The Clinical Core will provide a common mechanism through which study subjects are characterized, and subject and family information (including biologic samples) is collected. Centralizing and coordinating these activities in the Clinical Core will create efficiencies for the planned projects and should stimulate additional collaborations between STAART autism researchers as well as, to a limited degree, researchers not funded by STAART. A shared core dataset including basic descriptive information on all potential participants in the STAART studies will be generated. In addition, the core will assist in project-specific data management and statistical analyses. Although there will be two sites for the clinical core (Kennedy Krieger Institute and Children's National Medical Center), the operations of the clinical activities complement each other and are conceptually similar. Specific objectives of this core include: 1. identifying and recruiting STAART research participants; 2. determining eligibility of participants; 3. conducting diagnostic assessments of subjects; 4. conducting inter-rater reliability trials for autism diagnostic assessments; 5. monitoring the fidelity of test administration; 6. conducting outcome data collection; 7. facilitating the collection and distribution of biological samples; 8. providing data storage and data management support.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
1U54MH066417-01A1
Application #
6670933
Study Section
Special Emphasis Panel (ZRG1-BBBP-6 (50))
Project Start
2003-07-01
Project End
2007-06-30
Budget Start
Budget End
2004-04-30
Support Year
1
Fiscal Year
2003
Total Cost
$264,617
Indirect Cost
Name
Hugo W. Moser Research Institute Kennedy Krieger
Department
Type
DUNS #
155342439
City
Baltimore
State
MD
Country
United States
Zip Code
21205
Yerys, Benjamin E; Gordon, Evan M; Abrams, Danielle N et al. (2015) Default mode network segregation and social deficits in autism spectrum disorder: Evidence from non-medicated children. Neuroimage Clin 9:223-32
Yerys, Benjamin E; Antezana, Ligia; Weinblatt, Rachel et al. (2015) Neural Correlates of Set-Shifting in Children With Autism. Autism Res 8:386-97
Washington, Stuart D; VanMeter, John W (2015) Anterior-Posterior Connectivity within the Default Mode Network Increases During Maturation. Int J Med Biol Front 21:207-218
Washington, Stuart D; Gordon, Evan M; Brar, Jasmit et al. (2014) Dysmaturation of the default mode network in autism. Hum Brain Mapp 35:1284-96
Freilich, Emily R; Schreiber, John M; Zelleke, Tesfaye et al. (2014) Pediatric status epilepticus: identification and evaluation. Curr Opin Pediatr 26:655-61
Landa, Rebecca J; Gross, Alden L; Stuart, Elizabeth A et al. (2013) Developmental trajectories in children with and without autism spectrum disorders: the first 3 years. Child Dev 84:429-42
Anthony, Laura Gutermuth; Kenworthy, Lauren; Yerys, Benjamin E et al. (2013) Interests in high-functioning autism are more intense, interfering, and idiosyncratic than those in neurotypical development. Dev Psychopathol 25:643-52
Messinger, Daniel; Young, Gregory S; Ozonoff, Sally et al. (2013) Beyond autism: a baby siblings research consortium study of high-risk children at three years of age. J Am Acad Child Adolesc Psychiatry 52:300-308.e1
Bal, Elgiz; Yerys, Benjamin E; Sokoloff, Jennifer L et al. (2013) Do Social Attribution Skills Improve with Age in Children with High Functioning Autism Spectrum Disorders? Res Autism Spectr Disord 7:9-16
Tek, Saime; Landa, Rebecca J (2012) Differences in autism symptoms between minority and non-minority toddlers. J Autism Dev Disord 42:1967-73

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