Abstract
The first edition of Human Genome Epidemiology, published in 2004, discussed how the epidemiologic approach provides an important scientific foundation for studying the continuum from gene discovery to the development, application and evaluation of human genome information in improving health and preventing disease. Since that time, advances in human genomics have continued to occur at a breathtaking pace. With contributions from leaders in the field from around the world, this new edition is a fully updated look at the ways in which genetic factors in common diseases are studied. Methodologic developments in collection, analysis and synthesis of data, as well as issues surrounding specific applications of human genomic information for medicine and public health are all discussed. In addition, the book focuses on practical applications of human genome variation in clinical practice and disease prevention. The book is a useful tool for understanding the rapidly evolving methods of the discovery and use of genetic information in medicine and public health in the 21st century.
| Original language | English |
|---|---|
| Publisher | Oxford University Press |
| Number of pages | 704 |
| ISBN (Print) | 9780199776023, 9780195398441 |
| DOIs | |
| Publication status | Published - 1 May 2010 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Common diseases
- Gene discovery
- Genetic factors
- Human genomics
- Improving health
- Medicine
- Preventing disease
- Public health
- Synthesis of data
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