| scholarly article | Q13442814 |
| P356 | DOI | 10.1093/HMG/DDL089 |
| P8608 | Fatcat ID | release_bibnuikp4jcunmx7nx53tsdhly |
| P3181 | OpenCitations bibliographic resource ID | 2179626 |
| P698 | PubMed publication ID | 16600991 |
| P5875 | ResearchGate publication ID | 7178804 |
| P50 | author | Richard Wade-Martins | Q60537481 |
| Anthony Monaco | Q4773127 | ||
| Silvia Paracchini | Q21264679 | ||
| Andrew J Copp | Q37386184 | ||
| Julian C Knight | Q40247846 | ||
| Clyde Francks | Q42305970 | ||
| P2093 | author name string | Yu Wang | |
| Alex J Richardson | |||
| Brendan J Keating | |||
| Jennifer M Taylor | |||
| John F Stein | |||
| Sandra Castro | |||
| Douglas F Hacking | |||
| Thomas Scerri | |||
| Ankur Thomas | |||
| Cecilia Lai | |||
| Joseph Loturco | |||
| Murugan Paramasivam | |||
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | dyslexia | Q132971 |
| P304 | page(s) | 1659-66 | |
| P577 | publication date | 2006-05-15 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration | |
| P478 | volume | 15 |
| Q33965244 | A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children |
| Q33422937 | A common variant associated with dyslexia reduces expression of the KIAA0319 gene |
| Q34648864 | A dyslexia-associated variant in DCDC2 changes gene expression |
| Q34144455 | A theoretical molecular network for dyslexia: integrating available genetic findings |
| Q35804580 | A versatile ligation-independent cloning method suitable for high-throughput expression screening applications |
| Q37156121 | A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12 |
| Q37010437 | Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment |
| Q47605875 | Alpha-synuclein induces the unfolded protein response in Parkinson's disease SNCA triplication iPSC-derived neurons |
| Q28248178 | Alternative splicing in the dyslexia-associated gene KIAA0319 |
| Q33749322 | An allele-specific gene expression assay to test the functional basis of genetic associations |
| Q39797226 | An examination of candidate gene SNPs for dyslexia in an Indian sample |
| Q34886032 | Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population |
| Q50744254 | Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population. |
| Q50154711 | Ancestral Variations of the PCDHG Gene Cluster Predispose to Dyslexia in a Multiplex Family |
| Q40505104 | Approach to epigenetic analysis in language disorders |
| Q91785231 | Assessment for familial pattern and association of polymorphisms in KIAA0319 gene with specific reading disorder in children from North India visiting a tertiary care centre: A case-control study |
| Q36803173 | Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region |
| Q42292717 | Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319. |
| Q35068099 | Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children |
| Q48827312 | Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population |
| Q39553271 | Associations Between the KIAA0319 Dyslexia Susceptibility Gene Variants, Antenatal Maternal Stress, and Reading Ability in a Longitudinal Birth Cohort |
| Q36591712 | Atypical Sulcal Pattern in Children with Developmental Dyslexia and At-Risk Kindergarteners |
| Q28716605 | CNVs leading to fusion transcripts in individuals with autism spectrum disorder |
| Q41729389 | CTNND2-a candidate gene for reading problems and mild intellectual disability |
| Q37141088 | Cell biology in neuroscience: mechanisms of cell migration in the nervous system |
| Q26779317 | Cellullar insights into cerebral cortical development: focusing on the locomotion mode of neuronal migration |
| Q30580491 | Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ |
| Q37258809 | Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs |
| Q47707873 | Cognitive genomics: Searching for the genetic roots of neuropsychological functioning |
| Q30492191 | Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment |
| Q24672124 | Cullin 5 regulates Dab1 protein levels and neuron positioning during cortical development |
| Q24631427 | DCDC2, KIAA0319 and CMIP are associated with reading-related traits |
| Q24304124 | DYX1C1 functions in neuronal migration in developing neocortex |
| Q38774522 | Deazaflavin Inhibitors of Tyrosyl-DNA Phosphodiesterase 2 (TDP2) Specific for the Human Enzyme and Active against Cellular TDP2. |
| Q58227234 | Dislexias evolutivas: qué pueden decirnos la neurología y la genética al respecto |
| Q37091458 | Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations |
| Q35592928 | Dissection of genetic associations with language-related traits in population-based cohorts |
| Q36491354 | Distinct genomic signatures of adaptation in pre- and postnatal environments during human evolution |
| Q24598131 | Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample |
| Q27346928 | Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children |
| Q38969390 | Dyslexia risk gene relates to representation of sound in the auditory brainstem. |
| Q52809303 | Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1. |
| Q36733870 | Dyslexia susceptibility genes influence brain atrophy in frontotemporal dementia |
| Q24294865 | Dyslexia-associated kiaa0319-like protein interacts with axon guidance receptor nogo receptor 1 |
| Q42953075 | Dyslexia: the Role of Vision and Visual Attention |
| Q37350966 | Embryonic disruption of the candidate dyslexia susceptibility gene homolog Kiaa0319-like results in neuronal migration disorders. |
| Q27349866 | Endocytosis regulates cell soma translocation and the distribution of adhesion proteins in migrating neurons |
| Q34146699 | Etiologies and Molecular Mechanisms of Communication Disorders |
| Q34568893 | From genes to behavior in developmental dyslexia |
| Q42132595 | Frontotemporal dementia and language networks: cortical thickness reduction is driven by dyslexia susceptibility genes. |
| Q24651392 | Functional MAPT haplotypes: bridging the gap between genotype and neuropathology |
| Q30505176 | Functional characteristics of developmental dyslexia in left-hemispheric posterior brain regions predate reading onset |
| Q24322880 | Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia |
| Q50712194 | Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. |
| Q81430138 | Gene x Environment interactions in speech sound disorder predict language and preliteracy outcomes |
| Q35965426 | Gene-environment interaction on neural mechanisms of orthographic processing in Chinese children |
| Q24647393 | Genes, cognition, and communication: insights from neurodevelopmental disorders |
| Q38839666 | Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort |
| Q34248551 | Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. |
| Q33793644 | Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia |
| Q37678978 | Genetics of developmental dyslexia |
| Q22306529 | Genetics of dyslexia: the evolving landscape |
| Q33785862 | Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci |
| Q40113301 | Haplotype-specific expression of the N-terminal exons 2 and 3 at the human MAPT locus |
| Q36071412 | Heritability of high reading ability and its interaction with parental education |
| Q36042505 | Human cell adhesion molecules: annotated functional subtypes and overrepresentation of addiction-associated genes |
| Q33742226 | Identification of candidate genes for dyslexia susceptibility on chromosome 18. |
| Q28672682 | Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments |
| Q24307517 | Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons |
| Q38322139 | Insights into the genetic foundations of human communication |
| Q30498012 | Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. |
| Q44835472 | Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample |
| Q50695616 | KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia. |
| Q37208967 | KIAA0319 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children |
| Q30439977 | Knockdown of the candidate dyslexia susceptibility gene homolog dyx1c1 in rodents: effects on auditory processing, visual attention, and cortical and thalamic anatomy |
| Q30407725 | Knockdown of the dyslexia-associated gene Kiaa0319 impairs temporal responses to speech stimuli in rat primary auditory cortex |
| Q47633155 | Knockout Mice for Dyslexia Susceptibility Gene Homologs KIAA0319 and KIAA0319L have Unaffected Neuronal Migration but Display Abnormal Auditory Processing. |
| Q35547385 | Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders |
| Q38986771 | Lessons to be learned: how a comprehensive neurobiological framework of atypical reading development can inform educational practice |
| Q51862601 | Molecular genetics and molecular biology of dyslexia. |
| Q38153350 | Molecular genetics of dyslexia: an overview |
| Q24630169 | Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice |
| Q30454040 | Neocortical disruption and behavioral impairments in rats following in utero RNAi of candidate dyslexia risk gene Kiaa0319. |
| Q30378092 | Neural Biomarkers for Dyslexia, ADHD, and ADD in the Auditory Cortex of Children. |
| Q39235595 | Neural Noise Hypothesis of Developmental Dyslexia |
| Q61449263 | Neurobiological Sex Differences in Developmental Dyslexia |
| Q44597775 | Neurobiological bases of reading disorder Part I: Etiological investigations |
| Q58227231 | Neurobiology and neurogenetics of dyslexia |
| Q58764687 | Neurochemistry Predicts Convergence of Written and Spoken Language: A Proton Magnetic Resonance Spectroscopy Study of Cross-Modal Language Integration |
| Q39932335 | Newborn event-related potentials predict poorer pre-reading skills in children at risk for dyslexia |
| Q33601252 | Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment |
| Q30358905 | Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice. |
| Q37202517 | OKCAM: an ontology-based, human-centered knowledgebase for cell adhesion molecules |
| Q27322845 | Opposite Associations between Individual KIAA0319 Polymorphisms and Developmental Dyslexia Risk across Populations: A Stratified Meta-Analysis by the Study Population |
| Q30469964 | Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1 |
| Q35600743 | Pleiotropic functions of EAPII/TTRAP/TDP2: cancer development, chemoresistance and beyond |
| Q34750026 | Position of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes |
| Q32872058 | Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat |
| Q30475697 | Progress towards a cellular neurobiology of reading disability |
| Q33891684 | Reading and language disorders: the importance of both quantity and quality. |
| Q27326690 | Speech sound processing deficits and training-induced neural plasticity in rats with dyslexia gene knockdown |
| Q35913343 | Spherical harmonic analysis of cortical complexity in autism and dyslexia |
| Q30528399 | Structural brain alterations associated with dyslexia predate reading onset |
| Q42707804 | Study of Genetic Association With DCDC2 and Developmental Dyslexia in Hong Kong Chinese Children. |
| Q30362517 | Tackling the 'dyslexia paradox': reading brain and behavior for early markers of developmental dyslexiax. |
| Q38711030 | The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling |
| Q42219905 | The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities |
| Q41577410 | The Roles of Genes in the Neuronal Migration and Neurite Outgrowth Network in Developmental Dyslexia: Single- and Multiple-Risk Genetic Variants |
| Q30515982 | The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language |
| Q30482949 | The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia |
| Q92867236 | The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration |
| Q41130845 | The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage |
| Q39739344 | The dyslexia-associated gene DCDC2 is required for spike-timing precision in mouse neocortex |
| Q40038611 | The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms |
| Q24322732 | The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway |
| Q24324779 | The effect of variation in expression of the candidate dyslexia susceptibility gene homolog Kiaa0319 on neuronal migration and dendritic morphology in the rat. |
| Q30440802 | The effects of Kiaa0319 knockdown on cortical and subcortical anatomy in male rats |
| Q34441478 | The effects of embryonic knockdown of the candidate dyslexia susceptibility gene homologue Dyx1c1 on the distribution of GABAergic neurons in the cerebral cortex. |
| Q28603746 | The evolutionary history of genes involved in spoken and written language: beyond FOXP2. |
| Q30459192 | The genetics of reading disabilities: from phenotypes to candidate genes |
| Q37419588 | The genetics of reading disability |
| Q24653501 | The human lexinome: genes of language and reading |
| Q57384485 | The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on |
| Q27317078 | The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles. |
| Q34708502 | The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function |
| Q28118826 | Transcriptional program of ciliated epithelial cells reveals new cilium and centrosome components and links to human disease |
| Q50735365 | Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero. |
| Q33875792 | Tyrosyl-DNA-phosphodiesterases (TDP1 and TDP2). |
| Q34023768 | Understanding the Complex Etiologies of Developmental Disorders: Behavioral and Molecular Genetic Approaches |
| Q30529633 | Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability |
| Q47911640 | White Matter Alterations in Infants at Risk for Developmental Dyslexia |
| Q21198726 | Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech. |
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