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References AMA (American Medical Association). 2011. Request for molecular pathology code re- view and feedback. http://www.ama-assn.org/ama1/pub/upload/mm/362/request-for- molecular-pathology-code-review-and-feedback.pdf (accessed February 2, 2012). Andriole, G. L., E. D. Crawford, R. L. Grubb, III, S. S. Buys, D. Chia, T. R. Church, M. N. Fouad, E. P. Gelmann, P. A. Kvale, D. J. Reding, J. L. Weissfeld, L. A. Yokochi, B. O’Brien, J. D. Clapp, J. M. Rathmell, T. L. Riley, R. B. Hayes, B. S. Kramer, G. Izmirlian, A. B. Miller, P. F. Pinsky, P. C. Prorok, J. K. Gohagan, and C. D. Berg, for the PLCO Project Team. 2009. Mortality results from a randomized prostate-cancer screening trial. New England Journal of Medicine 360(13):1310-1319. Buyse, M., S. Loi, L. van ‘t Veer, G. Viale, M. Delorenzi, A. M. Glas, M. S. d’Assignies, J. Bergh, R. Lidereau, P. Ellis, A. Harris, J. Bogaerts, P. Therasse, A. Floore, M. Amakrane, F. Piette, E. Rutgers, C. Sotiriou, F. Cardoso, and M. J. Piccart. 2006. Validation and clinical utility of a 70-gene prognostic signature for women with node-negative breast cancer. Journal of the National Cancer Institute 98(17):1183-1192. CMS (Center for Medicare & Medicaid Services). 2012. Summary of policies in the calendar year 2012 medicare physician fee schedule final rule and the telehealth originating site facility fee payment amount. MLN Matters MM7671. Fisher, B., J. Dignam, N. Wolmark, A. DeCillis, B. Emir, D. L. Wickerham, J. Bryant, N. V. Dimitrov, N. Abramson, J. N. Atkins, H. Shibata, L. Deschenes, and R. G. Margolese. 1997. Tamoxifen and chemotherapy for lymph node-negative, estrogen receptor-positive breast cancer. Journal of the National Cancer Institute 89(22):1673-1682. IOM (Institute of Medicine). 2011a. Establishing precompetitive collaborations to stimulate genomics-driven product development: Workshop summary. Washington, DC: The Na- tional Academies Press. IOM. 2011b. Generating evidence for genomic diagnostic test development: Workshop sum- mary. Washington, DC: The National Academies Press. IOM. 2012. Evolution of translational omics: Lessons learned and the path forward. Wash- ington, DC: The National Academies Press. 61
OCR for page 62
62 GENOME-BASED DIAGNOSTICS Meyers, M. F. 2011. Health care providers and direct-to-consumer access and advertising of genetic testing in the United States. Genome Medicine 3(12):81. NIH (National Institutes of Health). 2010. NIH announces genetic testing registry. http:// www.nih.gov/news/health/mar2010/od-18.htm (accessed February 2, 2012). NVCA (National Venture Capital Association). 2011a. Venture impact: The economic impor- tance of venture capital-backed companies to the U.S. economy. www.nvca.org/index. php?option=com_docman&task (accessed March 19, 2012). NVCA. 2011b. Vital signs: The crisis in investment in U.S. medical innovation and the im- perative of FDA reform. www.nvca.org/vital_signs_data_slides.pdf (accessed March 19, 2012). NVCA. 2011c. Yearbook. New York: Thomson Reuters. Peterson, C., and R. Burton. 2007. U.S. health care spending: Comparison with other OECD countries. Paper 311, Congressional Research Service. SACGHS (Secretary’s Advisory Committee on Genetics, Health, and Society). 2008. U.S. sys- tem of oversight of genetic testing: A response to the charge of the Secretary of Health and Human Services. Bethesda, MD: Department of Health and Human Services. Schully, S. D., C. B. Benedicto, E. M. Gillanders, S. S. Wang, and M. J. Khoury. 2011. Trans- lational research in cancer genetics: The road less traveled. Public Health Genomics 14(1):1-8. Siegel, R., D. Naishadham, and A. Jemal. 2012. Cancer statistics, 2012. CA: A Cancer Journal for Clinicians 62(1):10-29. Simon, R. M., S. Park, and D. F. Hayes. 2009. Use of archived specimens in evaluation of prognostic and predictive biomarkers. Journal of the National Cancer Institute 101(21): 1446-1452. Slamon, D. J., B. Leyland-Jones, S. Shak, H. Fuchs, V. Paton, A. Bajamonde, T. Fleming, W. Eiermann, J. Wolter, M. Pegram, J. Baselga, and L. Norton. 2001. Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. New England Journal of Medicine 344(11):783-792. SSAB (Social Security Advisory Board). 2009. The unsustainable cost of health care. http:// www.ssab.gov/documents/TheUnsustainableCostofHealthCare_508.pdf (accessed Janu- ary 26, 2012). Teutsch, S. M., L. A. Bradley, G. E. Palomaki, J. E. Haddow, M. Piper, N. Calonge, W. D. Dotson, M. P. Douglas, A. O. Berg, and EGAPP Working Group. 2009. The evaluation of genomic applications in practice and prevention (EGAPP) initiative: Methods of the EGAPP working group. Genetic Medicine 11(1):3-14. Thygesen, K., J. Mair, H. Katus, M. Plebani, P. Venge, P. Collinson, B. Lindahl, E. Giannitsis, Y. Hasin, M. Galvani, M. Tubaro, J. S. Alpert, L. M. Biasucci, W. Koenig, C. Mueller, K. Huber, C. Hamm, and A. S. Jaffe. 2010. Recommendations for the use of cardiac troponin measurement in acute cardiac care. European Heart Journal 31(18):2197-2204. USPSTF (U.S. Preventive Services Task Force). 2005. Genetic risk assessment and BRCA mu- tation testing for breast and ovarian cancer susceptibility: Recommendation statement. Annals of Internal Medicine 143(5):355-361. West, D. M. 2011. Enabling personalized medicine through health information tech- nology: Advancing the integration of information. http://www.brookings.edu/ papers/2011/0128_personalized_medicine_west.aspx (accessed February 2, 2012). Wright, C. F., and M. Kroese. 2009. Evaluation of genetic tests for susceptibility to common complex diseases: Why, when and how? Human Genetics 127(2):125-134.