Equal access to pharmacogenomics testing: The ethical imperative for population‐wide access in the UK NHS

Author:

Magavern Emma F.1ORCID,Caulfield Mark J.1

Affiliation:

1. William Harvey Research Institute Queen Mary University of London London UK

Funder

Barts Charity

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference17 articles.

1. NHS England.Accelerating Genomic Medicine in the NHS: A Strategy for Embedding Genomics in the NHS over the next 5 Years.2022.

2. Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study

3. Rapid Point-of-Care Genotyping to Avoid Aminoglycoside-Induced Ototoxicity in Neonatal Intensive Care

4. Genomics Education Programme.Reducing stroke risk with a genetic test: NHS Tayside introduces UK's first routine genetic test for stroke patients estimated to bring improved outcomes to thousands of patients each year.https://www.genomicseducation.hee.nhs.uk/blog/reducing-stroke-risk-with-a-genetic-test/. Published August 22 2022. Accessed February 14 2023.

5. McDermottJH NewmanW.Rapid genetic testing to avoid hearing loss in neonates.ENT Audiol News.https://www.entandaudiologynews.com/features/audiology-features/post/rapid-genetic-testing-to-avoid-hearing-loss-in-neonates. Published September 2 2022. Accessed February 14 2023.

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1. The British Journal of Clinical Pharmacology: The first 50 years;British Journal of Clinical Pharmacology;2023-12-28

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