Nervous System Diseases - Dyslexia PubMed MeSh Term

Overview

subject area of

• DCDC2 is associated with reading disability and modulates neuronal development in the brain  Journal Article
• A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States  Journal Article
• A Cognitive Dimensional Approach to Understanding Shared and Unique Contributions to Reading, Math, and Attention Skills  Journal Article
• A comparison of the cognitive deficits in reading disability and attention-deficit/hyperactivity disorder  Journal Article
• Applying eye movement miscue analysis to the reading patterns of children with language impairment  Journal Article
• Avoidance strategies in an exceptional child during unsuccessful reading performances  Journal Article
• Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci.  Journal Article
• Causal models of reading disability: A twin study  Journal Article
• Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ  Journal Article
• Colorado longitudinal twin study of reading disability  Journal Article
• Comorbidity Between Reading Disability and Math Disability: Concurrent Psychopathology, Functional Impairment, and Neuropsychological Functioning  Journal Article
• Comorbidity of reading disability and attention-deficit/hyperactivity disorder: differences by gender and subtype.  Journal Article
• DEVELOPMENT OF PHONETIC MEMORY IN DISABLED AND NORMAL READERS  Journal Article
• DYSLEXIC AND NORMAL READERS EYE-MOVEMENTS  Journal Article
• DeFries-Fulker Analysis of Longitudinal Reading Performance Data from Twin Pairs Ascertained for Reading Difficulties and from Their Nontwin Siblings  Journal Article
• Differential Genetic Etiology of Reading Difficulties as a Function of IQ: An Update  Journal Article
• Differential genetic etiology of reading component processes as a function of IQ  Journal Article
• Differential genetic etiology of reading disability as a function of IQ  Journal Article
• Discovery of 42 genome-wide significant loci associated with dyslexia  Journal Article
• Dyslexia: nature and nurture.  Journal Article
• EYE FIXATION PATTERNS AMONG DYSLEXIC AND NORMAL READERS - EFFECTS OF WORD-LENGTH AND WORD-FREQUENCY  Journal Article
• Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC  Journal Article
• Etiologies and Molecular Mechanisms of Communication Disorders  Journal Article
• Etiology and neuropsychology of comorbidity between RD and ADHD: The case for multiple-deficit models  Journal Article
• Etiology of reading difficulties and rapid naming: The Colorado twin study of reading disability  Journal Article
• Etiology of the comorbidity between RD and ADHD: Exploration of the non-random mating hypothesis  Journal Article
• Etiology of the stability of reading difficulties: The longitudinal twin study of reading disabilities  Journal Article
• Evidence for linkage and association with reading disability, on 6p21.3-22  Journal Article
• Explaining the sex difference in dyslexia  Journal Article
• Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1  Journal Article
• GENDER RATIOS AMONG READING-DISABLED CHILDREN AND THEIR SIBLINGS AS A FUNCTION OF PARENTAL IMPAIRMENT  Journal Article
• Gender Ratios for Reading Difficulties  Journal Article
• Gene X Environment Interactions in Reading Disability and Attention-Deficit/Hyperactivity Disorder  Journal Article
• Gene by environment interactions influencing reading disability and the inattentive symptom dimension of attention deficit/hyperactivity disorder  Journal Article
• Gene x environment interactions in speech sound disorder predict language and preliteracy outcomes  Journal Article
• Genes, environment, and dyslexia - The 2005 Norman Geschwind memorial lecture  Journal Article
• Genetic Etiologies of Comorbidity and Stability for Reading Difficulties and ADHD: A Replication Study  Journal Article
• Genetic and environmental influences on orthographic and phonological skills in children with reading disabilities  Journal Article
• Genetic influences on reading difficulties in boys and girls: The Colorado twin study  Journal Article
• Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia  Journal Article
• Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia  Journal Article
• Genome-wide screening for DNA variants associated with reading and language traits  Journal Article
• Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities  Journal Article
• Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18  Journal Article
• Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia  Journal Article
• Individual Prediction of Dyslexia by Single Versus Multiple Deficit Models  Journal Article
• Multivariate behavioral genetic analysis of achievement and cognitive measures in reading-disabled and control twin pairs  Journal Article
• Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth  Journal Article
• Neuropsychological analyses of comorbidity between reading disability and attention deficit hyperactivity disorder: In search of the common deficit  Journal Article
• Parental Education Moderates Genetic Influences on Reading Disability  Journal Article
• Processing speed deficits in attention deficit/hyperactivity disorder and reading disability  Journal Article
• Psychiatric comorbidity in children and adolescents with reading disability  Journal Article
• Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit hyperactivity disorder  Journal Article
• Quantitative-trait locus for specific language and reading deficits on chromosome 6p  Journal Article
• Reaction Time Variability Associated with Reading Skills in Poor Readers with ADHD  Journal Article
• Reading disability and chromosome 6p21.3: Evaluation of MOG as a candidate gene  Journal Article
• Reading disability: Evidence for a genetic etiology  Journal Article
• Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses  Journal Article
• Self-reported reading problems in parents of twins with reading difficulties.  Journal Article
• Subtypes of developmental dyslexia: Testing the predictions of the dual-route and connectionist frameworks  Journal Article
• TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort  Journal Article
• THE EXTERNAL VALIDITY OF AGE-DISCREPANCY VERSUS IQ-DISCREPANCY DEFINITIONS OF READING-DISABILITY - LESSONS FROM A TWIN STUDY  Journal Article
• Testing hypotheses regarding the causes of comorbidity: Examining the underlying deficits of comorbid disorders  Journal Article
• The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language  Journal Article
• The Colorado Longitudinal Twin Study of Reading Difficulties and ADHD: Etiologies of Comorbidity and Stability  Journal Article
• The genetics of children's oral reading performance  Journal Article
• Twin study of the etiology of comorbidity between reading disability and attention-deficit/hyperactivity disorder  Journal Article
• Understanding Comorbidity Between Specific Learning Disabilities  Journal Article
• Understanding comorbidity: A twin study of reading disability and attention-deficit/hyperactivity disorder  Journal Article
• Understanding the Complex Etiologies of Developmental Disorders: Behavioral and Molecular Genetic Approaches  Journal Article
• Varieties of developmental reading disorder: Genetic and environmental influences  Journal Article

broader concept

• Nervous System Diseases - Language Disorders  PubMed MeSh Term