-
1
-
-
33645174874
-
Evidence that dyslexia may represent the lower tail of a normal distribution of reading ability
-
Shaywitz SE, Escobar MD, Shaywitz BA, et al.: Evidence that dyslexia may represent the lower tail of a normal distribution of reading ability. N Engl J Med 1992, 326:145-150.
-
(1992)
N Engl J Med
, vol.326
, pp. 145-150
-
-
Shaywitz, S.E.1
Escobar, M.D.2
Shaywitz, B.A.3
-
2
-
-
0041524990
-
Emerging issues in the genetics of dyslexia: A methodological preview
-
Wood FB, Grigorenko EL: Emerging issuesAin the genetics of dyslexia: a methodological preview. J Learn Disabil 2001, 34:503-511.
-
(2001)
J Learn Disabil
, vol.34
, pp. 503-511
-
-
Wood, F.B.1
Grigorenko, E.L.2
-
3
-
-
33744455435
-
The genetics of developmental dyslexia
-
Williams J, O'Donovan MC: The genetics of developmental dyslexia. Eur J Hum Genet 2006, 14:681-689.
-
(2006)
Eur J Hum Genet
, vol.14
, pp. 681-689
-
-
Williams, J.1
ODonovan, M.C.2
-
4
-
-
0035163547
-
Extent and distribution of linkage disequilibrium in three genomic regions
-
Abecasis GR, Noguchi E, Heinzmann A, et al.: Extent and distribution of linkage disequilibrium in three genomic regions. Am J Hum Genet 2001, 68:191-197.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 191-197
-
-
Abecasis, G.R.1
Noguchi, E.2
Heinzmann, A.3
-
5
-
-
0035837267
-
Linkage disequilibrium in the human genome
-
Reich DE, Cargill M, Bolk S, et al.: Linkage disequilibrium in the human genome. Nature 2001, 411:199-204.
-
(2001)
Nature
, vol.411
, pp. 199-204
-
-
Reich, D.E.1
Cargill, M.2
Bolk, S.3
-
6
-
-
0034660559
-
Searching for genetic determinants in the new millennium
-
Risch NJ: Searching for genetic determinants in the new millennium. Nature 2000, 405:847-856.
-
(2000)
Nature
, vol.405
, pp. 847-856
-
-
Risch, N.J.1
-
7
-
-
43049146524
-
A HapMap harvest of insights into the genetics of common disease
-
Manolio TA, Brooks LD, Collins FS: A HapMap harvest of insights into the genetics of common disease. J Clin Invest 2008, 118:1590-1605.
-
(2008)
J Clin Invest
, vol.118
, pp. 1590-1605
-
-
Manolio, T.A.1
Brooks, L.D.2
Collins, F.S.3
-
8
-
-
0141482054
-
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain
-
Taipale M, Kaminen N, Nopola-Hemmi J, et al.: A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proc Natl Acad Sci U S A 2003,100: 11553-11558.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 11553-11558
-
-
Taipale, M.1
Kaminen, N.2
Nopola-Hemmi, J.3
-
9
-
-
33745343959
-
The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia
-
Hannula-Jouppi K, Kaminen-Ahola N, Taipale M, et al.: The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS Genet 2005, 1:e50.
-
(2005)
PLoS Genet
, vol.1
-
-
Hannula-Jouppi, K.1
Kaminen-Ahola, N.2
Taipale, M.3
-
10
-
-
54049144653
-
Copy-number variations associated with neuropsychiatric conditions
-
Cook EH Jr, Scherer SW: Copy-number variations associated with neuropsychiatric conditions. Nature 2008, 455:919-923.
-
(2008)
Nature
, vol.455
, pp. 919-923
-
-
Cook Jr., E.H.1
Scherer, S.W.2
-
11
-
-
0020622130
-
Specific reading disability: Identification of an inherited form through linkage analysis
-
Smith SD, Kimberling WJ, Pennington BF, et al.: Specific reading disability: Identification of an inherited form through linkage analysis. Science 1983, 219:1345-1347.
-
(1983)
Science
, vol.219
, pp. 1345-1347
-
-
Smith, S.D.1
Kimberling, W.J.2
Pennington, B.F.3
-
12
-
-
0031027824
-
Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
-
Grigorenko EL, Wood FB, Meyer MS, et al.: Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15. Am J Hum Genet 1997, 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
-
13
-
-
0032231443
-
Evidence for linkage of spelling disability to chromosome 15
-
Schulte-Korne G, Grimm T, Nothen MM, et al.: Evidence for linkage of spelling disability to chromosome 15. Am J Hum Genet 1998, 63:279-282.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 279-282
-
-
Schulte-Korne, G.1
Grimm, T.2
Nothen, M.M.3
-
14
-
-
0034701254
-
Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q
-
Morris DW, Robinson L, Turic D, et al.: Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q. Hum Mol Genet 2000, 9:843-848.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 843-848
-
-
Morris, D.W.1
Robinson, L.2
Turic, D.3
-
15
-
-
7644236039
-
Linkage analyses of four regions previously implicated in dyslexia: Confirmation of a locus on chromosome 15q
-
Chapman NH, Igo RP, Thomson JB, et al.: Linkage analyses of four regions previously implicated in dyslexia: Confirmation of a locus on chromosome 15q. Am J Med Genet B Neuropsychiatr Genet 2004, 131B:67-75.
-
(2004)
Am J Med Genet B Neuropsychiatr Genet
, vol.131 B
, pp. 67-75
-
-
Chapman, N.H.1
Igo, R.P.2
Thomson, J.B.3
-
16
-
-
42149141765
-
Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection
-
de Kovel CG, Franke B, Hol FA, et al.: Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection. Am J Med Genet B Neuropsychiatr Genet 2008, 147:294-300.
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147
, pp. 294-300
-
-
de Kovel, C.G.1
Franke, B.2
Hol, F.A.3
-
17
-
-
55349100227
-
Association of reading disability on chromosome 6p22 in the Afrikaner population
-
Platko JV, Wood FB, Pelser I, et al.: Association of reading disability on chromosome 6p22 in the Afrikaner population. Am J Med Genet B Neuropsychiatr Genet 2008, 147B:1278-1287.
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147 B
, pp. 1278-1287
-
-
Platko, J.V.1
Wood, F.B.2
Pelser, I.3
-
18
-
-
0033792625
-
Two translocations of chromosome 15q associated with dyslexia
-
Nopola-Hemmi J, Taipale M, Haltia T, et al.: Two translocations of chromosome 15q associated with dyslexia. J Med Genet 2000, 37:771-775.
-
(2000)
J Med Genet
, vol.37
, pp. 771-775
-
-
Nopola-Hemmi, J.1
Taipale, M.2
Haltia, T.3
-
19
-
-
19944428926
-
Support for EKN1 as the susceptibility locus for dyslexia on 15q21
-
Wigg KG, Couto JM, Feng Y, et al.: Support for EKN1 as the susceptibility locus for dyslexia on 15q21. Mol Psychiatry 2004, 9:1111-1121.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 1111-1121
-
-
Wigg, K.G.1
Couto, J.M.2
Feng, Y.3
-
20
-
-
34748875368
-
Association of short-term memory with a variant within DYX1C1 in developmental dyslexia
-
Marino C, Citterio A, Giorda R, et al.: Association of short-term memory with a variant within DYX1C1 in developmental dyslexia. Genes Brain Behav 2007, 6:640-646.
-
(2007)
Genes Brain Behav
, vol.6
, pp. 640-646
-
-
Marino, C.1
Citterio, A.2
Giorda, R.3
-
21
-
-
0028030006
-
Quantitative trait locus for reading disability on chromosome 6
-
Cardon LR, Smith SD, Fulker DW, et al.: Quantitative trait locus for reading disability on chromosome 6. Science 1994, 266:276-279.
-
(1994)
Science
, vol.266
, pp. 276-279
-
-
Cardon, L.R.1
Smith, S.D.2
Fulker, D.W.3
-
22
-
-
0033912869
-
Absence of significant linkage between phonological coding dyslexia and chromosome 6p23-21.3, as determined by use of quantitative-trait methods: Confirmation of qualitative analyses
-
Petryshen TL, Kaplan BJ, Liu MF, et al.: Absence of significant linkage between phonological coding dyslexia and chromosome 6p23-21.3, as determined by use of quantitative-trait methods: Confirmation of qualitative analyses. Am J Hum Genet 2000, 66:708-714.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 708-714
-
-
Petryshen, T.L.1
Kaplan, B.J.2
Liu, M.F.3
-
23
-
-
3543029197
-
Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: Linkage and association analyses
-
Deffenbacher KE, Kenyon JB, Hoover DM, et al.: Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: Linkage and association analyses. Hum Genet 2004, 115:128-138.
-
(2004)
Hum Genet
, vol.115
, pp. 128-138
-
-
Deffenbacher, K.E.1
Kenyon, J.B.2
Hoover, D.M.3
-
24
-
-
28044465597
-
DCDC2 is associated with reading disability and modulates neuronal development in the brain
-
(Published erratum appears in Proc Natl Acad Sci U S A 2005, 102: 18763
-
Meng H, Smith SD, Hager K, et al.: DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci U S A 2005, 102: 17053-17058. (Published erratum appears in Proc Natl Acad Sci U S A 2005, 102:18763.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 17053-17058
-
-
Meng, H.1
Smith, S.D.2
Hager, K.3
-
25
-
-
15944372645
-
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia
-
(Published erratum appears in Am J Hum Genet 2005, 77: 898.)
-
Cope N, Harold D, Hill G, et al.: Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am J Hum Genet 2005, 76: 581-591 (Published erratum appears in Am J Hum Genet 2005, 77:898.)
-
(2005)
Am J Hum Genet
, vol.76
, pp. 581-591
-
-
Cope, N.1
Harold, D.2
Hill, G.3
-
26
-
-
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, 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 2004, 75:1046-1058.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 1046-1058
-
-
Francks, C.1
Paracchini, S.2
Smith, S.D.3
-
27
-
-
0032877882
-
A new gene (DYX3) for dyslexia is located on chromosome 2
-
Fagerheim T, Raeymaekers P, Tonnessen FE, et al.: A new gene (DYX3) for dyslexia is located on chromosome 2. J Med Genet 1999, 36:664-669.
-
(1999)
J Med Genet
, vol.36
, pp. 664-669
-
-
Fagerheim, T.1
Raeymaekers, P.2
Tonnessen, F.E.3
-
28
-
-
0036168959
-
Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families
-
Petryshen TL, Kaplan BJ, Hughes ML, et al.: Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families. J Med Genet 2002, 39:125-126.
-
(2002)
J Med Genet
, vol.39
, pp. 125-126
-
-
Petryshen, T.L.1
Kaplan, B.J.2
Hughes, M.L.3
-
29
-
-
18544365699
-
Independent genome-wide scans identify a chromosome 18 quantitativetrait locus influencing dyslexia
-
Fisher SE, Francks C, Marlow AJ, et al.: Independent genome-wide scans identify a chromosome 18 quantitativetrait locus influencing dyslexia. Nat Genet 2002, 30:86-91.
-
(2002)
Nat Genet
, vol.30
, pp. 86-91
-
-
Fisher, S.E.1
Francks, C.2
Marlow, A.J.3
-
30
-
-
0035828096
-
Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia
-
Petryshen TL, Kaplan BJ, Fu Liu M, et al.: Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia. Am J Med Genet 2001, 105:507-517.
-
(2001)
Am J Med Genet
, vol.105
, pp. 507-517
-
-
Petryshen, T.L.1
Kaplan, B.J.2
Fu Liu, M.3
-
31
-
-
35748969320
-
Genetic correlates of brain aging on MRI and cognitive test measures: A genome-wide association and linkage analysis in the Framingham Study
-
Seshadri S, DeStefano AL, Au R, et al.: Genetic correlates of brain aging on MRI and cognitive test measures: A genome-wide association and linkage analysis in the Framingham Study. BMC Med Genet 2007, 19(Suppl 1):S15.
-
(2007)
BMC Med Genet
, vol.19
, Issue.SUPPL. 1
-
-
Seshadri, S.1
DeStefano, A.L.2
Au, R.3
-
32
-
-
0942301435
-
A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5
-
Hsiung GY, Kaplan BJ, Petryshen TL, et al.: A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5. Am J Med Genet B Neuropsychiatr Genet 2004, 125B:112-119.
-
(2004)
Am J Med Genet B Neuropsychiatr Genet
, vol.125 B
, pp. 112-119
-
-
Hsiung, G.Y.1
Kaplan, B.J.2
Petryshen, T.L.3
-
33
-
-
0027213075
-
Suggestive linkage of developmental dyslexia to chromosome 1p34-p36
-
Rabin M, Wen XL, Hepburn M, et al.: Suggestive linkage of developmental dyslexia to chromosome 1p34-p36. Lancet 1993, 342:178.
-
(1993)
Lancet
, vol.342
, pp. 178
-
-
Rabin, M.1
Wen, X.L.2
Hepburn, M.3
-
34
-
-
4444356020
-
Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family
-
de Kovel CG, Hol FA, Heister JG, et al.: Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family. J Med Genet 2004, 41:652-657.
-
(2004)
J Med Genet
, vol.41
, pp. 652-657
-
-
de Kovel, C.G.1
Hol, F.A.2
Heister, J.G.3
-
35
-
-
35148851563
-
Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations
-
Rosen GD, Bai J, Wang Y, et al.: Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations. Cereb Cortex 2007, 17:2562-2572.
-
(2007)
Cereb Cortex
, vol.17
, pp. 2562-2572
-
-
Rosen, G.D.1
Bai, J.2
Wang, Y.3
-
36
-
-
48749084615
-
The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia
-
Tapia-Paez I, Tammimies K, Massinen S, et al.: The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia. FASEB J 2008, 22:3001-3009.
-
(2008)
FASEB J
, vol.22
, pp. 3001-3009
-
-
Tapia-Paez, I.1
Tammimies, K.2
Massinen, S.3
-
37
-
-
33751251057
-
DYX1C1 functions in neuronal migration in developing neocortex
-
Wang Y, Paramasivam M, Thomas A, et al.: DYX1C1 functions in neuronal migration in developing neocortex. Neuroscience 2006, 143:515-522.
-
(2006)
Neuroscience
, vol.143
, pp. 515-522
-
-
Wang, Y.1
Paramasivam, M.2
Thomas, A.3
-
38
-
-
0021832834
-
Developmental dyslexia: Four consecutive patients with cortical anomalies
-
Galaburda AM, SherFan GF, Rosen GD, et al.: Developmental dyslexia: four consecutive patients with cortical anomalies. Ann Neurol 1985, 18:222-233.
-
(1985)
Ann Neurol
, vol.18
, pp. 222-233
-
-
Galaburda, A.M.1
Sherman, G.F.2
Rosen, G.D.3
-
39
-
-
29244468273
-
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
-
Schumacher J, Anthoni H, Dahdouh F, et al.: Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Am J Hum Genet 2006, 78:52-62.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 52-62
-
-
Schumacher, J.1
Anthoni, H.2
Dahdouh, F.3
-
40
-
-
0033397770
-
A new antigen recognized by cytolytic T lymphocytes on a human kidney tumor results from reverse strand transcription
-
Van Den Eynde BJ, Gaugler B, Probst-Kepper M, et al.: A new antigen recognized by cytolytic T lymphocytes on a human kidney tumor results from reverse strand transcription. J Exp Med 1999, 190:1793-1800.
-
(1999)
J Exp Med
, vol.190
, pp. 1793-1800
-
-
Van Den Eynde, B.J.1
Gaugler, B.2
Probst-Kepper, M.3
-
41
-
-
12444287449
-
Diversity of antisense regulation in eukaryotes: Multiple mechanisms, emerging patterns
-
Munroe SH: Diversity of antisense regulatioM in eukaryotes: multiple mechanisms, emerging patterns. J Cell Biochem 2004, 93:664-671.
-
(2004)
J Cell Biochem
, vol.93
, pp. 664-671
-
-
Munroe, S.H.1
-
42
-
-
28044465597
-
DCDC2 is associated with reading disability and modulates neuronal development in the brain
-
Meng H, Smith SD, Hager K, et al.: DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci U S A 2005, 102:17053-17058.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 17053-17058
-
-
Meng, H.1
Smith, S.D.2
Hager, K.3
-
43
-
-
40949114128
-
Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat
-
Burbridge TJ, Wang Y, Volz AJ, et al.: Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat. Neuroscience 2008, 152:723-733.
-
(2008)
Neuroscience
, vol.152
, pp. 723-733
-
-
Burbridge, T.J.1
Wang, Y.2
Volz, A.J.3
-
44
-
-
57349157021
-
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population
-
Paracchini S, Steer CD, Buckingham LL, et al.: Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. Am J Psychiatry 2008, 165:1576-1584.
-
(2008)
Am J Psychiatry
, vol.165
, pp. 1576-1584
-
-
Paracchini, S.1
Steer, C.D.2
Buckingham, L.L.3
-
45
-
-
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, et al.: The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum Mol Genet 2006, 15:1659-1666.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1659-1666
-
-
Paracchini, S.1
Thomas, A.2
Castro, S.3
-
46
-
-
35048813966
-
Alternative splicing in the dyslexia-associated gene KIAA0319
-
Velayos-Baeza A, Toma C, da Roza S, et al.: Alternative splicing in the dyslexia-associated gene KIAA0319. Mamm Genome 2007, 18:627-634.
-
(2007)
Mamm Genome
, vol.18
, pp. 627-634
-
-
Velayos-Baeza, A.1
Toma, C.2
da Roza, S.3
-
47
-
-
57349189085
-
Multivariate genomewide linkage scan of neurocognitive traits and ADHD symptoms: Suggestive linkage to 3q13
-
Doyle AE, Ferreira MA, Sklar PB, et al.: Multivariate genomewide linkage scan of neurocognitive traits and ADHD symptoms: Suggestive linkage to 3q13. Am J Med Genet B Neuropsychiatr Genet 2008, 147B:1399-1411.
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147 B
, pp. 1399-1411
-
-
Doyle, A.E.1
Ferreira, M.A.2
Sklar, P.B.3
-
48
-
-
0035831296
-
Hierarchical organization of guidance receptors: Silencing of netrin attraction by slit through a Robo/DCC receptor complex
-
Stein E, Tessier-Lavigne M: Hierarchical organization of guidance receptors: Silencing of netrin attraction by slit through a Robo/DCC receptor complex. Science 2001, 291:1928-1938.
-
(2001)
Science
, vol.291
, pp. 1928-1938
-
-
Stein, E.1
Tessier-Lavigne, M.2
-
49
-
-
37849003092
-
The role of Slit-Robo signaling in the generation, migration and morphological differentiation of cortical interneurons
-
Andrews W, Barber M, Hernadez-Miranda LR, et al.: The role of Slit-Robo signaling in the generation, migration and morphological differentiation of cortical interneurons. Dev Biol 2008, 313:648-658.
-
(2008)
Dev Biol
, vol.313
, pp. 648-658
-
-
Andrews, W.1
Barber, M.2
Hernadez-Miranda, L.R.3
-
50
-
-
34247092473
-
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia
-
Anthoni H, Zucchelli M, Matsson H, et al.: A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Hum Mol Genet 2007, 16:667-677.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 667-677
-
-
Anthoni, H.1
Zucchelli, M.2
Matsson, H.3
-
51
-
-
33747872677
-
Heterotopia formation in rat but not mouse neocortex after RNA interference knockdown of DCX
-
Ramos RL, Bai J, LoTurco JJ: Heterotopia formation in rat but not mouse neocortex after RNA interference knockdown of DCX. Cereb Cortex 2006, 16:1323-1331.
-
(2006)
Cereb Cortex
, vol.16
, pp. 1323-1331
-
-
Ramos, R.L.1
Bai, J.2
LoTurco, J.J.3
|