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Literature DB >> 19066388

An unwelcome side effect of direct-to-consumer personal genome testing: raiding the medical commons.

Amy L McGuire¹, Wylie Burke.

Abstract

Entities: Disease Gene Species

Mesh：

Year: 2008 PMID： 19066388 PMCID： PMC2789655 DOI： 10.1001/jama.2008.803

Source DB: PubMed Journal: JAMA ISSN： 0098-7484 Impact factor: 56.272

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10 in total

1. Protecting the medical commons: who is responsible?

Authors: H H Hiatt
Journal: N Engl J Med Date: 1975-07-31 Impact factor: 91.245

2. Primary care: is there enough time for prevention?

Authors: Kimberly S H Yarnall; Kathryn I Pollak; Truls Østbye; Katrina M Krause; J Lloyd Michener
Journal: Am J Public Health Date: 2003-04 Impact factor: 9.308

Review 3. Computed tomography--an increasing source of radiation exposure.

Authors: David J Brenner; Eric J Hall
Journal: N Engl J Med Date: 2007-11-29 Impact factor: 91.245

4. Essential elements of a technology and outcomes assessment initiative.

Authors: Ezekiel J Emanuel; Victor R Fuchs; Alan M Garber
Journal: JAMA Date: 2007-09-19 Impact factor: 56.272

5. Managing medical resources: return to the commons?

Authors: Christine K Cassel; Troyen E Brennan
Journal: JAMA Date: 2007-06-13 Impact factor: 56.272

6. Letting the genome out of the bottle--will we get our wish?

Authors: David J Hunter; Muin J Khoury; Jeffrey M Drazen
Journal: N Engl J Med Date: 2008-01-10 Impact factor: 91.245

7. Psychology. The unseen mind.

Authors: Timothy D Wilson; Yoav Bar-Anan
Journal: Science Date: 2008-08-22 Impact factor: 47.728

Review 8. Cascade effects of medical technology.

Authors: Richard A Deyo
Journal: Annu Rev Public Health Date: 2001-10-25 Impact factor: 21.981

Review 9. Patient self-referral for radiologic screening tests: clinical and ethical concerns.

Authors: Joshua J Fenton; Richard A Deyo
Journal: J Am Board Fam Pract Date: 2003 Nov-Dec

Review 10. 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?

Authors: Muin J Khoury; Marta Gwinn; Paula W Yoon; Nicole Dowling; Cynthia A Moore; Linda Bradley
Journal: Genet Med Date: 2007-10 Impact factor: 8.822

10 in total

121 in total

1. Racial and ethnic differences in direct-to-consumer genetic tests awareness in HINTS 2007: sociodemographic and numeracy correlates.

Authors: Aisha T Langford; Ken Resnicow; J Scott Roberts; Brian J Zikmund-Fisher
Journal: J Genet Couns Date: 2012-01-21 Impact factor: 2.537

2. Genetic counseling and the ethical issues around direct to consumer genetic testing.

Authors: Alice K Hawkins; Anita Ho
Journal: J Genet Couns Date: 2012-06 Impact factor: 2.537

3. Neither as harmful as feared by critics nor as empowering as promised by providers: risk information offered direct to consumer by personal genomics companies.

Authors: Anders Nordgren
Journal: J Community Genet Date: 2012-04-05

An unwelcome side effect of direct-to-consumer personal genome testing: raiding the medical commons.

1. Protecting the medical commons: who is responsible?

2. Primary care: is there enough time for prevention?

Review 3. Computed tomography--an increasing source of radiation exposure.

4. Essential elements of a technology and outcomes assessment initiative.

5. Managing medical resources: return to the commons?

6. Letting the genome out of the bottle--will we get our wish?

7. Psychology. The unseen mind.

Review 8. Cascade effects of medical technology.

Review 9. Patient self-referral for radiologic screening tests: clinical and ethical concerns.

Review 10. 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?

1. Racial and ethnic differences in direct-to-consumer genetic tests awareness in HINTS 2007: sociodemographic and numeracy correlates.

2. Genetic counseling and the ethical issues around direct to consumer genetic testing.

3. Neither as harmful as feared by critics nor as empowering as promised by providers: risk information offered direct to consumer by personal genomics companies.

4. Points to consider in assessing and appraising predictive genetic tests.

5. A population approach to precision medicine.

6. Genetic self knowledge and the future of epidemiologic confounding.

7. Translational medicine in the era of health care reform.

8. Debating clinical utility.

9. Health system implications of direct-to-consumer personal genome testing.

10. Personal genomics and individual identities: motivations and moral imperatives of early users.