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Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment
16 references·7 citing·50 second hopsampled
Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment (2013)Alleles of a Polymorphic ETV6 Binding Sit…Developmental dyslexia (2012)Developmental dyslexiaLearning Disabilities, Dyslexia, and Vision (2011)Learning Disabilities, Dyslex…DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits (2011)DCDC2, KIAA0319 and CMIP Are …DCDC2 genetic variants and susceptibility to developmental dyslexia (2011)DCDC2 genetic variants and su…A theoretical molecular network for dyslexia: integrating available genetic findings (2010)A theoretical molecular netwo…Genetics of developmental dyslexia (2009)Genetics of developmental dys…CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment (2009)CMIP and ATP2C2 Modulate Phon…A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene (2009)A Common Variant Associated w…Relations Among Speech, Language, and Reading Disorders (2008)Relations Among Speech, Langu…Association of the KIAA0319 Dyslexia Susceptibility Gene With Reading Skills in the General Population (2008)Association of the KIAA0319 D…A Haplotype Spanning KIAA0319 and TTRAP Is Associated with Normal Variation in Reading and Spelling Ability (2007)A Haplotype Spanning KIAA0319…The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration (2006)The chromosome 6p22 haplotype…Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia (2006)Further evidence that the KIA…DCDC2 is associated with reading disability and modulates neuronal development in the brain (2005)DCDC2 is associated with read…A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States (2004)A 77-Kilobase Region of Chrom…Nonword Repetition as a Behavioural Marker for Inherited Language Impairment: Evidence From a Twin Study (1996)Nonword Repetition as a Behav…White matter in infancy is prospectively associated with language outcomes in kindergarten (2021)White matter in infancy is pr…Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages (2018)Worldwide distribution of the…Dyslexia risk gene relates to representation of sound in the auditory brainstem (2017)Dyslexia risk gene relates to…Strong Motion Deficits in Dyslexia Associated withDCDC2Gene Alteration (2015)Strong Motion Deficits in Dys…The DCDC2/intron 2 deletion and white matter disorganization: Focus on developmental dyslexia (2014)The DCDC2/intron 2 deletion a…Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability (2014)Mutation of Dcdc2 in mice lea…Imaging-genetics in dyslexia: Connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments (2013)Imaging-genetics in dyslexia:…Developmental dyslexia: Four consecutive patients with cortical anomalies (1985)The Development and Well-Being Assessment: Description and Initial Validation of an Integrated Assessment of Child and Adolescent Psychopathology (2000)Developmental Dyslexia and Specific Language Impairment: Same or Different? (2004)Three Dyslexia Susceptibility Genes, DYX1C1, DCDC2, and KIAA0319, Affect Temporo-Parietal White Matter Structure (2012)Molecular Genetics of Dyslexia: An Overview (2013)Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms (2017)Evaluation of the role of phonological STM in the development of vocabulary in children: A longitudinal study (1989)A Prospective Study of the Relationship between Specific Language Impairment, Phonological Disorders and Reading Retardation (1990)Phonological memory deficits in language disordered children: Is there a causal connection? (1990)Working memory deficits in children with low achievements in the national curriculum at 7 years of age (2000)Is working memory still working? (2001)Are Specific Language Impairment and Dyslexia Distinct Disorders? (2005)Varieties of developmental dyslexia (1993)Quantitative Trait Locus for Reading Disability on Chromosome 6 (1994)Dyslexia: Cultural Diversity and Biological Unity (2001)Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia (2005)Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects (2010)The children's test of nonword repetition: A test of phonological working memory (1994)Development of the Children's Communication Checklist (CCC): A Method for Assessing Qualitative Aspects of Communicative Impairment in Children (1998)Genome‐wide screening for DNA variants associated with reading and language traits (2014)Prevalence of Specific Language Impairment in Kindergarten Children (1997)The double-deficit hypothesis for the developmental dyslexias. (1999)Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults (2003)Genetic Advances in the Study of Speech and Language Disorders (2010)Cerebellar Function in Developmental Dyslexia (2012)Dyslexia (Specific Reading Disability) (2005)The neural code for written words: a proposal (2005)From genes to behavior in developmental dyslexia (2006)The Education of Dyslexic Children from Childhood to Young Adulthood (2007)Cytoarchitectonic abnormalities in developmental dyslexia: A case study (1979)Structural brain alterations associated with dyslexia predate reading onset (2010)Functional characteristics of developmental dyslexia in left-hemispheric posterior brain regions predate reading onset (2012)Diagnostic and Statistical Manual of Mental Disorders. (2000)Why Most Published Research Findings Are False (2005)The dyslexia debate (2012)Diagnostic and Statistical Manual of Mental Disorders (2013)The current status of the magnocellular theory of developmental dyslexia (2018)Understanding Dyslexia in the Context of Developmental Language Disorders (2018)Matthew Effects in Reading: Some Consequences of Individual Differences in the Acquisition of Literacy (1986)Nature-nurture reconceptualized in developmental perspective: A bioecological model. (1994)Statistical Learning by 8-Month-Old Infants (1996)Phonological deficits in specific language impairment and developmental dyslexia: towards a multidimensional model (2013)Oral language deficits in familial dyslexia: A meta-analysis and review. (2016)Defining and understanding dyslexia: past, present and future (2020)Preventing Reading Difficulties in Young Children (1998)A definition of dyslexia (2003)Foundation literacy acquisition in European orthographies (2003)Action Video Games Make Dyslexic Children Read Better (2013)The construct of the multisensory temporal binding window and its dysregulation in developmental disabilities (2014)Music Training Increases Phonological Awareness and Reading Skills in Developmental Dyslexia: A Randomized Control Trial (2015)
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References

  • 2012Developmental dyslexia762 cited
  • 1996Nonword Repetition as a Behavioural Marker for Inherited Language Impairment: Evidence From a Twin Study668 cited
  • 2008Relations Among Speech, Language, and Reading Disorders524 cited
  • 2005DCDC2 is associated with reading disability and modulates neuronal development in the brain383 cited
  • 2006The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration270 cited
  • 2004A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States234 cited
  • 2009Genetics of developmental dyslexia230 cited
  • 2011Learning Disabilities, Dyslexia, and Vision216 cited
  • 2009CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment184 cited
  • 2011DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits174 cited
  • 2006Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia158 cited
  • 2008Association of the KIAA0319 Dyslexia Susceptibility Gene With Reading Skills in the General Population129 cited
  • 2010A theoretical molecular network for dyslexia: integrating available genetic findings119 cited
  • 2009A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene

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104 cited
  • 2007A Haplotype Spanning KIAA0319 and TTRAP Is Associated with Normal Variation in Reading and Spelling Ability94 cited
  • 2011DCDC2 genetic variants and susceptibility to developmental dyslexia80 cited
  • Cited by

    • 2021White matter in infancy is prospectively associated with language outcomes in kindergarten60 cited
    • 2017Dyslexia risk gene relates to representation of sound in the auditory brainstem54 cited
    • 2014Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability50 cited
    • 2013Imaging-genetics in dyslexia: Connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments47 cited
    • 2014The DCDC2/intron 2 deletion and white matter disorganization: Focus on developmental dyslexia46 cited
    • 2015Strong Motion Deficits in Dyslexia Associated withDCDC2Gene Alteration40 cited
    • 2018Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages12 cited