Clinical phenome scanning

Nader Ghebranious, Catherine A. McCarty, Russell A. Wilke

Research output: Contribution to journalArticle

10 Scopus citations

Abstract

Large population-based cohorts are ideal for the study of common, complex disorders because they allow characterization of gene-gene and gene-environment interactions. We propose a clinical phenome scanning approach to genotype-phenotype association studies, as this approach acknowledges the heterogeneous nature of common diseases and takes advantage of the unprecedented density of phenotypic data available in population-based DNA biobanks. By analogy to genome-wide scanning, the construction of a clinical phenome scan includes a complete scan of all clinically available information (housed in electronic medical records). This is done on a subject-by-subject basis and the resulting phenomes can subsequently be interrogated for association with a single allele for any given gene. By prioritizing phenotype (rather than genotype), this approach allows investigators to ask the question "Which disease is associated with a given gene?" rather than "Which gene is associated with a given disease?".

Original languageEnglish (US)
Pages (from-to)175-182
Number of pages8
JournalPersonalized Medicine
Volume4
Issue number2
DOIs
StatePublished - May 1 2007

Keywords

  • Biobank
  • Clinical phenome scan
  • Common diseases
  • DNA
  • Phenomic markers
  • Pleiotropy

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    Ghebranious, N., McCarty, C. A., & Wilke, R. A. (2007). Clinical phenome scanning. Personalized Medicine, 4(2), 175-182. https://doi.org/10.2217/17410541.4.2.175