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article · Annals of Human Genetics

Incorporating familial risk, lifestyle factors, and pharmacogenomic insights into personalized noncommunicable disease (NCD) reports for healthcare funder beneficiaries participating in the Open Genome Project

20243 citationsOpen accessStellenbosch University

Abstract

This study demonstrated the implementation of genomics into an evolving workflow for patients with a history of frequent clinic visits. Eliminating the cost barrier provided valuable insights to guide future reimbursement policy decisions.

Research topics

  • BRCA gene mutations in cancer
  • Genomics and Rare Diseases
  • Ethics in Clinical Research

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DOI: 10.1111/ahg.12582

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