-
1
-
-
0026801071
-
Hand preference and age in the United States
-
Gilbert, A.N. and Wysocki, C.J. (1992) Hand preference and age in the United States. Neuropsychologia, 30, 601-608.
-
(1992)
Neuropsychologia
, vol.30
, pp. 601-608
-
-
Gilbert, A.N.1
Wysocki, C.J.2
-
2
-
-
0032322951
-
Human handedness: an ethological perspective
-
Marchant, L.F. and McGrew, W.C. (1998) Human handedness: an ethological perspective. Hum. Evol., 13, 221-228.
-
(1998)
Hum. Evol.
, vol.13
, pp. 221-228
-
-
Marchant, L.F.1
McGrew, W.C.2
-
3
-
-
0442304444
-
Is there geographical variation in human handedness?
-
Raymond, M. and Pontier, D. (2004) Is there geographical variation in human handedness? Laterality, 9, 35-51.
-
(2004)
Laterality
, vol.9
, pp. 35-51
-
-
Raymond, M.1
Pontier, D.2
-
4
-
-
0000841833
-
Remarques sur le siége de la faculté du language articulé, suivies d'une observation d'aphémie (perte de la parole)
-
Broca, P. (1861) Remarques sur le siége de la faculté du language articulé, suivies d'une observation d'aphémie (perte de la parole). Bull. Soc. Anatom., 6, 330-357.
-
(1861)
Bull. Soc. Anatom.
, vol.6
, pp. 330-357
-
-
Broca, P.1
-
7
-
-
60549109887
-
Relations among speech, language, and reading disorders
-
Pennington, B.F. and Bishop, D.V. (2009) Relations among speech, language, and reading disorders. Annu. Rev. Psychol., 60, 283-306.
-
(2009)
Annu. Rev. Psychol.
, vol.60
, pp. 283-306
-
-
Pennington, B.F.1
Bishop, D.V.2
-
9
-
-
0347075619
-
Familial and genetic effects on motor coordination, laterality, and reading-related cognition
-
Francks, C., Fisher, S.E., Marlow, A.J., MacPhie, I.L., Taylor, K.E., Richardson, A.J., Stein, J.F. and Monaco, A.P. (2003) Familial and genetic effects on motor coordination, laterality, and reading-related cognition. Am. J. Psychiatry, 160, 1970-1977.
-
(2003)
Am. J. Psychiatry
, vol.160
, pp. 1970-1977
-
-
Francks, C.1
Fisher, S.E.2
Marlow, A.J.3
MacPhie, I.L.4
Taylor, K.E.5
Richardson, A.J.6
Stein, J.F.7
Monaco, A.P.8
-
10
-
-
0033637516
-
Handedness and hemispheric language dominance in healthy humans
-
Knecht, S., Drager, B., Deppe, M., Bobe, L., Lohmann, H., Floel, A., Ringelstein, E.B. and Henningsen, H. (2000) Handedness and hemispheric language dominance in healthy humans. Brain, 123, 2512-2518.
-
(2000)
Brain
, vol.123
, pp. 2512-2518
-
-
Knecht, S.1
Drager, B.2
Deppe, M.3
Bobe, L.4
Lohmann, H.5
Floel, A.6
Ringelstein, E.B.7
Henningsen, H.8
-
12
-
-
33845409811
-
The neural basis of language development and its impairment
-
Friederici, A.D. (2006) The neural basis of language development and its impairment. Neuron, 52, 941-952.
-
(2006)
Neuron
, vol.52
, pp. 941-952
-
-
Friederici, A.D.1
-
13
-
-
0021832834
-
Developmental dyslexia: four consecutive patients with cortical anomalies
-
Galaburda, A.M., Sherman, G.F., Rosen, G.D., Aboitiz, F. and Geschwind, N. (1985) Developmental dyslexia: four consecutive patients with cortical anomalies. Ann. Neurol., 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
-
14
-
-
51649154738
-
Ordinary and extraordinary brain development: anatomical variation in developmental dyslexia
-
Galaburda, A.M. (1989) Ordinary and extraordinary brain development: anatomical variation in developmental dyslexia. Ann. Dyslexia, 39, 65-80.
-
(1989)
Ann. Dyslexia
, vol.39
, pp. 65-80
-
-
Galaburda, A.M.1
-
15
-
-
70349314562
-
Functional abnormalities in the dyslexic brain: a quantitative meta-analysis of neuroimaging studies
-
Richlan, F., Kronbichler, M. and Wimmer, H. (2009) Functional abnormalities in the dyslexic brain: a quantitative meta-analysis of neuroimaging studies. Hum. Brain Mapp., 30, 3299-3308.
-
(2009)
Hum. Brain Mapp.
, vol.30
, pp. 3299-3308
-
-
Richlan, F.1
Kronbichler, M.2
Wimmer, H.3
-
16
-
-
0035896358
-
Dyslexia: cultural diversity and biological unity
-
Paulesu, E., Demonet, J.F., Fazio, F., McCrory, E., Chanoine, V., Brunswick, N., Cappa, S.F., Cossu, G., Habib, M., Frith, C.D. et al. (2001) Dyslexia: cultural diversity and biological unity. Science, 291, 2165-2167.
-
(2001)
Science
, vol.291
, pp. 2165-2167
-
-
Paulesu, E.1
Demonet, J.F.2
Fazio, F.3
McCrory, E.4
Chanoine, V.5
Brunswick, N.6
Cappa, S.F.7
Cossu, G.8
Habib, M.9
Frith, C.D.10
-
17
-
-
26044460165
-
Brain abnormalities underlying altered activation in dyslexia: a voxel based morphometry study
-
Silani, G., Frith, U., Demonet, J.F., Fazio, F., Perani, D., Price, C., Frith, C.D. and Paulesu, E. (2005) Brain abnormalities underlying altered activation in dyslexia: a voxel based morphometry study. Brain, 128, 2453-2461.
-
(2005)
Brain
, vol.128
, pp. 2453-2461
-
-
Silani, G.1
Frith, U.2
Demonet, J.F.3
Fazio, F.4
Perani, D.5
Price, C.6
Frith, C.D.7
Paulesu, E.8
-
18
-
-
58849122655
-
Genetic influences on handedness: data from 25,732 Australian and Dutch twin families
-
Medland, S.E., Duffy, D.L., Wright, M.J., Geffen, G.M., Hay, D.A., Levy, F., Van-Beijsterveldt, C.E.M., Willemsen, G., Townsend, G.C., White, V. et al. (2009) Genetic influences on handedness: data from 25,732 Australian and Dutch twin families. Neuropsychologia, 47, 330-337.
-
(2009)
Neuropsychologia
, vol.47
, pp. 330-337
-
-
Medland, S.E.1
Duffy, D.L.2
Wright, M.J.3
Geffen, G.M.4
Hay, D.A.5
Levy, F.6
Van-Beijsterveldt, C.E.M.7
Willemsen, G.8
Townsend, G.C.9
White, V.10
-
19
-
-
0036182240
-
A genomewide linkage screen for relative hand skill in sibling pairs
-
Francks, C., Fisher, S.E., MacPhie, I.L., Richardson, A.J., Marlow, A.J., Stein, J.F. and Monaco, A.P. (2002) A genomewide linkage screen for relative hand skill in sibling pairs. Am. J. Hum. Genet., 70, 800-805.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 800-805
-
-
Francks, C.1
Fisher, S.E.2
MacPhie, I.L.3
Richardson, A.J.4
Marlow, A.J.5
Stein, J.F.6
Monaco, A.P.7
-
20
-
-
0037318808
-
Confirmatory evidence for linkage of relative hand skill to 2p12-q11
-
Francks, C., DeLisi, L.E., Fisher, S.E., Laval, S.H., Rue, J.E., Stein, J.F. and Monaco, A.P. (2003) Confirmatory evidence for linkage of relative hand skill to 2p12-q11. Am. J. Hum. Genet., 72, 499-502.
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 499-502
-
-
Francks, C.1
DeLisi, L.E.2
Fisher, S.E.3
Laval, S.H.4
Rue, J.E.5
Stein, J.F.6
Monaco, A.P.7
-
21
-
-
0036802940
-
Parametric and non-parametric linkage analysis of several candidate regions for genes for human handedness
-
Van Agtmael, T., Forrest, S.M. and Williamson, R. (2002) Parametric and non-parametric linkage analysis of several candidate regions for genes for human handedness. Eur. J. Hum. Genet., 10, 623-630.
-
(2002)
Eur. J. Hum. Genet.
, vol.10
, pp. 623-630
-
-
Van Agtmael, T.1
Forrest, S.M.2
Williamson, R.3
-
22
-
-
33748529289
-
Heritability and linkage analysis of hand, foot, and eye preference in Mexican Americans
-
Warren, D.M., Stern, M., Duggirala, R., Dyer, T.D. and Almasy, L. (2006) Heritability and linkage analysis of hand, foot, and eye preference in Mexican Americans. Laterality, 11, 508-524.
-
(2006)
Laterality
, vol.11
, pp. 508-524
-
-
Warren, D.M.1
Stern, M.2
Duggirala, R.3
Dyer, T.D.4
Almasy, L.5
-
23
-
-
36549060114
-
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
-
Francks, C., Maegawa, S., Lauren, J., Abrahams, B.S., Velayos-Baeza, A., Medland, S.E., Colella, S., Groszer, M., McAuley, E.Z., Caffrey, T.M. et al. (2007) LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Mol. Psychiatry, 12, 1129-1139.
-
(2007)
Mol. Psychiatry
, vol.12
, pp. 1129-1139
-
-
Francks, C.1
Maegawa, S.2
Lauren, J.3
Abrahams, B.S.4
Velayos-Baeza, A.5
Medland, S.E.6
Colella, S.7
Groszer, M.8
McAuley, E.Z.9
Caffrey, T.M.10
-
24
-
-
27844533502
-
Opposite effects of androgen receptor CAG repeat length on increased risk of left-handedness in males and females
-
Medland, S.E., Duffy, D.L., Spurdle, A.B., Wright, M.J., Geffen, G.M., Montgomery, G.W. and Martin, N.G. (2005) Opposite effects of androgen receptor CAG repeat length on increased risk of left-handedness in males and females. Behav. Genet., 35, 735-744.
-
(2005)
Behav. Genet.
, vol.35
, pp. 735-744
-
-
Medland, S.E.1
Duffy, D.L.2
Spurdle, A.B.3
Wright, M.J.4
Geffen, G.M.5
Montgomery, G.W.6
Martin, N.G.7
-
25
-
-
77954167176
-
Web-based, participant-driven studies yield novel genetic associations for common traits
-
Eriksson, N., Macpherson, J.M., Tung, J.Y., Hon, L.S., Naughton, B., Saxonov, S., Avey, L., Wojcicki, A., Pe'er, I. and Mountain, J. (2010) Web-based, participant-driven studies yield novel genetic associations for common traits. PLoS Genet., 6, e1000993.
-
(2010)
PLoS Genet.
, vol.6
-
-
Eriksson, N.1
Macpherson, J.M.2
Tung, J.Y.3
Hon, L.S.4
Naughton, B.5
Saxonov, S.6
Avey, L.7
Wojcicki, A.8
Pe'er, I.9
Mountain, J.10
-
26
-
-
0034194471
-
SPC4/PACE4 regulates a TGFbeta signaling network during axis formation
-
Constam, D.B. and Robertson, E.J. (2000) SPC4/PACE4 regulates a TGFbeta signaling network during axis formation. Genes Dev., 14, 1146-1155.
-
(2000)
Genes Dev.
, vol.14
, pp. 1146-1155
-
-
Constam, D.B.1
Robertson, E.J.2
-
27
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
Howie, B.N., Donnelly, P. and Marchini, J. (2009) A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet., 5, e1000529.
-
(2009)
PLoS Genet.
, vol.5
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
28
-
-
0033366739
-
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia
-
Fisher, S.E., Marlow, A.J., Lamb, J., Maestrini, E., Williams, D.F., Richardson, A.J., Weeks, D.E., Stein, J.F. and Monaco, A.P. (1999) A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. Am. J. Hum. Genet., 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
Weeks, D.E.7
Stein, J.F.8
Monaco, A.P.9
-
29
-
-
0034863552
-
Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK
-
Marlow, A.J., Fisher, S.E., Richardson, A.J., Francks, C., Talcott, J.B., Monaco, A.P., Stein, J.F. and Cardon, L.R. (2001) Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK. Behav. Genet., 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
Stein, J.F.7
Cardon, L.R.8
-
31
-
-
0026348132
-
Identification of a second human subtilisin-like protease gene in the fes/fps region of chromosome 15
-
Kiefer, M.C., Tucker, J.E., Joh, R., Landsberg, K.E., Saltman, D. and Barr, P.J. (1991) Identification of a second human subtilisin-like protease gene in the fes/fps region of chromosome 15. DNA Cell Biol., 10, 757-769.
-
(1991)
DNA Cell Biol.
, vol.10
, pp. 757-769
-
-
Kiefer, M.C.1
Tucker, J.E.2
Joh, R.3
Landsberg, K.E.4
Saltman, D.5
Barr, P.J.6
-
32
-
-
0036902759
-
Extraembryonic proteases regulate Nodal signalling during gastrulation
-
Beck, S., Le Good, J.A., Guzman, M., Ben Haim, N., Roy, K., Beermann, F. and Constam, D.B. (2002) Extraembryonic proteases regulate Nodal signalling during gastrulation. Nat. Cell Biol., 4, 981-985.
-
(2002)
Nat. Cell Biol.
, vol.4
, pp. 981-985
-
-
Beck, S.1
Le Good, J.A.2
Guzman, M.3
Ben Haim, N.4
Roy, K.5
Beermann, F.6
Constam, D.B.7
-
33
-
-
0347623371
-
Genome-wide survey of human alternative pre-mRNA splicing with exon junction microarrays
-
Johnson, J.M., Castle, J., Garrett-Engele, P., Kan, Z., Loerch, P.M., Armour, C.D., Santos, R., Schadt, E.E., Stoughton, R. and Shoemaker, D.D. (2003) Genome-wide survey of human alternative pre-mRNA splicing with exon junction microarrays. Science, 302, 2141-2144.
-
(2003)
Science
, vol.302
, pp. 2141-2144
-
-
Johnson, J.M.1
Castle, J.2
Garrett-Engele, P.3
Kan, Z.4
Loerch, P.M.5
Armour, C.D.6
Santos, R.7
Schadt, E.E.8
Stoughton, R.9
Shoemaker, D.D.10
-
34
-
-
46149123644
-
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly
-
Roessler, E., Ouspenskaia, M.V., Karkera, J.D., Velez, J.I., Kantipong, A., Lacbawan, F., Bowers, P., Belmont, J.W., Towbin, J.A., Goldmuntz, E. et al. (2008) Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly. Am. J. Hum. Genet., 83, 18-29.
-
(2008)
Am. J. Hum. Genet.
, vol.83
, pp. 18-29
-
-
Roessler, E.1
Ouspenskaia, M.V.2
Karkera, J.D.3
Velez, J.I.4
Kantipong, A.5
Lacbawan, F.6
Bowers, P.7
Belmont, J.W.8
Towbin, J.A.9
Goldmuntz, E.10
-
35
-
-
60549091742
-
Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations
-
Mohapatra, B., Casey, B., Li, H., Ho-Dawson, T., Smith, L., Fernbach, S.D., Molinari, L., Niesh, S.R., Jefferies, J.L., Craigen, W.J. et al. (2009) Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations. Hum. Mol. Genet., 18, 861-871.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 861-871
-
-
Mohapatra, B.1
Casey, B.2
Li, H.3
Ho-Dawson, T.4
Smith, L.5
Fernbach, S.D.6
Molinari, L.7
Niesh, S.R.8
Jefferies, J.L.9
Craigen, W.J.10
-
36
-
-
28044465597
-
DCDC2 is associated with reading disability and modulates neuronal development in the brain
-
Meng, H., Smith, S.D., Hager, K., Held, M., Liu, J., Olson, R.K., Pennington, B.F., DeFries, J.C., Gelernter, J., O'Reilly-Pol, T. et al. (2005) DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc. Natl Acad. Sci. USA, 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
Pennington, B.F.7
DeFries, J.C.8
Gelernter, J.9
O'Reilly-Pol, T.10
-
37
-
-
29244468273
-
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
-
Schumacher, J., Anthoni, H., Dahdouh, F., Konig, I.R., Hillmer, A.M., Kluck, N., Manthey, M., Plume, E., Warnke, A., Remschmidt, H. et al. (2006) Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Am. J. Hum. Genet., 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
Manthey, M.7
Plume, E.8
Warnke, A.9
Remschmidt, H.10
-
38
-
-
0141482054
-
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain
-
Taipale, M., Kaminen, N., Nopola-Hemmi, J., Haltia, T., Myllyluoma, B., Lyytinen, H., Muller, K., Kaaranen, M., Lindsberg, P.J., Hannula-Jouppi, K. et al. (2003) A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proc. Natl Acad. Sci. USA, 100, 11553-11558.
-
(2003)
Proc. Natl Acad. Sci. USA
, vol.100
, 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
-
39
-
-
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, S.D., Richardson, A.J., Scerri, T.S., Cardon, L.R., Marlow, A.J., MacPhie, I.L., Walter, J., Pennington, B.F. et al. (2004) 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., 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
Marlow, A.J.7
MacPhie, I.L.8
Walter, J.9
Pennington, B.F.10
-
40
-
-
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., Owen, M.J., O'Donovan, M.C. and Williams, J. (2005) Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am. J. Hum. Genet., 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
Owen, M.J.7
O'Donovan, M.C.8
Williams, J.9
-
41
-
-
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. and 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
-
42
-
-
33749071999
-
From genes to behavior in developmental dyslexia
-
Galaburda, A.M., LoTurco, J., Ramus, F., Fitch, R.H. and Rosen, G.D. (2006) From genes to behavior in developmental dyslexia. Nat. Neurosci., 9, 1213-1217.
-
(2006)
Nat. Neurosci.
, vol.9
, pp. 1213-1217
-
-
Galaburda, A.M.1
LoTurco, J.2
Ramus, F.3
Fitch, R.H.4
Rosen, G.D.5
-
43
-
-
36749013035
-
High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders
-
Vernes, S.C., Spiteri, E., Nicod, J., Groszer, M., Taylor, J.M., Davies, K.E., Geschwind, D.H. and Fisher, S.E. (2007) High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. Am. J. Hum. Genet., 81, 1232-1250.
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 1232-1250
-
-
Vernes, S.C.1
Spiteri, E.2
Nicod, J.3
Groszer, M.4
Taylor, J.M.5
Davies, K.E.6
Geschwind, D.H.7
Fisher, S.E.8
-
44
-
-
56049086389
-
Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR
-
Royer-Zemmour, B., Ponsole-Lenfant, M., Gara, H., Roll, P., Leveque, C., Massacrier, A., Ferracci, G., Cillario, J., Robaglia-Schlupp, A., Vincentelli, R. et al. (2008) Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR. Hum. Mol. Genet., 17, 3617-3630.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 3617-3630
-
-
Royer-Zemmour, B.1
Ponsole-Lenfant, M.2
Gara, H.3
Roll, P.4
Leveque, C.5
Massacrier, A.6
Ferracci, G.7
Cillario, J.8
Robaglia-Schlupp, A.9
Vincentelli, R.10
-
45
-
-
18544365699
-
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
-
Fisher, S.E., Francks, C., Marlow, A.J., MacPhie, I.L., Newbury, D.F., Cardon, L.R., Ishikawa-Brush, Y., Richardson, A.J., Talcott, J.B., Gayan, J. et al. (2002) Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nat. Genet., 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
Ishikawa-Brush, Y.7
Richardson, A.J.8
Talcott, J.B.9
Gayan, J.10
-
46
-
-
0035130957
-
ALSPAC-the Avon Longitudinal Study of Parents and Children. I. Study methodology
-
Golding, J., Pembrey, M. and Jones, R. (2001) ALSPAC-the Avon Longitudinal Study of Parents and Children. I. Study methodology. Paediatr. Perinat. Epidemiol., 15, 74-87.
-
(2001)
Paediatr. Perinat. Epidemiol.
, vol.15
, pp. 74-87
-
-
Golding, J.1
Pembrey, M.2
Jones, R.3
-
47
-
-
0014871284
-
The growth of manual preference and speed
-
Annett, M. (1970) The growth of manual preference and speed. Br. J. Psychol., 61, 545-558.
-
(1970)
Br. J. Psychol.
, vol.61
, pp. 545-558
-
-
Annett, M.1
-
49
-
-
78651100696
-
Data quality control in genetic case-control association studies
-
Anderson, C.A., Pettersson, F.H., Clarke, G.M., Cardon, L.R., Morris, A.P. and Zondervan, K.T. (2010) Data quality control in genetic case-control association studies. Nat. Protoc., 5, 1564-1573.
-
(2010)
Nat. Protoc.
, vol.5
, pp. 1564-1573
-
-
Anderson, C.A.1
Pettersson, F.H.2
Clarke, G.M.3
Cardon, L.R.4
Morris, A.P.5
Zondervan, K.T.6
-
50
-
-
33646547251
-
An integrated system for genetic analysis
-
Fiddy, S., Cattermole, D., Xie, D., Duan, X.Y. and Mott, R. (2006) An integrated system for genetic analysis. BMC Bioinformatics, 7, 210.
-
(2006)
BMC Bioinformatics
, vol.7
, pp. 210
-
-
Fiddy, S.1
Cattermole, D.2
Xie, D.3
Duan, X.Y.4
Mott, R.5
-
51
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
Marchini, J., Howie, B., Myers, S., McVean, G. and Donnelly, P. (2007) A new multipoint method for genome-wide association studies by imputation of genotypes. Nat. Genet., 39, 906-913.
-
(2007)
Nat. Genet.
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
52
-
-
77952714079
-
GWAMA: software for genome-wide association meta-analysis
-
Magi, R. and Morris, A.P. (2010) GWAMA: software for genome-wide association meta-analysis. BMC Bioinformatics, 11, 288.
-
(2010)
BMC Bioinformatics
, vol.11
, pp. 288
-
-
Magi, R.1
Morris, A.P.2
-
53
-
-
77956586071
-
LocusZoom: regional visualization of genome-wide association scan results
-
Pruim, R.J., Welch, R.P., Sanna, S., Teslovich, T.M., Chines, P.S., Gliedt, T.P., Boehnke, M., Abecasis, G.R. and Willer, C.J. (2010) LocusZoom: regional visualization of genome-wide association scan results. Bioinformatics, 26, 2336-2337.
-
(2010)
Bioinformatics
, vol.26
, pp. 2336-2337
-
-
Pruim, R.J.1
Welch, R.P.2
Sanna, S.3
Teslovich, T.M.4
Chines, P.S.5
Gliedt, T.P.6
Boehnke, M.7
Abecasis, G.R.8
Willer, C.J.9
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