Beyond base pairs to bedside: a population perspective on how genomics can improve health (Q28390595)

Clinical assessment incorporating a personal genome

PubMed

volume

102

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issue

1

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page(s)

34-7

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cites work

1 reference

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20 March 2017

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Genetic susceptibility to occupational exposures

20 March 2017

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Do we need genomic research for the prevention of common diseases with environmental causes?

20 March 2017

1 reference

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What Is Population Health?

20 March 2017

1 reference

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Mendelian Randomization for Strengthening Causal Inference in Observational Studies

23 March 2017

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Current Priorities for Public Health Practice in Addressing the Role of Human Genomics in Improving Population Health

6 April 2017

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Charting a course for genomic medicine from base pairs to bedside

29 September 2017

1 reference

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Horizon scanning for new genomic tests

29 September 2017

1 reference

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Effect of direct-to-consumer genomewide profiling to assess disease risk

29 September 2017

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Long-term follow-up in newborn screening: A systems approach for improving health outcomes

29 September 2017

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Being more realistic about the public health impact of genomic medicine

29 September 2017

1 reference

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A formal risk-benefit framework for genomic tests: Facilitating the appropriate translation of genomics into clinical practice

29 September 2017

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Testicular cancer survivorship: research strategies and recommendations

29 September 2017

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Future health applications of genomics: priorities for communication, behavioral, and social sciences research

29 September 2017

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Translational research in cancer genetics: the road less traveled

29 September 2017

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Causal thinking and complex system approaches in epidemiology

29 September 2017

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The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop

29 September 2017

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Epigenetics - potential contribution to fetal programming

29 September 2017

1 reference

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Does comparative-effectiveness research threaten personalized medicine?

29 September 2017

1 reference

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Closing the evidence gap in the use of emerging testing technologies in clinical practice

29 September 2017

1 reference

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Systems thinking to improve the public's health

29 September 2017

1 reference

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The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention?

29 September 2017

1 reference

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Dissecting complex disease: the quest for the Philosopher's Stone?

29 September 2017

1 reference

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Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: systematic evidence review for the U.S. Preventive Services Task Force

29 September 2017

1 reference

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Central Challenges Facing the National Clinical Research Enterprise

29 September 2017

1 reference

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Extending the reach of public health genomics: what should be the agenda for public health in an era of genome-based and “personalized” medicine?

29 September 2017

1 reference

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Awareness and utilization of BRCA1/2 testing among U.S. primary care physicians

27 November 2018

1 reference

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Dealing with the evidence dilemma in genomics and personalized medicine

27 November 2018

1 reference

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Genomics and public health: translating research into public benefit

27 November 2018

1 reference

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The evidence dilemma in genomic medicine

27 November 2018

1 reference

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Genomics and the public health code of ethics.

27 November 2018

1 reference

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A code of ethics for public health.

27 November 2018

1 reference

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Racial differences in the use of BRCA1/2 testing among women with a family history of breast or ovarian cancer

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22095352