WASHINGTON UNIVERSITY INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH CENTER
Project Number5U54HD087011-04
Contact PI/Project LeaderCONSTANTINO, JOHN N.
Awardee OrganizationWASHINGTON UNIVERSITY
Description
Abstract Text
DESCRIPTION (provided by applicant): The last decade of research in intellectual and developmental disabilities (IDD) has beennotably characterized by rapid advances in understanding the nature and complexity of inherited susceptibilities to IDD, but genetic discovery has not yet fulfilled the promise of more effective intervention, even for monogenic IDD syndromes. It is the immediate priority of a next generation of research to capitalize upon knowledge about causation in IDD (both genetic and environmental) and translate it into higher-impact intervention for as many individuals and families affected as possible. In the second cycle of the IDDRC at Washington University in St. Louis (IDDRC@WUSTL), our strategy for contributing to this effort preserves our Center's original focus on characterization of white matter injury to the newborn brain, but extends the scope of Core activity to facilitate a comprehensive approach to understanding and preventing developmental disorders of neural connectivity at the respective levels of cell, synapse, circuit, and behavior, and brings on line major strengths of WUSTL in genomics, behavioral/cognitive neuroscience, and clinical-translational science. The overarching goals of our Center are as follows: (1) To facilitate high-caliber, translational research on the pathogenesis and treatment of IDDs by sustaining an innovative Core structure that attracts and supports qualified, collaborative investigators, and interacts synergistically with complementary Core facilities of other U.S. IDDRCs. We propose to support an Administrative Core, a Developmental Neuroimaging Core, a Model Systems Core (encompassing capacity and expertise for both animal and cellular models of IDD), and a Clinical Translational Core. (2) To cultivate nodes of interdisciplinary scientific activity in frotiers of IDD research which are critical for the derivation of higher-impact treatment and preventive intervention, across 4 major themes: (i) The prevention of prematurity and its neurodevelopmental consequences; (ii) The elucidation of robust intermediate DD phenotypes (as markers of pathogenic processes, targets of early intervention, and indices of response to treatment); (iii) In-depth characterization of the developing human brain, and (iv) Functional genomic approaches to elucidating convergent mechanisms of IDD pathogenesis. (3) To conduct a signature research project that represents a bold, critical step toward higher-impact intervention for IDD, capitalizes upon both the Core structure of our IDDRC and institutional strengths at WUSTL, and epitomizes the manner in which our IDDRC facilitates trans-disciplinary research. Our project is designed to elucidate mechanisms of sex-specific modulation-of-expression of inherited risk for autism spectrum disorders, at the respective levels of cell, brain, and behavior. A goal is to identify compensatory mechanisms underlying resilience among females in ASD-affected families, for the purpose of recapitulating those mechanisms innovel interventions which would be of major relevance to a large proportion of the population of individuals at risk or affected by familial autistic syndromes.
Public Health Relevance Statement
PUBLIC HEALTH RELEVANCE: Intellectual and Developmental Disabilities adversely affect 1 in 6 U.S. children and their families. The Intellectual and Developmental Disabilities Research Center at the Washington University School of Medicine (IDDRC@WUSTL) is a scientific program composed of three core facilities, one dedicated to studies of cellular and molecular mechanisms of causation in IDD, one dedicated to the identification of "signatures" of developmental disability that can be imaged in the developing brain, and one dedicated to in-depth clinical assessment of human subjects and the translation of new understanding of causal mechanisms into higher impact intervention.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AffectAnimal ModelBehaviorBehavioralBiological MarkersBiological ModelsBrainCaliberCell modelCellsChildClinicalClinical and Translational Science AwardsClinical assessmentsCollectionCore FacilityDataDerivation procedureDevelopmentDevelopmental DisabilitiesEarly InterventionEnvironmentEpigenetic ProcessEtiologyFamilyFemaleFosteringGenerationsGeneticGenetic Predisposition to DiseaseGenomic approachGenomicsGoalsHumanImageIndividualInheritedIntellectual functioning disabilityInterruptionInterventionKnowledgeMental Retardation and Developmental Disabilities Research CentersMolecularNatureNeurodevelopmental DisabilityNeurologyNewborn InfantPathogenesisPathogenicityPatientsPhenotypePopulationPopulation Attributable RisksPredispositionPreventionPreventive InterventionProcessPsychiatryResearchResearch PersonnelResearch Project GrantsResourcesRiskScienceScientific Advances and AccomplishmentsStructureSynapsesSyndromeTranslatingTranslational ResearchTranslationsUniversitiesVariantWashingtonautism spectrum disorderbrain behaviorcognitive neurosciencedesigndevelopmental diseaseeffective interventionfrontierfunctional genomicshuman subjectindexinginnovationmedical schoolsneuroimagingnext generationnovelprematureprenatalpreventprogramspublic health relevancerelating to nervous systemresiliencesextreatment responsewhite matter injury
Eunice Kennedy Shriver National Institute of Child Health and Human Development
CFDA Code
865
DUNS Number
068552207
UEI
L6NFUM28LQM5
Project Start Date
18-September-2015
Project End Date
31-May-2020
Budget Start Date
01-June-2018
Budget End Date
31-May-2019
Project Funding Information for 2018
Total Funding
$1,326,839
Direct Costs
$874,541
Indirect Costs
$459,135
Year
Funding IC
FY Total Cost by IC
2018
Eunice Kennedy Shriver National Institute of Child Health and Human Development
$1,326,839
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5U54HD087011-04
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 5U54HD087011-04
Patents
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Outcomes
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No Outcomes available for 5U54HD087011-04
Clinical Studies
No Clinical Studies information available for 5U54HD087011-04
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History
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Similar Projects
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