Abstract

This describes our work in the program on Neurochemistry and Childhood Psychopathology. Progress in the five component areas is described, along with a brief summary of our plans for the coming year. The program is currently in its first year; funding began in March, 1985. The component sections of the program include: Core Facilities, Biochemical Regulation; Neurotransmitter Receptors; Narcolepsy and Clinical Neurochemistry.

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Program Projects (P01)
Project #
5P01MH039437-02
Application #
3099042
Study Section
(SRC)
Project Start
1985-03-01
Project End
1988-02-29
Budget Start
1986-03-01
Budget End
1987-02-28
Support Year
2
Fiscal Year
1986
Total Cost
Indirect Cost

  Institution

Name
Stanford University
Department
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305

  Publications

Tsang, Kathryn M; Croen, Lisa A; Torres, Anthony R et al. (2013) A genome-wide survey of transgenerational genetic effects in autism. PLoS One 8:e76978
Sampath, Srirangan; Bhat, Shambu; Gupta, Simone et al. (2013) Defining the contribution of CNTNAP2 to autism susceptibility. PLoS One 8:e77906
Fradin, Delphine; Cheslack-Postava, Keely; Ladd-Acosta, Christine et al. (2010) Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs. PLoS One 5:
Weiss, Lauren A; Arking, Dan E; Gene Discovery Project of Johns Hopkins & the Autism Consortium et al. (2009) A genome-wide linkage and association scan reveals novel loci for autism. Nature 461:802-8
Arking, Dan E; Cutler, David J; Brune, Camille W et al. (2008) A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am J Hum Genet 82:160-4
Benayed, Rym; Gharani, Neda; Rossman, Ian et al. (2005) Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus. Am J Hum Genet 77:851-68
Spiker, Donna; Lotspeich, Linda J; Dimiceli, Sue et al. (2002) Behavioral phenotypic variation in autism multiplex families: evidence for a continuous severity gradient. Am J Med Genet 114:129-36
Spiker, D; Lotspeich, L J; Dimiceli, S et al. (2001) Birth order effects on nonverbal IQ scores in autism multiplex families. J Autism Dev Disord 31:449-60
Salmon, B; Hallmayer, J; Rogers, T et al. (1999) Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism. Am J Med Genet 88:551-6
Risch, N; Spiker, D; Lotspeich, L et al. (1999) A genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet 65:493-507

Showing the most recent 10 out of 58 publications