feldman, E. and Duara, R. (1993) Suggestive linkage of developmental dyslexia to chromosome 1p34-p36. Lancet, 342, 178.
    • (1993) Lancet , vol.342 , pp. 178
    • Rabin, M.1    Wen, X.L.2    Hepburn, M.3    Lubs, H.A.4    Feldman, E.5    Duara, R.6
  • 24
    • 0023254230 scopus 로고
    • Dyslexia and chromosome 15 heteromorphism - Negative lod in a Danish material
    • Bisgaard, M.L., Eiberg, H., Moller, N., Niebuhr, E. and Mohr, J. (1987) Dyslexia and chromosome 15 heteromorphism - negative lod in a Danish material. Clin. Genet., 32, 118-119.
    • (1987) Clin. Genet. , vol.32 , pp. 118-119
    • Bisgaard, M.L.1    Eiberg, H.2    Moller, N.3    Niebuhr, E.4    Mohr, J.5
  • 25
    • 0002877401 scopus 로고
    • Dyslexia subtypes: Genetics, behaviour and brain imaging
    • Duane, D. and Gray, D. (eds), York, Parkton, MD
    • Lubs, H.A. (1991) Dyslexia subtypes: genetics, behaviour and brain imaging. In Duane, D. and Gray, D. (eds), The Biological Basis of Dyslexia, York, Parkton, MD, pp. 89-118.
    • (1991) The Biological Basis of Dyslexia , pp. 89-118
    • Lubs, H.A.1
  • 26
    • 0028340175 scopus 로고
    • The genetic basis of complex human behaviour
    • Plomin, R., Owen, M.J. and McCuffin, P. (1994) The genetic basis of complex human behaviour. Science, 264, 1733-1739.
    • (1994) Science , vol.264 , pp. 1733-1739
    • Plomin, R.1    Owen, M.J.2    McCuffin, P.3
  • 27
    • 0029741063 scopus 로고    scopus 로고
    • The future of genetic studies of complex human diseases
    • Risch, N. and Merikangas, K. (1996) The future of genetic studies of complex human diseases. Science, 273, 1516-1517.
    • (1996) Science , vol.273 , pp. 1516-1517
    • Risch, N.1    Merikangas, K.2
  • 28
    • 19544378885 scopus 로고    scopus 로고
    • Linkage disequilibrium mapping of complex disease: Fantasy or reality?
    • Terwilliger, J.D. and Weiss, K.M. (1998) Linkage disequilibrium mapping of complex disease: fantasy or reality? Pharmaceut. Biol., 8, 579-598.
    • (1998) Pharmaceut. Biol. , vol.8 , pp. 579-598
    • Terwilliger, J.D.1    Weiss, K.M.2
  • 29
    • 0033039497 scopus 로고    scopus 로고
    • Prospects for whole-genome linkage disequilibrium mapping of common disease genes
    • Kruglyak, L. (1999) Prospects for whole-genome linkage disequilibrium mapping of common disease genes. Nature Genet., 22, 139.
    • (1999) Nature Genet. , vol.22 , pp. 139
    • Kruglyak, L.1
  • 31
    • 85037454267 scopus 로고    scopus 로고
    • Using late-onset Alzheimer's disease (LOAD) as a model to study the application of single nucleotide polymorphisms (SNPs) for complex association studies: Genotyping and analysis of 65 SNPs in a 4-megabase region surrounding apolipoprotein e (APOE)
    • Vance, J.M., Martin, E.R., Gilbert, J.R., Rogala, A.R., Afshari, A., Slotterbeck, B.D., Grubber, J.M. Saunders, A.M., Riley, J., Purvis, I. et al. (1999) Using late-onset Alzheimer's disease (LOAD) as a model to study the application of single nucleotide polymorphisms (SNPs) for complex association studies: genotyping and analysis of 65 SNPs in a 4-megabase region surrounding apolipoprotein E (APOE). Am. J. Hum. Genet., 65, 2673.
    • (1999) Am. J. Hum. Genet. , vol.65 , pp. 2673
    • Vance, J.M.1    Martin, E.R.2    Gilbert, J.R.3    Rogala, A.R.4    Afshari, A.5    Slotterbeck, B.D.6    Grubber, J.M.7    Saunders, A.M.8    Riley, J.9    Purvis, I.10
  • 32
    • 0033525152 scopus 로고    scopus 로고
    • Marker-to-marker linkage disequilibrium on chromosomes 5q, 6p and 8p in Irish high-density schizophrenia pedigrees
    • Kendler, K.S., MacLean, C.J., Ma, Y.L., Oneill, F.A., Walsh, D. and Straub, R.E. (1999) Marker-to-marker linkage disequilibrium on chromosomes 5q, 6p and 8p in Irish high-density schizophrenia pedigrees. Am. J. Med. Genet., 88, 29-33.
    • (1999) Am. J. Med. Genet. , vol.88 , pp. 29-33
    • Kendler, K.S.1    MacLean, C.J.2    Ma, Y.L.3    Oneill, F.A.4    Walsh, D.5    Straub, R.E.6
  • 33
    • 0032697536 scopus 로고    scopus 로고
    • Association analysis using refined microsatellite markers localizes a susceptibility locus for psoriasis vulgaris within a 111 kb segment telomeric to the HLA-C gene
    • Oka, A., Tamiya, G., Tomizawa, M., Ota, M., Katsuyama, Y., Makino, S., Shiina, T., Yoshitome, M., Lizuka, M., Sasao, Y. et al. (1999) Association analysis using refined microsatellite markers localizes a susceptibility locus for psoriasis vulgaris within a 111 kb segment telomeric to the HLA-C gene. Hum. Mol. Genet., 8, 2165-2170.
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 2165-2170
    • Oka, A.1    Tamiya, G.2    Tomizawa, M.3    Ota, M.4    Katsuyama, Y.5    Makino, S.6    Shiina, T.7    Yoshitome, M.8    Lizuka, M.9    Sasao, Y.10
  • 37
    • 0029858544 scopus 로고    scopus 로고
    • The TDT and other family-based tests for linkage disequilibrium and association
    • Spielman, R.S. and Ewens, W.J. (1996). The TDT and other family-based tests for linkage disequilibrium and association. Am. J. Hum. Genet., 59, 983-989.
    • (1996) Am. J. Hum. Genet. , vol.59 , pp. 983-989
    • Spielman, R.S.1    Ewens, W.J.2
  • 38
    • 0023758528 scopus 로고
    • Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families
    • Krawczak, M., Konecki, D.S., Schmidtke, J., Duck, M., Engel, W., Nutzenadel, W. and Trefz, F.K. (1988) Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families. Hum. Genet., 80, 78-80.
    • (1988) Hum. Genet. , vol.80 , pp. 78-80
    • Krawczak, M.1    Konecki, D.S.2    Schmidtke, J.3    Duck, M.4    Engel, W.5    Nutzenadel, W.6    Trefz, F.K.7
  • 39
    • 0028981182 scopus 로고
    • An extended transmission/disequilibrium test (TDT) for multi-allele marker loci
    • Sham, P.C. and Curtis, D. (1995) An extended transmission/disequilibrium test (TDT) for multi-allele marker loci. Ann. Hum. Genet., 59, 323-336.
    • (1995) Ann. Hum. Genet. , vol.59 , pp. 323-336
    • Sham, P.C.1    Curtis, D.2
  • 40
    • 0343113249 scopus 로고
    • The Psychological Corporation, Harcourt Brace, London, UK
    • Wechsler, D. (1992) WISC III UK, 3rd edn. The Psychological Corporation, Harcourt Brace, London, UK.
    • (1992) WISC III UK, 3rd Edn.
    • Wechsler, D.1
  • 41
    • 0003615334 scopus 로고
    • (British adaptation and standardisation by Una Christophers and Chris Whetton). NFER-Nelson Publishing, Windsor, UK
    • Neale, M.D. (1989) Neale Analysis of Reading Ability, revised British edition (British adaptation and standardisation by Una Christophers and Chris Whetton). NFER-Nelson Publishing, Windsor, UK.
    • (1989) Neale Analysis of Reading Ability, Revised British Edition
    • Neale, M.D.1


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