Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH052223-02
Application #
2251835
Study Section
Child Psychopathology and Treatment Review Committee (CPT)
Project Start
1995-09-30
Project End
2000-04-30
Budget Start
1996-09-01
Budget End
1997-04-30
Support Year
2
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Chicago
Department
Psychiatry
Type
Schools of Medicine
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Brune, Camille W; Kim, Soo-Jeong; Salt, Jeff et al. (2006) 5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism. Am J Psychiatry 163:2148-56
Herzing, Laura B K; Cook Jr, Edwin H; Ledbetter, David H (2002) Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11- q13 duplications. Hum Mol Genet 11:1707-18
Veenstra-VanderWeele, Jeremy; Kim, Soo-Jeong; Lord, Catherine et al. (2002) Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism. Am J Med Genet 114:277-83
Kim, S-J; Young, L J; Gonen, D et al. (2002) Transmission disequilibrium testing of arginine vasopressin receptor 1A (AVPR1A) polymorphisms in autism. Mol Psychiatry 7:503-7
Kim, S-J; Cox, N; Courchesne, R et al. (2002) Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder. Mol Psychiatry 7:278-88
Kim, Soo-Jeong; Herzing, Laura B K; Veenstra-VanderWeele, Jeremy et al. (2002) Mutation screening and transmission disequilibrium study of ATP10C in autism. Am J Med Genet 114:137-43
Herzing, L B; Kim, S J; Cook Jr, E H et al. (2001) The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression. Am J Hum Genet 68:1501-5
Cook Jr, E H (2001) Genetics of autism. Child Adolesc Psychiatr Clin N Am 10:333-50
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
Kim, S J; Cook Jr, E H (2000) Novel de novo nonsense mutation of MECP2 in a patient with Rett syndrome. Hum Mutat 15:382-3

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