-
1
-
-
0024364215
-
Educational interventions in learning disabilities
-
10.1097/00004583-198905000-00004, 2661524
-
Lerner JW. Educational interventions in learning disabilities. J Am Acad Child Adolesc Psychiatry 1989, 28(3):326-331. 10.1097/00004583-198905000-00004, 2661524.
-
(1989)
J Am Acad Child Adolesc Psychiatry
, vol.28
, Issue.3
, pp. 326-331
-
-
Lerner, J.W.1
-
2
-
-
0032576678
-
Dyslexia
-
10.1056/NEJM199801293380507, 9445412
-
Shaywitz SE. Dyslexia. N Engl J Med 1998, 338(5):307-312. 10.1056/NEJM199801293380507, 9445412.
-
(1998)
N Engl J Med
, vol.338
, Issue.5
, pp. 307-312
-
-
Shaywitz, S.E.1
-
3
-
-
33846630374
-
Developmental dyslexia: an update
-
10.1007/s10038-006-0088-z, 17111266
-
Shastry BS. Developmental dyslexia: an update. J Hum Genet 2007, 52(2):104-109. 10.1007/s10038-006-0088-z, 17111266.
-
(2007)
J Hum Genet
, vol.52
, Issue.2
, pp. 104-109
-
-
Shastry, B.S.1
-
4
-
-
34247092473
-
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia
-
Anthoni H, Zucchelli M, Matsson H, Muller-Myhsok B, Fransson I, Schumacher J, Massinen S, Onkamo P, Warnke A, Griesemann H, Hoffmann P, Nopola-Hemmi J, Lyytinen H, Schulte-Korne G, Kere J, Nothen MM, Peyrard-Janvid M. A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Hum Mol Genet 2007, 16(6):667-677.
-
(2007)
Hum Mol Genet
, vol.16
, Issue.6
, pp. 667-677
-
-
Anthoni, H.1
Zucchelli, M.2
Matsson, H.3
Muller-Myhsok, B.4
Fransson, I.5
Schumacher, J.6
Massinen, S.7
Onkamo, P.8
Warnke, A.9
Griesemann, H.10
Hoffmann, P.11
Nopola-Hemmi, J.12
Lyytinen, H.13
Schulte-Korne, G.14
Kere, J.15
Nothen, M.M.16
Peyrard-Janvid, M.17
-
5
-
-
57649136416
-
The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities
-
10.1080/01677060802354328, 19085271
-
Couto JM, Gomez L, Wigg K, Cate-Carter T, Archibald J, Anderson B, Tannock R, Kerr EN, Lovett MW, Humphries T, Barr CL. The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities. J Neurogenet 2008, 22(4):295-313. 10.1080/01677060802354328, 19085271.
-
(2008)
J Neurogenet
, vol.22
, Issue.4
, pp. 295-313
-
-
Couto, J.M.1
Gomez, L.2
Wigg, K.3
Cate-Carter, T.4
Archibald, J.5
Anderson, B.6
Tannock, R.7
Kerr, E.N.8
Lovett, M.W.9
Humphries, T.10
Barr, C.L.11
-
6
-
-
77349127347
-
Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia
-
Ludwig KU, Roeske D, Herms S, Schumacher J, Warnke A, Plume E, Neuhoff N, Bruder J, Remschmidt H, Schulte-Korne G, Muller-Myhsok B, Nothen MM, Hoffmann P. Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia. Am J Med Genet B Neuropsychiatr Genet 2010, 153B(2):503-511.
-
(2010)
Am J Med Genet B Neuropsychiatr Genet
, vol.153 B
, Issue.2
, pp. 503-511
-
-
Ludwig, K.U.1
Roeske, D.2
Herms, S.3
Schumacher, J.4
Warnke, A.5
Plume, E.6
Neuhoff, N.7
Bruder, J.8
Remschmidt, H.9
Schulte-Korne, G.10
Muller-Myhsok, B.11
Nothen, M.M.12
Hoffmann, P.13
-
7
-
-
0033792625
-
Two translocations of chromosome 15q associated with dyslexia
-
10.1136/jmg.37.10.771, 1757170, 11015455
-
Nopola-Hemmi J, Taipale M, Haltia T, Lehesjoki AE, Voutilainen A, Kere J. Two translocations of chromosome 15q associated with dyslexia. J Med Genet 2000, 37(10):771-775. 10.1136/jmg.37.10.771, 1757170, 11015455.
-
(2000)
J Med Genet
, vol.37
, Issue.10
, pp. 771-775
-
-
Nopola-Hemmi, J.1
Taipale, M.2
Haltia, T.3
Lehesjoki, A.E.4
Voutilainen, A.5
Kere, J.6
-
8
-
-
0141482054
-
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain
-
10.1073/pnas.1833911100, 208796, 12954984
-
Taipale M, Kaminen N, Nopola-Hemmi J, Haltia T, Myllyluoma B, Lyytinen H, Muller K, Kaaranen M, Lindsberg PJ, Hannula-Jouppi K, Kere J. A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proc Natl Acad Sci USA 2003, 100(20):11553-11558. 10.1073/pnas.1833911100, 208796, 12954984.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, Issue.20
, pp. 11553-11558
-
-
Taipale, M.1
Kaminen, N.2
Nopola-Hemmi, J.3
Haltia, T.4
Myllyluoma, B.5
Lyytinen, H.6
Muller, K.7
Kaaranen, M.8
Lindsberg, P.J.9
Hannula-Jouppi, K.10
Kere, J.11
-
9
-
-
34748875368
-
Association of short-term memory with a variant within DYX1C1 in developmental dyslexia
-
10.1111/j.1601-183X.2006.00291.x, 17309662
-
Marino C, Citterio A, Giorda R, Facoetti A, Menozzi G, Vanzin L, Lorusso ML, Nobile M, Molteni M. Association of short-term memory with a variant within DYX1C1 in developmental dyslexia. Genes Brain Behav 2007, 6(7):640-646. 10.1111/j.1601-183X.2006.00291.x, 17309662.
-
(2007)
Genes Brain Behav
, vol.6
, Issue.7
, pp. 640-646
-
-
Marino, C.1
Citterio, A.2
Giorda, R.3
Facoetti, A.4
Menozzi, G.5
Vanzin, L.6
Lorusso, M.L.7
Nobile, M.8
Molteni, M.9
-
10
-
-
19944428926
-
Support for EKN1 as the susceptibility locus for dyslexia on 15q21
-
10.1038/sj.mp.4001543, 15249932
-
Wigg KG, Couto JM, Feng Y, Anderson B, Cate-Carter TD, Macciardi F, Tannock R, Lovett MW, Humphries TW, Barr CL. Support for EKN1 as the susceptibility locus for dyslexia on 15q21. Mol Psychiatry 2004, 9(12):1111-1121. 10.1038/sj.mp.4001543, 15249932.
-
(2004)
Mol Psychiatry
, vol.9
, Issue.12
, 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
Tannock, R.7
Lovett, M.W.8
Humphries, T.W.9
Barr, C.L.10
-
11
-
-
8744255235
-
Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK
-
10.1136/jmg.2004.018341, 1735619, 15520411
-
Scerri TS, Fisher SE, Francks C, MacPhie IL, Paracchini S, Richardson AJ, Stein JF, Monaco AP. 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(11):853-857. 10.1136/jmg.2004.018341, 1735619, 15520411.
-
(2004)
J Med Genet
, vol.41
, Issue.11
, 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
Stein, J.F.7
Monaco, A.P.8
-
12
-
-
63149196656
-
Further evidence for DYX1C1 as a susceptibility factor for dyslexia
-
10.1097/YPG.0b013e32832080e1, 19240663
-
Dahdouh F, Anthoni H, Tapia-Paez I, Peyrard-Janvid M, Schulte-Korne G, Warnke A, Remschmidt H, Ziegler A, Kere J, Muller-Myhsok B, Nothen MM, Schumacher J, Zucchelli M. Further evidence for DYX1C1 as a susceptibility factor for dyslexia. Psychiatr Genet 2009, 19(2):59-63. 10.1097/YPG.0b013e32832080e1, 19240663.
-
(2009)
Psychiatr Genet
, vol.19
, Issue.2
, pp. 59-63
-
-
Dahdouh, F.1
Anthoni, H.2
Tapia-Paez, I.3
Peyrard-Janvid, M.4
Schulte-Korne, G.5
Warnke, A.6
Remschmidt, H.7
Ziegler, A.8
Kere, J.9
Muller-Myhsok, B.10
Nothen, M.M.11
Schumacher, J.12
Zucchelli, M.13
-
13
-
-
15944363095
-
No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia
-
10.1038/sj.mp.4001596, 15477871
-
Cope N, Hill G, van den Bree M, Harold D, Moskvina V, Green EK, Owen MJ, Williams J, O'Donovan MC. No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia. Mol Psychiatry 2005, 10(3):237-238. 10.1038/sj.mp.4001596, 15477871.
-
(2005)
Mol Psychiatry
, vol.10
, Issue.3
, pp. 237-238
-
-
Cope, N.1
Hill, G.2
van den Bree, M.3
Harold, D.4
Moskvina, V.5
Green, E.K.6
Owen, M.J.7
Williams, J.8
O'Donovan, M.C.9
-
14
-
-
27644480838
-
No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy
-
10.1385/JMN:27:3:311, 16280601
-
Bellini G, Bravaccio C, Calamoneri F, Donatella Cocuzza M, Fiorillo P, Gagliano A, Mazzone D, del Giudice EM, Scuccimarra G, Militerni R, Pascotto A. 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(3):311-314. 10.1385/JMN:27:3:311, 16280601.
-
(2005)
J Mol Neurosci
, vol.27
, Issue.3
, pp. 311-314
-
-
Bellini, G.1
Bravaccio, C.2
Calamoneri, F.3
Donatella Cocuzza, M.4
Fiorillo, P.5
Gagliano, A.6
Mazzone, D.7
del Giudice, E.M.8
Scuccimarra, G.9
Militerni, R.10
Pascotto, A.11
-
15
-
-
33744733429
-
TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort
-
10.1007/s00439-005-0017-9, 16133186
-
Meng H, Hager K, Held M, Page GP, Olson RK, Pennington BF, DeFries JC, Smith SD, Gruen JR. TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort. Hum Genet 2005, 118(1):87-90. 10.1007/s00439-005-0017-9, 16133186.
-
(2005)
Hum Genet
, vol.118
, Issue.1
, pp. 87-90
-
-
Meng, H.1
Hager, K.2
Held, M.3
Page, G.P.4
Olson, R.K.5
Pennington, B.F.6
DeFries, J.C.7
Smith, S.D.8
Gruen, J.R.9
-
16
-
-
34250810249
-
Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia
-
10.1002/ajmg.b.30471, 17450541
-
Brkanac Z, Chapman NH, Matsushita MM, Chun L, Nielsen K, Cochrane E, Berninger VW, Wijsman EM, Raskind WH. Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia. Am J Med Genet B Neuropsychiatr Genet 2007, 144B(4):556-560. 10.1002/ajmg.b.30471, 17450541.
-
(2007)
Am J Med Genet B Neuropsychiatr Genet
, vol.144 B
, Issue.4
, pp. 556-560
-
-
Brkanac, Z.1
Chapman, N.H.2
Matsushita, M.M.3
Chun, L.4
Nielsen, K.5
Cochrane, E.6
Berninger, V.W.7
Wijsman, E.M.8
Raskind, W.H.9
-
17
-
-
35148851563
-
Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations
-
10.1093/cercor/bhl162, 17218481
-
Rosen GD, Bai J, Wang Y, Fiondella CG, Threlkeld SW, LoTurco JJ, Galaburda AM. Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations. Cereb Cortex 2007, 17(11):2562-2572. 10.1093/cercor/bhl162, 17218481.
-
(2007)
Cereb Cortex
, vol.17
, Issue.11
, pp. 2562-2572
-
-
Rosen, G.D.1
Bai, J.2
Wang, Y.3
Fiondella, C.G.4
Threlkeld, S.W.5
LoTurco, J.J.6
Galaburda, A.M.7
-
18
-
-
33846440958
-
Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1
-
10.1016/j.brainresbull.2006.11.005, 1893003, 17259020
-
Threlkeld SW, McClure MM, Bai J, Wang Y, LoTurco JJ, Rosen GD, Fitch RH. Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1. Brain Res Bull 2007, 71(5):508-514. 10.1016/j.brainresbull.2006.11.005, 1893003, 17259020.
-
(2007)
Brain Res Bull
, vol.71
, Issue.5
, pp. 508-514
-
-
Threlkeld, S.W.1
McClure, M.M.2
Bai, J.3
Wang, Y.4
LoTurco, J.J.5
Rosen, G.D.6
Fitch, R.H.7
-
19
-
-
33744920683
-
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
-
10.1093/hmg/ddl089, 16600991
-
Paracchini S, Thomas A, Castro S, Lai C, Paramasivam M, Wang Y, Keating BJ, Taylor JM, Hacking DF, Scerri T, Francks C, Richardson AJ, Wade-Martins R, Stein JF, Knight JC, Copp AJ, Loturco J, Monaco AP. The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum Mol Genet 2006, 15(10):1659-1666. 10.1093/hmg/ddl089, 16600991.
-
(2006)
Hum Mol Genet
, vol.15
, Issue.10
, pp. 1659-1666
-
-
Paracchini, S.1
Thomas, A.2
Castro, S.3
Lai, C.4
Paramasivam, M.5
Wang, Y.6
Keating, B.J.7
Taylor, J.M.8
Hacking, D.F.9
Scerri, T.10
Francks, C.11
Richardson, A.J.12
Wade-Martins, R.13
Stein, J.F.14
Knight, J.C.15
Copp, A.J.16
Loturco, J.17
Monaco, A.P.18
-
20
-
-
28044465597
-
DCDC2 is associated with reading disability and modulates neuronal development in the brain
-
10.1073/pnas.0508591102, 1278934, 16278297
-
Meng H, Smith SD, Hager K, Held M, Liu J, Olson RK, Pennington BF, DeFries JC, Gelernter J, O'Reilly-Pol T, Somlo S, Skudlarski P, Shaywitz SE, Shaywitz BA, Marchione K, Wang Y, Paramasivam M, LoTurco JJ, Page GP, Gruen JR. DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci USA 2005, 102(47):17053-17058. 10.1073/pnas.0508591102, 1278934, 16278297.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, Issue.47
, 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
Somlo, S.11
Skudlarski, P.12
Shaywitz, S.E.13
Shaywitz, B.A.14
Marchione, K.15
Wang, Y.16
Paramasivam, M.17
LoTurco, J.J.18
Page, G.P.19
Gruen, J.R.20
more..
-
21
-
-
48749084615
-
The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia
-
10.1096/fj.07-104455, 2493457, 18445785
-
Tapia-Paez I, Tammimies K, Massinen S, Roy AL, Kere J. The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia. FASEB J 2008, 22(8):3001-3009. 10.1096/fj.07-104455, 2493457, 18445785.
-
(2008)
FASEB J
, vol.22
, Issue.8
, pp. 3001-3009
-
-
Tapia-Paez, I.1
Tammimies, K.2
Massinen, S.3
Roy, A.L.4
Kere, J.5
-
22
-
-
67650763685
-
Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia
-
10.1093/hmg/ddp215, 19423554
-
Massinen S, Tammimies K, Tapia-Paez I, Matsson H, Hokkanen ME, Soderberg O, Landegren U, Castren E, Gustafsson JA, Treuter E, Kere J. Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia. Hum Mol Genet 2009, 18(15):2802-2812. 10.1093/hmg/ddp215, 19423554.
-
(2009)
Hum Mol Genet
, vol.18
, Issue.15
, pp. 2802-2812
-
-
Massinen, S.1
Tammimies, K.2
Tapia-Paez, I.3
Matsson, H.4
Hokkanen, M.E.5
Soderberg, O.6
Landegren, U.7
Castren, E.8
Gustafsson, J.A.9
Treuter, E.10
Kere, J.11
-
23
-
-
68649089236
-
A novel role for DYX1C1, a chaperone protein for both Hsp70 and Hsp90, in breast cancer
-
10.1007/s00432-009-0568-6, 19277710
-
Chen Y, Zhao M, Wang S, Chen J, Wang Y, Cao Q, Zhou W, Liu J, Xu Z, Tong G, Li J. A novel role for DYX1C1, a chaperone protein for both Hsp70 and Hsp90, in breast cancer. J Cancer Res Clin Oncol 2009, 135(9):1265-1276. 10.1007/s00432-009-0568-6, 19277710.
-
(2009)
J Cancer Res Clin Oncol
, vol.135
, Issue.9
, pp. 1265-1276
-
-
Chen, Y.1
Zhao, M.2
Wang, S.3
Chen, J.4
Wang, Y.5
Cao, Q.6
Zhou, W.7
Liu, J.8
Xu, Z.9
Tong, G.10
Li, J.11
-
24
-
-
38349049457
-
Estradiol and the developing brain
-
10.1152/physrev.00010.2007, 2754262, 18195084
-
McCarthy MM. Estradiol and the developing brain. Physiol Rev 2008, 88(1):91-124. 10.1152/physrev.00010.2007, 2754262, 18195084.
-
(2008)
Physiol Rev
, vol.88
, Issue.1
, pp. 91-124
-
-
McCarthy, M.M.1
-
25
-
-
39349110405
-
Rapid estrogen signaling in the brain
-
10.1159/000111559, 18253054
-
Raz L, Khan MM, Mahesh VB, Vadlamudi RK, Brann DW. Rapid estrogen signaling in the brain. Neurosignals 2008, 16(2-3):140-153. 10.1159/000111559, 18253054.
-
(2008)
Neurosignals
, vol.16
, Issue.2-3
, pp. 140-153
-
-
Raz, L.1
Khan, M.M.2
Mahesh, V.B.3
Vadlamudi, R.K.4
Brann, D.W.5
-
26
-
-
67649659873
-
Estrogens, brain, and behavior: lessons from knockout mouse models
-
10.1055/s-0029-1216275, 19401953
-
Hill RA, Boon WC. Estrogens, brain, and behavior: lessons from knockout mouse models. Semin Reprod Med 2009, 27(3):218-228. 10.1055/s-0029-1216275, 19401953.
-
(2009)
Semin Reprod Med
, vol.27
, Issue.3
, pp. 218-228
-
-
Hill, R.A.1
Boon, W.C.2
-
27
-
-
34247853254
-
Prevalence, Gender Ratio and Gender Differences in Reading-Related Cognitive Abilities among Chinese Children with Dyslexia in Hong Kong
-
Chan DW, Ho CS, Tsang S, Lee S, Chung KKH. Prevalence, Gender Ratio and Gender Differences in Reading-Related Cognitive Abilities among Chinese Children with Dyslexia in Hong Kong. Educational Studies 2007, 33(2):249-265.
-
(2007)
Educational Studies
, vol.33
, Issue.2
, pp. 249-265
-
-
Chan, D.W.1
Ho, C.S.2
Tsang, S.3
Lee, S.4
Chung, K.K.H.5
-
28
-
-
0000964806
-
Learning to read Chinese beyond the logographic phase
-
Ho CS, Bryant P. Learning to read Chinese beyond the logographic phase. Reading Research Quarterly 1997, 32(3):276.
-
(1997)
Reading Research Quarterly
, vol.32
, Issue.3
, pp. 276
-
-
Ho, C.S.1
Bryant, P.2
-
29
-
-
34247101559
-
In search of subtypes of Chinese developmental dyslexia
-
10.1016/j.jecp.2007.01.002, 17320097
-
Ho CS, Chan DW, Chung KKH, Lee S, Tsang S. In search of subtypes of Chinese developmental dyslexia. J Exp Child Psychol 2007, 97(1):61-83. 10.1016/j.jecp.2007.01.002, 17320097.
-
(2007)
J Exp Child Psychol
, vol.97
, Issue.1
, pp. 61-83
-
-
Ho, C.S.1
Chan, D.W.2
Chung, K.K.H.3
Lee, S.4
Tsang, S.5
-
30
-
-
0346997964
-
Cognitive profiling and preliminary subtyping in Chinese developmental dyslexia
-
10.1016/S0010-0277(03)00163-X, 14711491
-
Ho CS, Chan DW, Lee S, Tsang S, Luan VH. Cognitive profiling and preliminary subtyping in Chinese developmental dyslexia. Cognition 2004, 91(1):43-75. 10.1016/S0010-0277(03)00163-X, 14711491.
-
(2004)
Cognition
, vol.91
, Issue.1
, pp. 43-75
-
-
Ho, C.S.1
Chan, D.W.2
Lee, S.3
Tsang, S.4
Luan, V.H.5
-
31
-
-
44449161302
-
A structural-functional basis for dyslexia in the cortex of Chinese readers
-
10.1073/pnas.0801750105, 2291101, 18391194
-
Siok WT, Niu Z, Jin Z, Perfetti CA, Tan LH. A structural-functional basis for dyslexia in the cortex of Chinese readers. Proc Natl Acad Sci USA 2008, 105(14):5561-5566. 10.1073/pnas.0801750105, 2291101, 18391194.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, Issue.14
, pp. 5561-5566
-
-
Siok, W.T.1
Niu, Z.2
Jin, Z.3
Perfetti, C.A.4
Tan, L.H.5
-
32
-
-
4544271479
-
Biological abnormality of impaired reading is constrained by culture
-
10.1038/nature02865, 15343334
-
Siok WT, Perfetti CA, Jin Z, Tan LH. Biological abnormality of impaired reading is constrained by culture. Nature 2004, 431(7004):71-76. 10.1038/nature02865, 15343334.
-
(2004)
Nature
, vol.431
, Issue.7004
, pp. 71-76
-
-
Siok, W.T.1
Perfetti, C.A.2
Jin, Z.3
Tan, L.H.4
-
34
-
-
13444269543
-
Haploview: analysis and visualization of LD and haplotype maps
-
10.1093/bioinformatics/bth457, 15297300
-
Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005, 21(2):263-265. 10.1093/bioinformatics/bth457, 15297300.
-
(2005)
Bioinformatics
, vol.21
, Issue.2
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
35
-
-
24044550689
-
PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data
-
10.1093/bioinformatics/bti529, 15947021
-
Wigginton JE, Abecasis GR. PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data. Bioinformatics 2005, 21(16):3445-3447. 10.1093/bioinformatics/bti529, 15947021.
-
(2005)
Bioinformatics
, vol.21
, Issue.16
, pp. 3445-3447
-
-
Wigginton, J.E.1
Abecasis, G.R.2
-
36
-
-
0041857847
-
Pedigree disequilibrium tests for multilocus haplotypes
-
10.1002/gepi.10252, 12916020
-
Dudbridge F. Pedigree disequilibrium tests for multilocus haplotypes. Genet Epidemiol 2003, 25(2):115-121. 10.1002/gepi.10252, 12916020.
-
(2003)
Genet Epidemiol
, vol.25
, Issue.2
, pp. 115-121
-
-
Dudbridge, F.1
-
37
-
-
0042424602
-
Statistical significance for genomewide studies
-
10.1073/pnas.1530509100, 170937, 12883005
-
Storey JD, Tibshirani R. Statistical significance for genomewide studies. Proc Natl Acad Sci USA 2003, 100(16):9440-9445. 10.1073/pnas.1530509100, 170937, 12883005.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, Issue.16
, pp. 9440-9445
-
-
Storey, J.D.1
Tibshirani, R.2
-
38
-
-
0035956960
-
Morphological abnormalities in the brains of estrogen receptor beta knockout mice
-
10.1073/pnas.041617498, 30218, 11226319
-
Wang L, Andersson S, Warner M, Gustafsson JA. Morphological abnormalities in the brains of estrogen receptor beta knockout mice. Proc Natl Acad Sci USA 2001, 98(5):2792-2796. 10.1073/pnas.041617498, 30218, 11226319.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, Issue.5
, pp. 2792-2796
-
-
Wang, L.1
Andersson, S.2
Warner, M.3
Gustafsson, J.A.4
-
39
-
-
0032695442
-
Sex differences in cell migration in the preoptic area/anterior hypothalamus of mice
-
10.1002/(SICI)1097-4695(19991105)41:2<252::AID-NEU8>3.0.CO;2-W, 10512982
-
Henderson RG, Brown AE, Tobet SA. Sex differences in cell migration in the preoptic area/anterior hypothalamus of mice. J Neurobiol 1999, 41(2):252-266. 10.1002/(SICI)1097-4695(19991105)41:2<252::AID-NEU8>3.0.CO;2-W, 10512982.
-
(1999)
J Neurobiol
, vol.41
, Issue.2
, pp. 252-266
-
-
Henderson, R.G.1
Brown, A.E.2
Tobet, S.A.3
-
40
-
-
20444434726
-
Sex differences in the location of immunochemically defined cell populations in the mouse preoptic area/anterior hypothalamus
-
Wolfe CA, Van Doren M, Walker HJ, Seney ML, McClellan KM, Tobet SA. Sex differences in the location of immunochemically defined cell populations in the mouse preoptic area/anterior hypothalamus. Brain Res Dev Brain Res 2005, 157(1):34-41.
-
(2005)
Brain Res Dev Brain Res
, vol.157
, Issue.1
, pp. 34-41
-
-
Wolfe, C.A.1
Van Doren, M.2
Walker, H.J.3
Seney, M.L.4
McClellan, K.M.5
Tobet, S.A.6
-
41
-
-
34548319266
-
Estrogen modulates neuronal movements within the developing preoptic area-anterior hypothalamus
-
10.1111/j.1460-9568.2007.05751.x, 2295210, 17767488
-
Knoll JG, Wolfe CA, Tobet SA. Estrogen modulates neuronal movements within the developing preoptic area-anterior hypothalamus. Eur J Neurosci 2007, 26(5):1091-1099. 10.1111/j.1460-9568.2007.05751.x, 2295210, 17767488.
-
(2007)
Eur J Neurosci
, vol.26
, Issue.5
, pp. 1091-1099
-
-
Knoll, J.G.1
Wolfe, C.A.2
Tobet, S.A.3
-
42
-
-
78650241792
-
Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation
-
10.1038/mp.2009.120, 19901951
-
Bates TC, Lind PA, Luciano M, Montgomery GW, Martin NG, Wright MJ. Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation. Mol Psychiatry 2010, 15(12):1190-1196. 10.1038/mp.2009.120, 19901951.
-
(2010)
Mol Psychiatry
, vol.15
, Issue.12
, pp. 1190-1196
-
-
Bates, T.C.1
Lind, P.A.2
Luciano, M.3
Montgomery, G.W.4
Martin, N.G.5
Wright, M.J.6
-
43
-
-
0033473785
-
Naming-speed deficits and phonological memory deficits in Chinese developmental dyslexia
-
Ho CS, Lai DN. Naming-speed deficits and phonological memory deficits in Chinese developmental dyslexia. Learning and Individual Differences 1999, 11(2):173-186.
-
(1999)
Learning and Individual Differences
, vol.11
, Issue.2
, pp. 173-186
-
-
Ho, C.S.1
Lai, D.N.2
-
44
-
-
84937331359
-
The phonological deficit hypothesis in Chinese developmental dyslexia
-
Ho CS, Law TP, Ng PM. The phonological deficit hypothesis in Chinese developmental dyslexia. Reading and Writing 2000, 13(1):57-79.
-
(2000)
Reading and Writing
, vol.13
, Issue.1
, pp. 57-79
-
-
Ho, C.S.1
Law, T.P.2
Ng, P.M.3
|