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The role of gene DCDC2 in German dyslexics
15 references·11 citing·46 second hop
The role of gene DCDC2 in German dyslexics (2009)The role of gene DCDC2 in German dyslexicsEvaluation of candidate genes for DYX1 and DYX2 in families with dyslexia (2007)Evaluation of candidate genes…A Haplotype Spanning KIAA0319 and TTRAP Is Associated with Normal Variation in Reading and Spelling Ability (2007)A Haplotype Spanning KIAA0319…Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia (2006)Further evidence that the KIA…Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia (2005)Strong Genetic Evidence of DC…Strong Evidence That KIAA0319 on Chromosome 6p Is a Susceptibility Gene for Developmental Dyslexia (2005)Strong Evidence That KIAA0319…DCDC2 is associated with reading disability and modulates neuronal development in the brain (2005)DCDC2 is associated with read…Evidence for Linkage of Spelling Disability to Chromosome 15 (1998)Evidence for Linkage of Spell…Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15. (1997)Susceptibility loci for disti…Genes, Environment, and the Development of Orthographic Skills (1994)Genes, Environment, and the D…Evidence for a Magnocellular Defect in Developmental Dyslexia a (1993)Evidence for a Magnocellular …Bilingual Biscriptal Deep Dyslexia (1984)Bilingual Biscriptal Deep Dys…Surface Dyslexia (1983)Surface DyslexiaProgress in Learning Disabilities (1982)Progress in Learning Disabili…4. Developmental dyslexia—prevailing diagnostic concepts and a new diagnostic approach (1973)4. Developmental dyslexia—pre…Progress in Learning Disabilities (1972)Progress in Learning Disabili…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…Imaging-genetics in dyslexia: Connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments (2013)Imaging-genetics in dyslexia:…Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort (2013)Genetic analysis of dyslexia …Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment (2013)Alleles of a Polymorphic ETV6…Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability (2012)Variants in the DYX2 locus ar…Imaging genetics of FOXP2 in dyslexia (2011)Imaging genetics of FOXP2 in …Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population (2010)Analysis of dyslexia candidat…A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression (2010)A Dyslexia-Associated Variant…Progress towards a cellular neurobiology of reading disability (2009)Progress towards a cellular n…Explaining the Differences Between the Dyslexic and the Garden-Variety Poor Reader (1988)Prevalence of reading disability in boys and girls. Results of the Connecticut Longitudinal Study (1990)Longitudinal Studies of Phonological Processing and Reading (1994)Developmental dyslexia: genetic dissection of a complex cognitive trait (2002)Developmental dyslexia (2004)The Dimensional Yale–Brown Obsessive–Compulsive Scale (DY-BOCS): an instrument for assessing obsessive–compulsive symptom dimensions (2006)Quantitative Trait Locus for Reading Disability on Chromosome 6 (1994)The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration (2006)Genetics of developmental dyslexia (2009)British Ability Scales 3 (2013)Rapid “Automatized” Naming of Pictured Objects, Colors, Letters and Numbers by Normal Children (1974)Sex Differences in Developmental Reading Disability (2004)The contribution of white and gray matter differences to developmental dyslexia: Insights from DTI and VBM at 3.0T (2008)Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects (2010)Reading, Writing and Speech Problems in Children. (1937)Auditory temporal perception, phonics, and reading disabilities in children (1980)Dyslexia: Theory and Research (1981)Impaired neuronal timing in developmental dyslexia—the magnocellular hypothesis (1999)The relationship between visuo-spatial attention and nonword reading in developmental dyslexia (2006)Grey Matter Alterations Co-Localize with Functional Abnormalities in Developmental Dyslexia: An ALE Meta-Analysis (2012)Grundintelligenztest Skala 2 CFT 20 (1998)A dominant gene for developmental dyslexia on chromosome 3 (2001)Genetics of dyslexia: the evolving landscape (2007)Molecular Genetics of Dyslexia: An Overview (2013)Developmental dyslexia: Four consecutive patients with cortical anomalies (1985)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)A distributed, developmental model of word recognition and naming. (1989)Beginning to read: thinking and learning about print (1990)Beginning to read : Thinking and learning about print. By Marilyn Jager Adams. Cambridge, MA: The MIT Press, 1990. Pp. x, 494. Cloth $29.95. (1991)Not All Reading Disabilities Are Alike (1999)Training Phonological Awareness with and without Explicit Attention to Articulation (1999)Varieties of Developmental Reading Disorder: Genetic and Environmental Influences (1999)Patterns of paralexia: A psycholinguistic approach (1973)The organization and activation of orthographic knowledge in reading aloud. (1979)Cognitive processes in spelling (1981)Phonological Dyslexia and Dysgraphia in a Highly Literate Subject: A Developmental Case with Associated Deficits of Phonemic Processing and Awareness (1985)Mechanisms for accessing lexical representations for output: Evidence from a category-specific semantic deficit (1991)Eye movements of dyslexic children when reading in a regular orthography (2004)Phonology and the Problems of Learning to Read and Write (1985)Specific Deficits in Component Reading and Language Skills (1989)The impact of orthographic consistency on dyslexia: A German-English comparison (1997)Substance over Style: Assessing the Efficacy of Modality Testing and Teaching (1987)Genetic Factors in Child Psychiatric Disorders—II. Empirical Findings (1990)
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References

  • 1982Progress in Learning Disabilities575 cited
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  • 2005DCDC2 is associated with reading disability and modulates neuronal development in the brain383 cited
  • 1983Surface Dyslexia305 cited
  • 2005Strong Evidence That KIAA0319 on Chromosome 6p Is a Susceptibility Gene for Developmental Dyslexia293 cited
  • 1972Progress in Learning Disabilities262 cited
  • 1993Evidence for a Magnocellular Defect in Developmental Dyslexia a255 cited
  • 2005Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia236 cited
  • 1994Genes, Environment, and the Development of Orthographic Skills198 cited
  • 1998Evidence for Linkage of Spelling Disability to Chromosome 15171 cited
  • 2006Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia158 cited
  • 19734. Developmental dyslexia—prevailing diagnostic concepts and a new diagnostic approach150 cited
  • 1984Bilingual Biscriptal Deep Dyslexia144 cited
  • 2007A Haplotype Spanning KIAA0319 and TTRAP Is Associated with Normal Variation in Reading and Spelling Ability94 cited
  • 2007Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

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Cited by

  • 2013Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort67 cited
  • 2013Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment65 cited
  • 2012Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability62 cited
  • 2010A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression58 cited
  • 2010Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population55 cited
  • 2017Dyslexia risk gene relates to representation of sound in the auditory brainstem54 cited
  • 2011Imaging genetics of FOXP2 in dyslexia52 cited
  • 2009Progress towards a cellular neurobiology of reading disability49 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