Search results for "dyslexi"

showing 10 items of 276 documents

Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings.

2008

Contains fulltext : 69485.pdf (Publisher’s version ) (Closed access) BACKGROUND: Limited success has been achieved through previous attention-deficit/hyperactivity disorder (ADHD) linkage scans, which were all designed to map genes underlying the dichotomous phenotype. The International Multi-centre ADHD Genetics (IMAGE) project performed a whole genome linkage scan specifically designed to map ADHD quantitative trait loci (QTL). METHODS: A set of 1094 single selected Caucasian ADHD nuclear families was genotyped on a highly accurate and informative single nucleotide polymorphism (SNP) panel. Two quantitative traits measuring the children's symptoms in home and school settings were collecte…

MaleAdolescentGenetics and epigenetic pathways of disease [NCMLS 6]Genetic LinkageMedizin610 Medicine & healthSingle-nucleotide polymorphismLocus (genetics)Quantitative trait locusNeuroinformatics [DCN 3]Social EnvironmentMental health [NCEBP 9]ArticleWhite PeopleDyslexiaGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciences0302 clinical medicineCognitive neurosciences [UMCN 3.2]Genetic linkagemental disordersmedicinePerception and Action [DCN 1]HumansAttention deficit hyperactivity disorderddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersChildBiological PsychiatryGenetics0303 health sciencesSchools030305 genetics & heredityDyslexia10058 Department of Child and Adolescent PsychiatryHeritabilitymedicine.disease030227 psychiatryPhenotypeGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with HyperactivityChromosomes Human Pair 1Child PreschoolTraitFemalePsychology2803 Biological PsychiatryFunctional Neurogenomics [DCN 2]
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Aetiology for the covariation between combined type ADHD and reading difficulties in a family study: the role of IQ.

2012

Twin studies using both clinical and population-based samples suggest that the frequent co-occurrence of attention deficit hyperactivity disorder (ADHD) and reading ability/disability (RD) is largely driven by shared genetic influences. While both disorders are associated with lower IQ, recent twin data suggest that the shared genetic variability between reading difficulties and ADHD inattention symptoms is largely independent from genetic influences contributing to general cognitive ability. The current study aimed to extend the previous findings that were based on rating scale measures in a population sample by examining the generalisability of the findings to a clinical population, and b…

MaleAdolescentSiblingsIntelligenceWechsler ScalesArticleDyslexiaYoung AdultAptitude TestsAttention Deficit Disorder with HyperactivitySurveys and QuestionnairesHumansFemaleChildJournal of child psychology and psychiatry, and allied disciplines
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Towards text simplification for poor readers with intellectual disability: When do connectives enhance text cohesion?

2013

Abstract Cohesive elements of texts such as connectives (e.g., but, in contrast) are expected to facilitate inferential comprehension in poor readers. Two experiments tested this prediction in poor readers with intellectual disability (ID) by: (a) comparing literal and inferential text comprehension of texts with and without connectives and/or high frequency content words (Experiment 1) and (b) exploring the effects of type and familiarity of connectives on two-clause text comprehension by means of a cloze task (Experiment 2). Neither the addition of high frequency content words nor connectives in general produced inferential comprehension improvements. However, although readers with ID wer…

MaleAdolescentText simplificationTeaching methodSpecial educationDyslexiaYoung AdultIntellectual DisabilityIntellectual disabilityDevelopmental and Educational PsychologymedicineHumansChildRecognition Psychologymedicine.diseaseLinguisticsEducation of Intellectually DisabledCohesion (linguistics)ComprehensionClinical PsychologyWord lists by frequencyReading comprehensionCase-Control StudiesFemaleComprehensionPsychologyResearch in Developmental Disabilities
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Auditory event-related potentials measured in kindergarten predict later reading problems at school age.

2013

Identifying children at risk for reading problems or dyslexia at kindergarten age could improve support for beginning readers. Brain event-related potentials (ERPs) were measured for temporally complex pseudowords and corresponding non-speech stimuli from 6.5-year-old children who participated in behavioral literacy tests again at 9 years in the second grade. Children who had reading problems at school age had larger N250 responses to speech and non-speech stimuli particularly at the left hemisphere. The brain responses also correlated with reading skills. The results suggest that atypical auditory and speech processing are a neural-level risk factor for future reading problems. [Supplement…

MaleAuditory eventmedia_common.quotation_subjectSpeech soundsLateralization of brain functionLiteracyDevelopmental psychologyDyslexiaPhoneticsotorhinolaryngologic diseasesDevelopmental and Educational PsychologymedicineHumansSpeechChildta515media_commonAnalysis of VarianceBrain MappingSchool age childDyslexiaBrainElectroencephalographymedicine.diseaseSpeech processingReading ProblemsNeuropsychology and Physiological PsychologyAcoustic StimulationReadingCase-Control StudiesEvoked Potentials AuditorySpeech PerceptionFemalePsychologyDevelopmental neuropsychology
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Reading skill and neural processing accuracy improvement after a 3-hour intervention in preschoolers with difficulties in reading-related skills

2012

This study aimed at determining whether an intervention game developed for strengthening phonological awareness has a remediating effect on reading skills and central auditory processing in 6-year-old preschool children with difficulties in reading-related skills. After a 3-hour training only, these children made a greater progress in reading-related skills than did their matched controls who did mathematical exercises following comparable training format. Furthermore, the results suggest that this brief intervention might be beneficial in modulating the neural basis of phonetic discrimination as an enhanced speech-elicited mismatch negativity (MMN) was seen in the intervention group, indic…

MaleBrain activity and meditationmedia_common.quotation_subjecteducationMismatch negativityRecognition (Psychology)behavioral disciplines and activitiesEarly Intervention (Education)050105 experimental psychologyDevelopmental psychologyDyslexia03 medical and health sciencesDiscrimination Psychological0302 clinical medicinePhoneticsPhonological awarenessEvent-related potentialIntervention (counseling)Reading (process)Early Intervention EducationalmedicineHumansRemedial Teaching0501 psychology and cognitive sciencesChildEvoked PotentialsMolecular Biologyta515media_commonAuditory CortexDiscrimination (Psychology)General Neuroscience05 social sciencesDyslexiaRecognition PsychologyElectroencephalographymedicine.diseaseGames ExperimentalReadingData Interpretation StatisticalAuditory PerceptionFemaleNeurology (clinical)Brief interventionPsychologyPsychomotor Performance030217 neurology & neurosurgeryDevelopmental BiologyBrain Research
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A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32

2003

Developmental dyslexia is a distinct learning disability with unexpected difficulty in learning to read despite adequate intelligence, education, and environment, and normal senses. The genetic aetiology of dyslexia is heterogeneous and loci on chromosomes 2, 3, 6, 15, and 18 have been repeatedly linked to it. We have conducted a genome scan with 376 markers in 11 families with 38 dyslexic subjects ascertained in Finland. Linkage of dyslexia to the vicinity of DYX3 on 2p was confirmed with a non-parametric linkage (NPL) score of 2.55 and a lod score of 3.01 for a dominant model, and a novel locus on 7q32 close to the SPCH1 locus was suggested with an NPL score of 2.77. The SPCH1 locus has p…

MaleCandidate geneGenotypeDNA Mutational AnalysisShort ReportLocus (genetics)BiologyDyslexia03 medical and health sciences0302 clinical medicineCommunication disorderDCDC2mental disordersGeneticsmedicineHumansLanguage disorderFinlandGenetics (clinical)030304 developmental biologyGenetics0303 health sciencesGenome HumanDyslexiaChromosome MappingForkhead Transcription FactorsFOXP2medicine.diseasePedigreeRepressor ProteinsChromosomes Human Pair 2Learning disabilityFemaleLod Scoremedicine.symptomChromosomes Human Pair 7030217 neurology & neurosurgeryTranscription FactorsJournal of Medical Genetics
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The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language

2012

Inspired by the localization, on 15q21.2 of the CYP19A1 gene in the linkage region of speech and language disorders, and a rare translocation in a dyslexic individual that was brought to our attention, we conducted a series of studies on the properties of CYP19A1 as a candidate gene for dyslexia and related conditions. The aromatase enzyme is a member of the cytochrome P450 super family, and it serves several key functions: it catalyzes the conversion of androgens into estrogens; during early mammalian development it controls the differentiation of specific brain areas (e.g. local estrogen synthesis in the hippocampus regulates synaptic plasticity and axonal growth); it is involved in sexua…

MaleCandidate geneSLIEstrogen synthesisTranslocation GeneticDyslexiaCohort StudiesMice0302 clinical medicineGenetics(clinical)Receptors ImmunologicAromatasePromoter Regions GeneticGenetics (clinical)Original ResearchQuantitative trait analysisMice KnockoutGeneticsRegulation of gene expression0303 health sciencesbiologyBrainNuclear ProteinsHuman brainmedicine.anatomical_structureTranslocation breakpointFemaleendocrine systemmedicine.drug_classQuantitative Trait LociNerve Tissue ProteinsPolymorphism Single NucleotideSpeech Disorders03 medical and health sciencesAromataseROBO1GeneticsmedicineAnimalsHumansGenetic Predisposition to DiseaseRNA MessengerEcology Evolution Behavior and SystematicsSSD030304 developmental biologyLanguage DisordersAromatase inhibitorCategorical trait associationDyslexiamedicine.diseaseCytoskeletal ProteinsGene Expression RegulationSynaptic plasticitybiology.protein030217 neurology & neurosurgeryBehavior Genetics
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A computer-based Pinyin intervention for disadvantaged children in China: Effects on Pinyin skills, phonological awareness, and character reading.

2019

Pinyin is an alphabetic script that denotes pronunciations of Chinese characters. Studies have shown that Pinyin instruction enhances both phonological awareness (e.g., Shu et al., Developmental Science, 2008, 11, 171-181) and character reading (e.g., Lin et al., Psychological Science, 2010, 21, 1117-1122) in Chinese children. In the present study, we provided a 3-week Pinyin intervention with a computer-based Pinyin GraphoGame to disadvantaged migrant children with poor Pinyin skills. A total of 252 first graders who were children of migrant workers in a large Chinese city were assessed to identify poor Pinyin readers. Fifty-six 7-year-old children with poor Pinyin skills were selected and…

MaleChinamedia_common.quotation_subjectExperimental and Cognitive PsychologyVulnerable Populations050105 experimental psychologyLiteracyEducationDevelopmental psychologyDyslexiaFluencyPhonological awarenessPhoneticsReading (process)Developmental and Educational PsychologymedicineHumans0501 psychology and cognitive sciencesChildmedia_commonPhonemic awareness4. Education05 social sciencesPinyinDyslexia050301 educationGeneral MedicineAwarenessmedicine.diseaseCognitive RemediationReadingTherapy Computer-AssistedLanguage TherapyFemaleChinese charactersPsychology0503 educationDyslexia (Chichester, England)REFERENCES
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Brain responses to changes in speech sound durations differ between infants with and without familial risk for dyslexia

2002

A specific learning disability, developmental dyslexia, is a language-based disorder that is shown to be strongly familial. Therefore, infants born to families with a history of the disorder are at an elevated risk for the disorder. However, little is known of the potential early markers of dyslexia. Here we report differences between 6-month-old infants with and without high risk of familial dyslexia in brain electrical activation generated by changes in the temporal structure of speech sounds, a critical cueing feature in speech. We measured event-related brain responses to consonant duration changes embedded in ata pseudowords applying an oddball paradigm, in which pseudoword tokens with…

MaleConsonantDyslexiaBrainInfantElectroencephalographyStimulus (physiology)medicine.diseaseDevelopmental psychologyDyslexiaPseudowordLanguage developmentNeuropsychology and Physiological PsychologyAcoustic StimulationCommunication disorderEvoked Potentials AuditorySpeech PerceptionDevelopmental and Educational PsychologymedicineHumansFemaleGenetic Predisposition to DiseaseLanguage disorderPsychologyOddball paradigm
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Event-Related Potentials and Consonant Differentiation in Newborns with Familial Risk for Dyslexia

2004

We measured event-related potentials (ERPs) to synthetic consonant-vowel syllables (/ba/, /da/, /ga/) from 26 newborns with familial risk for dyslexia and 23 control infants participating in the Jyväskylä Longitudinal Study of Dyslexia. The syllables were presented with equal probability and with interstimulus intervals ranging from 3,010 to 7,285 ms. Analyses of averaged ERPs from the latencies identified on the basis of principal component analysis (PCA) revealed significant group differences in stop-consonant processing in several latency ranges. At the latencies of 50-170 ms and 540-630 ms, the responses to /ga/ were larger and more positive than those to /ba/ and /da/ in the right hem…

MaleConsonantmedicine.medical_specialtyHealth (social science)050109 social psychologyAudiologyElectroencephalographyRisk Assessmentbehavioral disciplines and activities050105 experimental psychologyEducationDevelopmental psychologyDyslexiaPhoneticsCommunication disorderEvent-related potentialReaction TimemedicineHumans0501 psychology and cognitive sciencesLanguage disorderDominance CerebralCerebral CortexPrincipal Component Analysismedicine.diagnostic_testAuditory Perceptual Disorders05 social sciencesInfant NewbornDyslexiamedicine.diseaseElectrophysiologyGeneral Health ProfessionsEvoked Potentials AuditorySpeech PerceptionFemaleSyllablePsychologypsychological phenomena and processesJournal of Learning Disabilities
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