-
1
-
-
0025602128
-
A prospective study of the relationship between specific language impairment, phonological disorders and reading retardation
-
Bishop, D. V. & Adams, C. A prospective study of the relationship between specific language impairment, phonological disorders and reading retardation. J. Child. Psychol. Psychiatry 31, 1027-1050 (1990
-
(1990)
J. Child. Psychol. Psychiatry
, vol.31
, pp. 1027-1050
-
-
Bishop, D.V.1
Adams, C.2
-
2
-
-
2142645060
-
The development of early literacy skills among children with speech difficulties: A test of the 'critical age hypo thesis'
-
Nathan, L., Stackhouse, J., Goulandris, N. & Snowling, M. J. The development of early literacy skills among children with speech difficulties: A test of the 'critical age hypothesis'. J. Speech. Lang. Hear. Res. 47, 377-391 (2004
-
(2004)
J. Speech. Lang. Hear. Res
, vol.47
, pp. 377-391
-
-
Nathan, L.1
Stackhouse, J.2
Goulandris, N.3
Snowling, M.J.4
-
3
-
-
0031976625
-
Language-impaired preschoolers: A follow-up into adolescence
-
Stothard, S. E., Snowling, M. J., Bishop, D. V., Chipchase, B. B. & Kaplan, C. A. Language-impaired preschoolers: A follow-up into adolescence. J. Speech. Lang. Hear. Res. 41, 407-418 (1998
-
(1998)
J. Speech. Lang. Hear. Res
, vol.41
, pp. 407-418
-
-
Stothard, S.E.1
Snowling, M.J.2
Bishop, D.V.3
Chipchase, B.B.4
Kaplan, C.A.5
-
4
-
-
0033943099
-
Is preschool language impairment a risk factor for dyslexia in adolescence
-
Snowling, M., Bishop, D. V. & Stothard, S. E. Is preschool language impairment a risk factor for dyslexia in adolescence? J. Child. Psychol. Psychiatry 41, 587-600 (2000
-
(2000)
J. Child. Psychol. Psychiatry
, vol.41
, pp. 587-600
-
-
Snowling, M.1
Bishop, D.V.2
Stothard, S.E.3
-
5
-
-
0035430299
-
Language development and symbolic play in children with and without familial risk for dyslexia
-
Lyytinen, P., Poikkeus, A. M., Laakso, M. L., Eklund, K. & Lyytinen, H. Language development and symbolic play in children with and without familial risk for dyslexia. J. Speech. Lang. Hear. Res. 44, 873-885 (2001
-
(2001)
J. Speech. Lang. Hear. Res
, vol.44
, pp. 873-885
-
-
Lyytinen, P.1
Poikkeus, A.M.2
Laakso, M.L.3
Eklund, K.4
Lyytinen, H.5
-
6
-
-
31144448452
-
Language development and literacy skills in late-Talking toddlers with and without familial risk for dyslexia
-
Lyytinen, P., Eklund, K. & Lyytinen, H. Language development and literacy skills in late-Talking toddlers with and without familial risk for dyslexia. Ann. Dyslexia 55, 166-192 (2001
-
(2001)
Ann. Dyslexia
, vol.55
, pp. 166-192
-
-
Lyytinen, P.1
Eklund, K.2
Lyytinen, H.3
-
7
-
-
22944466707
-
Age 13 language and reading outcomes in late-Talking toddlers
-
Rescorla, L. Age 13 language and reading outcomes in late-Talking toddlers. J. Speech. Lang. Hear. Res. 48, 459-472 (2005
-
(2005)
J. Speech. Lang. Hear. Res
, vol.48
, pp. 459-472
-
-
Rescorla, L.1
-
8
-
-
28544444164
-
The etiology of mathematical and reading (dis)ability covariation in a sample of dutch twins
-
Markowitz, E. M., Willemsen, G., Trumbetta, S. L., van Beijsterveldt, T. C. & Boomsma, D. I. The etiology of mathematical and reading (dis)ability covariation in a sample of Dutch twins. Twin Res. Hum. Genet. 8, 585-593 (2005
-
(2005)
Twin Res. Hum. Genet
, vol.8
, pp. 585-593
-
-
Markowitz, E.M.1
Willemsen, G.2
Trumbetta, S.L.3
Van Beijsterveldt, T.C.4
Boomsma, D.I.5
-
9
-
-
0029246289
-
Comorbidity of reading and mathematics disabilities: Genetic and environmental etiologies
-
Light, J. G. & DeFries, J. C. Comorbidity of reading and mathematics disabilities: Genetic and environmental etiologies. J. Learn. Disabil. 28, 96-106 (1995
-
(1995)
J. Learn. Disabil
, vol.28
, pp. 96-106
-
-
Light, J.G.1
Defries, J.C.2
-
10
-
-
0032858773
-
Etiology of covariation between reading and mathematics performance: A twin study
-
Knopik, V. S. & DeFries, J. C. Etiology of covariation between reading and mathematics performance: A twin study. Twin Res. 2, 226-234 (1999
-
(1999)
Twin Res
, vol.2
, pp. 226-234
-
-
Knopik, V.S.1
Defries, J.C.2
-
11
-
-
0026180712
-
Longitudinal prediction of specific cognitive abilities from infant novelty preference
-
Thompson, L. A., Fagan, J. F. & Fulker, D. W. Longitudinal prediction of specific cognitive abilities from infant novelty preference. Child Dev. 62, 530-538 (1991
-
(1991)
Child Dev
, vol.62
, pp. 530-538
-
-
Thompson, L.A.1
Fagan, J.F.2
Fulker, D.W.3
-
12
-
-
0033087303
-
The structure of genetic influences on general cognitive, language, phonological, and reading abilities
-
Hohnen, B. & Stevenson, J. The structure of genetic influences on general cognitive, language, phonological, and reading abilities. Dev. Psychol. 35, 590-603 (1999
-
(1999)
Dev. Psychol
, vol.35
, pp. 590-603
-
-
Hohnen, B.1
Stevenson, J.2
-
13
-
-
34547851575
-
Overlap and specificity of genetic and environmental influences on mathematics and reading disability in 10-year-old twins
-
Kovas, Y., Haworth, C. M., Harlaar, N., Petrill, S. A., Dale, P. S. & Plomin, R. Overlap and specificity of genetic and environmental influences on mathematics and reading disability in 10-year-old twins. J. Child. Psychol. Psychiatry 48, 914-922 (2007
-
(2007)
J. Child. Psychol. Psychiatry
, vol.48
, pp. 914-922
-
-
Kovas, Y.1
Haworth, C.M.2
Harlaar, N.3
Petrill, S.A.4
Dale, P.S.5
Plomin, R.6
-
14
-
-
0035080409
-
Genetic influences on language impairment and literacy problems in children: Same or different
-
Bishop, D. V. Genetic influences on language impairment and literacy problems in children: Same or different? J. Child. Psychol. Psychiatry 42, 189-198 (2001
-
(2001)
J. Child. Psychol. Psychiatry
, vol.42
, pp. 189-198
-
-
Bishop, D.V.1
-
15
-
-
23844450016
-
Generalist genes and learning disabilities
-
Plomin, R. & Kovas, Y. Generalist genes and learning disabilities. Psychol. Bull. 131, 592-617 (2005
-
(2005)
Psychol. Bull
, vol.131
, pp. 592-617
-
-
Plomin, R.1
Kovas, Y.2
-
16
-
-
33646352936
-
Generalist genes: Implications for the cognitive sciences
-
Kovas, Y. & Plomin, R. Generalist genes: Implications for the cognitive sciences. Trends Cogn. Sci. 10, 198-203 (2006
-
(2006)
Trends Cogn. Sci
, vol.10
, pp. 198-203
-
-
Kovas, Y.1
Plomin, R.2
-
17
-
-
84879603668
-
Dna evidence for strong genome-wide pleiotropy of cognitive and learning abilities
-
Trzaskowski, M., Davis, O. S., DeFries, J. C., Yang, J., Visscher, P. M. & Plomin, R. DNA evidence for strong genome-wide pleiotropy of cognitive and learning abilities. Behav. Genet. 43, 267-273 (2013
-
(2013)
Behav. Genet
, vol.43
, pp. 267-273
-
-
Trzaskowski, M.1
Davis, O.S.2
Defries, J.C.3
Yang, J.4
Visscher, P.M.5
Plomin, R.6
-
18
-
-
63849314154
-
Speaking genes or genes for speaking? Deciphering the genetics of speech and language
-
Grigorenko, E. L. Speaking genes or genes for speaking? Deciphering the genetics of speech and language. J. Child. Psychol. Psychiatry 50, 116-125 (2009
-
(2009)
J. Child. Psychol. Psychiatry
, vol.50
, pp. 116-125
-
-
Grigorenko, E.L.1
-
19
-
-
77949416390
-
A genome-wide association study identifies multiple loci associated with mathematics ability and disability
-
Docherty, S. J., Davis, O. S., Kovas, Y., Meaburn, E. L., Dale, P. S., Petrill, S. A. et al. A genome-wide association study identifies multiple loci associated with mathematics ability and disability. Genes Brain Behav. 9, 234-247 (2010
-
(2010)
Genes Brain Behav
, vol.9
, pp. 234-247
-
-
Docherty, S.J.1
Davis, O.S.2
Kovas, Y.3
Meaburn, E.L.4
Dale, P.S.5
Petrill, S.A.6
-
20
-
-
0036779497
-
Developmental dyslexia: Genetic dissection of a complex cognitive trait
-
Fisher, S. E. & DeFries, J. C. Developmental dyslexia: Genetic dissection of a complex cognitive trait. Nat. Rev. Neurosci. 3, 767-780 (2002
-
(2002)
Nat. Rev. Neurosci
, vol.3
, pp. 767-780
-
-
Fisher, S.E.1
Defries, J.C.2
-
22
-
-
18344374003
-
Evidence for linkage and association with reading disability on 6p21.3-22
-
Kaplan, D. E., Gayan, J., Ahn, J., Won, T. W., Pauls, D., Olson, R. K. et al. Evidence for linkage and association with reading disability on 6p21.3-22. Am. J. Hum. Genet. 70, 1287-1298 (2002
-
(2002)
Am. J. Hum. Genet
, vol.70
, pp. 1287-1298
-
-
Kaplan, D.E.1
Gayan, J.2
Ahn, J.3
Won, T.W.4
Pauls, D.5
Olson, R.K.6
-
23
-
-
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, S. D., Richardson, A. J., Scerri, T. S., Cardon, L. R. et al. 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
-
(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
-
24
-
-
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. et al. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am. J. Hum. Genet. 76, 581-591 (2005
-
(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
-
25
-
-
33845246158
-
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. 11, 1085-1091 (2006
-
(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
-
26
-
-
34548473808
-
A haplotype spanning kiaa0319 and ttrap is associated with normal variation in reading and spelling ability
-
Luciano, M., Lind, P. A., Duffy, D. L., Castles, A., Wright, M. J., Montgomery, G. W. et al. A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biol. Psychiatry 62, 811-817 (2007
-
(2007)
Biol. Psychiatry
, vol.62
, pp. 811-817
-
-
Luciano, M.1
Lind, P.A.2
Duffy, D.L.3
Castles, A.4
Wright, M.J.5
Montgomery, G.W.6
-
27
-
-
55349131289
-
Investigation of interaction between dcdc2 and kiaa0319 in a large german dyslexia sample
-
Ludwig, K. U., Roeske, D., Schumacher, J., Schulte-Korne, G., Konig, I. R., Warnke, A. et al. Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample. J. Neural Transm. 115, 1587-1589 (2008
-
(2008)
J. Neural Transm
, vol.115
, pp. 1587-1589
-
-
Ludwig, K.U.1
Roeske, D.2
Schumacher, J.3
Schulte-Korne, G.4
Konig, I.R.5
Warnke, A.6
-
28
-
-
63449106260
-
A common variant associated with dyslexia reduces expression of the kiaa0319 gene
-
Dennis, M., Paracchini, S., Scerri, T. S., Prokunina-Olsson, L., Knight, J. C., Wade-Martins, R. et al. A common variant associated with dyslexia reduces expression of the KIAA0319 gene. PLoS Genet. 5, e1000436 (2009
-
(2009)
PLoS Genet
, vol.5
-
-
Dennis, M.1
Paracchini, S.2
Scerri, T.S.3
Prokunina-Olsson, L.4
Knight, J.C.5
Wade-Martins, R.6
-
29
-
-
77349092836
-
Association of reading disabilities with regions marked by acetylated h3 histones in kiaa0319
-
Couto, J. M., Livne-Bar, I., Huang, K., Xu, Z., Cate-Carter, T., Feng, Y. et al. Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 153B, 447-462 (2010
-
(2010)
Am. J. Med. Genet. B. Neuropsychiatr. Genet
, pp. 447-462
-
-
Couto, J.M.1
Livne-Bar, I.2
Huang, K.3
Xu, Z.4
Cate-Carter, T.5
Feng, Y.6
-
30
-
-
79952440240
-
Genetic variation in the KIAA0319 5- region as a possible contributor to dyslexia
-
Elbert, A., Lovett, M. W., Cate-Carter, T., Pitch, A., Kerr, E. N. & Barr, C. L. Genetic variation in the KIAA0319 5- region as a possible contributor to dyslexia. Behav. Genet. 41, 77-89 (2011
-
(2011)
Behav. Genet
, vol.41
, pp. 77-89
-
-
Elbert, A.1
Lovett, M.W.2
Cate-Carter, T.3
Pitch, A.4
Kerr, E.N.5
Barr, C.L.6
-
31
-
-
84863500479
-
Association study of a functional genetic variant in kiaa0319 in german dyslexics
-
Kirsten, H., Wilcke, A., Ligges, C., Boltze, J. & Ahnert, P. Association study of a functional genetic variant in KIAA0319 in German dyslexics. Psychiatr. Genet. 22, 216-217 (2012
-
(2012)
Psychiatr. Genet
, vol.22
, pp. 216-217
-
-
Kirsten, H.1
Wilcke, A.2
Ligges, C.3
Boltze, J.4
Ahnert, P.5
-
32
-
-
84883274320
-
Analysis of genetic variats of dyslexia candidate genes kiaa0319 and dcdc2 in indian population
-
Venkatesh, S. K., Siddaiah, A., Padakannaya, P. & Ramachandra, N. B. Analysis of genetic variats of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population. J. Hum. Genet. 58, 531-538 (2013
-
(2013)
J. Hum. Genet
, vol.58
, pp. 531-538
-
-
Venkatesh, S.K.1
Siddaiah, A.2
Padakannaya, P.3
Ramachandra, N.B.4
-
33
-
-
84869072315
-
Genetic variants in kiaa0319, but not in dyx1c1, is associated with risk of dyslexia: An integrated metaamalysis
-
Zou, L., Chen, W., Shao, S., Sun, Z., Zhong, R., Shi, J. et al. Genetic variants in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: An integrated metaamalysis. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 159B, 970-976 (2012
-
(2012)
Am. J. Med. Genet. B. Neuropsychiatr. Genet
, pp. 970-976
-
-
Zou, L.1
Chen, W.2
Shao, S.3
Sun, Z.4
Zhong, R.5
Shi, J.6
-
34
-
-
34250810249
-
Evaluation of candidate genes for dyx1 and dyx2 in families with dyslexia
-
Brkanac, Z., Chapman, N. H., Matsushita, M. M., Chun, L., Nielsen, K., Cochrane, E. et al. Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 144B, 556-560 (2007
-
(2007)
Am. J. Med. Genet. B. Neuropsychiatr. Genet
, pp. 556-560
-
-
Brkanac, Z.1
Chapman, N.H.2
Matsushita, M.M.3
Chun, L.4
Nielsen, K.5
Cochrane, E.6
-
35
-
-
84887346281
-
Study of candidate genes for dyslexia in Brazilian individuals
-
Svidnicki, M.C., Salgado, C.A., Lima, R.F., Ciasca, S.M., Secolin, R., Pomilio, M.C. et al. Study of candidate genes for dyslexia in Brazilian individuals. Genet. Mol. Res. 12, 5356-5364 (2013
-
(2013)
Genet. Mol. Res
, vol.12
, pp. 5356-5364
-
-
Svidnicki, M.C.1
Salgado, C.A.2
Lima, R.F.3
Ciasca, S.M.4
Secolin, R.5
Pomilio, M.C.6
-
36
-
-
57349157021
-
Association of the kiaa0319 dyslexia susceptibility gene with reading skills in the general population
-
Paracchini, S., Steer, C. D., Buckingham, L. L., Morris, A. P., Ring, S., Scerri, T. et al. Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. Am. J. Psychiatry 165, 1576-1584 (2008
-
(2008)
Am. J. Psychiatry
, vol.165
, pp. 1576-1584
-
-
Paracchini, S.1
Steer, C.D.2
Buckingham, L.L.3
Morris, A.P.4
Ring, S.5
Scerri, T.6
-
37
-
-
79960220393
-
Dcdc2 kiaa0319 and cmip are associated with reading-related traits
-
Scerri, T. S., Morris, A. P., Buckingham, L. L., Newbury, D. F., Miller, L. L., Monaco, A. P. et al. DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Biol. Psychiatry 70, 237-245 (2011
-
(2011)
Biol. Psychiatry
, vol.70
, pp. 237-245
-
-
Scerri, T.S.1
Morris, A.P.2
Buckingham, L.L.3
Newbury, D.F.4
Miller, L.L.5
Monaco, A.P.6
-
38
-
-
77950852556
-
Convergent genetic linkage and associations to language, speech and reading measures in families of probands with specific language impairment
-
Rice, M. L., Smith, S. D. & Gayan, J. Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment. J. Neurodev. Disord. 1, 264-282 (2009
-
(2009)
J. Neurodev. Disord
, vol.1
, pp. 264-282
-
-
Rice, M.L.1
Smith, S.D.2
Gayan, J.3
-
39
-
-
79952443636
-
Investigation of dyslexia and SLI risk variants in reading-And language-impaired subjects
-
Newbury, D. F., Paracchini, S., Scerri, T. S., Winchester, L., Addis, L., Richardson, A. J. et al. Investigation of dyslexia and SLI risk variants in reading-And language-impaired subjects. Behav. Genet. 41, 90-104 (2011
-
(2011)
Behav. Genet
, vol.41
, pp. 90-104
-
-
Newbury, D.F.1
Paracchini, S.2
Scerri, T.S.3
Winchester, L.4
Addis, L.5
Richardson, A.J.6
-
40
-
-
29144466474
-
Linkage of speech sound disorder to reading disability loci
-
Smith, S. D., Pennington, B. F., Boada, R. & Shriberg, L. D. Linkage of speech sound disorder to reading disability loci. J. Child. Psychol. Psychiatry 46, 1057-1066 (2005
-
(2005)
J. Child. Psychol. Psychiatry
, vol.46
, pp. 1057-1066
-
-
Smith, S.D.1
Pennington, B.F.2
Boada, R.3
Shriberg, L.D.4
-
41
-
-
0034785618
-
A dominant gene for developmental dyslexia on chromosome 3
-
Nopola-Hemmi, J., Myllyluoma, B., Haltia, T., Taipale, M., Ollikainen, V., Ahonen, T. et al. A dominant gene for developmental dyslexia on chromosome 3. J. Med. Genet. 38, 658-664 (2001
-
(2001)
J. Med. Genet
, vol.38
, pp. 658-664
-
-
Nopola-Hemmi, J.1
Myllyluoma, B.2
Haltia, T.3
Taipale, M.4
Ollikainen, V.5
Ahonen, T.6
-
42
-
-
33745343959
-
The axon guidance receptor gene robo1 is a candidate gene for developmental dyslexia
-
Hannula-Jouppi, K., Kaminen-Ahola, N., Taipale, M., Eklund, R., Nopola-Hemmi, J., Kaariainen, H. et al. The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS Genet. 1, e50 (2005
-
(2005)
PLoS Genet
, vol.1
-
-
Hannula-Jouppi, K.1
Kaminen-Ahola, N.2
Taipale, M.3
Eklund, R.4
Nopola-Hemmi, J.5
Kaariainen, H.6
-
43
-
-
79952443930
-
Genetic variance in a component of the language acquisition device: Robo1 polymorphisms associated with phonological buffer deficits
-
Bates, T. C., Luciano, M., Medland, S. E., Montgomery, G. W., Wright, M. J. & Martin, N. G. Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. Behav. Genet. 41, 50-57 (2011
-
(2011)
Behav. Genet
, vol.41
, pp. 50-57
-
-
Bates, T.C.1
Luciano, M.2
Medland, S.E.3
Montgomery, G.W.4
Wright, M.J.5
Martin, N.G.6
-
44
-
-
84883786565
-
Lack of association between genetic polymorphisms in robo1 mrpl19/c2orf3 and them2 with developmental dyslexia
-
Venkatesh, S. K., Siddaiah, A., Padakannaya, P. & Ramachandra, N. B. Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with developmental dyslexia. Gene 529, 215-219 (2013
-
(2013)
Gene
, vol.529
, pp. 215-219
-
-
Venkatesh, S.K.1
Siddaiah, A.2
Padakannaya, P.3
Ramachandra, N.B.4
-
45
-
-
10744233099
-
Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading
-
Stein, C. M., Schick, J. H., Gerry Taylor, H., Shriberg, L. D., Millard, C., Kundtz-Kluge, A. et al. Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading. Am. J. Hum. Genet. 74, 283-297 (2004
-
(2004)
Am. J. Hum. Genet
, vol.74
, pp. 283-297
-
-
Stein, C.M.1
Schick, J.H.2
Gerry Taylor, H.3
Shriberg, L.D.4
Millard, C.5
Kundtz-Kluge, A.6
-
46
-
-
33744920683
-
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of kiaa0319, a novel gene involved in neuronal migration
-
Paracchini, S., Thomas, A., Castro, S., Lai, C., Paramasivam, M., Wang, Y. et al. The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum. Mol. Genet. 15, 1659-1666 (2006
-
(2006)
Hum. Mol. Genet
, vol.15
, pp. 1659-1666
-
-
Paracchini, S.1
Thomas, A.2
Castro, S.3
Lai, C.4
Paramasivam, M.5
Wang, Y.6
-
47
-
-
78650072090
-
The dyslexia-Associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage
-
Velayos-Baeza, A., Levecque, C., Kobayashi, K., Holloway, Z. G. & Monaco, A. P. The dyslexia-Associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage. J. Biol. Chem. 285, 40148-40162 (2010
-
(2010)
J. Biol. Chem
, vol.285
, pp. 40148-40162
-
-
Velayos-Baeza, A.1
Levecque, C.2
Kobayashi, K.3
Holloway, Z.G.4
Monaco, A.P.5
-
48
-
-
77949357854
-
The effect of variation in expression of the candidate dyslexia susceptibility gene homolog Kiaa0319 on neuronal migration and dendritic morphology in the rat
-
Peschansky, V. J., Burbridge, T. J., Volz, A. J., Fiondella, C., Wissner-Gross, Z., Galaburda, A. M. et al. The effect of variation in expression of the candidate dyslexia susceptibility gene homolog Kiaa0319 on neuronal migration and dendritic morphology in the rat. Cereb. Cortex 20, 884-897 (2010
-
(2010)
Cereb. Cortex
, vol.20
, pp. 884-897
-
-
Peschansky, V.J.1
Burbridge, T.J.2
Volz, A.J.3
Fiondella, C.4
Wissner-Gross, Z.5
Galaburda, A.M.6
-
49
-
-
78650743180
-
The effects of embryonic knockdown of the candidate dyslexia susceptibility gene homologue dyx1c1 on the distribution of gabaergic neurons in the cerebral cortex
-
Currier, T. A., Etchegaray, M. A., Haight, J. L., Galaburda, A. M. & Rosen, G. D. The effects of embryonic knockdown of the candidate dyslexia susceptibility gene homologue Dyx1c1 on the distribution of GABAergic neurons in the cerebral cortex. Neuroscience 172, 535-546 (2011
-
(2011)
Neuroscience
, vol.172
, pp. 535-546
-
-
Currier, T.A.1
Etchegaray, M.A.2
Haight, J.L.3
Galaburda, A.M.4
Rosen, G.D.5
-
50
-
-
79151472367
-
Dyslexiaassociated kiaa0319-like protein interacts with axon guidance receptor nogo receptor 1
-
Poon, M. W., Tsang, W. H., Chan, S. O., Li, H. M., Ng, H. K. & Waye, M. M. Dyslexiaassociated kiaa0319-like protein interacts with axon guidance receptor nogo receptor 1. Cell. Mol. Neurobiol. 31, 27-35 (2011
-
(2011)
Cell. Mol. Neurobiol
, vol.31
, pp. 27-35
-
-
Poon, M.W.1
Tsang, W.H.2
Chan, S.O.3
Li, H.M.4
Ng, H.K.5
Waye, M.M.6
-
51
-
-
84871734920
-
The effects of Kiaa0319 knockdown on cortical and subcortical anatomy in male rats
-
Szalkowski, C. E., Fiondella, C. F., Truong, D. T., Rosen, G. D., Loturco, J. J. & Fitch, R. H. The effects of Kiaa0319 knockdown on cortical and subcortical anatomy in male rats. Int. J. Dev. Neurosci. 31, 116-122 (2012
-
(2012)
Int. J. Dev. Neurosci
, vol.31
, pp. 116-122
-
-
Szalkowski, C.E.1
Fiondella, C.F.2
Truong, D.T.3
Rosen, G.D.4
Loturco, J.J.5
Fitch, R.H.6
-
52
-
-
84860522828
-
Neocortical disruption and behavioral impairments in rats following in utero rnai of candidate dyslexia risk gene kiaa0319
-
Szalkowski, C. E., Fiondella, C. G., Galaburda, A. M., Rosen, G. D., Loturco, J. J. & Fitch, R. H. Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319. Int. J. Dev. Neurosci. 30, 293-302 (2012
-
(2012)
Int. J. Dev. Neurosci
, vol.30
, pp. 293-302
-
-
Szalkowski, C.E.1
Fiondella, C.G.2
Galaburda, A.M.3
Rosen, G.D.4
Loturco, J.J.5
Fitch, R.H.6
-
53
-
-
84879651845
-
Cortical speech-evoked response patterns in multiple auditory fields are correlated with behavioral discrimination ability
-
Centanni, T. M., Engineer, C. T. & Kilgard, M. P. Cortical speech-evoked response patterns in multiple auditory fields are correlated with behavioral discrimination ability. J. Neurophysiol. 110, 177-189 (2013
-
(2013)
J. Neurophysiol
, vol.110
, pp. 177-189
-
-
Centanni, T.M.1
Engineer, C.T.2
Kilgard, M.P.3
-
54
-
-
84880942384
-
Embryonic disruption of the candidate dyslexia susceptibility gene homolog Kiaa0319-like results in neuronal migration disorders
-
Platt, M. P., Adler, W. T., Mehlhorn, A. J., Johnson, G. C., Wright, K. A., Choi, R. T. et al. Embryonic disruption of the candidate dyslexia susceptibility gene homolog Kiaa0319-like results in neuronal migration disorders. Neuroscience 248C, 585-593 (2013
-
(2013)
Neuroscience
, pp. 585-593
-
-
Platt, M.P.1
Adler, W.T.2
Mehlhorn, A.J.3
Johnson, G.C.4
Wright, K.A.5
Choi, R.T.6
-
55
-
-
84878403099
-
Position of neocortical neurons transfected at different gestational ages with shrna targeted against candidate dyslexia susceptibility genes
-
Adler, W. T., Platt, M. P., Mehlhorn, A. J., Haight, J. L., Currier, T. A., Etchegaray, M. A. et al. Position of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes. PLoS One 8, e65179 (2013
-
(2013)
PLoS One
, vol.8
-
-
Adler, W.T.1
Platt, M.P.2
Mehlhorn, A.J.3
Haight, J.L.4
Currier, T.A.5
Etchegaray, M.A.6
-
56
-
-
0018356659
-
Cytoarchitectonic abnormalities in developmental dyslexia: A case study
-
Galaburda, A. M. & Kemper, T. L. Cytoarchitectonic abnormalities in developmental dyslexia: A case study. Ann. Neurol. 6, 94-100 (1979
-
(1979)
Ann. Neurol
, vol.6
, pp. 94-100
-
-
Galaburda, A.M.1
Kemper, T.L.2
-
57
-
-
0021832834
-
Developmental dyslexia: Four consecutive patients with cortical anomalies
-
Galaburda, A. M., Sherman, G. F., Rosen, G. D., Aboitiz, F. & Geschwind, N. Developmental dyslexia: Four consecutive patients with cortical anomalies. Ann. Neurol. 18, 222-233 (1985
-
(1985)
Ann. Neurol
, vol.18
, pp. 222-233
-
-
Galaburda, A.M.1
Sherman, G.F.2
Rosen, G.D.3
Aboitiz, F.4
Geschwind, N.5
-
58
-
-
34748875368
-
Association of short-Term memory with a variant within dyx1c1 in developmental dyslexia
-
Marino, C., Citterio, A., Giorda, R., Facoetti, A., Menozzi, G., Vanzin, L. et al. Association of short-Term memory with a variant within DYX1C1 in developmental dyslexia. Genes Brain Behav. 6, 640-646 (2007
-
(2007)
Genes Brain Behav
, vol.6
, pp. 640-646
-
-
Marino, C.1
Citterio, A.2
Giorda, R.3
Facoetti, A.4
Menozzi, G.5
Vanzin, L.6
-
59
-
-
79952442429
-
Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia
-
Marino, C., Mascheretti, S., Riva, V., Cattaneo, F., Rigoletto, C., Rusconi, M. et al. Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia. Behav. Genet. 41, 67-76 (2011
-
(2011)
Behav. Genet
, vol.41
, pp. 67-76
-
-
Marino, C.1
Mascheretti, S.2
Riva, V.3
Cattaneo, F.4
Rigoletto, C.5
Rusconi, M.6
-
60
-
-
84655169217
-
DCDC2 genetic variants and susceptibility to developmental dyslexia
-
Marino, C., Meng, H., Mascheretti, S., Rusconi, M., Cope, N., Giorda, R. et al. DCDC2 genetic variants and susceptibility to developmental dyslexia. Psychiatr. Genet. 22, 25-30 (2012
-
(2012)
Psychiatr. Genet
, vol.22
, pp. 25-30
-
-
Marino, C.1
Meng, H.2
Mascheretti, S.3
Rusconi, M.4
Cope, N.5
Giorda, R.6
-
61
-
-
0041370144
-
No evidence for association and linkage disequilibrium between dyslexia and markers of four dopamine-related genes
-
Marino, C., Giorda, R., Vanzin, L., Molteni, M., Lorusso, M. L., Nobile, M. et al. No evidence for association and linkage disequilibrium between dyslexia and markers of four dopamine-related genes. Eur. Child Adolesc. Psychiatry 12, 198-202 (2003
-
(2003)
Eur. Child Adolesc. Psychiatry
, vol.12
, pp. 198-202
-
-
Marino, C.1
Giorda, R.2
Vanzin, L.3
Molteni, M.4
Lorusso, M.L.5
Nobile, M.6
-
62
-
-
1642574231
-
A locus on 15q15-15qter influences dyslexia: Further support from a transmission/ disequilibrium study in an Italian speaking population
-
Marino, C., Giorda, R., Vanzin, L., Nobile, M., Lorusso, M. L., Baschirotto, C. et al. A locus on 15q15-15qter influences dyslexia: Further support from a transmission/ disequilibrium study in an Italian speaking population. J. Med. Genet. 41, 42-46 (2004
-
(2004)
J. Med. Genet
, vol.41
, pp. 42-46
-
-
Marino, C.1
Giorda, R.2
Vanzin, L.3
Nobile, M.4
Lorusso, M.L.5
Baschirotto, C.6
-
63
-
-
20244377078
-
A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia
-
Marino, C., Giorda, R., Lorusso, L. M., 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. 13, 491-499 (2005
-
(2005)
Eur. J. Hum. Genet
, vol.13
, pp. 491-499
-
-
Marino, C.1
Giorda, R.2
Lorusso, L.M.3
Vanzin, L.4
Salandi, N.5
Nobile, M.6
-
64
-
-
84872678669
-
An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes
-
Mascheretti, S., Bureau, A., Battaglia, M., Simone, D., Quadrelli, E., Croteau, J. et al. An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes. Genes Brain Behav. 12, 47-55 (2013
-
(2013)
Genes Brain Behav
, vol.12
, pp. 47-55
-
-
Mascheretti, S.1
Bureau, A.2
Battaglia, M.3
Simone, D.4
Quadrelli, E.5
Croteau, J.6
-
68
-
-
0003735958
-
-
Firenze, Italy: Organizzazioni Speciali
-
Sartori, G., Job, R. & Tressoldi, P. E. Batteria per la valutazione della dislessia e della disortografia evolutiva (Firenze, Italy: Organizzazioni Speciali, 1995
-
(1995)
Batteria per la Valutazione della Dislessia e della Disortografia Evolutiva
-
-
Sartori, G.1
Job, R.2
Tressoldi, P.E.3
-
70
-
-
84938749474
-
Awareness of phonological segments and reading ability in Italian children
-
Cossu, G., Shankweiler, D., Liberman, I. Y., Katz, L. & Tola, G. Awareness of phonological segments and reading ability in Italian children. Appl. Psycholinguist. 9, 1-16 (1988
-
(1988)
Appl. Psycholinguist
, vol.9
, pp. 1-16
-
-
Cossu, G.1
Shankweiler, D.2
Liberman, I.Y.3
Katz, L.4
Tola, G.5
-
71
-
-
0032802466
-
Neurolinguistica e neuropsicologia dei disturbi specifici del linguaggio nel bambino: Proposta di un esame del linguaggio saggi
-
Fabbro, F. Neurolinguistica e Neuropsicologia Dei Disturbi Specifici Del Linguaggio Nel Bambino: Proposta Di Un Esame Del Linguaggio. Saggi. Neuropsicologia Infantile, psicopedagogia, riabilitazione 1, 11-23 (1999
-
(1999)
Neuropsicologia Infantile Psicopedagogia Riabilitazione
, vol.1
, pp. 11-23
-
-
Fabbro, F.1
-
72
-
-
34249814552
-
-
Trento, Italy: Erickson
-
Cornoldi, C., Lucangeli, D. & Bellina, M. AC-MT, Test Di Valutazione Delle Abilità Di Calcolo-Gruppo MT (Trento, Italy: Erickson, 2003
-
(2003)
AC-MT Test di Valutazione Delle Abilità di Calcolo-Gruppo MT
-
-
Cornoldi, C.1
Lucangeli, D.2
Bellina, M.3
-
73
-
-
0742288695
-
Arithmetic education and learning disabilities in Italy
-
Cornoldi, C. & Lucangeli, D. Arithmetic education and learning disabilities in Italy. J. Learn Disabil. 37, 42-49 (2004
-
(2004)
J. Learn Disabil
, vol.37
, pp. 42-49
-
-
Cornoldi, C.1
Lucangeli, D.2
-
76
-
-
24044550689
-
Pedstats: Descriptive statistics, graphics and quality assessment for gene mapping data
-
Wigginton, J. E. & Abecasis, G. R. PEDSTATS: Descriptive statistics, graphics and quality assessment for gene mapping data. Bioinformatics 21, 3445-3447 (2004
-
(2004)
Bioinformatics
, vol.21
, pp. 3445-3447
-
-
Wigginton, J.E.1
Abecasis, G.R.2
-
77
-
-
0033909546
-
A general test of association for quantitative traits in nuclear families
-
Abecasis, G. R., Cardon, L. R. & Cookson, W. O. A general test of association for quantitative traits in nuclear families. Am. J. Hum. Genet. 66, 279-292 (2000
-
(2000)
Am. J. Hum. Genet
, vol.66
, pp. 279-292
-
-
Abecasis, G.R.1
Cardon, L.R.2
Cookson, W.O.3
-
78
-
-
84899549024
-
-
in press
-
Eicher, J. D., Powers, N. R., Miller, L. L., Mueller, K. L, Marino, C., Smith, S. D. et al. Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and overall cognition. (in press
-
Characterization of the Dyx2 Locus on Chromosome 6p22 with Reading Disability, Language Impairment, and Overall Cognition
-
-
Eicher, J.D.1
Powers, N.R.2
Miller, L.L.3
Mueller, K.L.4
Marino, C.5
Smith, S.D.6
-
79
-
-
77349127347
-
Variation in grin2b contributes to weak performance in verbal short-Term memory in children with dyslexia
-
Ludwig, K. U., Roeske, D., Herms, S., Schumacher, J., Warnke, A. & Plume, E. Variation in GRIN2B contributes to weak performance in verbal short-Term memory in children with dyslexia. Am. J. Med. Genet. B. Neuropsychiatr. Genet 153, 503-511 (2009
-
(2009)
Am. J. Med. Genet. B. Neuropsychiatr. Genet
, vol.153
, pp. 503-511
-
-
Ludwig, K.U.1
Roeske, D.2
Herms, S.3
Schumacher, J.4
Warnke, A.5
Plume, E.6
-
80
-
-
0842307348
-
Pbat: Tools for family-based association studies
-
Lange, C., DeMeo, D., Silverman, E. K., Weiss, S. T. & Laird, N. M. PBAT: Tools for family-based association studies. Am. J. Hum. Genet. 74, 367-369 (2004
-
(2004)
Am. J. Hum. Genet
, vol.74
, pp. 367-369
-
-
Lange, C.1
Demeo, D.2
Silverman, E.K.3
Weiss, S.T.4
Laird, N.M.5
-
81
-
-
0033814928
-
Implementing a unified approach to family-based tests of association
-
Laird, N. M., Horvath, S. & Xu, X. Implementing a unified approach to family-based tests of association. Genet. Epidemiol. 19 (Suppl 1), S36-S42 (2000
-
(2000)
Genet. Epidemiol
, vol.19
, Issue.SUPPL. 1
-
-
Laird, N.M.1
Horvath, S.2
Xu, X.3
-
82
-
-
3543029197
-
Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: Linkage and association analyses
-
Deffenbacher, K. E., Kenyon, J. B., Hoover, D. M., Olson, R. K., Pennington, B. F., DeFries, J. C. et al. Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: Linkage and association analyses. Hum. Genet. 115, 128-138 (2004
-
(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
-
83
-
-
28044465597
-
DCDC2 is associated with reading disability and modulates neuronal development in the brain
-
Meng, H., Smith, S. D., Hager, K., Held, M., Liu, J., Olson, R. K. et al. DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc. Natl Acad. Sci. USA 102, 17053-17058 (2005
-
(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
-
84
-
-
29244468273
-
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
-
Schumacher, J., Anthoni, H., Dahdouh, F., Konig, I. R., Hillmer, A. M., Kluck, N. et al. Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Am. J. Hum. Genet. 78, 52-62 (2006
-
(2006)
Am. J. Hum. Genet
, vol.78
, pp. 52-62
-
-
Schumacher, J.1
Anthoni, H.2
Dahdouh, F.3
Konig, I.R.4
Hillmer, A.M.5
Kluck, N.6
-
85
-
-
0036020892
-
A direct approach to false discovery rates
-
Storey, J.D. A direct approach to false discovery rates. J. R. Stat. Soc. Ser. B 64, 479-498 (2002
-
(2002)
J. R. Stat. Soc. Ser
, vol.B64
, pp. 479-498
-
-
Storey, J.D.1
-
86
-
-
0035829361
-
Controlling the false discovery rate in behavior genetics research
-
Benjamini, Y., Drai, D., Elmer, G., Kafkafi, N. & Golani, I. Controlling the false discovery rate in behavior genetics research. Behav. Brain Res. 125, 279-284 (2001
-
(2001)
Behav. Brain Res
, vol.125
, pp. 279-284
-
-
Benjamini, Y.1
Drai, D.2
Elmer, G.3
Kafkafi, N.4
Golani, I.5
-
87
-
-
19944428926
-
Support for ekn1 as the susceptibility locus for dyslexia on 15q21
-
Wigg, K.G., Couto, J.M., Feng, Y., Anderson, B., Cate-Carter, T.D., Macciardi, F. et al. Support for EKN1 as the susceptibility locus for dyslexia on 15q21. Mol. Psychiatry 9, 1111-1121 (2004
-
(2004)
Mol. Psychiatry
, vol.9
, pp. 1111-1121
-
-
Wigg, K.G.1
Couto, J.M.2
Feng, Y.3
Anderson, B.4
Cate-Carter, T.D.5
MacCiardi, F.6
-
88
-
-
27544473473
-
Quantitative trait loci analysis using the false discovery rate
-
Benjamini, Y. & Yekutieli, D. Quantitative trait loci analysis using the false discovery rate. Genetics 171, 783-790 (2005
-
(2005)
Genetics
, vol.171
, pp. 783-790
-
-
Benjamini, Y.1
Yekutieli, D.2
-
89
-
-
84872678669
-
An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes
-
Mascheretti, S., Bureau, A., Battaglia, M., Simone, D., Quadrelli, E., Croteau, J. et al. An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes. Genes Brain Behav. 12, 47-55 (2013
-
(2013)
Genes Brain Behav
, vol.12
, pp. 47-55
-
-
Mascheretti, S.1
Bureau, A.2
Battaglia, M.3
Simone, D.4
Quadrelli, E.5
Croteau, J.6
-
90
-
-
45849097619
-
Generalist genes: Genetic links between brain mind and education
-
Plomin, R., Kovas, Y. & Haworth, C. M. Generalist Genes: Genetic Links Between Brain, Mind, and Education. Mind Brain Educ. 1, 11-19 (2007.
-
(2007)
Mind Brain Educ
, vol.1
, pp. 11-19
-
-
Plomin, R.1
Kovas, Y.2
Haworth, C.M.3
|