-
1
-
-
0242439277
-
Localization of a gene for migraine without aura to chromosome 4q21
-
Bjornsson A, Gudmundsson G, Gudfinnsson E, Hrafnsdottir M, Benedikz J, Skuladottir S, Kristjansson K, Frigge M, Kong A, Stefansson K., et al. 2003. Localization of a gene for migraine without aura to chromosome 4q21. Am J Hum Genet 73: 986-993.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 986-993
-
-
Bjornsson, A.1
Gudmundsson, G.2
Gudfinnsson, E.3
Hrafnsdottir, M.4
Benedikz, J.5
Skuladottir, S.6
Kristjansson, K.7
Frigge, M.8
Kong, A.9
Stefansson, K.10
-
2
-
-
84937384492
-
Life-span data on continuous-naming speeds of numbers, letters, colors, and pictured objects, and word-reading speed
-
van den Bos KP, Zijlstra BJH, Spelberg HC. 2002. Life-span data on continuous-naming speeds of numbers, letters, colors, and pictured objects, and word-reading speed. Sci Stud Read 6: 25-49.
-
(2002)
Sci Stud Read
, vol.6
, pp. 25-49
-
-
van den Bos, K.P.1
Zijlstra, B.J.H.2
Spelberg, H.C.3
-
3
-
-
0028071382
-
The power of interval mapping of quantitative trait loci, using selected sib pairs
-
Cardon LR, Fulker DW. 1994. The power of interval mapping of quantitative trait loci, using selected sib pairs. Am J Hum Genet 55: 825-833.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 825-833
-
-
Cardon, L.R.1
Fulker, D.W.2
-
4
-
-
0026047218
-
Linkage analysis of quantitative traits: Increased power by using selected samples
-
Carey G, Williamson J. 1991. Linkage analysis of quantitative traits: Increased power by using selected samples. Am J Hum Genet 49: 786-796.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 786-796
-
-
Carey, G.1
Williamson, J.2
-
5
-
-
15944372645
-
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, Owen MJ, O'Donovan MC, Williams J. 2005. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am J Hum Genet 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
Owen, M.J.7
O'Donovan, M.C.8
Williams, J.9
-
6
-
-
3543029197
-
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, Smith SD. 2004. Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: Linkage and association analyses. Hum Genet 115: 128-138.
-
(2004)
Hum Genet
, vol.115
, 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
-
7
-
-
0016150610
-
Rapid "automatized" naming of pictured objects, colors, letters and numbers by normal children
-
Denckla MB, Rudel R. 1974. Rapid "automatized" naming of pictured objects, colors, letters and numbers by normal children. Cortex 10: 186-202.
-
(1974)
Cortex
, vol.10
, pp. 186-202
-
-
Denckla, M.B.1
Rudel, R.2
-
9
-
-
0036779497
-
Developmental dyslexia: Genetic dissection of a complex cognitive trait
-
Fisher SE, DeFries JC. 2002. Developmental dyslexia: Genetic dissection of a complex cognitive trait. Nat Rev Neurosci 3: 767-780.
-
(2002)
Nat Rev Neurosci
, vol.3
, pp. 767-780
-
-
Fisher, S.E.1
DeFries, J.C.2
-
10
-
-
18544365699
-
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, Ishikawa-Brush Y, Richardson AJ, Talcott JB, Gayan J., et al. 2002. Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nat Genet 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
Ishikawa-Brush, Y.7
Richardson, A.J.8
Talcott, J.B.9
Gayan, J.10
-
11
-
-
8844258018
-
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. 2004. 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 75: 1046-1058.
-
(2004)
Am J Hum Genet
, vol.75
, 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
-
13
-
-
0035571529
-
Genetic and environmental influences on orthographic and phonological skills in children with reading disabilities
-
Gayan J, Olson RK. 2001. Genetic and environmental influences on orthographic and phonological skills in children with reading disabilities. Dev Neuropsychol 20: 483-507.
-
(2001)
Dev Neuropsychol
, vol.20
, pp. 483-507
-
-
Gayan, J.1
Olson, R.K.2
-
14
-
-
0033364213
-
Quantitative-trait locus for specific language and reading deficits on chromosome 6p
-
Gayan J, Smith SD, Cherny SS, Cherny SS, Cardon LR, Fulker DW, Brower AM, Olson RK, Pennington BF, DeFries JC. 1999. Quantitative-trait locus for specific language and reading deficits on chromosome 6p. Am J Hum Genet 64: 157-164.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 157-164
-
-
Gayan, J.1
Smith, S.D.2
Cherny, S.S.3
Cherny, S.S.4
Cardon, L.R.5
Fulker, D.W.6
Brower, A.M.7
Olson, R.K.8
Pennington, B.F.9
DeFries, J.C.10
-
15
-
-
33645154439
-
Genetic bases of developmental dyslexia: A capsule review of heritability estimates
-
Grigorenko EL. 2004. Genetic bases of developmental dyslexia: A capsule review of heritability estimates. Enfance 3: 273-287.
-
(2004)
Enfance
, vol.3
, pp. 273-287
-
-
Grigorenko, E.L.1
-
16
-
-
0042319316
-
Continuing the search for dyslexia genes on 6p
-
Grigorenko EL, Wood FB, Golovyan L, Golovyan L, Meyer M, Romano C, Pauls D. 2003. Continuing the search for dyslexia genes on 6p. Am J Med Genet Part B 118B: 89-98.
-
(2003)
Am J Med Genet Part B
, vol.118
, pp. 89-98
-
-
Grigorenko, E.L.1
Wood, F.B.2
Golovyan, L.3
Golovyan, L.4
Meyer, M.5
Romano, C.6
Pauls, D.7
-
17
-
-
30344454660
-
Genomewide scan for real-word reading subphenotypes of dyslexia: Novel chromosome 13 locus and genetic complexity
-
Igo RP Jr, Chapman NH, Berninger VW, Matsushita M, Brkanac Z, Rothstein JH, Holzman T, Nielsen K, Raskind WH, Wijsman EM. 2006. Genomewide scan for real-word reading subphenotypes of dyslexia: Novel chromosome 13 locus and genetic complexity. Am J Med Genet Part B 141B: 15-27.
-
(2006)
Am J Med Genet Part B
, vol.141
, pp. 15-27
-
-
Igo Jr., R.P.1
Chapman, N.H.2
Berninger, V.W.3
Matsushita, M.4
Brkanac, Z.5
Rothstein, J.H.6
Holzman, T.7
Nielsen, K.8
Raskind, W.H.9
Wijsman, E.M.10
-
18
-
-
0034758491
-
Incidence of reading disability in a population-based birth cohort
-
Katusic SK, Colligan RC, Barbaresi WJ, Schaid DJ, Jacobsen SJ. 2001. Incidence of reading disability in a population-based birth cohort. Minn Mayo Clin Proc 76: 1081-1092.
-
(2001)
Minn Mayo Clin Proc
, vol.76
, pp. 1081-1092
-
-
Katusic, S.K.1
Colligan, R.C.2
Barbaresi, W.J.3
Schaid, D.J.4
Jacobsen, S.J.5
-
19
-
-
33745664813
-
Reading fluency: The whole is more than the parts
-
Katzir T, Kim Y, Wolf M, O'Brien B, Kennedy B, Lovett M., et al. 2006. Reading fluency: The whole is more than the parts. Ann Dyslexia 56: 51-82.
-
(2006)
Ann Dyslexia
, vol.56
, pp. 51-82
-
-
Katzir, T.1
Kim, Y.2
Wolf, M.3
O'Brien, B.4
Kennedy, B.5
Lovett, M.6
-
20
-
-
0029282257
-
The persistence of rapid naming problems in children with reading disabilities-A 9-year follow-up
-
Korhonen TT. 1995. The persistence of rapid naming problems in children with reading disabilities-A 9-year follow-up. J Learn Disabil 28: 232-239.
-
(1995)
J Learn Disabil
, vol.28
, pp. 232-239
-
-
Korhonen, T.T.1
-
21
-
-
0029886532
-
Parametric and nonparametric linkage analysis: A unified multipoint approach
-
Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. 1996. Parametric and nonparametric linkage analysis: A unified multipoint approach. Am J Hum Genet 58: 1347-1363.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
22
-
-
0032055958
-
Multivariate behavioural genetic analysis of achievement and cognitive measures in reading disabled and control twin pairs
-
Light JG, DeFries JC, Olson RK. 1998. Multivariate behavioural genetic analysis of achievement and cognitive measures in reading disabled and control twin pairs. Hum Biol 70: 215-237.
-
(1998)
Hum Biol
, vol.70
, pp. 215-237
-
-
Light, J.G.1
DeFries, J.C.2
Olson, R.K.3
-
23
-
-
0034863552
-
Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK
-
Marlow AJ, Fisher SE, Richardson AJ, Francks C, Talcott JB, Monaco AP, et al. 2001. Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK. Behav Genet 31: 219-230.
-
(2001)
Behav Genet
, vol.31
, pp. 219-230
-
-
Marlow, A.J.1
Fisher, S.E.2
Richardson, A.J.3
Francks, C.4
Talcott, J.B.5
Monaco, A.P.6
-
24
-
-
28044465597
-
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, Pennington BF, DeFries JC, Gelernter J, O'Reilly-Pol T., et al. 2005. DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci USA 102: 17053-17058.
-
(2005)
Proc Natl Acad Sci USA
, 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
Pennington, B.F.7
DeFries, J.C.8
Gelernter, J.9
O'Reilly-Pol, T.10
-
25
-
-
0032013270
-
Selective predictive value of rapid automatized naming in poor readers
-
Meyer MS, Wood FB, Hart LA, Felton RH. 1998. Selective predictive value of rapid automatized naming in poor readers. J Learn Disabil 31: 106-117.
-
(1998)
J Learn Disabil
, vol.31
, pp. 106-117
-
-
Meyer, M.S.1
Wood, F.B.2
Hart, L.A.3
Felton, R.H.4
-
26
-
-
4043048837
-
Neural systems for rapid automatized naming in skilled readers: Unravelling the RAN-reading relationship
-
Misra M, Katzir T, Wolf M, Poldrack R. 2004. Neural systems for rapid automatized naming in skilled readers: Unravelling the RAN-reading relationship. Sci Stud Read 8: 241-256.
-
(2004)
Sci Stud Read
, vol.8
, pp. 241-256
-
-
Misra, M.1
Katzir, T.2
Wolf, M.3
Poldrack, R.4
-
27
-
-
0025423228
-
Automaticity: A new framework for dyslexia research?
-
Nicolson RI, Fawcett AJ. 1990. Automaticity: A new framework for dyslexia research? Cognition 35: 159-182.
-
(1990)
Cognition
, vol.35
, pp. 159-182
-
-
Nicolson, R.I.1
Fawcett, A.J.2
-
28
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell JR, Weeks DE. 1998. PedCheck: A program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 63: 259-266.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
29
-
-
0036637040
-
Dyslexia: Nature and nurture
-
Olson RK. 2002. Dyslexia: Nature and nurture. Dyslexia 8: 143-159.
-
(2002)
Dyslexia
, vol.8
, pp. 143-159
-
-
Olson, R.K.1
-
30
-
-
0035828096
-
Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia
-
Petryshen TL, Kaplan BJ, Liu MF, Schmill de French N, Tobias R, Hughes ML, Field LL. 2001. Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia. Am J Med Genet 105: 507-517.
-
(2001)
Am J Med Genet
, vol.105
, pp. 507-517
-
-
Petryshen, T.L.1
Kaplan, B.J.2
Liu, M.F.3
Schmill de French, N.4
Tobias, R.5
Hughes, M.L.6
Field, L.L.7
-
31
-
-
0034472038
-
Familial aggregation of dyslexia phenotypes
-
Raskind WH, Hsu L, Berninger VW, Thomson JB, Wijsman EM. 2000. Familial aggregation of dyslexia phenotypes. Behav Genet 30: 385-396.
-
(2000)
Behav Genet
, vol.30
, pp. 385-396
-
-
Raskind, W.H.1
Hsu, L.2
Berninger, V.W.3
Thomson, J.B.4
Wijsman, E.M.5
-
32
-
-
21844460777
-
A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency
-
Raskind WH, Igo RP, Chapman NH, Berninger VW, Thomson JB, Matsushita M, Brkanac Z, Holzman T, Brown M, Wijsman EM. 2005. A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency. Mol Psychiatry 10: 699-711.
-
(2005)
Mol Psychiatry
, vol.10
, pp. 699-711
-
-
Raskind, W.H.1
Igo, R.P.2
Chapman, N.H.3
Berninger, V.W.4
Thomson, J.B.5
Matsushita, M.6
Brkanac, Z.7
Holzman, T.8
Brown, M.9
Wijsman, E.M.10
-
33
-
-
78650510385
-
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children
-
Epub ahead of print].
-
Roeske D, Ludwig KU, Neuhoff N, Becker J, Bartling J, Bruder J, Brockschmidt FF, Warnke A, Remschmidt H, Hoffmann P, Müller-Myhsok B, Nöthen MM, Schulte-Körne G. 2009. First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. Mol Psychiatry [Epub ahead of print].
-
(2009)
Mol Psychiatry
-
-
Roeske, D.1
Ludwig, K.U.2
Neuhoff, N.3
Becker, J.4
Bartling, J.5
Bruder, J.6
Brockschmidt, F.F.7
Warnke, A.8
Remschmidt, H.9
Hoffmann, P.10
Müller-Myhsok, B.11
Nöthen, M.M.12
Schulte-Körne, G.13
-
34
-
-
0004509186
-
Regression using fractional polynomials of continuous covariates: Parsimonious parametric modelling
-
Royston P, Altman DG. 1994. Regression using fractional polynomials of continuous covariates: Parsimonious parametric modelling. Appl Stat 43: 429-467.
-
(1994)
Appl Stat
, vol.43
, pp. 429-467
-
-
Royston, P.1
Altman, D.G.2
-
35
-
-
15744385942
-
Evidence of a highly specific relationship between rapid automatic naming of digits and text-reading speed
-
Savage RS, Frederickson N. 2005. Evidence of a highly specific relationship between rapid automatic naming of digits and text-reading speed. Brain Lang 93: 152-159.
-
(2005)
Brain Lang
, vol.93
, pp. 152-159
-
-
Savage, R.S.1
Frederickson, N.2
-
40
-
-
0032231443
-
Evidence for linkage of spelling disability to chromosome 15
-
Schulte-Körne G, Grimm T, Nöthen MM, Müller-Myhsok B, Cichon S, Vogt IR, Propping P, 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-Körne, G.1
Grimm, T.2
Nöthen, M.M.3
Müller-Myhsok, B.4
Cichon, S.5
Vogt, I.R.6
Propping, P.7
Remschmidt, H.8
-
41
-
-
34047255228
-
Interrelationship and familiality of dyslexia related quantitative measures
-
Schulte-Körne G, Ziegler A, Deimel W, Plume E, Bachmann C, Kleensang A, Propping P, Nöthen MM, Warnke A, Remschmidt H., et al. 2006. Interrelationship and familiality of dyslexia related quantitative measures. Ann Hum Genet 71: 160-175.
-
(2006)
Ann Hum Genet
, vol.71
, pp. 160-175
-
-
Schulte-Körne, G.1
Ziegler, A.2
Deimel, W.3
Plume, E.4
Bachmann, C.5
Kleensang, A.6
Propping, P.7
Nöthen, M.M.8
Warnke, A.9
Remschmidt, H.10
-
42
-
-
29244468273
-
Strong genetic evidence for DCDC2 as a susceptibility gene for dyslexia
-
Schumacher J, Anthoni H, Dahdouh F, König IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H., et al. 2006. Strong genetic evidence for DCDC2 as a susceptibility gene for dyslexia. Am J Hum Genet 78: 52-62.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 52-62
-
-
Schumacher, J.1
Anthoni, H.2
Dahdouh, F.3
König, I.R.4
Hillmer, A.M.5
Kluck, N.6
Manthey, M.7
Plume, E.8
Warnke, A.9
Remschmidt, H.10
-
43
-
-
34248337476
-
Genetics of dyslexia: The evolving landscape
-
Schumacher J, Hoffmann P, Schmal C, Schulte-Körne G, Nöthen MM. 2007. Genetics of dyslexia: The evolving landscape. J Med Genet 44: 289-297.
-
(2007)
J Med Genet
, vol.44
, pp. 289-297
-
-
Schumacher, J.1
Hoffmann, P.2
Schmal, C.3
Schulte-Körne, G.4
Nöthen, M.M.5
-
44
-
-
49049110163
-
Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21
-
Schumacher J, König IR, Schröder T, Duell M, Plume E, Propping P, Warnke A, Libertus C, Ziegler A, Müller-Myhsok B, Schulte-Körne G, Nöthen MM. 2008. Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21. Psychiatr Genet 18: 137-142.
-
(2008)
Psychiatr Genet
, vol.18
, pp. 137-142
-
-
Schumacher, J.1
König, I.R.2
Schröder, T.3
Duell, M.4
Plume, E.5
Propping, P.6
Warnke, A.7
Libertus, C.8
Ziegler, A.9
Müller-Myhsok, B.10
Schulte-Körne, G.11
Nöthen, M.M.12
-
45
-
-
0033852095
-
Rapid naming deficits in children and adolescents with reading disabilities and attention deficit hyperactivity disorder
-
Semrud-Clikeman M, Guy K, Griffin JD, Hynd GW. 2000. Rapid naming deficits in children and adolescents with reading disabilities and attention deficit hyperactivity disorder. Brain Lang 74: 70-83.
-
(2000)
Brain Lang
, vol.74
, pp. 70-83
-
-
Semrud-Clikeman, M.1
Guy, K.2
Griffin, J.D.3
Hynd, G.W.4
-
46
-
-
0032712319
-
Persistence of dyslexia: The Connecticut Longitudinal Study at adolescence
-
Shaywitz SE, Fletcher JM, Holahan JM, Shneider AE, Marchione KE, Stuebing KK, Francis DJ, Pugh KR, Shaywitz BA. 1999. Persistence of dyslexia: The Connecticut Longitudinal Study at adolescence. Pediatrics 104: 1351-1359.
-
(1999)
Pediatrics
, vol.104
, pp. 1351-1359
-
-
Shaywitz, S.E.1
Fletcher, J.M.2
Holahan, J.M.3
Shneider, A.E.4
Marchione, K.E.5
Stuebing, K.K.6
Francis, D.J.7
Pugh, K.R.8
Shaywitz, B.A.9
-
47
-
-
41549165267
-
The education of dyslexic children from childhood to young adulthood
-
Shaywitz SE, Morris R, Shaywitz BA. 2008. The education of dyslexic children from childhood to young adulthood. Annu Rev Psychol 59: 451-475.
-
(2008)
Annu Rev Psychol
, vol.59
, pp. 451-475
-
-
Shaywitz, S.E.1
Morris, R.2
Shaywitz, B.A.3
-
49
-
-
0028432432
-
Longitudinal studies of phonological processing and reading
-
Torgesen JK, Wagner RK, Rashotte CA. 1994. Longitudinal studies of phonological processing and reading. J Learn Disabil 27: 276-286.
-
(1994)
J Learn Disabil
, vol.27
, pp. 276-286
-
-
Torgesen, J.K.1
Wagner, R.K.2
Rashotte, C.A.3
-
50
-
-
33750704625
-
Predicting delayed letter knowledge development and its relation to grade 1 reading achievement among children with and without familial risk for dyslexia
-
Torppa M, Poikkeus A-M, Laakso M-L, Eklund K, Lyytinen H. 2006. Predicting delayed letter knowledge development and its relation to grade 1 reading achievement among children with and without familial risk for dyslexia. Dev Psychol 42: 1128-1142.
-
(2006)
Dev Psychol
, vol.42
, pp. 1128-1142
-
-
Torppa, M.1
Poikkeus, A.-M.2
Laakso, M.-L.3
Eklund, K.4
Lyytinen, H.5
-
52
-
-
58149206162
-
Development of young readers' phonological processing abilities
-
Wagner RK, Torgesen JK, Laughon PL, Simmons K, Rashotte CA. 1993. Development of young readers' phonological processing abilities. J Educ Psychol 85: 83-103.
-
(1993)
J Educ Psychol
, vol.85
, pp. 83-103
-
-
Wagner, R.K.1
Torgesen, J.K.2
Laughon, P.L.3
Simmons, K.4
Rashotte, C.A.5
-
53
-
-
0031136030
-
Changing relations between phonological processing abilities and word-level reading as children develop from beginning to skilled readers: A 5-year longitudinal study
-
Wagner RK, Torgesen JK, Rashotte CA, Hecht SA, Barker TA, Burgess SR., et al. 1997. Changing relations between phonological processing abilities and word-level reading as children develop from beginning to skilled readers: A 5-year longitudinal study. Dev Psychol 33: 468-479.
-
(1997)
Dev Psychol
, vol.33
, pp. 468-479
-
-
Wagner, R.K.1
Torgesen, J.K.2
Rashotte, C.A.3
Hecht, S.A.4
Barker, T.A.5
Burgess, S.R.6
-
56
-
-
24044550689
-
PEDSTATS: Descriptive statistics, graphics and quality assessment for gene mapping data
-
Wigginton JE, Abecasis GR. 2005. PEDSTATS: Descriptive statistics, graphics and quality assessment for gene mapping data. Bioinformatics 21: 3445-3447.
-
(2005)
Bioinformatics
, vol.21
, pp. 3445-3447
-
-
Wigginton, J.E.1
Abecasis, G.R.2
-
57
-
-
34247258570
-
Phonology, rapid naming and academic achievement in very preterm children at eight years of age
-
Wocadlo C, Rieger I. 2007. Phonology, rapid naming and academic achievement in very preterm children at eight years of age. Early Hum Dev 83: 367-377.
-
(2007)
Early Hum Dev
, vol.83
, pp. 367-377
-
-
Wocadlo, C.1
Rieger, I.2
-
58
-
-
0022760427
-
Automaticity, retrieval processes, and reading: A longitudinal study in average and impaired readers
-
Wolf M, Bally H, Morris R. 1986. Automaticity, retrieval processes, and reading: A longitudinal study in average and impaired readers. Child Devel 57: 988-1000.
-
(1986)
Child Devel
, vol.57
, pp. 988-1000
-
-
Wolf, M.1
Bally, H.2
Morris, R.3
-
59
-
-
21044457554
-
Developmental dyslexia-Recurrence risk estimates from a German bi-center study using the single proband sib pair design
-
Ziegler A, König IR, Deimel W, Plume E, Nöthen MM, Propping P, Kleensang A, Müller-Myhsok B, Warnke A, Remschmidt H., et al. 2005. Developmental dyslexia-Recurrence risk estimates from a German bi-center study using the single proband sib pair design. Hum Hered 59: 136-143.
-
(2005)
Hum Hered
, vol.59
, pp. 136-143
-
-
Ziegler, A.1
König, I.R.2
Deimel, W.3
Plume, E.4
Nöthen, M.M.5
Propping, P.6
Kleensang, A.7
Müller-Myhsok, B.8
Warnke, A.9
Remschmidt, H.10
|