Common genetic variation and human disease

Nick Orr, Stephen Chanock

Research output: Contribution to journalReview article

47 Citations (Scopus)

Abstract

The landscape of human genetics has changed remarkably in a relatively short space of time. The field has progressed from comparatively small studies of rare genetic diseases to vast consortia based efforts that target the inherited components of common complex diseases and which typically involve thousands of individual samples. In particular, genome wide association studies have become possible as a result of a new generation of genotyping platforms. At the time of writing, these have led to the discovery of more than 150 novel susceptibility loci across a broad spectrum of diseases, a few in genes with high biological plausibility but the majority in others that had not been considered candidates. Here, we provide an overview of the field of complex disease genetics pertaining to mapping by association and consider the many pitfalls and caveats that have arisen.

Original languageEnglish
Pages (from-to)1-32
Number of pages32
JournalCurrent Genetics
Volume62
DOIs
Publication statusPublished - 2008
Externally publishedYes

Keywords

  • Chromosome Mapping
  • Disease
  • Genetic Predisposition to Disease
  • Genetic Variation
  • Genome, Human
  • Genome-Wide Association Study
  • Humans
  • Linkage Disequilibrium
  • Models, Biological
  • Polymorphism, Single Nucleotide
  • Public Health
  • Journal Article
  • Review

Fingerprint Dive into the research topics of 'Common genetic variation and human disease'. Together they form a unique fingerprint.

  • Cite this