Human difference in the genomic era: Facilitating a socially responsible dialogue

BMC Med Genomics. 2010 May 26:3:20. doi: 10.1186/1755-8794-3-20.

Abstract

Background: The study of human genetic variation has been advanced by research such as genome-wide association studies, which aim to identify variants associated with common, complex diseases and traits. Significant strides have already been made in gleaning information on susceptibility, treatment, and prevention of a number of disorders. However, as genetic researchers continue to uncover underlying differences between individuals, there is growing concern that observed population-level differences will be inappropriately generalized as inherent to particular racial or ethnic groups and potentially perpetuate negative stereotypes.

Discussion: We caution that imprecision of language when conveying research conclusions, compounded by the potential distortion of findings by the media, can lead to the stigmatization of racial and ethnic groups.

Summary: It is essential that the scientific community and with those reporting and disseminating research findings continue to foster a socially responsible dialogue about genetic variation and human difference.

MeSH terms

  • Genetic Variation*
  • Genome, Human
  • Genome-Wide Association Study*
  • Humans