-
1
-
-
1642343512
-
The Nature of Phonological Awareness: Converging Evidence From Four Studies of Preschool and Early Grade School Children
-
DOI 10.1037/0022-0663.96.1.43
-
JL Anothny CJ Lonigan 2004 The nature of phonological awareness: converging evidence from four studies of preschool and early grade school children J Educ Psychol 96 43 55 10.1037/0022-0663.96.1.43 (Pubitemid 38397486)
-
(2004)
Journal of Educational Psychology
, vol.96
, Issue.1
, pp. 43-55
-
-
Anthony, J.L.1
Lonigan, C.J.2
-
2
-
-
34247092473
-
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia
-
DOI 10.1093/hmg/ddm009
-
H Anthoni M Zucchelli H Matsson B Muller-Myhsok I Fransson J Schumacher S Massinen P Onkamo A Warnke H Griesemann P Hoffmann J Nopola-Hemmi H Lyytinen G Schulte-Korne J Kere MM Nothen M Peyrard-Janvid 2007 A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia Hum Mol Genet 16 667 677 17309879 10.1093/hmg/ddm009 (Pubitemid 46585666)
-
(2007)
Human Molecular Genetics
, 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
Nthen, M.M.16
Peyrard-Janvid, M.17
-
4
-
-
33846297701
-
Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17
-
DOI 10.1038/sj.ejhg.5201739, PII 5201739
-
TC Bates M Luciano A Castles M Coltheart MJ Wright NG Martin 2007 Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17 Eur J Hum Genet 15 194 203 17119535 10.1038/sj.ejhg.5201739 (Pubitemid 46111858)
-
(2007)
European Journal of Human Genetics
, vol.15
, Issue.2
, pp. 194-203
-
-
Bates, T.C.1
Luciano, M.2
Castles, A.3
Coltheart, M.4
Wright, M.J.5
Martin, N.G.6
-
5
-
-
53849127147
-
Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language
-
10.1016/j.intell.2008.04.001
-
TC Bates M Luciano PA Lind MJ Wright GW Montgomery NG Martin 2008 Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language Intelligence 3 689 693 10.1016/j.intell.2008.04.001
-
(2008)
Intelligence
, vol.3
, pp. 689-693
-
-
Bates, T.C.1
Luciano, M.2
Lind, P.A.3
Wright, M.J.4
Montgomery, G.W.5
Martin, N.G.6
-
6
-
-
78650241792
-
Dyslexia and DYX1C1: Deficits in reading and spelling associated with a missense mutation
-
19901951 10.1038/mp.2009.120
-
TC Bates PA Lind M Luciano GW Montgomery NG Martin MJ Wright 2010 Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation Mol Psychiatry 15 1190 1196 19901951 10.1038/mp.2009.120
-
(2010)
Mol Psychiatry
, vol.15
, 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
-
7
-
-
79952443930
-
Genes for a component of the language acquisition mechanism: ROBO1 polymorphisms associated with phonological buffer deficit
-
this issue
-
Bates TC, Luciano M, Montgomery GW, Wright MJ, Martin NG (2011) Genes for a component of the language acquisition mechanism: ROBO1 polymorphisms associated with phonological buffer deficit. Behav Genet this issue
-
(2011)
Behav Genet
-
-
Bates, T.C.1
Luciano, M.2
Montgomery, G.W.3
Wright, M.J.4
Martin, N.G.5
-
8
-
-
27644480838
-
No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy
-
DOI 10.1385/JMN:27:3:311
-
G Bellini C Bravaccio F Calamoneri MD Cocuzza P Fiorillo A Gagliano D Mazzone EM del Giudice G Scuccimarra R Militerni A Pascotto 2005 No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy J Mol Neurosci 27 311 314 16280601 10.1385/JMN:27:3:311 (Pubitemid 41572678)
-
(2005)
Journal of Molecular Neuroscience
, vol.27
, Issue.3
, pp. 311-314
-
-
Bellini, G.1
Bravaccio, C.2
Calamoneri, F.3
Cocuzza, M.D.4
Fiorillo, P.5
Gagliano, A.6
Mazzone, D.7
Del Giudice, E.M.8
Scuccimarra, G.9
Militerni, R.10
Pascotto, A.11
-
9
-
-
79952441187
-
A family based association study of DRD4, DAT1, and 5HTT and continuous traits of Attention-Deficit Hyperactivity Disorder
-
this issue
-
Bidwell LC, Willcutt EG, McQueen MB, DeFries JC, Olson RK, Smith SD, Pennington BF (2011) A family based association study of DRD4, DAT1, and 5HTT and continuous traits of Attention-Deficit Hyperactivity Disorder. Behav Genet this issue
-
(2011)
Behav Genet
-
-
Bidwell, L.C.1
Willcutt, E.G.2
McQueen, M.B.3
Defries, J.C.4
Olson, R.K.5
Smith, S.D.6
Pennington, B.F.7
-
10
-
-
84974220771
-
Metalinguistic ability and early reading achievement
-
10.1017/S0142716400008067
-
JA Bowey RK Patel 1988 Metalinguistic ability and early reading achievement Appl Psycholinguist 9 367 383 10.1017/S0142716400008067
-
(1988)
Appl Psycholinguist
, vol.9
, pp. 367-383
-
-
Bowey, J.A.1
Patel, R.K.2
-
11
-
-
34250810249
-
Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia
-
DOI 10.1002/ajmg.b.30471
-
Z Brkanac NH Chapman MM Matsushita L Chun K Nielsen E Cochrane VW Berninger EM Wijsman WH Raskind 2007 Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia Am J Med Genet (Neuropsychiatr Genet) 144 556 560 (Pubitemid 46983168)
-
(2007)
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
, vol.144
, 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
-
12
-
-
52549109216
-
Genome scan of a nonword repetition phenotype in families with dyslexia: Evidence for multiple loci
-
18607713 10.1007/s10519-008-9215-2
-
Z Brkanac NH Chapman RP Igo MM Matsushita K Nielsen VW Berninger E Wijsman WH Raskind 2008 Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci Behav Genet 38 462 475 18607713 10.1007/s10519-008-9215-2
-
(2008)
Behav Genet
, vol.38
, pp. 462-475
-
-
Brkanac, Z.1
Chapman, N.H.2
Igo, R.P.3
Matsushita, M.M.4
Nielsen, K.5
Berninger, V.W.6
Wijsman, E.7
Raskind, W.H.8
-
13
-
-
33750192577
-
Word recognition skills of adults with childhood diagnoses of dyslexia
-
10.1037/0012-1649.26.3.439
-
M Bruck 1990 Word recognition skills of adults with childhood diagnoses of dyslexia Dev Psychol 26 439 454 10.1037/0012-1649.26.3.439
-
(1990)
Dev Psychol
, vol.26
, pp. 439-454
-
-
Bruck, M.1
-
14
-
-
79952450048
-
A cohort of balanced reciprocal translocations associated with dyslexia: Identification of two putative candidate genes at DYX1
-
this issue
-
Buonincontri R, Bache I, Silahtaroglu A, Elbro C, Veber Nielsen A-M, Ullmann R, Arkesteijn G, Tommerup N (2011) A cohort of balanced reciprocal translocations associated with dyslexia: identification of two putative candidate genes at DYX1. Behav Genet this issue
-
(2011)
Behav Genet
-
-
Buonincontri, R.1
Bache, I.2
Silahtaroglu, A.3
Elbro, C.4
Veber Nielsen, A.-M.5
Ullmann, R.6
Arkesteijn, G.7
Tommerup, N.8
-
17
-
-
0027598525
-
Varieties of developmental dyslexia
-
8324999 10.1016/0010-0277(93)90003-E
-
A Castles M Coltheart 1993 Varieties of developmental dyslexia Cognition 47 149 180 8324999 10.1016/0010-0277(93)90003-E
-
(1993)
Cognition
, vol.47
, pp. 149-180
-
-
Castles, A.1
Coltheart, M.2
-
19
-
-
7644236039
-
Linkage analyses of four regions previously implicated in dyslexia: Confirmation of a locus on chromosome 15q
-
DOI 10.1002/ajmg.b.30018
-
NH Chapman RP Igo JB Thomson M Matsushita Z Brkanac T Holzman VW Berninger EM Wijsman WH Raskind 2004 Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q Am J Med Genet (Neuropsychiatr Genet) 131B 67 75 10.1002/ajmg.b.30018 (Pubitemid 39458440)
-
(2004)
American Journal of Medical Genetics - Neuropsychiatric Genetics
, vol.131 B
, Issue.1
, pp. 67-75
-
-
Chapman, N.H.1
Igo, R.P.2
Thomson, J.B.3
Matsushita, M.4
Brkanac, Z.5
Holzman, T.6
Berninger, V.W.7
Wijsman, E.M.8
Raskind, W.H.9
-
20
-
-
15944363095
-
No support for association between Dyslexia Susceptibility 1 Candidate 1 and developmental dyslexia
-
10.1038/sj.mp.4001596
-
N Cope G Hill M van den Bree D Harold V Moskvina EK Green MJ Owen J Williams MC O'Donovan 2004 No support for association between Dyslexia Susceptibility 1 Candidate 1 and developmental dyslexia Mol Psychiatry 10 237 238 10.1038/sj.mp.4001596
-
(2004)
Mol Psychiatry
, vol.10
, 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
-
21
-
-
15944372645
-
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia
-
DOI 10.1086/429131
-
N Cope D Harold G Hill V Moskvina J Stevenson P Holmans MJ Owen MC O'Donovan J Williams 2005 Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia Am J Hum Genet 76 581 591 15717286 10.1086/429131 (Pubitemid 40432166)
-
(2005)
American Journal of Human Genetics
, vol.76
, Issue.4
, pp. 581-591
-
-
Cope, N.1
Harold, D.2
Hill, G.3
Moskvina, V.4
Stevenson, J.5
Holmans, P.6
Owen, M.J.7
O'Donovan, M.C.8
Williams, J.9
-
22
-
-
57649136416
-
The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities
-
19085271 10.1080/01677060802354328
-
JM Couto L Gomez K Wigg T Cate-Carter J Archibald B Anderson R Tannock E Kerr M Lovett T Humphries C Barr 2008 The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities J Neurogenet 22 295 313 19085271 10.1080/01677060802354328
-
(2008)
J Neurogenet
, vol.22
, 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.8
Lovett, M.9
Humphries, T.10
Barr, C.11
-
23
-
-
77349092836
-
Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319
-
19588467
-
JM Couto I Livne-Bar K Huang Z Xu T Cate-Carter Y Feng K Wigg T Humphries R Tannock EN Kerr MW Lovett R Bremner CL Barr 2010 Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319 Am J Med Genet 153B 447 462 19588467
-
(2010)
Am J Med Genet
, vol.153
, pp. 447-462
-
-
Couto, J.M.1
Livne-Bar, I.2
Huang, K.3
Xu, Z.4
Cate-Carter, T.5
Feng, Y.6
Wigg, K.7
Humphries, T.8
Tannock, R.9
Kerr, E.N.10
Lovett, M.W.11
Bremner, R.12
Barr, C.L.13
-
24
-
-
79952437992
-
Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia
-
this issue
-
Czamara D, Bruder J, Becker J, Bartling J, Hoffmann P, Ludwig KU, Müller-Myhsok B, Schulte-Körne G (2011) Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia. Behav Genet this issue
-
(2011)
Behav Genet
-
-
Czamara, D.1
Bruder, J.2
Becker, J.3
Bartling, J.4
Hoffmann, P.5
Ludwig, K.U.6
Müller-Myhsok, B.7
Schulte-Körne, G.8
-
25
-
-
63149196656
-
Further evidence for DYX1C1 as a susceptibility factor for dyslexia
-
19240663 10.1097/YPG.0b013e32832080e1
-
F Dahdouh H Anthoni I Tapia-Páez M Peyrard-Janvid G Schulte-Körne A Warnke H Remschmidt A Ziegler J Kere B Müller-Myhsok M Nöthen J Schumacher M Zucchelli 2009 Further evidence for DYX1C1 as a susceptibility factor for dyslexia Psychiatr Genet 19 59 63 19240663 10.1097/YPG.0b013e32832080e1
-
(2009)
Psychiatr Genet
, vol.19
, pp. 59-63
-
-
Dahdouh, F.1
Anthoni, H.2
Tapia-Páez, I.3
Peyrard-Janvid, M.4
Schulte-Körne, G.5
Warnke, A.6
Remschmidt, H.7
Ziegler, A.8
Kere, J.9
Müller-Myhsok, B.10
Nöthen, M.11
Schumacher, J.12
Zucchelli, M.13
-
26
-
-
26844510735
-
Telephone testing and teacher assessment of reading skills in 7-year-olds: I. Substantial correspondence for a sample of 5544 children and for extremes
-
DOI 10.1007/s11145-004-8130-z
-
PS Dale N Harlaar R Plomin 2005 Telephone testing and teacher assessment of reading skills in 7-year-olds: I. Substantial correspondence for a sample of 5808 children and for extremes Read Writ Interdiscip J 18 385 400 10.1007/s11145-004-8130-z (Pubitemid 41456303)
-
(2005)
Reading and Writing
, vol.18
, Issue.5
, pp. 385-400
-
-
Dale, P.S.1
Harlaar, N.2
Plomin, R.3
-
27
-
-
4444356020
-
Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family
-
DOI 10.1136/jmg.2003.012294
-
CGF de Kovel FA Hol J Heister J Willemen LA Sandkuijl B Franke GW Padberg 2004 Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family J Med Genet 41 652 657 15342694 10.1136/jmg.2003.012294 (Pubitemid 39208604)
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.9
, pp. 652-657
-
-
De Kovel, C.G.F.1
Hol, F.A.2
Heister, J.G.A.M.3
Willemen, J.J.H.T.4
Sandkuijl, L.A.5
Franke, B.6
Padberg, G.W.7
-
28
-
-
42149141765
-
Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection
-
DOI 10.1002/ajmg.b.30598
-
CGF de Kovel B Franke F Hol J Lebrec B Maassen H Brunner G Padberg J Platko D Pauls 2008 Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection Am J Med Genet (Neuropsychiatr Genet) 147B 294 300 10.1002/ajmg.b.30598 (Pubitemid 351536791)
-
(2008)
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
, vol.147
, Issue.3
, pp. 294-300
-
-
De Kovel, C.G.F.1
Franke, B.2
Hol, F.A.3
Lebrec, J.J.P.4
Maassen, B.5
Brunner, H.6
Padberg, G.W.7
Platko, J.8
Pauls, D.9
-
29
-
-
3543029197
-
Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: Linkage and association analyses
-
KE Deffenbacher JB Kenyon DM Hoover RK Olson BF Pennington JC DeFries SD Smith 2004 Refinement of the 6p21.3 QTL influencing dyslexia: linkage and association analyses Hum Genet 115 128 138 15138886 10.1007/s00439-004-1126-6 (Pubitemid 39010927)
-
(2004)
Human Genetics
, vol.115
, Issue.2
, 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
Smith, S.D.7
-
31
-
-
0016150610
-
Rapid "automatized" naming of pictured objects, colors, letters and numbers by normal children
-
4844470
-
M Denckla R Rudel 1974 Rapid "automatized" naming of pictured objects, colors, letters and numbers by normal children Cortex 10 186 202 4844470
-
(1974)
Cortex
, vol.10
, pp. 186-202
-
-
Denckla, M.1
Rudel, R.2
-
32
-
-
0017231374
-
Naming of object-drawings by dyslexic and other learning disabled children
-
773516 10.1016/0093-934X(76)90001-8
-
M Denckla R Rudel 1976 Naming of object-drawings by dyslexic and other learning disabled children Brain Lang 3 1 15 773516 10.1016/0093-934X(76)90001-8
-
(1976)
Brain Lang
, vol.3
, pp. 1-15
-
-
Denckla, M.1
Rudel, R.2
-
33
-
-
63449106260
-
A common variant associated with dyslexia reduces expression of the KIAA0319 gene
-
19325871 10.1371/journal.pgen.1000436
-
MY Dennis S Paracchini TS Scerri L Prokunina-Olsson JC Knight R Wade-Martins P Coggill S Beck ED Green AP Monaco 2009 A common variant associated with dyslexia reduces expression of the KIAA0319 gene PLoS Genet 5 e1000436 19325871 10.1371/journal.pgen.1000436
-
(2009)
PLoS Genet
, vol.5
, pp. 1000436
-
-
Dennis, M.Y.1
Paracchini, S.2
Scerri, T.S.3
Prokunina-Olsson, L.4
Knight, J.C.5
Wade-Martins, R.6
Coggill, P.7
Beck, S.8
Green, E.D.9
Monaco, A.P.10
-
34
-
-
79952442152
-
Gene-environment interaction in the etiology of mathematical ability using SNP sets
-
this issue
-
Docherty SJ, Kovas Y, Plomin R (2011) Gene-environment interaction in the etiology of mathematical ability using SNP sets. Behav Genet this issue
-
(2011)
Behav Genet
-
-
Docherty, S.J.1
Kovas, Y.2
Plomin, R.3
-
36
-
-
79952440240
-
Genetic variation in the KIAA0319 5′ region contributing to dyslexia
-
this issue
-
Elbert A, Lovett MW, Cate-Carter T, Pitch A, Kerr EN, Barr CL (2011) Genetic variation in the KIAA0319 5′ region contributing to dyslexia. Behav Genet this issue
-
(2011)
Behav Genet
-
-
Elbert, A.1
Lovett, M.W.2
Cate-Carter, T.3
Pitch, A.4
Kerr, E.N.5
Barr, C.L.6
-
39
-
-
0032231869
-
Absence of linkage of phonological coding dyslexia to chromosome 6p23- p21.3 in a large family data set
-
DOI 10.1086/302107
-
LL Field BJ Kaplan 1998 Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set Am J Hum Genet 63 1448 1456 9792873 10.1086/302107 (Pubitemid 30418543)
-
(1998)
American Journal of Human Genetics
, vol.63
, Issue.5
, pp. 1448-1456
-
-
Field, L.L.1
Kaplan, B.J.2
-
40
-
-
0033366739
-
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia
-
DOI 10.1086/302190
-
SE Fisher AJ Marlow J Lamb E Maestrini DF Williams AJ Richardson DE Weeks JF Stein AP Monaco 1999 A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia Am J Hum Genet 64 146 156 9915953 10.1086/302190 (Pubitemid 30428967)
-
(1999)
American Journal of Human Genetics
, vol.64
, Issue.1
, 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
Weeks, D.E.7
Stein, J.F.8
Monaco, A.P.9
-
41
-
-
18544365699
-
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
-
11743577 10.1038/ng792
-
SE Fisher C Francks AJ Marlow IL MacPhie DF Newbury LR Cardon Y Ishikawa-Brush AJ Richardson JB Talcott J Gayan RK Olson BF Pennington SD Smith JC DeFries JF Stein AP Monaco 2002 Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia Nat Genet 30 86 91 11743577 10.1038/ng792
-
(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
Ishikawa-Brush, Y.7
Richardson, A.J.8
Talcott, J.B.9
Gayan, J.10
Olson, R.K.11
Pennington, B.F.12
Smith, S.D.13
Defries, J.C.14
Stein, J.F.15
Monaco, A.P.16
-
42
-
-
70349421026
-
Dyslexia: The evolution of a scientific concept
-
19573267 10.1017/S1355617709090900
-
JM Fletcher 2009 Dyslexia: the evolution of a scientific concept J Int Neuropsychol Soc 15 501 508 19573267 10.1017/S1355617709090900
-
(2009)
J Int Neuropsychol Soc
, vol.15
, pp. 501-508
-
-
Fletcher, J.M.1
-
43
-
-
0036217207
-
Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: Quantitative association analysis and positional candidate genes SEMA4F and OTX1
-
DOI 10.1097/00041444-200203000-00005
-
C Francks SE Fisher RK Olson BF Pennington SD Smith JC DeFries AP Monaco 2002 Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1 Psychiatr Genet 12 35 41 11901358 10.1097/00041444-200203000-00005 (Pubitemid 34274492)
-
(2002)
Psychiatric Genetics
, vol.12
, Issue.1
, pp. 35-41
-
-
Francks, C.1
Fisher, S.E.2
Olson, R.K.3
Pennington, B.F.4
Smith, S.D.5
DeFries, J.C.6
Monaco, A.P.7
-
44
-
-
8844258018
-
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States
-
DOI 10.1086/426404
-
C Francks S Paracchini SD Smith AJ Richardson TS Scerri LR Cardon AJ Marlow IL MacPhie J Walter BF Pennington SE Fisher RK Olson JC DeFries JF Stein AP Monaco 2004 A 77-kilobase region on 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 15514892 10.1086/426404 (Pubitemid 39532073)
-
(2004)
American Journal of Human Genetics
, vol.75
, Issue.6
, 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
Marlow, A.J.7
MacPhie, I.L.8
Walter, J.9
Pennington, B.F.10
Fisher, S.E.11
Olson, R.K.12
DeFries, J.C.13
Stein, J.F.14
Monaco, A.P.15
-
45
-
-
0002109319
-
Unexpected spelling problems
-
U. Frith (eds). Academic Press London, UK
-
Frith U (1980) Unexpected spelling problems. In: Frith U (ed) Cognitive processes in spelling. Academic Press, London, UK, pp 495-517
-
(1980)
Cognitive Processes in Spelling
, pp. 495-517
-
-
Frith, U.1
-
46
-
-
0023282201
-
Strategies for visual word recognition and orthographical depth: A multilingual comparison
-
2951484 10.1037/0096-1523.13.1.104
-
R Frost L Katz S Bentin 1987 Strategies for visual word recognition and orthographical depth: a multilingual comparison J Exp Psychol Hum Percept Perform 13 104 115 2951484 10.1037/0096-1523.13.1.104
-
(1987)
J Exp Psychol Hum Percept Perform
, vol.13
, pp. 104-115
-
-
Frost, R.1
Katz, L.2
Bentin, S.3
-
48
-
-
0033364213
-
Quantitative-trait locus for specific language and reading deficits on chromosome 6p
-
DOI 10.1086/302191
-
J Gayán SD Smith SS Cherny LR Cardon DW Fulker AM Brower RK Olson BF Pennington JC DeFries 1999 Quantitative-trait locus for specific language and reading deficits on chromosome 6p Am J Hum Genet 64 157 164 9915954 10.1086/302191 (Pubitemid 30428968)
-
(1999)
American Journal of Human Genetics
, vol.64
, Issue.1
, 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
Olson, R.K.7
Pennington, B.F.8
DeFries, J.C.9
-
49
-
-
0035130957
-
ALSPAC - The Avon Longitudinal Study of Parents and Children I. Study methodology
-
DOI 10.1046/j.1365-3016.2001.00325.x
-
J Golding M Pembrey R Jones the ALSPAC Study Team 2001 ALSPAC-the Avon Longitudinal Study of Parents and Children I. Study methodology Pediatr Prenat Epidemiol 15 74 87 10.1046/j.1365-3016.2001.00325.x (Pubitemid 32155760)
-
(2001)
Paediatric and Perinatal Epidemiology
, vol.15
, Issue.1
, pp. 74-87
-
-
Golding, J.1
Pembrey, M.2
Jones, R.3
-
50
-
-
0038042381
-
Nonword reading across orthographies: How flexible is the choice of reading units?
-
DOI 10.1017/S0142716403000134
-
U Goswami JC Ziegler L Dalton W Schneider 2003 Nonword reading across orthographies: how flexible is the choice of reading units? Appl Psycholing 24 235 247 10.1017/S0142716403000134 (Pubitemid 36891785)
-
(2003)
Applied Psycholinguistics
, vol.24
, Issue.2
, pp. 235-247
-
-
Goswami, U.1
Ziegler, J.C.2
Dalton, L.3
Schneider, W.4
-
51
-
-
33645154439
-
Genetic bases of developmental dyslexia: A capsule review of heritability estimates
-
10.3917/enf.563.0273
-
EL Grigorenko 2004 Genetic bases of developmental dyslexia: a capsule review of heritability estimates Enfance 3 273 287 10.3917/enf.563.0273
-
(2004)
Enfance
, vol.3
, pp. 273-287
-
-
Grigorenko, E.L.1
-
52
-
-
79952448614
-
The devil is in the details: Decoding the genetics of reading
-
P. McCardle K. Pugh (eds). Psychological Press New York, NY
-
Grigorenko EL, Naples AJ (2009) The devil is in the details: decoding the genetics of reading. In: McCardle P, Pugh K (eds) Helping children learn to read: current issues and new directions in the integration of cognition, neurobiology and genetics of reading and dyslexia. Psychological Press, New York, NY, pp 133-148
-
(2009)
Helping Children Learn to Read: Current Issues and New Directions in the Integration of Cognition, Neurobiology and Genetics of Reading and Dyslexia
, pp. 133-148
-
-
Grigorenko, E.L.1
Naples, A.J.2
-
53
-
-
0031027824
-
Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
-
EL Grigorenko F Wood M Meyer L Hart W Speed A Shuster D Pauls 1997 Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15 Am J Hum Genet 60 27 39 8981944 (Pubitemid 26427775)
-
(1997)
American Journal of Human Genetics
, vol.60
, Issue.1
, 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
Pauls, D.L.7
-
54
-
-
0033928210
-
Chromosome 6p influences on different dyslexia-related cognitive processes: Further confirmation
-
DOI 10.1086/302755
-
EL Grigorenko FB Wood MS Meyer DL Pauls 2000 Chromosome 6p influences on different dyslexia related cognitive processes: further confirmation Am J Hum Genet 66 715 723 10677331 10.1086/302755 (Pubitemid 30468849)
-
(2000)
American Journal of Human Genetics
, vol.66
, Issue.2
, pp. 715-723
-
-
Grigorenko, E.L.1
Wood, F.B.2
Meyer, M.S.3
Pauls, D.L.4
-
55
-
-
0035825196
-
Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p
-
DOI 10.1002/1096-8628(20010108)105:1<120::AID-AJMG1075>3.0.CO;2-T
-
EL Grigorenko FB Wood MS Meyer JED Pauls LA Hart DL Pauls 2001 Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p Am J Med Genet (Neuropsychiatr Genet) 105 120 129 10.1002/1096-8628(20010108)105: 1<120::AID-AJMG1075>3.0.CO;2-T (Pubitemid 32105214)
-
(2001)
American Journal of Medical Genetics - Neuropsychiatric Genetics
, vol.105
, Issue.1
, pp. 120-129
-
-
Manor, I.1
Eisenberg, J.2
Tyano, S.3
Sever, Y.4
Cohen, H.5
Ebstein, R.P.6
Kotler, M.7
-
57
-
-
35348841532
-
Exploring interactive effects of genes and environments in etiology of individual differences in reading comprehension
-
DOI 10.1017/S0954579407000557
-
EL Grigorenko CG DeYoung M Getchell GJ Haeffel B af Klinteberg RA Koposov L Oreland A Pakstis VV Ruchkin CM Yrigollen 2007 Exploring interactive effects of genes and environments in etiology of individual differences in reading comprehension Dev Psychopathol 19 1089 1103 17931436 (Pubitemid 47578014)
-
(2007)
Development and Psychopathology
, vol.19
, Issue.4
, pp. 1089-1103
-
-
Grigorenko, E.L.1
Deyoung, C.G.2
Getchell, M.3
Haeffel, G.J.4
Klinteberg, B.A.F.5
Koposov, R.A.6
Oreland, L.7
Pakstis, A.J.8
Ruchkin, V.V.9
Yrigollen, C.M.10
-
58
-
-
33845774327
-
Back to Africa: Tracing dyslexia genes in East Africa
-
EL Grigorenko A Naples J Chang C Romano D Ngorosho S Kungulilo M Jukes D Bundy 2007 Back to Africa: tracing dyslexia genes in East Africa Read Writ Interdiscip J 1-2 27 49
-
(2007)
Read Writ Interdiscip J
, vol.12
, pp. 27-49
-
-
Grigorenko, E.L.1
Naples, A.2
Chang, J.3
Romano, C.4
Ngorosho, D.5
Kungulilo, S.6
Jukes, M.7
Bundy, D.8
-
60
-
-
33845246158
-
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia
-
DOI 10.1038/sj.mp.4001904, PII 4001904
-
D Harold S Paracchini TS Scerri M Dennis N Cope G Hill V Moskvina J Walter AJ Richardson MJ Owen JF Stein ED Green MC O'Donovan J Williams AP Monaco 2006 Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia Mol Psychiatry 11 1085 1091 17033633 10.1038/sj.mp. 4001904 (Pubitemid 44863433)
-
(2006)
Molecular Psychiatry
, vol.11
, Issue.12
, pp. 1085-1091
-
-
Harold, D.1
Paracchini, S.2
Scerri, T.3
Dennis, M.4
Cope, N.5
Hill, G.6
Moskvina, V.7
Walter, J.8
Richardson, A.J.9
Owen, M.J.10
Stein, J.F.11
Green, E.D.12
O'Donovan, M.C.13
Williams, J.14
Monaco, A.P.15
-
61
-
-
0041918341
-
Four cases of congenital word-blindness occuring in the same family
-
10.1136/bmj.1.2620.608
-
J Hinshelwood 1907 Four cases of congenital word-blindness occuring in the same family Br Med J 1 608 609 10.1136/bmj.1.2620.608
-
(1907)
Br Med J
, vol.1
, pp. 608-609
-
-
Hinshelwood, J.1
-
62
-
-
0036808179
-
The Australian Twin Registry
-
DOI 10.1375/136905202320906048
-
JL Hopper 2002 The Australian Twin Registry Twin Res 5 329 336 12537854 10.1375/136905202320906048 (Pubitemid 35315479)
-
(2002)
Twin Research
, vol.5
, Issue.5
, pp. 329-336
-
-
Hopper, J.L.1
-
64
-
-
30344454660
-
Genomewide scan for real-word reading subphenotypes of dyslexia: Novel chromosome 13 locus and genetic complexity
-
DOI 10.1002/ajmg.b.30245
-
RPJ Igo NH Chapman VW Berninger M Matsushita Z Brkanac JH Rothstein T Holzman K Nielsen WH Raskind EM Wijsman 2006 Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity Am J Med Genet (Neuropsychiatr Genet) 141 15 27 (Pubitemid 43062537)
-
(2006)
American Journal of Medical Genetics - Neuropsychiatric Genetics
, vol.141 B
, Issue.1
, pp. 15-27
-
-
Igo Jr., R.P.1
Chapman, N.H.2
Berninger, V.W.3
Matsushita, M.4
Brkanac, Z.5
Rothstein, J.H.6
Holzman, T.7
Nielsen, K.8
Raskind, W.H.9
Wijsman, E.M.10
-
67
-
-
0038577166
-
A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32
-
N Kaminen K Hannula-Jouppi M Kestila P Lahermo K Muller M Kaaranen B Myllyluoma A Voutilainen H Lyytinen J Nopola-Hemmi J Kere 2003 A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32 J Med Genet 40 340 345 12746395 10.1136/jmg.40.5.340 (Pubitemid 36613470)
-
(2003)
Journal of Medical Genetics
, vol.40
, Issue.5
, pp. 340-345
-
-
Kaminen, N.1
Hannula-Jouppi, K.2
Kestila, M.3
Lahermo, P.4
Muller, K.5
Kaaranen, M.6
Myllyluoma, B.7
Voutilainen, A.8
Lyytinen, H.9
Nopola-Hemmi, J.10
Kere, J.11
-
68
-
-
18344374003
-
Evidence for linkage and association with reading disability, on 6p21.3-22
-
DOI 10.1086/340449
-
DE Kaplan J Gayán J Ahn T-W Won D Pauls RK Olson JC DeFries F Wood BF Pennington GP Page SD Smith JR Gruen 2002 Evidence for linkage and association with reading disability, on 6p21.3-22 Am J Hum Genet 70 1287 1298 11951179 10.1086/340449 (Pubitemid 34450578)
-
(2002)
American Journal of Human Genetics
, vol.70
, Issue.5
, pp. 1287-1298
-
-
Kaplan, D.E.1
Gayan, J.2
Ahn, J.3
Won, T.-W.4
Pauls, D.5
Olson, R.K.6
DeFries, J.C.7
Wood, F.8
Pennington, B.F.9
Page, G.P.10
Smith, S.D.11
Gruen, J.R.12
-
70
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
7581446 10.1038/ng1195-241
-
E Lander L Kruglyak 1995 Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results Nat Genet 11 241 247 7581446 10.1038/ng1195-241
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
71
-
-
0031155426
-
The impact of orthographic consistency on dyslexia: A German-English comparison
-
PII S001002779700005X
-
K Landerl H Wimmer U Frith 1997 The impact of orthographic consistency on dyslexia: a German-English comparison Cognition 63 315 334 9265873 10.1016/S0010-0277(97)00005-X (Pubitemid 127432167)
-
(1997)
Cognition
, vol.63
, Issue.3
, pp. 315-334
-
-
Landerl, K.1
Wimmer, H.2
Frith, U.3
-
72
-
-
41549126540
-
On the replication of genetic associations: Timing can be everything!
-
18387595 10.1016/j.ajhg.2008.01.018
-
J Lasky-Su HN Lyon V Emilsson IM Heid C Molony BA Raby R Lazarus B Klanderman ME Soto-Quiros L Avila EK Silverman G Thorleifsson U Thorsteinsdottir F Kronenberg C Vollmert T Illig CS Fox D Levy N Laird X Ding MB McQueen J Butler K Ardlie C Papoutsakis G Dedoussis CJ O'Donnell HE Wichmann JC Celedón E Schadt J Hirschhorn ST Weiss K Stefansson C Lange 2008 On the replication of genetic associations: timing can be everything! Am J Hum Genet 82 849 858 18387595 10.1016/j.ajhg.2008.01.018
-
(2008)
Am J Hum Genet
, vol.82
, pp. 849-858
-
-
Lasky-Su, J.1
Lyon, H.N.2
Emilsson, V.3
Heid, I.M.4
Molony, C.5
Raby, B.A.6
Lazarus, R.7
Klanderman, B.8
Soto-Quiros, M.E.9
Avila, L.10
Silverman, E.K.11
Thorleifsson, G.12
Thorsteinsdottir, U.13
Kronenberg, F.14
Vollmert, C.15
Illig, T.16
Fox, C.S.17
Levy, D.18
Laird, N.19
Ding, X.20
McQueen, M.B.21
Butler, J.22
Ardlie, K.23
Papoutsakis, C.24
Dedoussis, G.25
O'Donnell, C.J.26
Wichmann, H.E.27
Celedón, J.C.28
Schadt, E.29
Hirschhorn, J.30
Weiss, S.T.31
Stefansson, K.32
Lange, C.33
more..
-
73
-
-
77952673657
-
Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample
-
20068590 10.1038/ejhg.2009.237
-
PA Lind M Luciano MJ Wright GW Montgomery NG Martin TC Bates 2010 Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample Eur J Hum Genet 18 668 673 20068590 10.1038/ejhg.2009.237
-
(2010)
Eur J Hum Genet
, vol.18
, pp. 668-673
-
-
Lind, P.A.1
Luciano, M.2
Wright, M.J.3
Montgomery, G.W.4
Martin, N.G.5
Bates, T.C.6
-
75
-
-
0942279598
-
A Genetic Investigation of the Covariation among Inspection Time, Choice Reaction Time, and IQ Subtest Scores
-
DOI 10.1023/B:BEGE.0000009475.35287.9d
-
M Luciano MJ Wright GM Geffen LB Geffen GA Smith NG Martin 2004 A genetic investigation of the covariation among inspection time, choice reaction time, and IQ subtest scores Behav Genet 34 41 50 14739695 10.1023/B:BEGE.0000009475. 35287.9d (Pubitemid 38141751)
-
(2004)
Behavior Genetics
, vol.34
, Issue.1
, pp. 41-50
-
-
Luciano, M.1
Wright, M.J.2
Geffen, G.M.3
Geffen, L.B.4
Smith, G.A.5
Martin, N.G.6
-
76
-
-
33846319378
-
Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins
-
DOI 10.1002/ajmg.b.30413
-
M Luciano E Hine MJ Wright DL Duffy J MacMillan NG Martin 2007 Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins Am J Med Genet (Neuropsychiatr Genet) 144B 95 100 10.1002/ajmg.b.30413 (Pubitemid 46122644)
-
(2007)
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
, vol.144
, Issue.1
, pp. 95-100
-
-
Luciano, M.1
Hine, E.2
Wright, M.J.3
Duffy, D.L.4
MacMillan, J.5
Martin, N.G.6
-
77
-
-
34548473808
-
A Haplotype Spanning KIAA0319 and TTRAP Is Associated with Normal Variation in Reading and Spelling Ability
-
DOI 10.1016/j.biopsych.2007.03.007, PII S000632230700234X, Molecular Mechanisms, Brain Development, and Novel Treatment Mechanisms for Schizophrenia
-
M Luciano PA Lind DL Duffy A Castles MJ Wright GW Montgomery NG Martin TC Bates 2007 A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability Biol Psychiatry 62 811 817 17597587 10.1016/j.biopsych.2007.03.007 (Pubitemid 47374651)
-
(2007)
Biological Psychiatry
, vol.62
, Issue.7
, 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
Martin, N.G.7
Bates, T.C.8
-
78
-
-
55349131289
-
Investigation of interaction between DCDC2, KIAA0319 in a large German dyslexia sample
-
18810304 10.1007/s00702-008-0124-6
-
K Ludwig D Roeske J Schumacher G Schulte-Körne I König A Warnke E Plume A Ziegler H Remschmidt B Müller-Myhsok M Nöthen P Hoffmann 2008 Investigation of interaction between DCDC2, KIAA0319 in a large German dyslexia sample J Neural Transm 115 1587 1589 18810304 10.1007/s00702-008-0124-6
-
(2008)
J Neural Transm
, vol.115
, pp. 1587-1589
-
-
Ludwig, K.1
Roeske, D.2
Schumacher, J.3
Schulte-Körne, G.4
König, I.5
Warnke, A.6
Plume, E.7
Ziegler, A.8
Remschmidt, H.9
Müller-Myhsok, B.10
Nöthen, M.11
Hoffmann, P.12
-
79
-
-
57149129848
-
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample
-
19018237 10.1097/YPG.0b013e3283063a78
-
KU Ludwig J Schumacher G Schulte-Körne I König A Warnke E Plume H Anthoni M Peyrard-Janvid H Meng A Ziegler H Remschmidt J Kere J Gruen B Müller-Myhsok M Nöthen P Hoffmann 2008 Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample Psychiatr Genet 18 310 312 19018237 10.1097/YPG.0b013e3283063a78
-
(2008)
Psychiatr Genet
, vol.18
, pp. 310-312
-
-
Ludwig, K.U.1
Schumacher, J.2
Schulte-Körne, G.3
König, I.4
Warnke, A.5
Plume, E.6
Anthoni, H.7
Peyrard-Janvid, M.8
Meng, H.9
Ziegler, A.10
Remschmidt, H.11
Kere, J.12
Gruen, J.13
Müller-Myhsok, B.14
Nöthen, M.15
Hoffmann, P.16
-
80
-
-
77349127347
-
Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia
-
KU Ludwig D Roeske S Kerms J Schumacher A Warnke E Plume N Neuhoff J Bruder H Remschmidt G Schulte-Körne B Müller-Myhsok MM Nöthen P Hoffmann 2010 Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia Am J Med Genet (Neuropsychiatr Genet) B153 503 511
-
(2010)
Am J Med Genet (Neuropsychiatr Genet)
, vol.153
, pp. 503-511
-
-
Ludwig, K.U.1
Roeske, D.2
Kerms, S.3
Schumacher, J.4
Warnke, A.5
Plume, E.6
Neuhoff, N.7
Bruder, J.8
Remschmidt, H.9
Schulte-Körne, G.10
Müller-Myhsok, B.11
Nöthen, M.M.12
Hoffmann, P.13
-
81
-
-
0041370144
-
No evidence for association and linkage disequilibrium between dyslexia and markers of four dopamine-related genes
-
DOI 10.1007/s00787-003-0332-4
-
C Marino R Giorda L Vanzin M Molteni ML Lorusso M Nobile C Baschirotto M Alda M Battaglia 2003 No evidence for association and linkage disequilibrium between dyslexia and markers of four dopamine-related genes Eur Child Adolesc Psychiatry 12 198 202 14505070 10.1007/s00787-003-0332-4 (Pubitemid 36903189)
-
(2003)
European Child and Adolescent Psychiatry
, vol.12
, Issue.4
, pp. 198-202
-
-
Marino, C.1
Giorda, R.2
Vanzin, L.3
Molteni, M.4
Lorusso, M.L.5
Nobile, M.6
Baschirotto, C.7
Alda, M.8
Battaglia, M.9
-
82
-
-
1642574231
-
A locus on 15q15-15qter influences dyslexia: Further support from a transmission/disequilibrium study in an Italian speaking population
-
C Marino R Giorda L Vanzin M Nobile ML Lorusso C Baschirotto L Riva M Molteni M Battaglia 2004 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 14729831 10.1136/jmg.2003.010603 (Pubitemid 38125686)
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.1
, pp. 42-46
-
-
Marino, C.1
Giorda, R.2
Vanzin, L.3
Nobile, M.4
Lorusso, M.L.5
Baschirotto, C.6
Riva, L.7
Molteni, M.8
Battaglia, M.9
-
83
-
-
20244377078
-
A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia
-
DOI 10.1038/sj.ejhg.5201356
-
C Marino R Giorda ML Lorusso L Vanzin N Salandi M Nobile M Battaglia M Molteni 2005 A family-based association study of the DYX1C1 gene on 15q21.1 in developmental dyslexia Eur J Hum Genet 13 491 499 15702132 10.1038/sj.ejhg. 5201356 (Pubitemid 40520941)
-
(2005)
European Journal of Human Genetics
, vol.13
, Issue.4
, pp. 491-499
-
-
Marino, C.1
Giorda, R.2
Lorusso, M.L.3
Vanzin, L.4
Salandi, N.5
Nobile, M.6
Citterio, A.7
Beri, S.8
Crespi, V.9
Battaglia, M.10
Molteni, M.11
-
84
-
-
34748875368
-
Association of short-term memory with a variant within DYX1C1 in developmental dyslexia
-
DOI 10.1111/j.1601-183X.2006.00291.x
-
C Marino A Citterio R Giorda A Facoetti G Menozzi L Vanzin ML Lorusso M Nobile M Molteni 2007 Association of short-term memory with a variant within DYX1C1 in developmental dyslexia Genes Brain Behav 6 640 646 17309662 10.1111/j.1601-183X.2006.00291.x (Pubitemid 47476184)
-
(2007)
Genes, Brain and Behavior
, 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
-
85
-
-
79952442429
-
Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia
-
this issue
-
Marino C, Mascheretti S, Riva V, Cattaneo F, Rigoletto C, Rusconi M, Gruen JF, Giorda R, Lazazzera C, Molteni M (2011) Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia. Behav Genet this issue
-
(2011)
Behav Genet
-
-
Marino, C.1
Mascheretti, S.2
Riva, V.3
Cattaneo, F.4
Rigoletto, C.5
Rusconi, M.6
Gruen, J.F.7
Giorda, R.8
Lazazzera, C.9
Molteni, M.10
-
86
-
-
0034863552
-
Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK
-
DOI 10.1023/A:1010209629021
-
AJ Marlow SE Fisher AJ Richardson C Francks JB Talcott AP Monaco JF Stein LR Cardon 2001 Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK Behav Genet 31 219 230 11545538 10.1023/A:1010209629021 (Pubitemid 32801383)
-
(2001)
Behavior Genetics
, vol.31
, Issue.2
, 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
Stein, J.F.7
Cardon, L.R.8
-
87
-
-
0037371605
-
Use of multivariate linkage analysis for dissection of a complex cognitive trait
-
DOI 10.1086/368201
-
AJ Marlow SE Fisher C Francks IL MacPhie SS Cherny AJ Richardson JB Talcott JF Stein AP Monaco LR Cardon 2003 Use of multivariate linkage analysis for dissection of a complex cognitive trait Am J Hum Genet 72 561 570 12587094 10.1086/368201 (Pubitemid 36255955)
-
(2003)
American Journal of Human Genetics
, vol.72
, Issue.3
, 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
Talcott, J.B.7
Stein, J.F.8
Monaco, A.P.9
Cardon, L.R.10
-
89
-
-
79952448889
-
SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations
-
doi: 10.1007/s10519-010-9431-4
-
Matsson H, Tammimies K, Zucchelli M, Anthoni H, Onkamo P, Nopola-Hemmi J, Lyytinen H, Leppanen PHT, Neuhoff N, Warnke A, Schulte-Körne G, Schumacher J, Nöthen MM, Kere J, Peyrard-Janvid M (2011) SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations. Behav Genet. doi: 10.1007/s10519-010-9431-4
-
(2011)
Behav Genet
-
-
Matsson, H.1
Tammimies, K.2
Zucchelli, M.3
Anthoni, H.4
Onkamo, P.5
Nopola-Hemmi, J.6
Lyytinen, H.7
Pht, L.8
Neuhoff, N.9
Warnke, A.10
Schulte-Körne, G.11
Schumacher, J.12
Nöthen, M.M.13
Kere, J.14
Peyrard-Janvid, M.15
-
90
-
-
42349112088
-
Genome-wide association studies for complex traits: Consensus, uncertainty and challenges
-
DOI 10.1038/nrg2344, PII NRG2344
-
MI McCarthy GR Abecasis LR Cardon DB Goldstein J Little JPA Ioannidis JN Hirschhorn 2008 Genome-wide association studies for complex traits: consensus, uncertainty and challenges Nat Rev Genet 9 356 369 18398418 10.1038/nrg2344 (Pubitemid 351556063)
-
(2008)
Nature Reviews Genetics
, vol.9
, Issue.5
, pp. 356-369
-
-
McCarthy, M.I.1
Abecasis, G.R.2
Cardon, L.R.3
Goldstein, D.B.4
Little, J.5
Ioannidis, J.P.A.6
Hirschhorn, J.N.7
-
91
-
-
45549087414
-
Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children
-
DOI 10.1038/sj.mp.4002063, PII 4002063
-
E Meaburn N Harlaar I Craig L Schalkwyk R Plomin 2008 Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100 K SNP microarrays in a sample of 5760 children Mol Psychiatry 13 729 740 17684495 10.1038/sj.mp.4002063 (Pubitemid 351861530)
-
(2008)
Molecular Psychiatry
, vol.13
, Issue.7
, pp. 729-740
-
-
Meaburn, E.L.1
Harlaar, N.2
Craig, I.W.3
Schalkwyk, L.C.4
Plomin, R.5
-
92
-
-
33744733429
-
TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort
-
16133186 10.1007/s00439-005-0017-9
-
H Meng K Hager M Held GP Page RK Olson BF Pennington JC DeFries SD Smith JR Gruen 2005 TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort Hum Genet 118 87 90 16133186 10.1007/s00439-005-0017-9
-
(2005)
Hum Genet
, vol.118
, 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
-
93
-
-
28044465597
-
DCDC2 is associated with reading disability and modulates neuronal development in the brain
-
DOI 10.1073/pnas.0508591102
-
H Meng SD Smith K Hager M Held J Liu RK Olson BF Pennington JC DeFries J Gelernter T O'Reilly-Pol S Somlo P Skudlarski SE Shaywitz BA Shaywitz K Marchione Y Wang M Paramasivam JJ LoTurco GP Page JR Gruen 2005 DCDC2 is associated with reading disability and modulates neuronal development in the brain PNAS 102 17053 17058 16278297 10.1073/pnas.0508591102 (Pubitemid 41692682)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, 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
DeFriess, 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..
-
94
-
-
78651111073
-
Moving closer to a public health model of language and learning disabilities: The role of genetics and the search for etiologies
-
this issue
-
Miller B, McCardle P (2011) Moving closer to a public health model of language and learning disabilities: the role of genetics and the search for etiologies. Behav Genet this issue
-
(2011)
Behav Genet
-
-
Miller, B.1
McCardle, P.2
-
95
-
-
0001125623
-
A case of congenital word-blindness (inability to learn to read)
-
WP Morgan 1896 A case of congenital word-blindness (inability to learn to read) Br Med J 2 1543 1544
-
(1896)
Br Med J
, vol.2
, pp. 1543-1544
-
-
Morgan, W.P.1
-
96
-
-
0034701254
-
Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q
-
DW Morris L Robinson D Turic M Duke V Webb C Milham E Hopkin K Pound S Ferrnando M Easton M Hamshere N Williams P McGuffin MJ Owen MC O'Donovan J Williams 2000 Family-based association mapping provides evidence for reading disability on chromosome 15q Hum Mol Genet 9 843 848 10749993 10.1093/hmg/9.5.843 (Pubitemid 30162770)
-
(2000)
Human Molecular Genetics
, vol.9
, Issue.5
, pp. 843-848
-
-
Morris, D.W.1
Robinson, L.2
Turic, D.3
Duke, M.4
Webb, V.5
Milham, C.6
Hopkin, E.7
Pound, K.8
Fernando, S.9
Easton, M.10
Hamshere, M.11
Williams, N.12
McGuffin, P.13
Stevenson, J.14
Krawczak, M.15
Owen, M.J.16
O'Donovan, M.C.17
Williams, J.18
-
97
-
-
3342917210
-
Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1-15.3 region associated with reading disability
-
DW Morris D Ivanov L Robinson N Williams J Stevenson MJ Owen J Williams MC O'Donovan 2004 Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1-15.3 region associated with reading disability Am J Med Genet B129 97 103 10.1002/ajmg.b.30033 (Pubitemid 38989077)
-
(2004)
American Journal of Medical Genetics - Neuropsychiatric Genetics
, vol.129 B
, Issue.1
, pp. 97-103
-
-
Morris, D.W.1
Ivanov, D.2
Robinson, L.3
Williams, N.4
Stevenson, J.5
Owen, M.J.6
Williams, J.7
O'Donovan, M.C.8
-
101
-
-
79952443636
-
Investigation of dyslexia and SLI risk-variants in reading- and language-impaired subjects
-
this issue
-
Newbury DF, Paracchini S, Scerri TS, Winchester L, Addis L, Walter J, Stein JF, Talcott JB, Monaco AP (2011) Investigation of dyslexia and SLI risk-variants in reading- and language-impaired subjects. Behav Genet this issue
-
(2011)
Behav Genet
-
-
Newbury, D.F.1
Paracchini, S.2
Scerri, T.S.3
Winchester, L.4
Addis, L.5
Walter, J.6
Stein, J.F.7
Talcott, J.B.8
Monaco, A.P.9
-
103
-
-
0034785618
-
A dominant gene for developmental dyslexia on chromosome 3
-
J Nopola-Hemmi B Myllyluoma T Haltia M Taipale V Ollikainen T Ahonen A Voutilainen J Kere E Widen 2001 A dominant gene for developmental dyslexia on chromosome 3 J Med Genet 38 658 664 11584043 10.1136/jmg.38.10.658 (Pubitemid 32946786)
-
(2001)
Journal of Medical Genetics
, vol.38
, Issue.10
, pp. 658-664
-
-
Nopola-Hemmi, J.1
Myllyluoma, B.2
Haltia, T.3
Taipale, M.4
Ollikainen, V.5
Ahonen, T.6
Voutilainen, A.7
Kere, J.8
Widen, E.9
-
104
-
-
0344496507
-
Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15
-
10638372 10.1007/PL00010696
-
MM Nöthen G Schulte-Körne T Grimm S Cichon IR Vogt B Muller-Myhsok P Propping H Remschmidt 1999 Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15 Eur Child Adolesc Psychiatry 8 56 59 10638372 10.1007/PL00010696
-
(1999)
Eur Child Adolesc Psychiatry
, vol.8
, pp. 56-59
-
-
Nöthen, M.M.1
Schulte-Körne, G.2
Grimm, T.3
Cichon, S.4
Vogt, I.R.5
Muller-Myhsok, B.6
Propping, P.7
Remschmidt, H.8
-
105
-
-
33947284340
-
Twins' Early Development Study (TEDS): A multivariate, longitudinal genetic investigation of language, cognition and behavior problems from childhood through adolescence
-
DOI 10.1375/twin.10.1.96
-
B Oliver R Plomin 2007 Twins Early Development Study (TEDS): a multivariate, longitudinal genetic investigation of language, cognition and behavior problems from childhood through adolescence Twin Res Hum Genet 10 96 105 17539369 10.1375/twin.10.1.96 (Pubitemid 46423380)
-
(2007)
Twin Research and Human Genetics
, vol.10
, Issue.1
, pp. 96-105
-
-
Oliver, B.R.1
Plomin, R.2
-
106
-
-
0002098551
-
Individual and developmental differences in reading disability
-
G.E. MacKinnon T.G. Waller (eds). Academic Press New York, NY
-
Olson RK, Kliegl R, Davidson BJ, Foltz G (1985) Individual and developmental differences in reading disability. In: MacKinnon GE, Waller TG (eds) Reading research: advances in theory and practice. Academic Press, New York, NY, pp 1-64
-
(1985)
Reading Research: Advances in Theory and Practice
, pp. 1-64
-
-
Olson, R.K.1
Kliegl, R.2
Davidson, B.J.3
Foltz, G.4
-
107
-
-
0024689078
-
Specific deficits in component reading and language skills: Genetic and environmental influences
-
2738467 10.1177/002221948902200604
-
RK Olson BW Wise F Conners J Rack D Fulker 1989 Specific deficits in component reading and language skills: genetic and environmental influences J Learn Disabil 22 339 348 2738467 10.1177/002221948902200604
-
(1989)
J Learn Disabil
, vol.22
, pp. 339-348
-
-
Olson, R.K.1
Wise, B.W.2
Conners, F.3
Rack, J.4
Fulker, D.5
-
108
-
-
0002823885
-
Genes, environment, and the development of orthographic skills
-
V.W. Berninger (eds). Kluwer Dordrecht
-
Olson RK, Forsberg H, Wise B (1994) Genes, environment, and the development of orthographic skills. In: Berninger VW (ed) The varieties of orthographic knowledge I: theoretical and developmental issues. Kluwer, Dordrecht, pp 27-71
-
(1994)
The Varieties of Orthographic Knowledge I: Theoretical and Developmental Issues
, pp. 27-71
-
-
Olson, R.K.1
Forsberg, H.2
Wise, B.3
-
109
-
-
57349157021
-
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population
-
18829873 10.1176/appi.ajp.2008.07121872
-
S Paracchini CD Steer LL Buckingham AP Morris S Ring TS Scerri J Stein ME Pembrey J Ragoussis J Golding A Monaco 2008 Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population Am J Psychiatry 165 1576 1584 18829873 10.1176/appi.ajp.2008.07121872
-
(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.S.6
Stein, J.7
Pembrey, M.E.8
Ragoussis, J.9
Golding, J.10
Monaco, A.11
-
110
-
-
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
-
DOI 10.1086/302764
-
TL Petryshen BJ Kaplan MF Liu LL Field 2000 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 66 708 714 10677330 10.1086/302764 (Pubitemid 30468848)
-
(2000)
American Journal of Human Genetics
, vol.66
, Issue.2
, pp. 708-714
-
-
Petryshen, T.L.1
Kaplan, B.J.2
Liu, M.F.3
Field, L.L.4
-
111
-
-
0035828096
-
Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia
-
DOI 10.1002/ajmg.1475
-
TL Petryshen BJ Kaplan MF Liu NS de French R Tobias ML Hughes LL Field 2001 Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia Am J Med Genet 105 507 517 11496366 10.1002/ajmg.1475 (Pubitemid 32729817)
-
(2001)
American Journal of Medical Genetics - Neuropsychiatric Genetics
, vol.105
, Issue.6
, pp. 507-517
-
-
Petryshen, T.L.1
Kaplan, B.J.2
Liu, M.F.3
De French, N.S.4
Tobias, R.5
Hughes, M.L.6
Leigh Field, L.7
-
113
-
-
2542498767
-
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene
-
DOI 10.1007/s00439-004-1103-0
-
M Peyrard-Janvid H Anthoni P Onkamo P Lahermo M Zucchelli N Kaminen K Hannula-Jouppi J Nopola-Hemmi A Voutilainen H Lyytinen J Kere 2004 Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene Hum Genet 114 510 516 15007729 10.1007/s00439-004-1103-0 (Pubitemid 38678931)
-
(2004)
Human Genetics
, vol.114
, Issue.5
, pp. 510-516
-
-
Peyrard-Janvid, M.1
Anthoni, H.2
Onkamo, P.3
Lahermo, P.4
Zucchelli, M.5
Kaminen, N.6
Hannula-Jouppi, K.7
Nopola-Hemmi, J.8
Voutilainen, A.9
Lyytinen, H.10
Kere, J.11
-
114
-
-
55349100227
-
Association of reading disability on chromosome 6p22 in the Afrikaner population
-
10.1002/ajmg.b.30774
-
J Platko F Wood I Pelser M Meyer G Gericke J O'Rourke J Birns S Purcell DL Pauls 2008 Association of reading disability on chromosome 6p22 in the Afrikaner population Am J Med Genet (Neuropsychiatr Genet) 147B 1278 1287 10.1002/ajmg.b.30774
-
(2008)
Am J Med Genet (Neuropsychiatr Genet)
, vol.147
, pp. 1278-1287
-
-
Platko, J.1
Wood, F.2
Pelser, I.3
Meyer, M.4
Gericke, G.5
O'Rourke, J.6
Birns, J.7
Purcell, S.8
Pauls, D.L.9
-
115
-
-
58849148546
-
Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion
-
18521840 10.1002/ajmg.b.30787
-
G Poelmans JJ Engelen J Van Lent-Albrechts HJ Smeets E Schoenmakers B Franke JK Buitelaar M Wuisman-Frerker W Erens J Steyaert C Schrander-Stumpel 2009 Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion Am J Med Genet B Neuropsychiatr Genet 150B 1 140 147 18521840 10.1002/ajmg.b.30787
-
(2009)
Am J Med Genet B Neuropsychiatr Genet
, vol.150
, Issue.1
, pp. 140-147
-
-
Poelmans, G.1
Engelen, J.J.2
Van Lent-Albrechts, J.3
Smeets, H.J.4
Schoenmakers, E.5
Franke, B.6
Buitelaar, J.K.7
Wuisman-Frerker, M.8
Erens, W.9
Steyaert, J.10
Schrander-Stumpel, C.11
-
116
-
-
36549056933
-
What phonological deficit?
-
10.1080/17470210701508822
-
F Ramus G Szenkovits 2008 What phonological deficit? Q J Exp Psychol 61 129 141 10.1080/17470210701508822
-
(2008)
Q J Exp Psychol
, vol.61
, pp. 129-141
-
-
Ramus, F.1
Szenkovits, G.2
-
117
-
-
21844460777
-
A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency
-
DOI 10.1038/sj.mp.4001657
-
WH Raskind RPJ Igo NH Chapman VW Berninger JB Thomson M Matsushita Z Brkanac T Holzman M Brown EM Wijsman 2005 A genome scan in multigenerational families with dyslexia: identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency Mol Psychiatry 10 699 711 15753956 10.1038/sj.mp.4001657 (Pubitemid 40961740)
-
(2005)
Molecular Psychiatry
, vol.10
, Issue.7
, pp. 699-711
-
-
Raskind, W.H.1
Igo Jr., R.P.2
Chapman, N.H.3
Berninger, V.W.4
Thomson, J.B.5
Matsushita, M.6
Brkanac, Z.7
Holzman, T.8
Brown, M.9
Wijsman, E.M.10
-
120
-
-
0002229511
-
The Auditory Analysis Test: An initial report
-
10.1177/002221947100400706
-
J Rosner DP Simon 1971 The Auditory Analysis Test: an initial report J Learn Disabil 4 40 48 10.1177/002221947100400706
-
(1971)
J Learn Disabil
, vol.4
, pp. 40-48
-
-
Rosner, J.1
Simon, D.P.2
-
121
-
-
79952449113
-
Genome scan for spelling deficits: Effects of verbal IQ on models of transmission and trait gene localization
-
this issue
-
Rubenstein K, Matsushita M, Berninger VW, Raskind WH, Wijsman EM (2011) Genome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localization. Behav Genet this issue
-
(2011)
Behav Genet
-
-
Rubenstein, K.1
Matsushita, M.2
Berninger, V.W.3
Raskind, W.H.4
Wijsman, E.M.5
-
124
-
-
77950861146
-
Genetics of developmental dyslexia
-
20091194 10.1007/s00787-009-0081-0
-
TS Scerri G Schulte-Körne 2010 Genetics of developmental dyslexia Eur Child Adolesc Psychiatry 19 179 197 20091194 10.1007/s00787-009-0081-0
-
(2010)
Eur Child Adolesc Psychiatry
, vol.19
, pp. 179-197
-
-
Scerri, T.S.1
Schulte-Körne, G.2
-
125
-
-
8744255235
-
Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK
-
DOI 10.1136/jmg.2004.018341
-
TS Scerri SE Fisher C Francks IL MacPhie S Paracchini AJ Richardson JF Stein AP Monaco 2004 Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK J Med Genet 41 853 857 15520411 10.1136/jmg.2004.018341 (Pubitemid 39524313)
-
(2004)
Journal of Medical Genetics
, 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
-
127
-
-
0032231443
-
Evidence for linkage of spelling disability to chromosome 15 [6]
-
DOI 10.1086/301919
-
G Schulte-Körne T Grimm MM Nothen B Muller-Myhsok S Cichon IR Vogt P Propping H Remschmidt 1998 Evidence for linkage of spelling disability to chromosome 15 Am J Hum Genet 63 279 282 9634517 10.1086/301919 (Pubitemid 30428348)
-
(1998)
American Journal of Human Genetics
, vol.63
, Issue.1
, pp. 279-282
-
-
Schulte-Korne, G.1
Grimm, T.2
Nothen, M.M.3
Muller-Myhsok, B.4
Cichon, S.5
Vogt, I.R.6
Propping, P.7
Remschmidt, H.8
-
128
-
-
29244468273
-
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
-
DOI 10.1086/498992
-
J Schumacher H Anthoni F Dahdouh IR König HM Hillmer N Kluck M Manthey E Plume A Warnke H Remschmidt J Hülsmann S Cichon CM Lindgren P Propping M Zucchelli A Ziegler M Peyrard-Janvid G Schulte-Körne MM Nöthen J Kere 2006 Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia Am J Hum Genet 78 52 62 16385449 10.1086/498992 (Pubitemid 41833159)
-
(2006)
American Journal of Human Genetics
, vol.78
, Issue.1
, pp. 52-62
-
-
Schumacher, J.1
Anthoni, H.2
Dahdouh, F.3
Konig, I.R.4
Hillmer, A.M.5
Kluck, N.6
Manthey, M.7
Plume, E.8
Warnke, A.9
Remschmidt, H.10
Hulsmann, J.11
Cichon, S.12
Lindgren, C.M.13
Propping, P.14
Zucchelli, M.15
Ziegler, A.16
Peyrard-Janvid, M.17
Schulte-Korne, G.18
Nothen, M.M.19
Kere, J.20
more..
-
129
-
-
32044457133
-
Linkage analyses of chromosomal region 18p11-q12 in dyslexia
-
DOI 10.1007/s00702-005-0336-y
-
J Schumacher I König E Plume P Propping A Warnke M Manthey M Duell A Kleensang D Repsilber M Preis H Remschmidt A Ziegler MM Nöthen G Schulte-Körne 2006 Linkage analyses of chromosomal region 18p11-q12 in dyslexia J Neural Transm 113 417 423 16075186 10.1007/s00702-005-0336-y (Pubitemid 43201107)
-
(2006)
Journal of Neural Transmission
, vol.113
, Issue.3
, pp. 417-423
-
-
Schumacher, J.1
Konig, I.R.2
Plume, E.3
Propping, P.4
Warnke, A.5
Manthey, M.6
Duell, M.7
Kleensang, A.8
Repsilber, D.9
Preis, M.10
Remschmidt, H.11
Ziegler, A.12
Nothen, M.M.13
Schulte-Korne, G.14
-
131
-
-
49049110163
-
Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21
-
18496212 10.1097/YPG.0b013e3282fb7fc6
-
J Schumacher I König T Schröder M Duell E Plume P Propping A Warnke C Libertus A Ziegler B Müller-Myhsok G Schulte-Körne M Nöthen 2008 Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21 Psychiatr Genet 18 137 142 18496212 10.1097/YPG.0b013e3282fb7fc6
-
(2008)
Psychiatr Genet
, vol.18
, pp. 137-142
-
-
Schumacher, J.1
König, I.2
Schröder, T.3
Duell, M.4
Plume, E.5
Propping, P.6
Warnke, A.7
Libertus, C.8
Ziegler, A.9
Müller-Myhsok, B.10
Schulte-Körne, G.11
Nöthen, M.12
-
132
-
-
0020622130
-
Specific reading disability: Identifiction of an inherited form through linkage analysis
-
SD Smith WJ Kimberling BF Pennington HA Lubs 1983 Specific reading disability: identification of an inherited form through linkage analyses Science 219 1345 1347 6828864 10.1126/science.6828864 (Pubitemid 13109173)
-
(1983)
Science
, vol.219
, Issue.4590
, pp. 1345-1347
-
-
Smith, S.D.1
Kimberling, W.J.2
Pennington, B.F.3
Lubs, H.A.4
-
134
-
-
0001328240
-
Six cases of congenital word-blindness affecting three generations of one family
-
S Stephenson 1907 Six cases of congenital word-blindness affecting three generations of one family Ophthalmoscope 5 482 484
-
(1907)
Ophthalmoscope
, vol.5
, pp. 482-484
-
-
Stephenson, S.1
-
135
-
-
0141482054
-
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain
-
DOI 10.1073/pnas.1833911100
-
M Taipale N Kaminen J Nopola-Hemmi T Haltia B Myllyluoma H Lyytinen K Muller M Kaaranen P Lindsberg K Hannula-Jouppi J Kere 2003 A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain PNAS 20 11553 11558 10.1073/pnas.1833911100 (Pubitemid 37205974)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, 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
-
137
-
-
0037219324
-
Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22
-
DOI 10.1038/sj.mp.4001216
-
D Turic L Robinson M Duke DW Morris V Webb M Hamshere C Milham E Hopkin K Pound S Fernando A Grierson M Easton N Williams M Van Den Bree R Chowdhury J Gruen J Stevenson M Krawczak MJ Owen MC O'Donovan J Williams 2003 Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22 Mol Psychiatry 8 176 185 12610650 10.1038/sj.mp.4001216 (Pubitemid 36315226)
-
(2003)
Molecular Psychiatry
, vol.8
, Issue.2
, pp. 176-185
-
-
Turic, D.1
Robinson, L.2
Duke, M.3
Morris, D.W.4
Webb, V.5
Hamshere, M.6
Milham, C.7
Hopkin, E.8
Pound, K.9
Fernando, S.10
Grierson, A.11
Easton, M.12
Williams, N.13
Van Den Bree, M.14
Chowdhury, R.15
Gruen, J.16
Stevenson, J.17
Krawcza, M.18
Owen, M.J.19
O'Donovan, M.C.20
Williams, J.21
more..
-
142
-
-
0031136030
-
Changing causal relations between phonological processing abilities and word-level reading as children develop from beginning to fluent readers: A five-year longitudinal study
-
9149925 10.1037/0012-1649.33.3.468
-
RK Wagner JK Torgesen CA Rashotte SA Hecht TA Barker SR Burgess CA Donahue T Garon 1997 Changing causal relations between phonological processing abilities and word-level reading as children develop from beginning to fluent readers: a five-year longitudinal study Dev Psychol 33 468 479 9149925 10.1037/0012-1649.33.3.468
-
(1997)
Dev Psychol
, vol.33
, pp. 468-479
-
-
Wagner, R.K.1
Torgesen, J.K.2
Rashotte, C.A.3
Hecht, S.A.4
Barker, T.A.5
Burgess, S.R.6
Donahue, C.A.7
Garon, T.8
-
146
-
-
0012348429
-
-
3 The Psychological Corporation Ltd., Harcourt Brace & Co. London, UK
-
Wechsler D (1992) WISC III U.K, 3rd edn. The Psychological Corporation Ltd., Harcourt Brace & Co., London, UK
-
(1992)
WISC III U.K
-
-
Wechsler, D.1
-
147
-
-
19944428926
-
Support for EKN1 as the susceptibility locus for dyslexia on 15q21
-
DOI 10.1038/sj.mp.4001543
-
KG Wigg JM Couto Y Feng T Anderson D Cate-Carter F Macciardi R Tannock MW Lovett TW Humphries CL Barr 2004 Support for EKN1 as the susceptibility locus for dyslexia on 15q21 Mol Psychiatry 9 1111 1121 15249932 10.1038/sj.mp.4001543 (Pubitemid 40065456)
-
(2004)
Molecular 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
-
150
-
-
0030074350
-
The nonword reading deficit in developmental dyslexia: Evidence from children learning to read German
-
DOI 10.1006/jecp.1996.0004
-
H Wimmer 1996 The nonword reading deficit in developmental dyslexia: evidence from children learning to read German J Exp Child Psychol 61 80 90 8812031 10.1006/jecp.1996.0004 (Pubitemid 126385030)
-
(1996)
Journal of Experimental Child Psychology
, vol.61
, Issue.1
, pp. 80-90
-
-
Wimmer, H.1
-
154
-
-
4544359744
-
Brisbane adolescent twin study: Outline of study methods and research projects
-
DOI 10.1080/00049530410001734865
-
M Wright N Martin 2004 Brisbane Adolescent Twin Study: outline of study methods and research projects Aust J Psychol 56 65 78 10.1080/ 00049530410001734865 (Pubitemid 39216642)
-
(2004)
Australian Journal of Psychology
, vol.56
, Issue.2
, pp. 65-78
-
-
Wright, M.J.1
Martin, N.G.2
|