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1
Dynamic relationships between phonological memory and reading:a five year longitudinal study from age 4 to 9
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2
To Name or Not to Name:Eye Movements and Semantic Processing in RAN and Reading
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3
Auditory frequency discrimination in developmental dyslexia: a meta-analysis
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4
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
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5
On the neural basis of word reading:A meta-analysis of fMRI evidence using activation likelihood estimation
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6
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
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7
Auditory frequency discrimination in developmental dyslexia: A meta‐analysis
Witton, Caroline; Swoboda, Katy; Shapiro, Laura R.. - : John Wiley and Sons Inc., 2019
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8
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
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9
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
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10
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
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11
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
Pettigrew, Kerry A.; Frinton, Emily; Nudel, Ron. - : BioMed Central Ltd., 2016
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12
Genome-wide screening for DNA variants associated with reading and language traits
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13
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
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14
Deconstructing phonological tasks:the contribution of stimulus and response type to the prediction of early decoding skills
Abstract: Abstract Phonological tasks are highly predictive of reading development but their complexity obscures the underlying mechanisms driving this association. There are three key components hypothesised to drive the relationship between phonological tasks and reading; (a) the linguistic nature of the stimuli, (b) the phonological complexity of the stimuli, and (c) the production of a verbal response. We isolated the contribution of the stimulus and response components separately through the creation of latent variables to represent specially designed tasks that were matched for procedure. These tasks were administered to 570 6 to 7-year-old children along with standardised tests of regular word and non-word reading. A structural equation model, where tasks were grouped according to stimulus, revealed that the linguistic nature and the phonological complexity of the stimulus predicted unique variance in decoding, over and above matched comparison tasks without these components. An alternative model, grouped according to response mode, showed that the production of a verbal response was a unique predictor of decoding beyond matched tasks without a verbal response. In summary, we found that multiple factors contributed to reading development, supporting multivariate models over those that prioritize single factors. More broadly, we demonstrate the value of combining matched task designs with latent variable modelling to deconstruct the components of complex tasks.
URL: https://publications.aston.ac.uk/id/eprint/26247/2/Stimulus_and_response_type_to_the_prediction_of_early_decoding_skills.pdf
https://publications.aston.ac.uk/id/eprint/26247/1/Stimulus_and_response_type_prediction_of_early_decoding_skills.pdf
https://publications.aston.ac.uk/id/eprint/26247/
https://doi.org/10.1016/j.cognition.2015.06.013
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15
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
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16
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
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17
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
Becker, Jessica; Czamara, Darina; Scerri, Tom S. - : Nature Publishing Group, 2014
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18
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
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19
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
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20
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.
In: ISSN: 1018-4813 ; EISSN: 1476-5438 ; European Journal of Human Genetics ; https://hal.archives-ouvertes.fr/hal-00964958 ; European Journal of Human Genetics, Nature Publishing Group, 2013, epub ahead of print. ⟨10.1038/ejhg.2013.199⟩ (2013)
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