-
1
-
-
4544338684
-
Behaviour genetic analyses of reading and spelling: A component processes approach
-
DOI 10.1080/00049530410001734847
-
Bates, T. C., Castles, A., Coltheart, M., Gillespie, N., Wright, M., & Martin, N. G. (2004). Behaviour genetic analyses of reading and spelling: a component processes approach. Australian Journal of Psychology, 56, 115-126. (Pubitemid 39216646)
-
(2004)
Australian Journal of Psychology
, vol.56
, Issue.2
, pp. 115-126
-
-
Bates, T.C.1
Castles, A.2
Coltheart, M.3
Gillespie, N.4
Wright, M.5
Martin, N.G.6
-
2
-
-
78650241792
-
Dyslexia and DYX1C1: Deficits in reading and spelling associated with a missense mutation
-
Bates, T. C., Lind, P. A., Luciano, M., Montgomery, G. W., Martin, N. G., & Wright, M. J. (2010a). Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation. Molecular Psychiatry, 15, 1190-1196.
-
(2010)
Molecular 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
-
3
-
-
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
-
Bates, T. C., Luciano, M., Castles, A., Coltheart, M., Wright, M. J., & Martin, N. G. (2007). Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17. European Journal of Human Genetics, 15, 194-203. (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
-
4
-
-
79957643838
-
Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits
-
Bates, T. C., Luciano, M., Medland, S. E., Montgomery, G. W., Wright, M. J., & Martin, N. G. (2010b). Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. Behavior Genetics.
-
(2010)
Behavior Genetics
-
-
Bates, T.C.1
Luciano, M.2
Medland, S.E.3
Montgomery, G.W.4
Wright, M.J.5
Martin, N.G.6
-
5
-
-
58049202750
-
Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels
-
Benyamin, B., McRae, A. F., Zhu, G., Gordon, S., Henders, A. K., Palotie, A., Peltonen, L., Martin, N. G., Montgomery, G. W., Whitfield, J. B., & Visscher, P. M. (2009). Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. American Journal of Human Genetics, 84, 60-65.
-
(2009)
American Journal of Human Genetics
, vol.84
, pp. 60-65
-
-
Benyamin, B.1
McRae, A.F.2
Zhu, G.3
Gordon, S.4
Henders, A.K.5
Palotie, A.6
Peltonen, L.7
Martin, N.G.8
Montgomery, G.W.9
Whitfield, J.B.10
Visscher, P.M.11
-
6
-
-
0028030006
-
Quantitative trait locus for reading disability on chromosome 6
-
Cardon, L. R., Smith, S. D., Fulker, D. W., Kimberling, W. J., Pennington, B. F., & DeFries, J. C. (1994). Quantitative trait locus for reading disability on chromosome 6. Science, 266, 276-279. (Pubitemid 24343512)
-
(1994)
Science
, vol.266
, Issue.5183
, 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
-
7
-
-
0027598525
-
Varieties of developmental dyslexia
-
Castles, A., & Coltheart, M. (1993). Varieties of developmental dyslexia. Cognition, 47, 149-180.
-
(1993)
Cognition
, vol.47
, pp. 149-180
-
-
Castles, A.1
Coltheart, M.2
-
8
-
-
34547628858
-
Family-based association tests for genomewide association scans
-
Chen, W. M., & Abecasis, G. R. (2007). Family-based association tests for genomewide association scans. American Journal of Human Genetics, 81, 913-926.
-
(2007)
American Journal of Human Genetics
, vol.81
, pp. 913-926
-
-
Chen, W.M.1
Abecasis, G.R.2
-
9
-
-
52949093111
-
Systematic assessment of copy number variant detection via genome-wide SNP genotyping
-
Cooper, G. M., Zerr, T., Kidd, J. M., Eichler, E. E., & Nickerson, D. A. (2008). Systematic assessment of copy number variant detection via genome-wide SNP genotyping. Nature Genetics, 40, 1199-1203.
-
(2008)
Nature Genetics
, vol.40
, pp. 1199-1203
-
-
Cooper, G.M.1
Zerr, T.2
Kidd, J.M.3
Eichler, E.E.4
Nickerson, D.A.5
-
10
-
-
15944372645
-
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia
-
DOI 10.1086/429131
-
Cope, N., Harold, D., Hill, G., Moskvina, V., Stevenson, J., Holmans, P., Owen, M. J., O'Donovan, M.C., & Williams, J. (2005). Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. American Journal of Human Genetics, 76, 581-591. (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
-
11
-
-
63149196656
-
Further evidence for DYX1C1 as a susceptibility factor for dyslexia
-
Dahdouh, F., Anthoni, H., Tapia-Paez, I., Peyrard-Janvid, M., Schulte-Korne, G., Warnke, A., Remschmidt, H., Ziegler, A., Kere, J., Müller-Myhsok, B., Nöthen, M. M., Schumacher, J., & Zucchelli, M. (2009). Further evidence for DYX1C1 as a susceptibility factor for dyslexia. Psychiatric Genetics, 19, 59-63.
-
(2009)
Psychiatric Genetics
, vol.19
, 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
Müller-Myhsok, B.10
Nöthen, M.M.11
Schumacher, J.12
Zucchelli, M.13
-
12
-
-
78149383523
-
Mendelian randomization for strengthening causal inference in observational studies: Application to gene x environment interactions
-
Davey Smith, G. (2010). Mendelian randomization for strengthening causal inference in observational studies: Application to gene x environment interactions. Perspectives on Psychological Science, 527-545.
-
(2010)
Perspectives on Psychological Science
, pp. 527-545
-
-
Davey Smith, G.1
-
13
-
-
33745343959
-
The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia
-
Hannula-Jouppi, K., Kaminen-Ahola, N., Taipale, M., Eklund, R., Nopola-Hemmi, J., Kaariainen, H., & Kere, J. (2005). The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS Genet, 1, e50.
-
(2005)
PLoS Genet
, vol.1
-
-
Hannula-Jouppi, K.1
Kaminen-Ahola, N.2
Taipale, M.3
Eklund, R.4
Nopola-Hemmi, J.5
Kaariainen, H.6
Kere, J.7
-
14
-
-
33644670379
-
A behavioural genomic analysis of DNA markers associated with general cognitive ability in 7-year-olds
-
DOI 10.1111/j.1469-7610.2005.01515.x
-
Harlaar, N., Butcher, L. M., Meaburn, E., Sham, P., Craig, I. W., & Plomin, R. (2005). A behavioural genomic analysis of DNA markers associated with general cognitive ability in 7-year-olds. Journal of Child Psychology and Psychiatry, 46, 1097-1107. (Pubitemid 44201557)
-
(2005)
Journal of Child Psychology and Psychiatry and Allied Disciplines
, vol.46
, Issue.10
, pp. 1097-1107
-
-
Harlaar, N.1
Butcher, L.M.2
Meaburn, E.3
Sham, P.4
Craig, I.W.5
Plomin, R.6
-
15
-
-
77952673657
-
Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample
-
Lind, P., Luciano, M., Duffy, D., Castles, A., Wright, M. J., Martin, N. G., & Bates, T. C. (2009). Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. European Journal of Human Genetics, 18, 668-673.
-
(2009)
European Journal of Human Genetics
, vol.18
, pp. 668-673
-
-
Lind, P.1
Luciano, M.2
Duffy, D.3
Castles, A.4
Wright, M.J.5
Martin, N.G.6
Bates, T.C.7
-
16
-
-
77952673657
-
Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample
-
Lind, P. A., Luciano, M., Wright, M. J., Montgomery, G. W., Martin, N. G., & Bates, T. C. (2010). Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. European Journal of Human Genetics, 18, 668-673.
-
(2010)
European Journal of Human Genetics
, 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
-
17
-
-
54549108915
-
Testing replication of a 5-SNP set for general cognitive ability in six population samples
-
Luciano, M., Lind, P. A., Deary, I. J., Payton, A., Posthuma, D., Butcher, L. M., Bochdanovits, Z., Whalley, L. J., Visscher, P. M., Harris, S. E., Polderman, T. J., Davis, O. S., Wright, M. J., Starr, J. M., de Geus, E. J., Bates, T. C., Montgomery, G. W., Boomsma, D. I., Martin, N. G., & Plomin, R. (2008). Testing replication of a 5-SNP set for general cognitive ability in six population samples. European Journal of Human Genetics, 16, 1388-1395.
-
(2008)
European Journal of Human Genetics
, vol.16
, pp. 1388-1395
-
-
Luciano, M.1
Lind, P.A.2
Deary, I.J.3
Payton, A.4
Posthuma, D.5
Butcher, L.M.6
Bochdanovits, Z.7
Whalley, L.J.8
Visscher, P.M.9
Harris, S.E.10
Polderman, T.J.11
Davis, O.S.12
Wright, M.J.13
Starr, J.M.14
De Geus, E.J.15
Bates, T.C.16
Montgomery, G.W.17
Boomsma, D.I.18
Martin, N.G.19
Plomin, R.20
more..
-
18
-
-
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
-
Luciano, M., Lind, P. A., Duffy, D. L., Castles, A., Wright, M. J., Montgomery, G. W., Martin, N. G., & Bates, T. C. (2007). A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biological Psychiatry, 62, 811-817. (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
-
19
-
-
77949282354
-
Optimal selection of markers from DNA pooling experiments
-
discussion 48
-
Macgregor, S. (2010). Optimal selection of markers from DNA pooling experiments. Behavior Genetics, 40, 46-47; discussion 48.
-
(2010)
Behavior Genetics
, vol.40
, pp. 46-47
-
-
Macgregor, S.1
-
20
-
-
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
-
Meaburn, E. L., Harlaar, N., Craig, I. W., Schalkwyk, L. C., & Plomin, R. (2008). Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children. Molecular Psychiatry, 13, 729-740. (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
-
21
-
-
0034785618
-
A dominant gene for developmental dyslexia on chromosome 3
-
Nopola-Hemmi, J., Myllyluoma, B., Haltia, T., Taipale, M., Ollikainen, V., Ahonen, T., Voutilainen, A., Kere, J., & Widén, E. (2001). A dominant gene for developmental dyslexia on chromosome 3. Journal of Medical Genetics, 38, 658-664. (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
-
22
-
-
12244264435
-
Genetic power calculator: Design of linkage and association genetic mapping studies of complex traits
-
DOI 10.1093/bioinformatics/19.1.149
-
Purcell, S., Cherny, S. S., & Sham, P. C. (2003). Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics, 19, 149-150. (Pubitemid 36150192)
-
(2003)
Bioinformatics
, vol.19
, Issue.1
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
-
23
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
& the International Schizophrenia Consortium
-
Purcell, S. M., Wray, N. R., Stone, J. L., Visscher, P. M., O'Donovan, M. C., Sullivan, P. F., Sklar, P., & the International Schizophrenia Consortium. (2009). Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature, 460, 748-752.
-
(2009)
Nature
, vol.460
, pp. 748-752
-
-
Purcell, S.M.1
Wray, N.R.2
Stone, J.L.3
Visscher, P.M.4
O'Donovan, M.C.5
Sullivan, P.F.6
Sklar, P.7
-
24
-
-
79951480123
-
-
R Development Core Team. Vienna, Austria: R Foundation for Statistical Computing
-
R Development Core Team. (2010). R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing.
-
(2010)
R: A Language and Environment for Statistical Computing
-
-
-
25
-
-
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
-
Raskind, W. H., Igo, R. P., Chapman, N. H., Berninger, V. W., Thomson, J. B., Matsushita, M., Brkanac, Z., Holzman, T., Brown, M., & Wijsman, E. M. (2005). A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency. Molecular Psychiatry, 10, 699-711. (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
-
26
-
-
65549097274
-
Pathways from science findings to health benefits
-
Rutter, M., & Plomin, R. (2009). Pathways from science findings to health benefits. Psychological Medicine, 39, 529-542.
-
(2009)
Psychological Medicine
, vol.39
, pp. 529-542
-
-
Rutter, M.1
Plomin, R.2
-
27
-
-
0040443899
-
Naming-speed processes, timing, and reading: A conceptual review
-
Wolf, M., Bowers, P. G., & Biddle, K. (2000). Naming-speed processes, timing, and reading: A conceptual review. Journal of Learning Disabilities, 33, 387-407.
-
(2000)
Journal of Learning Disabilities
, vol.33
, pp. 387-407
-
-
Wolf, M.1
Bowers, P.G.2
Biddle, K.3
-
28
-
-
68049126142
-
Accurate, large-scale genotyping of 5HTTLPR and flanking single nucleotide polymorphisms in an association study of depression, anxiety, and personality measures
-
Wray, N. R., James, M. R., Gordon, S. D., Dumenil, T., Ryan, L., Coventry, W. L., Statham, D. J., Pergadia, M. L., Madden, P. A., Heath, A. C., Montgomery, G. W., & Martin, N. G. (2009). Accurate, large-scale genotyping of 5HTTLPR and flanking single nucleotide polymorphisms in an association study of depression, anxiety, and personality measures. Biological Psychiatry, 66, 468-476.
-
(2009)
Biological Psychiatry
, vol.66
, pp. 468-476
-
-
Wray, N.R.1
James, M.R.2
Gordon, S.D.3
Dumenil, T.4
Ryan, L.5
Coventry, W.L.6
Statham, D.J.7
Pergadia, M.L.8
Madden, P.A.9
Heath, A.C.10
Montgomery, G.W.11
Martin, N.G.12
-
29
-
-
17944377388
-
Genetics of cognition: Outline of a collaborative twin study
-
DOI 10.1375/1369052012146
-
Wright, M. J., De Geus, E., Ando, J., Luciano, M., Posthuma, D., Ono, Y., Hansell, N., Van Baal, C., Hiraishi, K., Hasegawa, T., Smith, G., Geffen, G., Geffen, L., Kanba, S., Miyake, A., Martin, N., & Boomsma, D. (2001). Genetics of cognition: Outline of a collaborative twin study. Twin Research, 4, 48-56. (Pubitemid 32910648)
-
(2001)
Twin Research
, vol.4
, Issue.1
, pp. 48-56
-
-
Wright, M.1
Geus, E.D.2
Ando, J.3
Luciano, M.4
Posthuma, D.5
Ono, Y.6
Hansell, N.7
Baal, C.V.8
Hiraishi, K.9
Hasegawa, T.10
Smith, G.11
Geffen, G.12
Geffen, L.13
Kanba, S.14
Miyake, A.15
Martin, N.16
Boomsma, D.17
|