| scholarly article | Q13442814 |
| P50 | author | Natalie R Powers | Q56869904 |
| P2093 | author name string | Susan M Ring | |
| Laura L Miller | |||
| Yong Kong | |||
| Richard K Olson | |||
| Erik G Willcutt | |||
| Bruce F Pennington | |||
| Shelley D Smith | |||
| Jeffrey R Gruen | |||
| John D Eicher | |||
| P2860 | cites work | DCDC2 is associated with reading disability and modulates neuronal development in the brain | Q24294360 |
| The effect of variation in expression of the candidate dyslexia susceptibility gene homolog Kiaa0319 on neuronal migration and dendritic morphology in the rat. | Q24324779 | ||
| A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States | Q24534152 | ||
| Quantitative-trait locus for specific language and reading deficits on chromosome 6p | Q24540062 | ||
| DCDC2, KIAA0319 and CMIP are associated with reading-related traits | Q24631427 | ||
| DCDC2 genetic variants and susceptibility to developmental dyslexia | Q24631569 | ||
| Developmental dyslexia | Q26992245 | ||
| Speech sound processing deficits and training-induced neural plasticity in rats with dyslexia gene knockdown | Q27326690 | ||
| Polymerization of the SAM domain of TEL in leukemogenesis and transcriptional repression | Q27633822 | ||
| The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration | Q28306226 | ||
| A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability | Q28307743 | ||
| Recent advances in the genetics of language impairment | Q28748712 | ||
| ALSPAC--the Avon Longitudinal Study of Parents and Children. I. Study methodology | Q29615794 | ||
| Cohort profile: the 'children of the 90s'—the index offspring of the Avon Longitudinal Study of Parents and Children | Q29615806 | ||
| Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability | Q30399796 | ||
| The genetics of reading disabilities: from phenotypes to candidate genes | Q30459192 | ||
| Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability | Q30529633 | ||
| Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ | Q30580491 | ||
| A common variant associated with dyslexia reduces expression of the KIAA0319 gene | Q33422937 | ||
| Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia | Q33793644 | ||
| DNA binding by the ETS protein TEL (ETV6) is regulated by autoinhibition and self-association | Q33897815 | ||
| Dyslexia and early intervention: what did we learn from the Dutch Dyslexia Programme? | Q34378214 | ||
| A dyslexia-associated variant in DCDC2 changes gene expression | Q34648864 | ||
| Uses and interpretations of non-word repetition tasks in children with and without specific language impairments (SLI). | Q34733333 | ||
| Position of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes | Q34750026 | ||
| Relations among speech, language, and reading disorders | Q34800205 | ||
| Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. | Q34842629 | ||
| The DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexia. | Q35187515 | ||
| Homologue pairing in flies and mammals: gene regulation when two are involved | Q35910233 | ||
| Language growth and genetics of specific language impairment | Q36933769 | ||
| Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment | Q37010437 | ||
| Polymorphism of DCDC2 Reveals Differences in Cortical Morphology of Healthy Individuals-A Preliminary Voxel Based Morphometry Study | Q37019218 | ||
| Modeling the Etiology of Individual Differences in Early Reading Development: Evidence for Strong Genetic Influences | Q37527226 | ||
| The dyslexia-associated gene DCDC2 is required for spike-timing precision in mouse neocortex | Q39739344 | ||
| The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage | Q41130845 | ||
| Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample | Q44835472 | ||
| Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample | Q46095410 | ||
| The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems. | Q47848734 | ||
| Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. | Q50712194 | ||
| The role of gene DCDC2 in German dyslexics. | Q51802890 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 163-171 | |
| P577 | publication date | 2015-12-11 | |
| P1433 | published in | Journal of Medical Genetics | Q14640281 |
| P1476 | title | The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles | |
| P478 | volume | 53 |
| Q47741728 | A common genetic variant in FOXP2 is associated with language-based learning (dis)abilities: Evidence from two Italian independent samples |
| Q90991148 | A molecular-genetic and imaging-genetic approach to specific comprehension difficulties in children |
| Q47964788 | Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples. |
| Q38969390 | Dyslexia risk gene relates to representation of sound in the auditory brainstem. |
| Q47151456 | Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC. |
| Q42707804 | Study of Genetic Association With DCDC2 and Developmental Dyslexia in Hong Kong Chinese Children. |
| Q38662599 | The DCDC2 deletion is not a risk factor for dyslexia |
| Q47589839 | The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effects |
| Q38890401 | Translating dyslexia across species |
| Q47638796 | Visual motion and rapid auditory processing are solid endophenotypes of developmental dyslexia |
| Q53280343 | Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages. |
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