| P50 | author | Glenn D. Rosen | Q42067423 |
| | Joshua L Haight | Q58324211 |
| P2093 | author name string | T A Currier | |
| | A M Galaburda | |
| | M A Etchegaray | |
| P2860 | cites work | DCDC2 is associated with reading disability and modulates neuronal development in the brain | Q24294360 |
| | DYX1C1 functions in neuronal migration in developing neocortex | Q24304124 |
| | The effect of variation in expression of the candidate dyslexia susceptibility gene homolog Kiaa0319 on neuronal migration and dendritic morphology in the rat. | Q24324779 |
| | Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia | Q24531462 |
| | A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States | Q24534152 |
| | Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia | Q24540508 |
| | Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample | Q24598131 |
| | Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1. | Q24671718 |
| | A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain | Q24673084 |
| | Alternative splicing in the dyslexia-associated gene KIAA0319 | Q28248178 |
| | Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes | Q28251621 |
| | A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia | Q28288993 |
| | The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration | Q28306226 |
| | RNAi reveals doublecortin is required for radial migration in rat neocortex | Q28567912 |
| | Postnatal shifts of interneuron position in the neocortex of normal and reeler mice: evidence for inward radial migration | Q28594989 |
| | The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia | Q30482949 |
| | Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat | Q32872058 |
| | Differential modulation of proliferation in the neocortical ventricular and subventricular zones | Q33911054 |
| | Developmental dyslexia: four consecutive patients with cortical anomalies | Q34199798 |
| | The role of GABA in the pathophysiology and treatment of anxiety disorders. | Q34319322 |
| | GABA and glutamate depolarize cortical progenitor cells and inhibit DNA synthesis | Q34400922 |
| | The role of GABA in the early neuronal development | Q34499030 |
| | Development of cortical GABAergic circuits and its implications for neurodevelopmental disorders | Q34642137 |
| | Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. | Q34842629 |
| | GABA, gamma-hydroxybutyric acid, and neurological disease | Q35189066 |
| | Neurotransmitters and brain maturation: early paracrine actions of GABA and glutamate modulate neuronal migration | Q36829173 |
| | Neurotransmitters and the development of neuronal circuits | Q37082717 |
| | Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations | Q37091458 |
| | Dcx reexpression reduces subcortical band heterotopia and seizure threshold in an animal model of neuronal migration disorder | Q37275380 |
| | Defining the role of GABA in cortical development. | Q37372212 |
| | The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms | Q40038611 |
| | Layer specification of transplanted interneurons in developing mouse neocortex. | Q40578050 |
| | GABA and mood disorders: a brief review and hypothesis | Q40940358 |
| | Four-dimensional migratory coordinates of GABAergic interneurons in the developing mouse cortex. | Q42170320 |
| | In utero fate mapping reveals distinct migratory pathways and fates of neurons born in the mammalian basal forebrain | Q42510928 |
| | Human GABA(B) receptor 1 gene: eight novel sequence variants | Q43570469 |
| | Are dyslexia and dyscalculia associated with Rolandic epilepsy? A short report on ten Italian patients | Q44802789 |
| | Postsynaptic currents prior to onset of epileptiform activity in rat microgyria | Q44929020 |
| | GABA-A receptors regulate neocortical neuronal migration in vitro and in vivo | Q46923535 |
| | Spatial genetic patterning of the embryonic neuroepithelium generates GABAergic interneuron diversity in the adult cortex | Q46956790 |
| | GABA and histogenesis in fetal and neonatal mouse brain lacking both the isoforms of glutamic acid decarboxylase | Q48231628 |
| | Effects of neonatal freeze lesions on expression of parvalbumin in rat neocortex | Q48322953 |
| | Written language skills in children with benign childhood epilepsy with centrotemporal spikes | Q48565970 |
| | Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia | Q48674496 |
| | Ventricle-directed migration in the developing cerebral cortex | Q48685047 |
| | Developmental dyslexia in women: neuropathological findings in three patients | Q48841230 |
| | The role of gene DCDC2 in German dyslexics. | Q51802890 |
| | A structural basis for reading fluency: white matter defects in a genetic brain malformation. | Q51970623 |
| | [Characterization of the linguistic profile of a family with Perisylvian Syndrome]. | Q52029774 |
| | A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia. | Q52058164 |
| | Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q. | Q52087318 |
| | GABA receptor antagonists modulate postmitotic cell migration in slice cultures of embryonic rat cortex | Q74303565 |
| | Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia | Q81489538 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | dyslexia | Q132971 |
| P304 | page(s) | 535-546 | |
| P577 | publication date | 2010-11-09 | |
| P1433 | published in | Neuroscience | Q15708571 |
| P1476 | title | The effects of embryonic knockdown of the candidate dyslexia susceptibility gene homologue Dyx1c1 on the distribution of GABAergic neurons in the cerebral cortex | |
| P478 | volume | 172 | |