This is a competitive renewal of our program project to dissect the genetics of neurological diseases. During the first four years of the most recent funding period, we have made significant progress in each of our projects, and published 53 papers and have 3 in press. With this resubmission, we will focus our attention completely on the difficult and very important problem of the genetics of autism, one of the most common neurodevelopmental disorders. To do this, we will integrate the latest in genetic and genomic technologies with detailed clinical assessments. """"""""Genetic Studies in Autism on Chromosome 7,"""""""" is a continuation of efforts from the current Program Project. We will examine in detail the most consistently identified chromosomal region in autism, 7q21-32. We will apply three complementary approaches that include a comprehensive SNP scan of the region, specific testing of the REELIN gene, and characterization of the translocation breakpoints identified in an autism multiplex family. """"""""Restricted and Repetitive Behaviors in Young Children with Autism"""""""", will characterize the extent and trajectory of a critical behavioral aspect of autism. Understanding the emergence and trajectory of these behaviors has significant implications for directing interventional treatment. """"""""Neurogenetics of Candidate Systems in Autism"""""""" will use a functional candidate approach to determine the role(s) of genes underlying the serotonin and GABA systems, two systems known to affect behaviors exhibited by autistic children. We will characterize the variation in each gene using a comprehensive set of SNPs defining haplotype blocks, and examine their potential role individually and jointly in autism and in specific subsets of autistic behavior. An administrative core, a clinical and bioinformatics core, and a molecular analysis core will serve these three Projects. This integrated approach toward autism will provide significant insight into the role that specific genes play in this complex genetic disorder.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
7P01NS026630-19
Application #
7214781
Study Section
National Institute of Neurological Disorders and Stroke Initial Review Group (NSD)
Program Officer
Mamounas, Laura
Project Start
1997-03-01
Project End
2009-03-31
Budget Start
2007-04-01
Budget End
2008-03-31
Support Year
19
Fiscal Year
2007
Total Cost
$1,293,410
Indirect Cost
Name
University of Miami School of Medicine
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
052780918
City
Coral Gables
State
FL
Country
United States
Zip Code
33146
Griswold, Anthony J; Van Booven, Derek; Cuccaro, Michael L et al. (2018) Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorder. Neurogenetics 19:17-26
Zhu, Zuobin; Lu, Xitong; Yuan, Dejian et al. (2017) Close genetic relationships between a spousal pair with autism-affected children and high minor allele content in cases in autism-associated SNPs. Genomics 109:9-15
Correia, Catarina; Oliveira, Guiomar; Vicente, Astrid M (2014) Protein interaction networks reveal novel autism risk genes within GWAS statistical noise. PLoS One 9:e112399
Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J et al. (2014) Most genetic risk for autism resides with common variation. Nat Genet 46:881-5
Hadjixenofontos, Athena; Schmidt, Michael A; Whitehead, Patrice L et al. (2013) Evaluating mitochondrial DNA variation in autism spectrum disorders. Ann Hum Genet 77:9-21
Casey, Jillian P; Magalhaes, Tiago; Conroy, Judith M et al. (2012) A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Hum Genet 131:565-79
Cuccaro, Michael L; Tuchman, Roberto F; Hamilton, Kara L et al. (2012) Exploring the relationship between autism spectrum disorder and epilepsy using latent class cluster analysis. J Autism Dev Disord 42:1630-41
Anney, Richard; Klei, Lambertus; Pinto, Dalila et al. (2012) Individual common variants exert weak effects on the risk for autism spectrum disorders. Hum Mol Genet 21:4781-92
Cukier, Holly N; Lee, Joycelyn M; Ma, Deqiong et al. (2012) The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1. Autism Res 5:385-97
Griswold, Anthony J; Ma, Deqiong; Cukier, Holly N et al. (2012) Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways. Hum Mol Genet 21:3513-23

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