Research Project V addresses the definition, classification and etiology of individual differences in comprehension and disabilities associated with reading comprehension deficits and oral language comprehension deficits. Project V proposes to continue administering extensive assessments of both listening and reading comprehension and passage fluency, across simple and complex discourse, and across ages 8-16, to understand the genetic, cognitive, and developmental aspects of comprehension. Twins and siblings selected for deficits either in reading, comprehension, writing, and/or ADHD, as well as normal- range control twins will be tested. There are 3 prongs to our approach to understanding the functional architecture of comprehension and the nature and etiology of deficits. One involves multivariate analyses of individual differences in both reading comprehension and listening comprehension, across different age groups and across different comprehension tests, using multiple measures of cognitive skills and knowledge. This modeling will be compared across our broad range of comprehension tests so that we can address the problem of why there are currently such dramatic inconsistencies in diagnosis of comprehension deficits and how the problem might be rectified. A second prong to understanding the components of comprehension skill and the origin of deficits is to use behavioral genetic analyses to assess their etiology in terms of genetic and environmental influences. These analyses will also show the degree to which component comprehension skills and other learning learning disabilities such as ADHD share genetic influences, and thus the degree to which they represent distinct or common deficits. The third prong is to further define the phenotype by finding variables often ignored by current tests that could be influencing comprehension performance, such as the centrality of ideas and how prior knowledge of the passage topic influences comprehension and fluency. In collaboration with other CLDRC projects, Project V will assess whether similar skills and similar genes may be influencing comprehension and writing (Project II), assess molecular genetic linkage and association for deficits in comprehension (Project IV), and longitudinally assess stability of comprehension problems (Project VI).Project V provides research on the cognitive, developmental, and genetic aspects of language comprehension that underiie some of the most prevalent learning disabilities. It advances knowledge about both biological and behavioral mechanisms in reading comprehension, listening comprehension, and their co-occurrence with other learning disabilities such as ADHD and writing difficulties.

Public Health Relevance

Project V provides research on the cognitive, developmental, and genetic aspects of language comprehension that underiie some ofthe most prevalent learning disabilities. It advances knowledge about both biological and behavioral mechanisms in reading comprehension, listening comprehension, and their co-occurrence with other learning disabilities such as ADHD and writing difficulties.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Specialized Center (P50)
Project #
2P50HD027802-21
Application #
8265392
Study Section
Special Emphasis Panel (ZHD1-DSR-H (53))
Project Start
Project End
Budget Start
2011-12-01
Budget End
2012-11-30
Support Year
21
Fiscal Year
2012
Total Cost
$242,645
Indirect Cost
$13,131
Name
University of Colorado at Boulder
Department
Type
DUNS #
007431505
City
Boulder
State
CO
Country
United States
Zip Code
80309
McGrath, Lauren M (2018) Two GWASs Are Better Than One: Enhancing Genetic Discovery for Developmental Phenotypes. J Am Acad Child Adolesc Psychiatry 57:77-79
Leopold, Daniel R; Christopher, Micaela E; Olson, Richard K et al. (2018) Invariance of ADHD Symptoms Across Sex and Age: a Latent Analysis of ADHD and Impairment Ratings from Early Childhood into Adolescence. J Abnorm Child Psychol :
Aboud, Katherine S; Barquero, Laura A; Cutting, Laurie E (2018) Prefrontal mediation of the reading network predicts intervention response in dyslexia. Cortex 101:96-106
Ricker, Ashley A; Corley, Robin; DeFries, John C et al. (2018) Examining the influence of perceived stress on developmental change in memory and perceptual speed for adopted and nonadopted individuals. Dev Psychol 54:138-150
DeMille, Mellissa M C; Tang, Kevin; Mehta, Chintan M et al. (2018) Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages. Proc Natl Acad Sci U S A 115:4951-4956
Wilkey, Eric D; Cutting, Laurie E; Price, Gavin R (2018) Neuroanatomical correlates of performance in a state-wide test of math achievement. Dev Sci 21:
Devanna, P; Chen, X S; Ho, J et al. (2018) Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders. Mol Psychiatry 23:1375-1384
Frijters, Jan C; Tsujimoto, Kimberley C; Boada, Richard et al. (2018) Reading-Related Causal Attributions for Success and Failure: Dynamic Links With Reading Skill. Read Res Q 53:127-148
Peterson, Robin L; Arnett, Anne B; Pennington, Bruce F et al. (2018) Literacy acquisition influences children's rapid automatized naming. Dev Sci 21:e12589
Becker, Stephen P; Willcutt, Erik G (2018) Advancing the study of sluggish cognitive tempo via DSM, RDoC, and hierarchical models of psychopathology. Eur Child Adolesc Psychiatry :

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