Abstract
Recent groundbreaking work in genetics has identified thousands of small-effect genetic variants throughout the genome that are associated with almost all major diseases. These genome-wide association studies (GWAS) are often proposed as a source of future medical breakthroughs. However, with several notable exceptions, the journey from a small-effect genetic variant to a functional drug has proven arduous, and few examples of actual contributions to drug discovery exist. Here, we discuss novel approaches of overcoming this hurdle by using instead public genetics resources as a pragmatic guide alongside existing drug discovery methods. Our aim is to evaluate human genetic confidence as a rationale for drug target selection.
| Original language | English |
|---|---|
| Journal | Drug Discovery Today |
| Volume | 20 |
| Issue number | 10 |
| Pages (from-to) | 1176-1181 |
| Number of pages | 6 |
| ISSN | 1359-6446 |
| DOIs | |
| Publication status | Published - 2015 |
Bibliographical note
Published under a Creative Commons license.UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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