Genetic advances in autism hinge on the method of measuring symptoms

Curr Psychiatry Rep. 2005 Apr;7(2):133-7. doi: 10.1007/s11920-005-0010-y.

Abstract

Advances in genotyping and related technologies and the study of families with two or more autistic siblings have allowed the reporting of various genetic linkage and candidate gene association studies for autism. Despite this significant research effort, there still is no general agreement on the role of particular genes that predispose to the risk of autism. One source of general debate is whether core symptoms studied in research on the heredity of autism include single or multiple independent genetic domains. In this review, it is argued that failure to control for co-existing dimensions of psychopathology and lack of assessment of parents may lead to misinterpretation of genetic findings from pedigrees involving multiple affected family members.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Attention Deficit Disorder with Hyperactivity / diagnosis
  • Attention Deficit Disorder with Hyperactivity / genetics
  • Attention Deficit Disorder with Hyperactivity / psychology
  • Autistic Disorder / diagnosis
  • Autistic Disorder / genetics*
  • Autistic Disorder / psychology
  • Child
  • Chromosome Mapping
  • Diseases in Twins / genetics
  • Diseases in Twins / psychology
  • Genetic Markers / genetics
  • Genetic Predisposition to Disease / genetics
  • Genetic Research
  • Genotype
  • Humans
  • Phenotype

Substances

  • Genetic Markers