-
1
-
-
0022289877
-
Cross-national comparisons of developmental dyslexia in Italy and the United States
-
Lindgren S.D., De Renzi E., Richman L.C. Cross-national comparisons of developmental dyslexia in Italy and the United States. Child Dev 1985, 56:1404-1417.
-
(1985)
Child Dev
, vol.56
, pp. 1404-1417
-
-
Lindgren, S.D.1
De Renzi, E.2
Richman, L.C.3
-
3
-
-
0027965056
-
Evidence for aberrant auditory anatomy in developmental dyslexia
-
Galaburda A.M., Menard M.T., Rosen G.D. Evidence for aberrant auditory anatomy in developmental dyslexia. Proc Natl Acad Sci U S A 1994, 91:8010-8013.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 8010-8013
-
-
Galaburda, A.M.1
Menard, M.T.2
Rosen, G.D.3
-
4
-
-
69149090139
-
Subcortical differentiation of stop consonants relates to reading and speech-in-noise perception
-
Hornickel J., Skoe E., Nicol T., Zecker S., Kraus N. Subcortical differentiation of stop consonants relates to reading and speech-in-noise perception. Proc Natl Acad Sci U S A 2009, 106:13022-13027.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 13022-13027
-
-
Hornickel, J.1
Skoe, E.2
Nicol, T.3
Zecker, S.4
Kraus, N.5
-
6
-
-
58849148546
-
Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion
-
Poelmans G., Engelen J.J., Van Lent-Albrechts J., Smeets H.J., Schoenmakers E., Franke B., Buitelaar J.K., Wuisman-Frerker M., Erens W., Steyaert J., Schrander-Stumpel C. Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion. Am J Med Genet B Neuropsychiatr Genet 2009, 150B:140-147.
-
(2009)
Am J Med Genet B Neuropsychiatr Genet
, vol.150 B
, 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
-
7
-
-
79953065216
-
A theoretical molecular network for dyslexia: integrating available genetic findings
-
Poelmans G., Buitelaar J.K., Pauls D.L., Franke B. A theoretical molecular network for dyslexia: integrating available genetic findings. Mol Psychiatry 2011, 16:365-382.
-
(2011)
Mol Psychiatry
, vol.16
, pp. 365-382
-
-
Poelmans, G.1
Buitelaar, J.K.2
Pauls, D.L.3
Franke, B.4
-
8
-
-
57349157021
-
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population
-
Paracchini S., Steer C.D., Buckingham L.L., Morris A.P., Ring S., Scerri T., Stein J., Pembrey M.E., Ragoussis J., Golding J., Monaco A.P. Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. Am J Psychiatry 2008, 165:1576-1584.
-
(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.6
Stein, J.7
Pembrey, M.E.8
Ragoussis, J.9
Golding, J.10
Monaco, A.P.11
-
9
-
-
79951807749
-
Analysis of dyslexia candidate genes in the raine cohort representing the general Australian population
-
Paracchini S., Ang Q.W., Stanley F.J., Monaco A.P., Pennell C.E., Whitehouse A.J. Analysis of dyslexia candidate genes in the raine cohort representing the general Australian population. Genes Brain Behav 2011, 10:158-165.
-
(2011)
Genes Brain Behav
, vol.10
, pp. 158-165
-
-
Paracchini, S.1
Ang, Q.W.2
Stanley, F.J.3
Monaco, A.P.4
Pennell, C.E.5
Whitehouse, A.J.6
-
10
-
-
34548473808
-
A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability
-
Luciano M., Lind P.A., Duffy D.L., Castles A., Wright M.J., Montgomery G.W., Martin N.G., Bates T.C. A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biol Psychiatry 2007, 62:811-817.
-
(2007)
Biol Psychiatry
, vol.62
, 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
-
11
-
-
79960220393
-
DCDC2, KIAA0319 and CMIP are associated with reading-related traits
-
Scerri T.S., Morris A.P., Buckingham L.L., Newbury D.F., Miller L.L., Monaco A.P., Bishop D.V., Paracchini S. DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Biol Psychiatry 2011.
-
(2011)
Biol Psychiatry
-
-
Scerri, T.S.1
Morris, A.P.2
Buckingham, L.L.3
Newbury, D.F.4
Miller, L.L.5
Monaco, A.P.6
Bishop, D.V.7
Paracchini, S.8
-
12
-
-
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. Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. Eur J Hum Genet 2010, 18:668-673.
-
(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
-
13
-
-
82755197778
-
Dissection of genetic associations with language-related traits in population-based cohorts
-
Paracchini S. Dissection of genetic associations with language-related traits in population-based cohorts. J Neurodev Disord 2011, 3:365-373.
-
(2011)
J Neurodev Disord
, vol.3
, pp. 365-373
-
-
Paracchini, S.1
-
14
-
-
34748875368
-
Association of short-term memory with a variant within DYX1C1 in developmental dyslexia
-
Marino C., Citterio A., Giorda R., Facoetti A., Menozzi G., Vanzin L., Lorusso M.L., Nobile M., Molteni M. Association of short-term memory with a variant within DYX1C1 in developmental dyslexia. Genes Brain Behav 2007, 6:640-646.
-
(2007)
Genes Brain Behav
, vol.6
, 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
-
15
-
-
84655169217
-
DCDC2 genetic variants and susceptibility to developmental dyslexia
-
Marino C., Meng H., Mascheretti S., Rusconi M., Cope N., Giorda R., Molteni M., Gruen J.R. DCDC2 genetic variants and susceptibility to developmental dyslexia. Psychiatr Genet 2011, 22:25-30.
-
(2011)
Psychiatr Genet
, vol.22
, pp. 25-30
-
-
Marino, C.1
Meng, H.2
Mascheretti, S.3
Rusconi, M.4
Cope, N.5
Giorda, R.6
Molteni, M.7
Gruen, J.R.8
-
16
-
-
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. Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation. Mol Psychiatry 2010, 15:1190-1196.
-
(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
-
17
-
-
79952443930
-
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. Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. Behav Genet 2011, 41:50-57.
-
(2011)
Behav Genet
, vol.41
, pp. 50-57
-
-
Bates, T.C.1
Luciano, M.2
Medland, S.E.3
Montgomery, G.W.4
Wright, M.J.5
Martin, N.G.6
-
18
-
-
79953661892
-
Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21
-
Konig I.R., Schumacher J., Hoffmann P., Kleensang A., Ludwig K.U., Grimm T., Neuhoff N., Preis M., Roeske D., Warnke A., et al. Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21. Am J Med Genet B Neuropsychiatr Genet 2011, 156B:36-43.
-
(2011)
Am J Med Genet B Neuropsychiatr Genet
, vol.156 B
, pp. 36-43
-
-
Konig, I.R.1
Schumacher, J.2
Hoffmann, P.3
Kleensang, A.4
Ludwig, K.U.5
Grimm, T.6
Neuhoff, N.7
Preis, M.8
Roeske, D.9
Warnke, A.10
-
19
-
-
77957822728
-
Surface area accounts for the relation of gray matter volume to reading-related skills and history of dyslexia
-
Frye R.E., Liederman J., Malmberg B., McLean J., Strickland D., Beauchamp M.S. Surface area accounts for the relation of gray matter volume to reading-related skills and history of dyslexia. Cereb Cortex 2010, 20:2625-2635.
-
(2010)
Cereb Cortex
, vol.20
, pp. 2625-2635
-
-
Frye, R.E.1
Liederman, J.2
Malmberg, B.3
McLean, J.4
Strickland, D.5
Beauchamp, M.S.6
-
20
-
-
50549091582
-
The contribution of white and gray matter differences to developmental dyslexia: insights from DTI and VBM at 3.0T
-
Steinbrink C., Vogt K., Kastrup A., Muller H.P., Juengling F.D., Kassubek J., Riecker A. The contribution of white and gray matter differences to developmental dyslexia: insights from DTI and VBM at 3.0T. Neuropsychologia 2008, 46:3170-3178.
-
(2008)
Neuropsychologia
, vol.46
, pp. 3170-3178
-
-
Steinbrink, C.1
Vogt, K.2
Kastrup, A.3
Muller, H.P.4
Juengling, F.D.5
Kassubek, J.6
Riecker, A.7
-
21
-
-
77949646703
-
Polymorphism of DCDC2 reveals differences in cortical morphology of healthy individuals-a preliminary voxel based morphometry study
-
Meda S.A., Gelernter J., Gruen J.R., Calhoun V.D., Meng H., Cope N.A., Pearlson G.D. Polymorphism of DCDC2 reveals differences in cortical morphology of healthy individuals-a preliminary voxel based morphometry study. Brain Imaging Behav 2008, 2:21-26.
-
(2008)
Brain Imaging Behav
, vol.2
, pp. 21-26
-
-
Meda, S.A.1
Gelernter, J.2
Gruen, J.R.3
Calhoun, V.D.4
Meng, H.5
Cope, N.A.6
Pearlson, G.D.7
-
22
-
-
0021832834
-
Developmental dyslexia: four consecutive patients with cortical anomalies
-
Galaburda A.M., Sherman G.F., Rosen G.D., Aboitiz F., Geschwind N. Developmental dyslexia: four consecutive patients with cortical anomalies. Ann Neurol 1985, 18:222-233.
-
(1985)
Ann Neurol
, vol.18
, pp. 222-233
-
-
Galaburda, A.M.1
Sherman, G.F.2
Rosen, G.D.3
Aboitiz, F.4
Geschwind, N.5
-
23
-
-
84866628802
-
Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure
-
Darki F., Peyrard-Janvid M., Matsson H., Kere J., Klingberg T. Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure. Biol Psychiatry 2012, 72:671-676.
-
(2012)
Biol Psychiatry
, vol.72
, pp. 671-676
-
-
Darki, F.1
Peyrard-Janvid, M.2
Matsson, H.3
Kere, J.4
Klingberg, T.5
-
24
-
-
84857515739
-
A tractography study in dyslexia: neuroanatomic correlates of orthographic, phonological and speech processing
-
Vandermosten M., Boets B., Poelmans H., Sunaert S., Wouters J., Ghesquiere P. A tractography study in dyslexia: neuroanatomic correlates of orthographic, phonological and speech processing. Brain 2012, 135(Pt 3):935-948.
-
(2012)
Brain
, vol.135
, Issue.PART 3
, pp. 935-948
-
-
Vandermosten, M.1
Boets, B.2
Poelmans, H.3
Sunaert, S.4
Wouters, J.5
Ghesquiere, P.6
-
25
-
-
42649115410
-
Impaired semantic processing during sentence reading in children with dyslexia: combined fMRI and ERP evidence
-
Schulz E., Maurer U., van der Mark S., Bucher K., Brem S., Martin E., Brandeis D. Impaired semantic processing during sentence reading in children with dyslexia: combined fMRI and ERP evidence. Neuroimage 2008, 41:153-168.
-
(2008)
Neuroimage
, vol.41
, pp. 153-168
-
-
Schulz, E.1
Maurer, U.2
van der Mark, S.3
Bucher, K.4
Brem, S.5
Martin, E.6
Brandeis, D.7
-
26
-
-
84858290155
-
Neural correlates of temporal auditory processing in developmental dyslexia during german vowel length discrimination: an fMRI study
-
Steinbrink C., Groth K., Lachmann T., Riecker A. Neural correlates of temporal auditory processing in developmental dyslexia during german vowel length discrimination: an fMRI study. Brain Lang 2012, 121:1-11.
-
(2012)
Brain Lang
, vol.121
, pp. 1-11
-
-
Steinbrink, C.1
Groth, K.2
Lachmann, T.3
Riecker, A.4
-
27
-
-
84856002114
-
Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions
-
Pinel P., Fauchereau F., Moreno A., Barbot A., Lathrop M., Zelenika D., Le Bihan D., Poline J.B., Bourgeron T., Dehaene S. Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. J Neurosci 2012, 32:817-825.
-
(2012)
J Neurosci
, vol.32
, pp. 817-825
-
-
Pinel, P.1
Fauchereau, F.2
Moreno, A.3
Barbot, A.4
Lathrop, M.5
Zelenika, D.6
Le Bihan, D.7
Poline, J.B.8
Bourgeron, T.9
Dehaene, S.10
-
28
-
-
0142153166
-
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder
-
Lai C.S., Gerrelli D., Monaco A.P., Fisher S.E., Copp A.J. FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain 2003, 126(Pt 11):2455-2462.
-
(2003)
Brain
, vol.126
, Issue.PSRT 11
, pp. 2455-2462
-
-
Lai, C.S.1
Gerrelli, D.2
Monaco, A.P.3
Fisher, S.E.4
Copp, A.J.5
-
29
-
-
79960955811
-
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain
-
Vernes S.C., Oliver P.L., Spiteri E., Lockstone H.E., Puliyadi R., Taylor J.M., Ho J., Mombereau C., Brewer A., Lowy E., et al. Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. PLoS Genet 2011, 7:e1002145.
-
(2011)
PLoS Genet
, vol.7
-
-
Vernes, S.C.1
Oliver, P.L.2
Spiteri, E.3
Lockstone, H.E.4
Puliyadi, R.5
Taylor, J.M.6
Ho, J.7
Mombereau, C.8
Brewer, A.9
Lowy, E.10
-
30
-
-
84855790585
-
Imaging genetics of FOXP2 in dyslexia
-
Wilcke A., Ligges C., Burkhardt J., Alexander M., Wolf C., Quente E., Ahnert P., Hoffmann P., Becker A., Muller-Myhsok B., et al. Imaging genetics of FOXP2 in dyslexia. Eur J Hum Genet 2012, 20:224-229.
-
(2012)
Eur J Hum Genet
, vol.20
, pp. 224-229
-
-
Wilcke, A.1
Ligges, C.2
Burkhardt, J.3
Alexander, M.4
Wolf, C.5
Quente, E.6
Ahnert, P.7
Hoffmann, P.8
Becker, A.9
Muller-Myhsok, B.10
-
31
-
-
78650513551
-
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children
-
Roeske D., Ludwig K.U., Neuhoff N., Becker J., Bartling J., Bruder J., Brockschmidt F.F., Warnke A., Remschmidt H., Hoffmann P., et al. First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. Mol Psychiatry 2011, 16:97-107.
-
(2011)
Mol Psychiatry
, vol.16
, pp. 97-107
-
-
Roeske, D.1
Ludwig, K.U.2
Neuhoff, N.3
Becker, J.4
Bartling, J.5
Bruder, J.6
Brockschmidt, F.F.7
Warnke, A.8
Remschmidt, H.9
Hoffmann, P.10
-
32
-
-
79952437992
-
Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia
-
Czamara D., Bruder J., Becker J., Bartling J., Hoffmann P., Ludwig K.U., Muller-Myhsok B., Schulte-Korne G. Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia. Behav Genet 2011, 41:110-119.
-
(2011)
Behav Genet
, vol.41
, pp. 110-119
-
-
Czamara, D.1
Bruder, J.2
Becker, J.3
Bartling, J.4
Hoffmann, P.5
Ludwig, K.U.6
Muller-Myhsok, B.7
Schulte-Korne, G.8
-
33
-
-
59949102432
-
Topography of syllable change-detection electrophysiological indices in children and adults with reading disabilities
-
Hommet C., Vidal J., Roux S., Blanc R., Barthez M.A., De Becque B., Barthelemy C., Bruneau N., Gomot M. Topography of syllable change-detection electrophysiological indices in children and adults with reading disabilities. Neuropsychologia 2009, 47:761-770.
-
(2009)
Neuropsychologia
, vol.47
, pp. 761-770
-
-
Hommet, C.1
Vidal, J.2
Roux, S.3
Blanc, R.4
Barthez, M.A.5
De Becque, B.6
Barthelemy, C.7
Bruneau, N.8
Gomot, M.9
-
34
-
-
84860995532
-
Evidence for the late mmn as a neurophysiological endophenotype for dyslexia
-
Neuhoff N., Bruder J., Bartling J., Warnke A., Remschmidt H., Muller-Myhsok B., Schulte-Korne G. Evidence for the late mmn as a neurophysiological endophenotype for dyslexia. PLoS One 2012, 7:e34909.
-
(2012)
PLoS One
, vol.7
-
-
Neuhoff, N.1
Bruder, J.2
Bartling, J.3
Warnke, A.4
Remschmidt, H.5
Muller-Myhsok, B.6
Schulte-Korne, G.7
-
35
-
-
80051591340
-
Dcdc2 knockout mice display exacerbated developmental disruptions following knockdown of doublecortin
-
Wang Y., Yin X., Rosen G., Gabel L., Guadiana S.M., Sarkisian M.R., Galaburda A.M., Loturco J.J. Dcdc2 knockout mice display exacerbated developmental disruptions following knockdown of doublecortin. Neuroscience 2011, 190:398-408.
-
(2011)
Neuroscience
, vol.190
, pp. 398-408
-
-
Wang, Y.1
Yin, X.2
Rosen, G.3
Gabel, L.4
Guadiana, S.M.5
Sarkisian, M.R.6
Galaburda, A.M.7
Loturco, J.J.8
-
36
-
-
33744920683
-
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
-
Paracchini S., Thomas A., Castro S., Lai C., Paramasivam M., Wang Y., Keating B.J., Taylor J.M., Hacking D.F., Scerri T., et al. The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum Mol Genet 2006, 15:1659-1666.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1659-1666
-
-
Paracchini, S.1
Thomas, A.2
Castro, S.3
Lai, C.4
Paramasivam, M.5
Wang, Y.6
Keating, B.J.7
Taylor, J.M.8
Hacking, D.F.9
Scerri, T.10
-
37
-
-
79952282346
-
Layer I neocortical ectopia: cellular organization and local cortical circuitry
-
Gabel L.A. Layer I neocortical ectopia: cellular organization and local cortical circuitry. Brain Res 2011, 1381:148-158.
-
(2011)
Brain Res
, vol.1381
, pp. 148-158
-
-
Gabel, L.A.1
-
38
-
-
0018356659
-
Cytoarchitectonic abnormalities in developmental dyslexia: a case study
-
Galaburda A.M., Kemper T.L. Cytoarchitectonic abnormalities in developmental dyslexia: a case study. Ann Neurol 1979, 6:94-100.
-
(1979)
Ann Neurol
, vol.6
, pp. 94-100
-
-
Galaburda, A.M.1
Kemper, T.L.2
-
39
-
-
35148851563
-
Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations
-
Rosen G.D., Bai J., Wang Y., Fiondella C.G., Threlkeld S.W., LoTurco J.J., Galaburda A.M. Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations. Cereb Cortex 2007, 17:2562-2572.
-
(2007)
Cereb Cortex
, vol.17
, pp. 2562-2572
-
-
Rosen, G.D.1
Bai, J.2
Wang, Y.3
Fiondella, C.G.4
Threlkeld, S.W.5
LoTurco, J.J.6
Galaburda, A.M.7
-
40
-
-
84860522828
-
Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319
-
Szalkowski C.E., Fiondella C.G., Galaburda A.M., Rosen G.D., Loturco J.J., Fitch R.H. Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319. Int J Dev Neurosci 2012, 30:293-302.
-
(2012)
Int J Dev Neurosci
, vol.30
, pp. 293-302
-
-
Szalkowski, C.E.1
Fiondella, C.G.2
Galaburda, A.M.3
Rosen, G.D.4
Loturco, J.J.5
Fitch, R.H.6
-
41
-
-
33846440958
-
Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1
-
Threlkeld S.W., McClure M.M., Bai J., Wang Y., LoTurco J.J., Rosen G.D., Fitch R.H. Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1. Brain Res Bull 2007, 71:508-514.
-
(2007)
Brain Res Bull
, vol.71
, pp. 508-514
-
-
Threlkeld, S.W.1
McClure, M.M.2
Bai, J.3
Wang, Y.4
LoTurco, J.J.5
Rosen, G.D.6
Fitch, R.H.7
-
42
-
-
80755172120
-
Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice
-
Gabel L.A., Marin I., LoTurco J.J., Che A., Murphy C., Manglani M., Kass S. Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice. Genes Brain Behav 2011, 10:868-875.
-
(2011)
Genes Brain Behav
, vol.10
, pp. 868-875
-
-
Gabel, L.A.1
Marin, I.2
LoTurco, J.J.3
Che, A.4
Murphy, C.5
Manglani, M.6
Kass, S.7
-
43
-
-
80053214827
-
Distribution of Kiaa0319-like immunoreactivity in the adult mouse brain-a novel protein encoded by the putative dyslexia susceptibility gene KIAA0319-like
-
Poon M.W., Tsang W.H., Waye M.M., Chan S.O. Distribution of Kiaa0319-like immunoreactivity in the adult mouse brain-a novel protein encoded by the putative dyslexia susceptibility gene KIAA0319-like. Histol Histopathol 2011, 26:953-963.
-
(2011)
Histol Histopathol
, vol.26
, pp. 953-963
-
-
Poon, M.W.1
Tsang, W.H.2
Waye, M.M.3
Chan, S.O.4
-
44
-
-
79955101961
-
A synaptic organizing principle for cortical neuronal groups
-
Perin R., Berger T.K., Markram H. A synaptic organizing principle for cortical neuronal groups. Proc Natl Acad Sci U S A 2011, 108:5419-5424.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 5419-5424
-
-
Perin, R.1
Berger, T.K.2
Markram, H.3
-
45
-
-
18844444770
-
Background gamma rhythmicity and attention in cortical local circuits: a computational study
-
Borgers C., Epstein S., Kopell N.J. Background gamma rhythmicity and attention in cortical local circuits: a computational study. Proc Natl Acad Sci U S A 2005, 102:7002-7007.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 7002-7007
-
-
Borgers, C.1
Epstein, S.2
Kopell, N.J.3
-
46
-
-
84155183272
-
Altered low-gamma sampling in auditory cortex accounts for the three main facets of dyslexia
-
Lehongre K., Ramus F., Villiermet N., Schwartz D., Giraud A.L. Altered low-gamma sampling in auditory cortex accounts for the three main facets of dyslexia. Neuron 2011, 72:1080-1090.
-
(2011)
Neuron
, vol.72
, pp. 1080-1090
-
-
Lehongre, K.1
Ramus, F.2
Villiermet, N.3
Schwartz, D.4
Giraud, A.L.5
-
47
-
-
81855186982
-
Dual gamma rhythm generators control interlaminar synchrony in auditory cortex
-
Ainsworth M., Lee S., Cunningham M.O., Roopun A.K., Traub R.D., Kopell N.J., Whittington M.A. Dual gamma rhythm generators control interlaminar synchrony in auditory cortex. J Neurosci 2011, 31:17040-17051.
-
(2011)
J Neurosci
, vol.31
, pp. 17040-17051
-
-
Ainsworth, M.1
Lee, S.2
Cunningham, M.O.3
Roopun, A.K.4
Traub, R.D.5
Kopell, N.J.6
Whittington, M.A.7
-
48
-
-
13444279102
-
Persistent gamma oscillations in superficial layers of rat auditory neocortex: experiment and model
-
Traub R.D., Bibbig A., LeBeau F.E., Cunningham M.O., Whittington M.A. Persistent gamma oscillations in superficial layers of rat auditory neocortex: experiment and model. J Physiol 2005, 562(Pt 1):3-8.
-
(2005)
J Physiol
, vol.562
, Issue.PART 1
, pp. 3-8
-
-
Traub, R.D.1
Bibbig, A.2
LeBeau, F.E.3
Cunningham, M.O.4
Whittington, M.A.5
-
49
-
-
84859217287
-
Cortical oscillations and speech processing: emerging computational principles and operations
-
Giraud A.L., Poeppel D. Cortical oscillations and speech processing: emerging computational principles and operations. Nat Neurosci 2012, 15:511-517.
-
(2012)
Nat Neurosci
, vol.15
, pp. 511-517
-
-
Giraud, A.L.1
Poeppel, D.2
-
50
-
-
79953009142
-
Gamma and theta rhythms in biophysical models of hippocampal circuits
-
Springer, Ch 15, V. Cutsuridis, B.P. Graham, S. Cobb, I. Vida (Eds.)
-
Kopell N., Börgers C., Pervouchine D., Malerba P., Tort A.B.L. Gamma and theta rhythms in biophysical models of hippocampal circuits. Hippocampal Microcircuits: A Computational Modeller's Resource Book 2010, Springer, Ch 15. V. Cutsuridis, B.P. Graham, S. Cobb, I. Vida (Eds.).
-
(2010)
Hippocampal Microcircuits: A Computational Modeller's Resource Book
-
-
Kopell, N.1
Börgers, C.2
Pervouchine, D.3
Malerba, P.4
Tort, A.B.L.5
-
51
-
-
78649815928
-
Neurophysiological origin of human brain asymmetry for speech and language
-
Morillon B., Lehongre K., Frackowiak R.S., Ducorps A., Kleinschmidt A., Poeppel D., Giraud A.L. Neurophysiological origin of human brain asymmetry for speech and language. Proc Natl Acad Sci U S A 2010, 107:18688-18693.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 18688-18693
-
-
Morillon, B.1
Lehongre, K.2
Frackowiak, R.S.3
Ducorps, A.4
Kleinschmidt, A.5
Poeppel, D.6
Giraud, A.L.7
-
52
-
-
0842325639
-
Dynamics of precise spike timing in primary auditory cortex
-
Elhilali M., Fritz J.B., Klein D.J., Simon J.Z., Shamma S.A. Dynamics of precise spike timing in primary auditory cortex. J Neurosci 2004, 24:1159-1172.
-
(2004)
J Neurosci
, vol.24
, pp. 1159-1172
-
-
Elhilali, M.1
Fritz, J.B.2
Klein, D.J.3
Simon, J.Z.4
Shamma, S.A.5
-
53
-
-
33751110464
-
Auditory brainstem timing predicts cerebral asymmetry for speech
-
Abrams D.A., Nicol T., Zecker S.G., Kraus N. Auditory brainstem timing predicts cerebral asymmetry for speech. J Neurosci 2006, 26:11131-11137.
-
(2006)
J Neurosci
, vol.26
, pp. 11131-11137
-
-
Abrams, D.A.1
Nicol, T.2
Zecker, S.G.3
Kraus, N.4
-
54
-
-
84855454342
-
Reduced phase locking to slow amplitude modulation in adults with dyslexia: an MEG study
-
Hamalainen J.A., Rupp A., Soltesz F., Szucs D., Goswami U. Reduced phase locking to slow amplitude modulation in adults with dyslexia: an MEG study. Neuroimage 2012, 59:2952-2961.
-
(2012)
Neuroimage
, vol.59
, pp. 2952-2961
-
-
Hamalainen, J.A.1
Rupp, A.2
Soltesz, F.3
Szucs, D.4
Goswami, U.5
-
55
-
-
78650722552
-
A temporal sampling framework for developmental dyslexia
-
Goswami U. A temporal sampling framework for developmental dyslexia. Trends Cogn Sci 2011, 15:3-10.
-
(2011)
Trends Cogn Sci
, vol.15
, pp. 3-10
-
-
Goswami, U.1
-
56
-
-
80053631366
-
Reduced sensitivity to slow-rate dynamic auditory information in children with dyslexia
-
Poelmans H., Luts H., Vandermosten M., Boets B., Ghesquiere P., Wouters J. Reduced sensitivity to slow-rate dynamic auditory information in children with dyslexia. Res Dev Disabil 2011, 32:2810-2819.
-
(2011)
Res Dev Disabil
, vol.32
, pp. 2810-2819
-
-
Poelmans, H.1
Luts, H.2
Vandermosten, M.3
Boets, B.4
Ghesquiere, P.5
Wouters, J.6
-
57
-
-
31144448452
-
Language development and literacy skills in late-talking toddlers with and without familial risk for dyslexia
-
Lyytinen P., Eklund K., Lyytinen H. Language development and literacy skills in late-talking toddlers with and without familial risk for dyslexia. Ann Dyslexia 2005, 55:166-192.
-
(2005)
Ann Dyslexia
, vol.55
, pp. 166-192
-
-
Lyytinen, P.1
Eklund, K.2
Lyytinen, H.3
-
58
-
-
79851510800
-
Preschool impairments in auditory processing and speech perception uniquely predict future reading problems
-
Boets B., Vandermosten M., Poelmans H., Luts H., Wouters J., Ghesquiere P. Preschool impairments in auditory processing and speech perception uniquely predict future reading problems. Res Dev Disabil 2011, 32:560-570.
-
(2011)
Res Dev Disabil
, vol.32
, pp. 560-570
-
-
Boets, B.1
Vandermosten, M.2
Poelmans, H.3
Luts, H.4
Wouters, J.5
Ghesquiere, P.6
-
60
-
-
74649087417
-
Dyslexia: a deficit in visuo-spatial attention, not in phonological processing
-
Vidyasagar T.R., Pammer K. Dyslexia: a deficit in visuo-spatial attention, not in phonological processing. Trends Cogn Sci 2010, 14:57-63.
-
(2010)
Trends Cogn Sci
, vol.14
, pp. 57-63
-
-
Vidyasagar, T.R.1
Pammer, K.2
-
61
-
-
8444230203
-
Neurobiology of dyslexia: a reinterpretation of the data
-
Ramus F. Neurobiology of dyslexia: a reinterpretation of the data. Trends Neurosci 2004, 27:720-726.
-
(2004)
Trends Neurosci
, vol.27
, pp. 720-726
-
-
Ramus, F.1
|