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Suggested Citation:"References." Institute of Medicine. 2009. Innovations in Service Delivery in the Age of Genomics: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/12601.
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Page 53
Suggested Citation:"References." Institute of Medicine. 2009. Innovations in Service Delivery in the Age of Genomics: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/12601.
×
Page 54
Suggested Citation:"References." Institute of Medicine. 2009. Innovations in Service Delivery in the Age of Genomics: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/12601.
×
Page 55
Suggested Citation:"References." Institute of Medicine. 2009. Innovations in Service Delivery in the Age of Genomics: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/12601.
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Page 56

Below is the uncorrected machine-read text of this chapter, intended to provide our own search engines and external engines with highly rich, chapter-representative searchable text of each book. Because it is UNCORRECTED material, please consider the following text as a useful but insufficient proxy for the authoritative book pages.

References American Board of Medical Geneticists. 2008a. Training options. http://www.abmg.org/pages/ training_options.shtml (accessed January 28, 2009). ———. 2008b. Specialties of genetics. http://www.abmg.org/pages/training_specialties.shtml (accessed January 28, 2009). ———. 2008c. Numbers of certified specialists in genetics—by specialty. http://www.abmg. org/pages/resources_byspecialty.htm (accessed January 29, 2009). Burke, W. 2008. Vision of the future. Presentation at Institute of Medicine workshop on in- novations in service delivery in the age of genomics. July 28. Washington, DC. Cabe, J., and S. Springer. 2008. National call to action on cancer prevention and survivorship. Tucson, AZ: Excel Print Communications. CDC (Centers for Disease Control and Prevention). 2000. National health information sur- vey cancer module. ftp://ftp.cdc.gov/pub/Health_Statistics/NCHS/Survey_Questionnaires/ NHIS/2000/qcancerx.pdf. Cooksey, J. A., G. Forte, P. A. Flanagan, J. Benkendorf, and M. G. Blitzer. 2006. The medical genetics workforce: An analysis of clinical geneticist subgroups. Genet Med 8(10):603-614. DesRoches, C. M., E. C. Campbell, S. R. Rao, K. Donelan, T. G. Ferris, A. Jha, R. Kaushal, D. Levy, S. Rosenbaum, A. Shields, and D. Blumenthal. 2008. Electronic health record adoption in the ambulatory setting: Findings from a national survey of physicians. N Engl J Med 359:50-60. Deyo, R. A. 2002. Cascade effects of medical technology. Annu Rev Public Health 23:23-44. Eisenberg, J. M. 1999. Ten lessons for evidence-based technology assessment. JAMA 282(19): 1865-1869. Fiscella, K., and H. J. Geiger. 2006. Health information technology and quality improvement for community health centers. Health Aff 25(2):405-412. Gennaccaro, M., S. E. Waisbren, and D. Marsden. 2005. The knowledge gap in expanded newborn screening: Survey results from paediatricians in Massachusetts. J Inherit Metab Dis 28(6):819-824. 53

54 INNOVATIONS IN SERVICE DELIVERY IN THE AGE OF GENOMICS Giardiello, F. M. 1997. Genetic testing in hereditary colorectal cancer. JAMA 278(15): 1278-1281. Gowda, G. A., S. Zhang, H. Gu, V. Asiago, N. Shanaiah, and D. Raftery. 2008. Metabolomics- based methods for early disease diagnostics. Expert Rev Mol Diagn 8(5):617-633. IOM. 1994. Assessing genetic risks: Implications for health and social policy. Washington, DC: National Academy Press. ———. 2000. America’s health care safety net: Intact but endangered. Washington, DC: National Academy Press. ———. 2001. Crossing the quality chasm. Washington, DC: National Academy Press. ———. 2003a. Who will keep the public healthy?: Educating public health professionals for the 21st century. Washington, DC: The National Academies Press. ———. 2003b. Unequal treatment: Confronting racial and ethnic disparities in health care. Washington, DC: The National Academies Press. Jarvinen, H. J., M. Aarnio, H. Mustonen, K. Aktan-Collan, L. A. Aaltonen, P. Peltomaki, A. De La Chapelle, and J. P. Mecklin. 2000. Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer. Gastroen- terology 118(5):829-834. Korf, B. 2008. Brainstorming on a service delivery model for the future. Presentation at Insti­ tute of Medicine workshop on innovations in service delivery in the age of genomics. July 28. Washington, DC. Korf, B. R., G. Feldman, and G. L. Wiesner. 2005. Report of Banbury Summit Meeting on train- ing of physicians in medical genetics, October 20-22, 2004. Genet Med 7(6):433-438. Korf, B. R., D. Ledbetter, and M. F. Murray. 2008. Report of the Banbury Summit Meet- ing on the evolving role of the medical geneticist, February 12-14, 2006. Genet Med 10(7):502-507. Latterich, M., M. Abramovitz, and B. Leyland-Jones. 2008. Proteomics: New technologies and clinical applications. Eur J Cancer 44(18):2737-2741. Levy, D. E., J. E. Garber, and A. E. Shields. (Unpublished). Underprovision of guideline recom- mended advice on genetic assessment of breast and ovarian cancer among U.S. women. Lochner Doyle, D., and C. Watts (Principal Investigators). 2008. Genetic services policy project final report. Seattle: Washington State Department of Health and the University of Washington. March of Dimes. 2007. Nearly 90 percent of babies receive recommended newborn screening tests. http://www.marchofdimes.com/aboutus/22663_25778.asp (accessed January 28, 2009). McGlynn, E. A., S. M. Asch, J. Adams, J. Keesey, J. Hicks, A. DeCristofaro, and E. A. Kerr. 2003. The quality of health care delivered to adults in the United States. N Engl J Med 348:2635-2645. Menasha, J. D., C. Schechter, and J. Willner. 2000. Genetic testing: A physician’s perspective. Mt Sinai J Med 67(2):144-151. National Library of Medicine. 2009. Colorectal cancer. http://www.nlm.nih.gov/medlineplus/ colorectalcancer.html (accessed January 30, 2009). Ota Wang, V. 2008. The strengths and challenges of the current system: Patient education and communication. Presentation at Institute of Medicine workshop on innovations in service delivery in the age of genomics. July 28. Washington, DC. Parrott, S., and M. DelVecchio. 2007. Professional status survey 2006. National Society of Genetic Counselors, Inc. www.nsgc.org/client_files/career/2006_PSS_Results.doc (ac- cessed January 30, 2009). Phelan, R., P. Borry, and H. C. Howard. 2008. Letter to the editor. Pers Med 5(5):425-426. Rosenbaum, S., P. Shin, and J. Darnell. 2004. Economic stress and the safety net: A health center update. Washington, DC: The Henry J. Kaiser Family Foundation.

REFERENCES 55 Roses, A. D., D. K. Burns, S. Chissoe, L. Middleton, and P. St. Jean. 2005. Disease-­specific target selection: A critical first step down the right road. Drug Discov Today 10(3):177-189. Royal College of Physicians. 2004. Consultant physicians working with patients: The du- ties, responsibilities and practice for physicians, 3rd ed. London: Royal College of Physicians. Secretary’s Advisory Committee on Genetics, Health, and Society. 2008. U.S. system of over- sight of genetic testing: A response to the charge of the secretary of Health and Human Services. Washington, DC: U.S. Department of Health and Human Services. Shields, A. E. (Unpublished). Provision of genetics services at community health centers: Re- sults from a national survey. ———. 2008. The strengths and challenges of the current system: Disparities and access. Presentation at Institute of Medicine workshop on innovations in service delivery in the age of genomics. July 28. Washington, DC. Shields, A. E., W. Burke, and D. E. Levy. 2008. Differential use of available genetic tests among primary care physicians in the United States: Results of a national survey. Genet Med 10(6):404-414. U.S. Department of Health and Human Services, Health Resources and Services Administra- tion, Maternal and Child Health Bureau. 2004. The national survey of children with special health care needs chartbook 2001. Rockville, MD: U.S. Department of Health and Human Services. Wang, G., and C. Watts. 2007. Utilization trends of genetic clinics excluding prenatal services in Washington State, 1995-2004. Genet Med 9(10):713-718. Wideroff, L., S. T. Vadaparampil, N. Breen, R. T. Croyle, and A. N. Freedman. 2003. Aware- ness of genetic testing for increased cancer risk in the year 2000 National Health Inter- view Survey. Comm Genet 6(3):147-156.

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New discoveries in genomics--that is, the study of the entire human genome--are changing how we diagnose and treat diseases. As the trend shifts from genetic testing largely being undertaken for rare genetic disorders to, increasingly, individuals being screened for common diseases, general practitioners, pediatricians, obstetricians/gynecologists, and other providers need to be knowledgeable about and comfortable using genetic information to improve their patients' health. To address these changes, the Roundtable on Translating Genomic-Based Research for Health held the public workshop "Innovations in Service Delivery in the Age of Genomics" on July 27, 2008.

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