For the journal, see Public Health Genomics (journal).
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Public health genomics is the use of genomics information to benefit public health. This is visualized as more effective preventive care and disease treatments with better specificity, tailored to the genetic makeup of each patient.[1] According to the Centers for Disease Control and Prevention (U.S.), Public Health genomics is an emerging field of study that assesses the impact of genes and their interaction with behavior, diet and the environment on the population's health.[2]
This field of public health genomics is less than a decade old. A number of think tanks, universities, and governments (including the U.S., UK, and Australia) have started public health genomics projects. Research on the human genome is generating new knowledge that is changing public health programs and policies. Advances in genomic sciences are increasingly being used to improve health, prevent disease, educate and train the public health workforce, other healthcare providers, and citizens.
^Bellagio Group on Public Health Genomics. "Genome-based Research and Population Health" (PDF). Archived from the original on January 7, 2008. Retrieved 3 September 2015.{{cite web}}: CS1 maint: unfit URL (link)
^Cite error: The named reference CDC was invoked but never defined (see the help page).
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