A unified genetic theory for sporadic and inherited autism Academic Article uri icon

Overview

MeSH Major

  • Autistic Disorder
  • Genetic Predisposition to Disease

abstract

  • Autism is among the most clearly genetically determined of all cognitive-developmental disorders, with males affected more often than females. We have analyzed autism risk in multiplex families from the Autism Genetic Resource Exchange (AGRE) and find strong evidence for dominant transmission to male offspring. By incorporating generally accepted rates of autism and sibling recurrence, we find good fit for a simple genetic model in which most families fall into two types: a small minority for whom the risk of autism in male offspring is near 50%, and the vast majority for whom male offspring have a low risk. We propose an explanation that links these two types of families: sporadic autism in the low-risk families is mainly caused by spontaneous mutation with high penetrance in males and relatively poor penetrance in females; and high-risk families are from those offspring, most often females, who carry a new causative mutation but are unaffected and in turn transmit the mutation in dominant fashion to their offspring.

publication date

  • July 31, 2007

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed Central ID

  • PMC1933261

Digital Object Identifier (DOI)

  • 10.1073/pnas.0705803104

PubMed ID

  • 17652511

Additional Document Info

start page

  • 12831

end page

  • 6

volume

  • 104

number

  • 31