-
1
-
-
0027014164
-
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
-
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
-
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
-
4
-
-
0029919288
-
Is developmental dyslexia a disconnection syndrome? Evidence from PET scanning
-
Paulesu, E., Frith, U., Snowling, M., Gallagher, A., Morton, J., Frackowiak, R.S.J. and Frith, C.D. (1996) Is developmental dyslexia a disconnection syndrome? Evidence from PET scanning. Brain, 119, 143-157.
-
(1996)
Brain
, vol.119
, pp. 143-157
-
-
Paulesu, E.1
Frith, U.2
Snowling, M.3
Gallagher, A.4
Morton, J.5
Frackowiak, R.S.J.6
Frith, C.D.7
-
5
-
-
0023299180
-
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
-
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
-
7
-
-
0003881317
-
-
Lewis & Son, London, UK
-
Hinshelwood, J. (1900) Letter-, Word-, and Mind-Blindness. Lewis & Son, London, UK.
-
(1900)
Letter-, Word-, and Mind-Blindness
-
-
Hinshelwood, J.1
-
8
-
-
0023179955
-
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
-
9
-
-
0025992157
-
Evidence for major gene transmission of developmental dyslexia
-
Pennington, B.F., Gilger, J.W., Pauls, D., Smith, S.A., Smith, S.D. and DeFries, J.C. (1991) Evidence for major gene transmission of developmental dyslexia. JAMA, 266, 1527-1534.
-
(1991)
JAMA
, vol.266
, pp. 1527-1534
-
-
Pennington, B.F.1
Gilger, J.W.2
Pauls, D.3
Smith, S.A.4
Smith, S.D.5
DeFries, J.C.6
-
10
-
-
0033087303
-
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
-
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
-
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
-
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
-
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
-
15
-
-
0031027824
-
Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
-
Grigorenko, E.L., Wood, F.B., Meyer, M.S., Hart, L.A., Speed, W.C., Shuster, A. and Pauls, D.L. (1997) Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15. Am. J. Hum. Genet., 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
Pauls, D.L.7
-
16
-
-
0020622130
-
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
-
17
-
-
0032231443
-
Evidence for linkage of spelling disability to chromosome 15
-
Schulte-Korne, G., Grimm, T., Nothen, N.M., Muller-Myshok, B., Cichon, S., Vogt, I.R., Propping, P. and Remschmidt, H. (1998) Evidence for linkage of spelling disability to chromosome 15. Am. J. Hum. Genet., 63, 279-282.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 279-282
-
-
Schulte-Korne, G.1
Grimm, T.2
Nothen, N.M.3
Muller-Myshok, B.4
Cichon, S.5
Vogt, I.R.6
Propping, P.7
Remschmidt, H.8
-
18
-
-
0029003528
-
Quantiative trait locus for reading disability
-
Cardon, L.R., Smith, S.D., Fulker, D.W., Kimberling, W.J., Pennington, B.F. and DeFries, J.C. (1995) Quantiative trait locus for reading disability. Science, 268, 1553.
-
(1995)
Science
, vol.268
, pp. 1553
-
-
Cardon, L.R.1
Smith, S.D.2
Fulker, D.W.3
Kimberling, W.J.4
Pennington, B.F.5
DeFries, J.C.6
-
19
-
-
0028030006
-
Quantitative trait locus for reading disability on chromosome 6
-
Cardon, L.R., Smith, S.D., Fulker, D.W., Kimberling, B.F. and DeFries, J.C. (1994) Quantitative trait locus for reading disability on chromosome 6. Science, 266, 276-279.
-
(1994)
Science
, vol.266
, pp. 276-279
-
-
Cardon, L.R.1
Smith, S.D.2
Fulker, D.W.3
Kimberling, B.F.4
DeFries, J.C.5
-
20
-
-
0033366739
-
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia
-
Fisher, S.E., Marlow, A.J., Lamb, J., Maesreini, E., Williams, D.F., Richardson, A.J., Weeks, D.E., Stein, J.F. and Monaco, A.P. (1999) A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. Am. J. Hum. Genet., 64, 156.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 156
-
-
Fisher, S.E.1
Marlow, A.J.2
Lamb, J.3
Maesreini, E.4
Williams, D.F.5
Richardson, A.J.6
Weeks, D.E.7
Stein, J.F.8
Monaco, A.P.9
-
21
-
-
0033364213
-
Quantitative-trait for specific language and reading deficits on chromosome 6p
-
Gayan, J., Smith, S.D., Cherny, S.S., Cardon, L.R., Fulker, D.W., Brower, A.M., Olson, R.K., Pennington, B.F. and DeFries, J.D. (1999) Quantitative-trait for specific language and reading deficits on chromosome 6p. Am. J. Hum. Genet., 64, 164.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 164
-
-
Gayan, J.1
Smith, S.D.2
Cherny, S.S.3
Cardon, L.R.4
Fulker, D.W.5
Brower, A.M.6
Olson, R.K.7
Pennington, B.F.8
DeFries, J.D.9
-
22
-
-
0027213075
-
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
-
23
-
-
0032877882
-
A new gene (DYX3) for dyslexia is located on chromosome 2
-
Fagerheim, T., Raeymaekers, P., Tonnessen, F.E., Pedersen, M., Tranebjaerg, L. and Lubs, H.A. (1999) A new gene (DYX3) for dyslexia is located on chromosome 2. J. Med. Genet., 36, 664-669.
-
(1999)
J. Med. Genet.
, vol.36
, pp. 664-669
-
-
Fagerheim, T.1
Raeymaekers, P.2
Tonnessen, F.E.3
Pedersen, M.4
Tranebjaerg, L.5
Lubs, H.A.6
-
24
-
-
0023254230
-
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
-
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
-
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
-
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
-
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
-
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
-
30
-
-
0029061755
-
The distribution of linkage disequilibrium over anonymous genome regions
-
Peterson, A.C., Di Rienzo, A., Lehesjoki, A.E., de la Chapelle, A., Slatkin, M. and Fremier, N.B. (1995) The distribution of linkage disequilibrium over anonymous genome regions. Hum. Mol. Genet., 4, 887-894.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 887-894
-
-
Peterson, A.C.1
Di Rienzo, A.2
Lehesjoki, A.E.3
De La Chapelle, A.4
Slatkin, M.5
Fremier, N.B.6
-
31
-
-
85037454267
-
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
-
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
-
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
-
34
-
-
0028843482
-
Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31-q33
-
Copeman, J.B., Cucca, F., Hearne, C.M., Comall, R.J., Reed, P.W., Ronningen, K.S., Undlien, D.E., Nistico, L., Buzzetti, R., Tosi, R. et al. (1995) Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31-q33. Nature Genet., 9, 80-85.
-
(1995)
Nature Genet.
, vol.9
, pp. 80-85
-
-
Copeman, J.B.1
Cucca, F.2
Hearne, C.M.3
Comall, R.J.4
Reed, P.W.5
Ronningen, K.S.6
Undlien, D.E.7
Nistico, L.8
Buzzetti, R.9
Tosi, R.10
-
35
-
-
6844241972
-
Transmission of haplotypes of microsatellite markers rather than single marker alleles in the mapping of a putative type 1 diabetes susceptibility gene (IDDM6)
-
Merriman, T.R., Eaves, I.A., Twells, R.C.J., Merriman, M.E., Danoy, P.A.C., Muxworthy, C.E., Cox, R.D., Cucca, F., McFinney, P.A., Shield, J.P.H. et al. (1998) Transmission of haplotypes of microsatellite markers rather than single marker alleles in the mapping of a putative type 1 diabetes susceptibility gene (IDDM6). Hum. Mol. Genet., 7, 517-524.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 517-524
-
-
Merriman, T.R.1
Eaves, I.A.2
Twells, R.C.J.3
Merriman, M.E.4
Danoy, P.A.C.5
Muxworthy, C.E.6
Cox, R.D.7
Cucca, F.8
McFinney, P.A.9
Shield, J.P.H.10
-
36
-
-
0032231640
-
Fine mapping of the diabetes-susceptibility locus, IDDM4, on chromosome 11q13
-
Nakagawa, Y., Kawaguchi, Y., Twells, R.C.J., Muxworthy, C., Hunter, K.M.D., Wilson, A., Merriman, M.E., Cucca, F., McKinney, P.A., Shield, J.P.H. et al. (1998) Fine mapping of the diabetes-susceptibility locus, IDDM4, on chromosome 11q13. Am. J. Hum. Genet., 63, 547-556.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 547-556
-
-
Nakagawa, Y.1
Kawaguchi, Y.2
Twells, R.C.J.3
Muxworthy, C.4
Hunter, K.M.D.5
Wilson, A.6
Merriman, M.E.7
Cucca, F.8
McKinney, P.A.9
Shield, J.P.H.10
-
37
-
-
0029858544
-
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
-
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
-
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
-
-
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
-
-
(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
|