The University of Washington's Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center (IDDRC), based at the Center on Human Development and Disability (CHDD), provides a comprehensive interdisciplinary research program in the field of intellectual/developmental disabilities and related aspects of human development. Research is carried out in three major domains: (1) Developmental and Molecular Genetics, (2) Developmental Neuroscience, and (3) Developmental Processes and Behavioral Science. Interdisciplinary collaborations are emphasized in research carried out in 12 Research Emphasis Areas;Autism, Craniofacial Malformations, Developmental Toxicology, Ecological Factors, Fetal Alcohol Syndrome, Fragile X Syndrome, Infectious Disease and Immunology, Joubert Syndrome, Learning Disabilities, Neurodegenerative Disorders, Neurodevelopmental Oncology, and Neuroinflammation. Through this grant mechanism, support is requested for six scientific core facilities and one administrative core to enhance the effectiveness of scientists carrying out their research as part of the IDDRC. The scientific core support facilities are as follows: (1) Genetics, (2) Brain Imaging, (3) Cellular Morphology, (4) Behavioral Science, (5) Infant Primate Research Laboratory, and (6) Instrument Development Laboratory. Other IDDRC objectives include training researchers in various disciplines, disseminating research findings, and maintaining linkages to clinical training activities and exemplary service programs.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Center Core Grants (P30)
Project #
5P30HD002274-45
Application #
8322796
Study Section
Special Emphasis Panel (ZHD1-MRG-C (16))
Program Officer
Parisi, Melissa
Project Start
1989-08-01
Project End
2014-06-30
Budget Start
2012-07-01
Budget End
2013-06-30
Support Year
45
Fiscal Year
2012
Total Cost
$2,828,342
Indirect Cost
$712,084
Name
University of Washington
Department
None
Type
Organized Research Units
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Pasalich, Dave S; Fleming, Charles B; Oxford, Monica L et al. (2016) Can Parenting Intervention Prevent Cascading Effects From Placement Instability to Insecure Attachment to Externalizing Problems in Maltreated Toddlers? Child Maltreat 21:175-85
Schueler, Markus; Halbritter, Jan; Phelps, Ian G et al. (2016) Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies. J Med Genet 53:208-14
Schneider, A; Johnston, C; Tassone, F et al. (2016) Broad autism spectrum and obsessive-compulsive symptoms in adults with the fragile X premutation. Clin Neuropsychol 30:929-43
Wheeler, Anne C; Sideris, John; Hagerman, Randi et al. (2016) Developmental profiles of infants with an FMR1 premutation. J Neurodev Disord 8:40
Boldenow, Erica; Gendrin, Claire; Ngo, Lisa et al. (2016) GROUP B STREPTOCOCCUS CIRCUMVENTS NEUTROPHILS AND NEUTROPHIL EXTRACELLULAR TRAPS DURING AMNIOTIC CAVITY INVASION AND PRETERM LABOR. Sci Immunol 1:
Slaats, Gisela G; Isabella, Christine R; Kroes, Hester Y et al. (2016) MKS1 regulates ciliary INPP5E levels in Joubert syndrome. J Med Genet 53:62-72
Su, Wei; Kang, John; Sopher, Bryce et al. (2016) Recombinant adeno-associated viral (rAAV) vectors mediate efficient gene transduction in cultured neonatal and adult microglia. J Neurochem 136 Suppl 1:49-62
Russell, Beth S; Lee, Jungeun Olivia; Spieker, Susan et al. (2016) Parenting and Preschool Self-Regulation as Predictors of Social Emotional Competence in 1st Grade. J Res Child Educ 30:153-169
Gonçalves, Thaís Fernandez; dos Santos, Jussara Mendonça; Gonçalves, Andressa Pereira et al. (2016) Finding FMR1 mosaicism in Fragile X syndrome. Expert Rev Mol Diagn 16:501-7
Tassone, Flora (2015) Advanced technologies for the molecular diagnosis of fragile X syndrome. Expert Rev Mol Diagn 15:1465-73

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