Genetic studies in autistic disorder and chromosome 15

Meredyth P. Bass, Marisa M. Menold, Chantelle M. Wolpert, Shannon L. Donnelly, Sarah A. Ravan, Elizabeth R. Hauser, Lewis O. Maddox, Jeffery M Vance, Ruth K. Abramson, Harry H. Wright, John Gilbert, Michael Cuccaro, G. Robert DeLong, Margaret A Pericak-Vance

Research output: Contribution to journalArticle

89 Scopus citations

Abstract

Autistic disorder (AD) is a developmental disorder affecting social interactions, communication, and behavior. AD is a disease of complex genetic architecture. It is postulated that several genes contribute to the underlying etiology of AD. Chromosome 15 is of particular interest due to numerous reports of AD in the presence of chromosomal abnormalities, located mainly in the 15q11-q13 region. There are also a number of plausible candidate genes in this area, including the gamma-aminobutyric acid(A) (GABA(A)) receptor gene complex. We have undertaken a study of tiffs region of chromosome 15 in a data set of 63 multiplex families (with 2 or more AD affected individuals per family). We found evidence in support of linkage to the 15q11-q13 region, as well as evidence of increased recombination in this region. These findings provide further support for the involvement of chromosome 15q11-q13 in the genetic etiology of AD.

Original languageEnglish
Pages (from-to)219-226
Number of pages8
JournalNeurogenetics
Volume2
Issue number4
StatePublished - Apr 20 2000
Externally publishedYes

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Keywords

  • Autistic disorder
  • Chromosome 15q11-q13
  • Gamma-aminobutyric acid(A)
  • Increased recombination
  • Linkage

ASJC Scopus subject areas

  • Genetics(clinical)
  • Neuroscience(all)

Cite this

Bass, M. P., Menold, M. M., Wolpert, C. M., Donnelly, S. L., Ravan, S. A., Hauser, E. R., Maddox, L. O., Vance, J. M., Abramson, R. K., Wright, H. H., Gilbert, J., Cuccaro, M., DeLong, G. R., & Pericak-Vance, M. A. (2000). Genetic studies in autistic disorder and chromosome 15. Neurogenetics, 2(4), 219-226.