-
1
-
-
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
O'Donovan, M.C.2
-
2
-
-
0000919168
-
Case of congenital word blindness (inability to learn to read)
-
Fisher JH. Case of congenital word blindness (inability to learn to read). Ophthal Rev 1905; 24: 315.
-
(1905)
Ophthal Rev
, vol.24
, pp. 315
-
-
Fisher, J.H.1
-
3
-
-
0000122211
-
Four cases of hereditary word-blindness occurring in the same family
-
Hinshelwood J. Four cases of hereditary word-blindness occurring in the same family. Br Med J 1907; 2: 1229-1232.
-
(1907)
Br Med J
, vol.2
, pp. 1229-1232
-
-
Hinshelwood, J.1
-
4
-
-
0023179955
-
Evidence for a genetic aetiology in reading disability of twins
-
DeFries JC, Fulker DW, LaBuda MC. Evidence for a genetic aetiology in reading disability of twins. Nature 1987; 329: 537-539.
-
(1987)
Nature
, vol.329
, pp. 537-539
-
-
DeFries, J.C.1
Fulker, D.W.2
LaBuda, M.C.3
-
6
-
-
0003160556
-
Colorado reading project: Past, present, and future
-
DeFries JC, Olson R, Pennington BF, Smith SD. Colorado reading project: past, present, and future. Learn Disabil 1991; 2: 37-46.
-
(1991)
Learn Disabil
, vol.2
, pp. 37-46
-
-
DeFries, J.C.1
Olson, R.2
Pennington, B.F.3
Smith, S.D.4
-
7
-
-
0025992157
-
Evidence for major gene transmission of developmental dyslexia
-
Pennington BF, Gilger JW, Pauls D, Smith SA, Smith SD, DeFries JC. Evidence for major gene transmission of developmental dyslexia. JAMA 1991; 266: 1527-1534.
-
(1991)
JAMA
, vol.266
, pp. 1527-1534
-
-
Pennington, B.F.1
Gilger, J.W.2
Pauls, D.3
Smith, S.A.4
Smith, S.D.5
DeFries, J.C.6
-
8
-
-
0029987489
-
Familial aggregation of spelling disability
-
Schulte-Korne G, Deimel W, Muller K, Gutenbrunner C, Remschmidt H. Familial aggregation of spelling disability. J Child Psychol Psychiatry 1996; 37: 817-822.
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 817-822
-
-
Schulte-Korne, G.1
Deimel, W.2
Muller, K.3
Gutenbrunner, C.4
Remschmidt, H.5
-
9
-
-
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: 276-279.
-
(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
-
10
-
-
0029003528
-
Quantitative trait locus for reading disability: Correction
-
Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, DeFries JC. Quantitative trait locus for reading disability: correction. Science 1995; 268: 1553.
-
(1995)
Science
, vol.268
, pp. 1553
-
-
Cardon, L.R.1
Smith, S.D.2
Fulker, D.W.3
Kimberling, W.J.4
Pennington, B.F.5
DeFries, J.C.6
-
11
-
-
0031027824
-
Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
-
Grigorenko EL, Wood FB, Meyer MS, Hart LA, Speed WC, Shuster A 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
Hart, L.A.4
Speed, W.C.5
Shuster, A.6
-
12
-
-
0033366739
-
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia
-
Fisher SE, Marlow AJ, Lamb J, Maestrini E, Williams DF, Richardson AJ et al. A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. Am J Hum Genet 1999; 64: 146-156.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 146-156
-
-
Fisher, S.E.1
Marlow, A.J.2
Lamb, J.3
Maestrini, E.4
Williams, D.F.5
Richardson, A.J.6
-
13
-
-
0033364213
-
Quantitative-trait locus for specific language and reading deficits on chromosome 6p
-
Gayan J, Smith SD, Cherny SS, Cardon LR, Fulker DW, Brower AM et al. Quantitative-trait locus for specific language and reading deficits on chromosome 6p. Am J Hum Genet 1999; 64: 157-164.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 157-164
-
-
Gayan, J.1
Smith, S.D.2
Cherny, S.S.3
Cardon, L.R.4
Fulker, D.W.5
Brower, A.M.6
-
14
-
-
0033928210
-
Chromosome 6p influences on different dyslexia-related cognitive processes: Further confirmation
-
Grigorenko EL, Wood FB, Meyer MS, Pauls DL. Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation. Am J Hum Genet 2000; 66: 715-723.
-
(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
-
15
-
-
18344374003
-
Evidence for linkage and association with reading disability on 6p21.3-22
-
Kaplan DE, Gayan J, Ahn J, Won TW, Pauls D, Olson RK et al. Evidence for linkage and association with reading disability on 6p21.3-22. Am J Hum Genet 2002; 70: 1287-1298.
-
(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
-
16
-
-
0042319316
-
Continuing the search for dyslexia genes on 6p
-
Grigorenko EL, Wood FB, Golovyan L, Meyer M, Romano C, Pauls D. Continuing the search for dyslexia genes on 6p. Am J Med Genet B Neuropsychiatr Genet 2003; 118: 89-98.
-
(2003)
Am J Med Genet B Neuropsychiatr Genet
, vol.118
, pp. 89-98
-
-
Grigorenko, E.L.1
Wood, F.B.2
Golovyan, L.3
Meyer, M.4
Romano, C.5
Pauls, D.6
-
17
-
-
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. 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
Richardson, A.J.4
Scerri, T.S.5
Cardon, L.R.6
-
18
-
-
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 2005; 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
-
19
-
-
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 2006; 15: 1659-1666.
-
(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
-
20
-
-
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 et al. DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci USA 2005; 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
-
21
-
-
29244468273
-
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
-
Schumacher J, Anthoni H, Dahdouh F, Konig IR, Hillmer AM, Kluck N 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
Konig, I.R.4
Hillmer, A.M.5
Kluck, N.6
-
22
-
-
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. Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK. Behav Genet 2001; 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
-
23
-
-
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 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, I.L.4
Newbury, D.F.5
Cardon, L.R.6
-
24
-
-
0037371605
-
Use of multivariate linkage analysis for dissection of a complex cognitive trait
-
Marlow AJ, Fisher SE, Francks C, MacPhie IL, Cherny SS, Richardson AJ et al. Use of multivariate linkage analysis for dissection of a complex cognitive trait. Am J Hum Genet 2003; 72: 561-570.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 561-570
-
-
Marlow, A.J.1
Fisher, S.E.2
Francks, C.3
MacPhie, I.L.4
Cherny, S.S.5
Richardson, A.J.6
-
25
-
-
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 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
Olson, R.K.4
Pennington, B.F.5
DeFries, J.C.6
-
28
-
-
0043066904
-
Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease
-
Harold D, Peirce T, Moskvina V, Myers A, Jones S, Hollingworth P et al. Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease. Hum Genet 2003; 113: 258-267.
-
(2003)
Hum Genet
, vol.113
, pp. 258-267
-
-
Harold, D.1
Peirce, T.2
Moskvina, V.3
Myers, A.4
Jones, S.5
Hollingworth, P.6
-
29
-
-
3242694931
-
Detecting highly conserved regions of the human genome by multispecies sequence comparisons
-
Margulies EH, Green ED. Detecting highly conserved regions of the human genome by multispecies sequence comparisons. Cold Spring Harb Symp Quant Biol 2003; 68: 255-263.
-
(2003)
Cold Spring Harb Symp Quant Biol
, vol.68
, pp. 255-263
-
-
Margulies, E.H.1
Green, E.D.2
-
30
-
-
0033909546
-
A general test of association for quantitative traits in nuclear families
-
Abecasis GR, Cardon LR, Cookson WO. A general test of association for quantitative traits in nuclear families. Am J Hum Genet 2000; 66: 279-292.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 279-292
-
-
Abecasis, G.R.1
Cardon, L.R.2
Cookson, W.O.3
-
31
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002; 30: 97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
32
-
-
0041857847
-
Pedigree disequilibrium tests for multilocus haplotypes
-
Dudbridge F. Pedigree disequilibrium tests for multilocus haplotypes. Genet Epidemiol 2003; 25: 115-121.
-
(2003)
Genet Epidemiol
, vol.25
, pp. 115-121
-
-
Dudbridge, F.1
-
34
-
-
33745438900
-
GAIA: An easy-to-use web-based application for interaction analysis of case-control data
-
Macgregor S, Khan IA. GAIA: an easy-to-use web-based application for interaction analysis of case-control data. BMC Med Genet 2006; 7: 34.
-
(2006)
BMC Med Genet
, vol.7
, pp. 34
-
-
Macgregor, S.1
Khan, I.A.2
-
35
-
-
10244245425
-
GOLDsurfer: Three dimensional display of linkage disequilibrium
-
Pettersson F, Jonsson O, Cardon LR. GOLDsurfer: three dimensional display of linkage disequilibrium. Bioinformatics 2004; 20: 3241-3243.
-
(2004)
Bioinformatics
, vol.20
, pp. 3241-3243
-
-
Pettersson, F.1
Jonsson, O.2
Cardon, L.R.3
-
36
-
-
0018356659
-
Cytoarchitectonic abnormalities in developmental dyslexia: A case study
-
Galaburda AM, Kemper TL. Cytoarchitectonic abnormalities in developmental dyslexia: a case study. Ann Neurol 1979; 6: 94-100.
-
(1979)
Ann Neurol
, vol.6
, pp. 94-100
-
-
Galaburda, A.M.1
Kemper, T.L.2
-
37
-
-
0021832834
-
Developmental dyslexia: Four consecutive patients with cortical anomalies
-
Galaburda AM, Sherman GF, Rosen GD, Aboitiz F, Geschwind N. 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
Aboitiz, F.4
Geschwind, N.5
|