Core Support for five years is requested for the competitive renewal of the Kansas Intellectual and Developmental Disabilities Research Center (KIDDRC). The KIDDRC, now in its 44th year, has played a major international role in generating highly effective biobehavioral interventions aimed at the causes, prevention, and treatment of intellectual and developmental disabilities and related secondary conditions, and in delineating basic knowledge of the underlying biology of typical and atypical development. Since its inception, the Center has supported a balanced portfolio of behavioral, biological, and biobehavioral research. Building on its rich history, a unique contribution of the Center in the future will be the development of biologically-informed interventions and treatments. The mission of the KIDDRC is to support high quality basic and applied research relevant to the causes and prevention of intellectual and developmental disabilities and the prevention and remediation of associated secondary conditions. To achieve this mission, the KIDDRC is designed to accomplish three objectives. First, to develop and support new interdisciplinary basic and applied research initiatives directly relevant to the Center's mission, bringing together scientists across the Kansas Center as well as promoting collaborative ventures with researchers at other institutions. Second, to provide cost-effective, scientifically generative, state of the art core services, resources, and facilities that directly enhance the quality and impact of science produced by center investigators and their collaborators. Third, to provide highly efficient, cost-effective systems for planning, developing, managing, coordinating, and disseminating research activities associated with the center. The KIDDRC's research program is organized around four integrated thematic areas that each reflects a topic of central importance to IDD, comports with our scientific directions, and draws upon our research strengths. These themes are: 1) language, communication, and cognition of IDD;2) risk, prevention, and intervention in IDD;3) neurobiology of IDD;4) cellular and molecular biology of early development. To coordinate and support the research activities of the 84 investigators and co-investigators and 88 research projects associated with these themes, four core units are proposed: a) Communication and Administration;b) Biobehavioral Measurement;c) Research Design and Analysis;d) Integrative Imaging.

Public Health Relevance

The Kansas Intellectual and Developmental Disabilities Research Center seeks to assist scientists in their pursuit of the causes, prevention, and amelioration of intellectual and developmental disabilities. The end goal of the work of scientists within the center is to improve the quality of life of individuals with intellectual and developmental disabilities.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Center Core Grants (P30)
Project #
5P30HD002528-47
Application #
8505509
Study Section
Special Emphasis Panel (ZHD1-DSR-Y (50))
Program Officer
Parisi, Melissa
Project Start
1997-08-01
Project End
2016-06-30
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
47
Fiscal Year
2013
Total Cost
$1,457,963
Indirect Cost
$467,332
Name
University of Kansas Lawrence
Department
Pediatrics
Type
Organized Research Units
DUNS #
076248616
City
Lawrence
State
KS
Country
United States
Zip Code
66045
Gan, Li; Ma, Delin; Li, Min et al. (2018) Region-specific differences in bioenergetic proteins and protein response to acute high fat diet in brains of low and high capacity runner rats. Neurosci Lett 674:49-53
Amundsen Huffmaster, Sommer L; Van Acker 3rd, Gustaf M; Luchies, Carl W et al. (2018) Muscle Synergies Obtained from Comprehensive Mapping of the Cortical Forelimb Representation Using Stimulus Triggered Averaging of EMG Activity. J Neurosci 38:8759-8771
Hartin, Samantha N; Hossain, Waheeda A; Manzardo, Ann M et al. (2018) A descriptive study on selected growth parameters and growth hormone receptor gene in healthy young adults from the American Midwest. Growth Horm IGF Res 41:48-53
Manzardo, Ann M; Loker, James; Heinemann, Janalee et al. (2018) Survival trends from the Prader-Willi Syndrome Association (USA) 40-year mortality survey. Genet Med 20:24-30
Kimler, Bruce F; Briley, Shawn M; Johnson, Brian W et al. (2018) Radiation-induced ovarian follicle loss occurs without overt stromal changes. Reproduction 155:553-562
Belousov, Andrei B; Nishimune, Hiroshi; Denisova, Janna V et al. (2018) A potential role for neuronal connexin 36 in the pathogenesis of amyotrophic lateral sclerosis. Neurosci Lett 666:1-4
Manzardo, A M; Weisensel, N; Ayala, S et al. (2018) Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults. Clin Genet 93:622-631
Moukarzel, Sara; Ozias, Marlies; Kerling, Elizabeth et al. (2018) Maternal Vitamin D Status and Infant Infection. Nutrients 10:
Chakrabarty, Anuradha; Liao, Zhaohui; Mu, Ying et al. (2018) Inflammatory Renin-Angiotensin System Disruption Attenuates Sensory Hyperinnervation and Mechanical Hypersensitivity in a Rat Model of Provoked Vestibulodynia. J Pain 19:264-277
Butler, Merlin G (2018) Pharmacogenetics and Psychiatric Care: A Review and Commentary. J Ment Health Clin Psychol 2:17-24

Showing the most recent 10 out of 534 publications