Contact PI/Project LeaderWALKLEY, STEVEN UPSHAW Other PIs
Awardee OrganizationALBERT EINSTEIN COLLEGE OF MEDICINE
Description
Abstract Text
PROJECT SUMMARY (OVERALL)
The overarching purpose of the Rose F. Kennedy Intellectual and Developmental Disabilities Research Center
(RFK IDDRC) is to improve the lives of children with intellectual and developmental disabilities (IDD). Fifty
years of distinguished progress in basic, translational and clinical research as one of NICHD's flagship
IDDRCs, coupled with important recent faculty recruitments and an historic merger between the Albert Einstein
College of Medicine and its University-Affiliated Hospital, Montefiore Medical Center, offer a solid platform for
continuing excellence in our commitment to IDD research. The Center's 4 highly integrated and complemen-
tary scientific Cores consist of: 1) our clinical translational core known as the Human Clinical Phenotyping
(Core B, HCP), which serves to facilitate both access to and characterization of participants for IDD relevant
research; 2) a Neurogenomics facility (Core C, NGEN) that provides cutting edge epigenetic and genomic
processing and analyses on both human and animal tissues; 3) a Neural Cell Engineering and Imaging facility
(Core D, NCEI) that provides state-of-the-art approaches to brain cell manipulation and visual-ization; and 4)
an Animal Phenotyping facility (Core E, AP) for evaluation of animal behavior, metabolism, imaging and brain
function in a manner with strong parallels to approaches taken in patients accessed through HCP. Each of our
scientific Cores is carefully overseen and monitored by the Administrative Core (Core A, ADM), which also
serves as the head ganglion of the entire IDDRC in its outreach programs to the Einstein/ Montefiore
community as well as nationally. Each scientific Core is tightly connected to our selected Research Project
which brings together a multidisciplinary team of investigators focused on intellectual disability in 22q11.2
Deletion Syndrome (22q11.2DS). A central function of the RFK IDDRC is to promote the substantive links
between Einstein research laboratories and clinics at the Children's Evaluation and Rehabilitation Center
(CERC) Children's and the Hospital at Montefiore (CHAM). Together, this set of Cores and our research
project form a dynamic network of IDD-focused programs and practices that interlink 19 different academic
departments and 20-plus IDD-relevant clinics at Einstein and Montefiore. The latter include 22q11.2DS, Rett
and Williams syndromes, tuberous sclerosis, neurofibromatosis, West syndrome and infantile spasms, autism
spectrum disorders, and a wide range of lysosomal diseases. New initiatives being set in motion involve
outcome assessments of premature birth in terms of IDD and newborn screening (NBS) and critical genotype/
phenotype issues in conditions of high relevance to such NBS programs in New York State (Krabbe disease
and adrenoleukodystrophy). Strong outreach programs driven by our ADM core help spread the word about
IDD research. Such efforts over the past 5 years have positioned the RFK IDDRC in a substantive leadership
role in coupling research and clinical strategic goals across the newly merged Einstein-Montefiore community,
and will play an essential role in promotion of new clinical-research partnerships going forward.
Public Health Relevance Statement
PROJECT NARRATIVE
The overarching mission of the Rose F. Kennedy IDDRC (RFK IDDRC) is to improve the lives of children with
intellectual and developmental disabilities (IDD) through research and clinical outreach. The RFK IDDRC
works tirelessly to support new and ongoing IDD relevant investigations, with the ultimate goal of translating
basic science discoveries into new therapies. This will be realized through Center-sponsored support of
collaborations between bench scientists and clinicians at Einstein and Montefiore, and with other IDDRCs and
related institutions; and the support of four scientific Cores that serve to promote basic science and clinical
studies in IDD. In addition, the Center will advance understanding of the biological pathways responsible for
intellectual disability in 22q11.2DS through a multi-investigator/multimodal research project.
NIH Spending Category
No NIH Spending Category available.
Project Terms
22q11AdrenoleukodystrophyAffectAnimal BehaviorAnimalsBasic ScienceBiologicalBrainCellular biologyChargeChildClinicClinicalClinical ResearchCollaborationsCommunication impairmentCommunitiesCoupledCouplingDevelopmentDiagnosisDiseaseEarly treatmentEpigenetic ProcessEvaluationFaculty RecruitmentFamilyFosteringGangliaGeneticGenomicsGenotypeGloboid cell leukodystrophyGoalsGroup MeetingsHeadHospitalsHumanHuman ResourcesImageImageryIndividualInfantile spasmsInstitutionIntellectual functioning disabilityIntelligenceInterest GroupInvestigationLaboratory ResearchLeadershipLearningLinkMedical centerMedicineMemoryMental Retardation and Developmental Disabilities Research CentersMetabolismMissionMonitorMotionNational Institute of Child Health and Human DevelopmentNeonatal ScreeningNeurofibromatosesNeuronsNew YorkOutcome AssessmentParticipantPathogenesisPathway interactionsPatient CarePatientsPediatric HospitalsPhenotypePilot ProjectsPlayPositioning AttributePremature BirthPreventionProcessQuality ControlRare DiseasesRehabilitation CentersResearchResearch PersonnelResearch Project GrantsRett SyndromeRewardsRoleScienceScientistServicesSolidStructureTechnologyTestingTranslatingTranslational ResearchTranslationsTuberous SclerosisUniversitiesUrsidae FamilyWilliams SyndromeWorkanimal tissueautism spectrum disorderbrain cellcellular engineeringcellular imagingclinical phenotypecollegeconotruncal anomaly face syndromecost effectivenessdesignhuman tissueimaging facilitiesimprovedinnovationinsightmultidisciplinarymultimodalityneurogenomicsnovel therapeuticsoutreachoutreach programpatient advocacy grouppreventprogramsscreening panelscreening programsymposium
Eunice Kennedy Shriver National Institute of Child Health and Human Development
CFDA Code
865
DUNS Number
081266487
UEI
H6N1ZF5HJ2G3
Project Start Date
22-September-2016
Project End Date
31-May-2021
Budget Start Date
01-June-2019
Budget End Date
31-May-2020
Project Funding Information for 2019
Total Funding
$1,202,400
Direct Costs
$862,238
Indirect Costs
$577,699
Year
Funding IC
FY Total Cost by IC
2019
Eunice Kennedy Shriver National Institute of Child Health and Human Development
$1,202,400
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5U54HD090260-05
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 5U54HD090260-05
Patents
No Patents information available for 5U54HD090260-05
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 5U54HD090260-05
Clinical Studies
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News and More
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History
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Similar Projects
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