-
2
-
-
13144279294
-
Functional disruption in the organization of the brain for reading in Dyslexia
-
Shaywitz SE, Shaywitz BA, Pugh KR, Fulbright RK, Constable RT, Mencl WE. Functional disruption in the organization of the brain for reading in Dyslexia. Proc Natl Acad Sci 1998;95:2636-41.
-
(1998)
Proc Natl Acad Sci
, vol.95
, pp. 2636-2641
-
-
Shaywitz, S.E.1
Shaywitz, B.A.2
Pugh, K.R.3
Fulbright, R.K.4
Constable, R.T.5
Mencl, W.E.6
-
4
-
-
0028030006
-
Quantitative trait locus for reading disability on Chromosome 6
-
Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, DeFries JC. Quantitative trait locus for reading disability on Chromosome 6. Science 1994;266:276-9.
-
(1994)
Science
, vol.266
, pp. 276-279
-
-
Cardon, L.R.1
Smith, S.D.2
Fulker, D.W.3
Kimberling, W.J.4
Pennington, B.F.5
DeFries, J.C.6
-
5
-
-
0032231443
-
Evidence for linkage of spelling disability to chromosome 15
-
Schulte-Körne G, Nöthen MM, Muller-Myhsok B, Cichon S, Vogt IR, Propping P, et al. Evidence for linkage of spelling disability to chromosome 15. Am J Hum Genet 1998;63:279-82.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 279-282
-
-
Schulte-Körne, G.1
Nöthen, M.M.2
Muller-Myhsok, B.3
Cichon, S.4
Vogt, I.R.5
Propping, P.6
-
6
-
-
0032877882
-
A new gene (DYX3) for Dyslexia is located on chromosome 2
-
Fagerheim T, Raeymaekers P, Tonnessen FE, Pedersen M, Tranebjaerg L, Lubs HA. A new gene (DYX3) for Dyslexia is located on chromosome 2. J Med Genet 1999;36:664-9.
-
(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
-
7
-
-
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 2001;38:658-64.
-
(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
-
8
-
-
18544365699
-
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
-
Fisher SE, Francks C, Marlow AJ, MacPhie LI, Newbury DF, Cardon LR, et al. Independent genome-wide scans identify a chromosome 18 quantitative-trait 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
MacPhie, L.I.4
Newbury, D.F.5
Cardon, L.R.6
-
9
-
-
33644605462
-
Biological basis of dyslexia: A maturing perspective
-
Saviour P, Ramachandra NB. Biological basis of dyslexia: A maturing perspective. Curr Sci 2006;90:168-75.
-
(2006)
Curr Sci
, vol.90
, pp. 168-175
-
-
Saviour, P.1
Ramachandra, N.B.2
-
10
-
-
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, Haltia T, Myllyluoma B, Lyytinen H, et al. A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proc Natl Acad Sci 2003;100:11553-8.
-
(2003)
Proc Natl Acad Sci
, vol.100
, pp. 11553-11558
-
-
Taipale, M.1
Kaminen, N.2
Nopola-Hemmi, J.3
Haltia, T.4
Myllyluoma, B.5
Lyytinen, H.6
-
11
-
-
0014089675
-
Children's behavior questionnaire for completion by teachers: Preliminary findings
-
Rutter M. Children's behavior questionnaire for completion by teachers: Preliminary findings. J Child Psychol Psychiatry 1967;8:1-11.
-
(1967)
J Child Psychol Psychiatry
, vol.8
, pp. 1-11
-
-
Rutter, M.1
-
12
-
-
58849116099
-
-
Rao SN, Reddy IK. Indian norms of Revan's A, AB, B form. J Psychol Studies 1968;13:2.
-
Rao SN, Reddy IK. Indian norms of Revan's A, AB, B form. J Psychol Studies 1968;13:2.
-
-
-
-
13
-
-
9144269126
-
A transcription map of the 6p22.3 reading disability locus identifying candidate genes
-
Londin ER, Meng H, Gruen JR. A transcription map of the 6p22.3 reading disability locus identifying candidate genes. BMC Genomics 2003;4:25-30.
-
(2003)
BMC Genomics
, vol.4
, pp. 25-30
-
-
Londin, E.R.1
Meng, H.2
Gruen, J.R.3
-
14
-
-
1642574231
-
A locus on 15q15-15qter influences dyslexia: Further support form a transmission / disequilibrium study in an Italian speaking population
-
Marino C, Giorda R, Vanzin L, Nobile R, Lorusso M, Baschirotto C, et al. A locus on 15q15-15qter influences dyslexia: Further support form a transmission / disequilibrium study in an Italian speaking population. J Med Genet 2004;41:42-6.
-
(2004)
J Med Genet
, vol.41
, pp. 42-46
-
-
Marino, C.1
Giorda, R.2
Vanzin, L.3
Nobile, R.4
Lorusso, M.5
Baschirotto, C.6
-
15
-
-
8744255235
-
Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK
-
Scerri TS, Fisher SE, Francks C, MacPhie IL, Paracchini S, Richardson AJ, et al. Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. J Med Genet 2004;41:853-7.
-
(2004)
J Med Genet
, vol.41
, pp. 853-857
-
-
Scerri, T.S.1
Fisher, S.E.2
Francks, C.3
MacPhie, I.L.4
Paracchini, S.5
Richardson, A.J.6
-
16
-
-
27644480838
-
No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy
-
Bellini G, Bravaccio C, Calamoneri F, Cocuzza DM, Filorillo P, Gagliano A, et al. No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy. J Mol Neurosci 2005;27:311-4.
-
(2005)
J Mol Neurosci
, vol.27
, pp. 311-314
-
-
Bellini, G.1
Bravaccio, C.2
Calamoneri, F.3
Cocuzza, D.M.4
Filorillo, P.5
Gagliano, A.6
-
17
-
-
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 2005;1:467-74.
-
(2005)
PLOS Genet
, vol.1
, pp. 467-474
-
-
Hannula-Jouppi, K.1
Kaminen-Ahola, N.2
Taipale, M.3
Eklund, R.4
Nopola-Hemmi, J.5
Kaariainen, H.6
-
18
-
-
28044465597
-
DCDC2 is associated with reading disability and modulates neuronal development in the brain
-
Meng H, Smith SD, Hager K, Keld M, Liu J, Olson RK, et al. DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci 2005;102:17053-8.
-
(2005)
Proc Natl Acad Sci
, vol.102
, pp. 17053-17058
-
-
Meng, H.1
Smith, S.D.2
Hager, K.3
Keld, M.4
Liu, J.5
Olson, R.K.6
-
19
-
-
0033928210
-
Chromosome 6p influences different Dyslexia- related processes: Further confirmation
-
Grigorenko EL, Wood FB, Meyer MS, Pauls DL. Chromosome 6p influences different Dyslexia- related processes: Further confirmation. Am J Hum Genet 2000;66:715-23.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 715-723
-
-
Grigorenko, E.L.1
Wood, F.B.2
Meyer, M.S.3
Pauls, D.L.4
-
20
-
-
0034701254
-
Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q
-
Morris DW, Robinson L, Turic D, Duke M, Webb V, Milham C, et al. Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q. Hum Mol Gene 2000;9:843-8.
-
(2000)
Hum Mol Gene
, vol.9
, pp. 843-848
-
-
Morris, D.W.1
Robinson, L.2
Turic, D.3
Duke, M.4
Webb, V.5
Milham, C.6
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