description): The goal of this project is to identify distinct subtypes of autism disorder and to map the loci biological or behavioral differences (neurobiological phenotypes) among patients diagnosed with AD. For stable differences they will study first-degree relatives to establish the trait is familial and to identify genetic patterns of transmission. Then they will apply linkage and association tests to an appropriate series of genome DNA markers. GRANT =P01HD354580002 Description(Adapted from the applicant's description): To further investigate the anomalous neural systems in autistic disorder as a phenotype for genetic analysis, the investigators will perform high- resolution three-dimensional magnetic resonance imaging (MRI) scans in two childhood AD populations as the basis for subsequent complete morphometric analysis for computation of volume of whole brain, individual substructures, hemispheric regions, and application of specialized method of cortical localization and parcellation.

Project Start
2002-03-01
Project End
2003-02-28
Budget Start
2002-03-01
Budget End
2003-02-28
Support Year
5
Fiscal Year
2002
Total Cost
$234,548
Indirect Cost
Name
University of California Irvine
Department
Type
DUNS #
161202122
City
Irvine
State
CA
Country
United States
Zip Code
92697
Fujikawa-Brooks, Sharon; Isenberg, A Lisette; Osann, Kathryn et al. (2010) The effect of rate stress on the auditory brainstem response in autism: a preliminary report. Int J Audiol 49:129-40
Ramanathan, Subhadra; Woodroffe, Abigail; Flodman, Pamela L et al. (2004) A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R. BMC Med Genet 5:10
Palmer, Abraham A; Breen, Laura L; Flodman, Pamela et al. (2003) Identification of quantitative trait loci for prepulse inhibition in rats. Psychopharmacology (Berl) 165:270-9
Smith, M; Woodroffe, A; Smith, R et al. (2002) Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits. Cytogenet Genome Res 98:233-9
Smith, M; Escamilla, J R; Filipek, P et al. (2001) Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR. Cytogenet Cell Genet 94:15-22
Owley, T; McMahon, W; Cook, E H et al. (2001) Multisite, double-blind, placebo-controlled trial of porcine secretin in autism. J Am Acad Child Adolesc Psychiatry 40:1293-9