UCSF

Publications

  1. Douglas MP, Parker SL, Trosman JR, Slavotinek AM, Phillips KA. Private Payer Coverage Policies for Exome Sequencing (ES) in Pediatric Patients: Trends Over Time and Analysis of Evidence Cited. Genet Med. 2019;21(1):152-160. https://www.ncbi.nlm.nih.gov/pubmed/29997388
  2. Phillips KA, Douglas MP. The Global Market for Next-Generation Sequencing Tests Continues Its Torrid Pace. Journal Precision Medicine. 2018; https://www.thejournalofprecisionmedicine.com/wp-content/uploads/2018/11/Phillips-Online.pdf
  3. Phillips KA, Trosman JR, Weldon CB, Douglas MP. The New Medicare Coverage Policy for Next Generation Tumor Sequencing: A Key Shift in Coverage Criteria with Broad Implications beyond Medicare. JCO Precis Oncol. 2018 :2, 1-5. https://ascopubs.org/doi/abs/10.1200/PO.18.00206
  4. Phillips KA. Assessing the Value of Next-Generation Sequencing Technologies: An Introduction. Value Health. 2018; 21(9):1031-1032. https://www.ncbi.nlm.nih.gov/pubmed/30224105
  5. Phillips KA, Deverka PA, Marshall DA, Wordsworth S, Regier DA, Christensen KD, Buchanan J. Methodological Challenges and Solutions for Assessing Economic Value of Next Generation Sequencing Tests. Value Health. 2018; 21(9):1033-1042. https://www.ncbi.nlm.nih.gov/pubmed/30224106
  6. Wordsworth S, Doble B, Payne K, Buchanan J, Marshall DA, McCabe C, Regier DA. Using ‘big’ data in the cost-effectiveness analysis of genomic-based diagnostic tests: challenges and potential solutions. Value Health. 2018; 21(9):1048-1053. https://www.ncbi.nlm.nih.gov/pubmed/30224108
  7. Reiger DA, Weymann D, Buchanan J, Marshall DA, Wordsworth S. Valuation of health and non-health Outcomes from Next-Generation Sequencing: Approaches, Challenges, and Solutions. Value Health 2018; 21(9):1043-1047. https://www.ncbi.nlm.nih.gov/pubmed/30224107
  8. Christensen KD, Phillips KA, Green RC, Dukhovny D. Cost Analyses of Genomic Sequencing – Lessons Learned from the MedSeq Project. Value Health. Value Health. 2018; 21(9):1054-1061. https://www.ncbi.nlm.nih.gov/pubmed/30224109
  9. Trosman JR, Weldon CB, Gradishar WJ, Benson AB III, Cristofanilli M, Kurian AW, Ford JM, Balch A, Watkins J, Phillips KA. From the Past to the Present: Insurer Coverage Frameworks for Next-Generation Tumor Sequencing. Value Health. 2018; 21(9):1062-1068. https://www.ncbi.nlm.nih.gov/pubmed/30224110
  10. Christensen KD, Vassy JL, Phillips KA, Blout CL, Azzariti DR, Lu CY, Robinson JO, Lee K, Douglas MP, Yeh JM, Machini K, Stout NK, Rehm HL, McGuire AL, Green RC, Dukhovny D. Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial. Genet Med. 2018; March 22. https://www.ncbi.nlm.nih.gov/pubmed/29565423
  11. Phillips KA, Deverka PA, Douglas MP, Hooker G. Genetic Test Availability and Spending. Where Are We Now? Where Are We Going? Health Affairs. 2018;37(5):710-716. https://www.ncbi.nlm.nih.gov/pubmed/29733704
  12. Ginsburg GS, Phillips KA. Precision Medicine: From Science to Value. Health Affairs. 2018;37(5):694-701. https://www.ncbi.nlm.nih.gov/pubmed/29733705
  13. Phillips KA. Evolving Payer Coverage Policies on Genomic Sequencing Tests: Beginning of the End or End of the Beginning? JAMA. 2018; Apr 16. [Epub ahead of print] https://www.ncbi.nlm.nih.gov/pubmed/29710095
  14. Phillips KA, Trosman JR, Deverka PA, Quinn B, Tunis S, Neumann PJ, Chambers JD, Garrison LP, Douglas MP, Weldon CB. Insurance Coverage for Genomic Tests. Science. 2018;360(6386):278-279. https://www.ncbi.nlm.nih.gov/pubmed/29674586
  15. Chambers J, Saret C, Anderson J, Deverka, PA, Douglas, MP, Phillips KA. Examining payer coverage policies for multi-gene panels and sequencing tests. IJTAHC. 2017;33(4):534-540. https://www.ncbi.nlm.nih.gov/pubmed/29065945
  16. Phillips KA, Deverka PA, Trosman JR, Douglas MP, Chambers JD, Weldon CB, Dervan AP. Payer Coverage Policies for Multigene Tests. Nature Biotechnol. 2017; 35(7):614-617. https://www.ncbi.nlm.nih.gov/pubmed/28700544
  17. Phillips KA, Deverka PA, Sox HC, Khoury MJ, Sandy LG, Ginsburg GS, Tunis SR, Orlando LA, Douglas MP. Making Genomic Medicine Evidence-Based and Patient-Centered: A Structured Review and Landscape Analysis of Comparative Effectiveness Research. Genet Med. 2017; 19(10):1081-1091. https://www.ncbi.nlm.nih.gov/pubmed/28406488
  18. Trosman JR, Weldon CB, Douglas MP, Kurian AW, Kelley RK, Deverka PA, Phillips KA. Payer Coverage for Hereditary Cancer Panels: Barriers, Opportunities, and Implications for the Precision Medicine Initiative. J Natl Compr Canc Netw. 2017; Feb;15(2):219-228. https://www.ncbi.nlm.nih.gov/pubmed/28188191
  19. Dervan AP, Deverka PA, Trosman JR, Weldon CB, Douglas MP, and Phillips KA. Payer Decision-Making for Next Generation Sequencing-Based Genetic Tests: Insights from Cell-Free DNA Prenatal Screening. Genet Med. 2017; May;19(5):559-567. https://www.ncbi.nlm.nih.gov/pubmed/27657682
  20. Marshall DA, Gonzalez JM, MacDonald KV, et al. Estimating Preferences for Complex Health Technologies: Lessons Learned and Implications for Personalized Medicine. Value Health. 2017;20(1): 32-39. https://www.ncbi.nlm.nih.gov/pubmed/28212966
  21. Phillips KA, Douglas MP, Trosman JR, et al. "What Goes Around Comes Around": Lessons Learned from Economic Evaluations of Personalized Medicine Applied to Digital Medicine. Value Health. 2017;20(1): 47-53. https://www.ncbi.nlm.nih.gov/pubmed/28212968
  22. Trosman JR, Weldon CB, Douglas MP, et al. Decision-Making on Medical Innovations in a Changing Health Environment: Insights from Accountable Care Organizations and Payers on Personalized Medicine and Other Technologies. Value Health. 2017;20(1): 40-46. https://www.ncbi.nlm.nih.gov/pubmed/28212967
  23. Marshall DA, MacDonald KV, Oliver Robinson J, Barcellos LF, Gianfrancesco M, Helm M, McGuire A, Green RC, Douglas MP, Goldman MA, Phillips KA. The price of whole genome sequencing may be decreasing, but who will be sequenced? Personalized Medicine. 2017; 14(2): 203-211. https://www.futuremedicine.com/doi/abs/10.2217/pme-2016-0075
  24. Phillips KA, Deverka PA, Sox HC, Khoury MJ, Sandy LG, Ginsburg GS, Tunis SR, Orlando LA, Douglas MP. Making genomic medicine evidence-based and patient-centered: a structured review and landscape analysis of comparative effectiveness research. Genet Med. 2017; 19:1081-1091. https://www.ncbi.nlm.nih.gov/pubmed/28406488
  25. Phillips KA, Deverka PA, Trosman JR, Douglas MP, Chambers JD, Weldon CB, Dervan AP. Payer coverage policies for multigene tests. Nat Biotechnol. 2017 Jul 12;35(7):614-617. https://www.ncbi.nlm.nih.gov/pubmed/28700544
  26. Marshall DA, Gonzalez JM, Johnson FR, MacDonald KV, Pugh A, Douglas MP, Phillips KA. What are people willing to pay for whole-genome sequencing information, and who decides what they receive? Genet Med. 2016, 18(2):1295-1302. http://www.ncbi.nlm.nih.gov/pubmed/27253734
  27. Phillips KA, Schleifer D, Hagelskamp C. Most Americans Do Not Believe That There Is An Association Between Health Care Prices And Quality Of Care. Health Affairs. 2016, 35:647-653. http://www.ncbi.nlm.nih.gov/pubmed/27044965
  28. Payne K, Redekop K, and Phillips KA. (2016) Personalized Medicine: Economic Evaluation and Evidence (book chapter). In World Scientific Handbook of Global Health Economics and Public Policy, Vol. 2, edited by Richard M. Scheffler. World Scientific, Imperial College Press. Hackensack, NJ.
  29. Phillips KA, Pletcher MJ, Ladabaum U. Is the “$1000 Genome” Really $1000? Understanding the Full Benefits and Costs of Genomic Sequencing. Technol Health Care 2015. 23(3)373-379. http://www.ncbi.nlm.nih.gov/pubmed/25669213
  30. Trosman JR, Weldon CB, Kelley RK, Phillips KA. Challenges of coverage policy development for next-generation tumor sequencing panels: Experts and Payers Weigh in. JNCCN. 2015. 13(3):311-8. http://www.ncbi.nlm.nih.gov/pubmed/25736008
  31. Phillips KA, Ladabaum U, Pletcher MJ, Marshall DA, Douglas MP. Key emerging themes for assessing the cost-effectiveness of reporting incidental findings. Genet Med. 2015. 17(4):314-5. http://www.ncbi.nlm.nih.gov/pubmed/25835195
  32. Douglas MP, Ladabaum U, Pletcher MJ, Marshall DA, Phillips KA. Economic evidence on identifying clinically actionable findings with whole-genome sequencing: a scoping review. Genet Med. 2016. 18(2):111-116. http://www.ncbi.nlm.nih.gov/pubmed/25996638
  33. Clain E, Trosman JR, Douglas MP, Weldon CB, and Phillips KA. Availability and payer coverage of BRCA1/2 tests and gene panels. Nat Biotechnol. 2015. 33(9):900-2. http://www.ncbi.nlm.nih.gov/pubmed/26348951
  34. Garfield, S., M. P. Douglas, K. V. MacDonald, D. A. Marshall and K. A. Phillips (2015). "Consumer familiarity, perspectives and expected value of personalized medicine with a focus on applications in oncology." Personalized Medicine. 12(1): 13-22. http://www.futuremedicine.com/doi/full/10.2217/pme.14.74
  35. Schink, J. C., J. R. Trosman, C. B. Weldon, K. P. Siziopikou, G. J. Tsongalis, A. W. Rademaker, J. D. Patel, A. B. Benson, 3rd, E. A. Perez and W. J. Gradishar (2014). "Biomarker testing for breast, lung, and gastroesophageal cancers at NCI designated cancer centers." J Natl Cancer Inst 106(10). PMCID: 4176043. http://www.ncbi.nlm.nih.gov/pubmed/25217578
  36. Phillips, K. A., J. R. Trosman, R. K. Kelley, M. J. Pletcher, M. P. Douglas and C. B. Weldon (2014). "Genomic sequencing: assessing the health care system, policy, and big-data implications." Health Aff (Millwood) 33(7): 1246-1253. PMCID: 4113721. http://www.ncbi.nlm.nih.gov/pubmed/25006153
  37. Phillips, K. A., J. Ann Sakowski, J. Trosman, M. P. Douglas, S. Y. Liang and P. Neumann (2014). "The economic value of personalized medicine tests: what we know and what we need to know." Genet Med 16(3): 251-257. PMCID: 3949119. http://www.ncbi.nlm.nih.gov/pubmed/24232413
  38. Phillips, K. A. and Labno, A. (2014). "“SHINING A LIGHT” on Companies Providing Healthcare Price Transparency Data. ." JMCM 17(4): 75-79. http://jmcmpub.org/pdf/17-4/?pdf_page=75
  39. Trosman, J. R., C. B. Weldon, J. C. Schink, W. J. Gradishar and A. B. Benson, 3rd (2013). "What do providers, payers and patients need from comparative effectiveness research on diagnostics? The case of HER2/Neu testing in breast cancer." J Comp Eff Res 2(4): 461-477. http://www.ncbi.nlm.nih.gov/pubmed/24236686
  40. Shin, J., S. Y. Liang, M. J. Hassett, K. A. Phillips and J. S. Haas (2013). "Utilization of cardiac monitoring tests in women with non-metastatic breast cancer treated with trastuzumab." Personalized Medicine 10(7): 703-708. http://www.futuremedicine.com/doi/full/10.2217/pme.13.68
  41. Phillips, K. A., J. S. Sakowski, S. Y. Liang and N. A. Ponce (2013). "Economic Perspectives on Personalized Health Care and Prevention. ." Forum for Health Economics and Policy. 16(2): S23-S52. http://www.degruyter.com/view/j/fhep.2013.16.issue-2/fhep-2013-0010/fhep-2013-0010.xml?rskey=dVaq6A&result=4
  42. Kuppermann, M., G. Wang, S. Wong, A. Blanco, P. Conrad, S. Nakagawa, J. Terdiman and U. Ladabaum (2013). "Preferences for outcomes associated with decisions to undergo or forgo genetic testing for Lynch syndrome." Cancer 119(1): 215-225. http://www.ncbi.nlm.nih.gov/pubmed/22786716
  43. Ferrusi, I. L., C. C. Earle, M. Trudeau, N. B. Leighl, E. Pullenayegum, H. Khong, J. S. Hoch and D. A. Marshall (2013). "Closing the personalized medicine information gap: HER2 test documentation practice." Am J Manag Care 19(1): 838-844. PMCID: 3919466. http://www.ncbi.nlm.nih.gov/pubmed/23379747
  44. Weldon, C. B., J. R. Trosman, W. J. Gradishar, A. B. Benson, 3rd and J. C. Schink (2012). "Barriers to the use of personalized medicine in breast cancer." J Oncol Pract 8(4): e24-31. PMCID: 3396824. http://www.ncbi.nlm.nih.gov/pubmed/23180995
  45. Wang, G., M. Kuppermann, B. Kim, K. A. Phillips and U. Ladabaum (2012). "Influence of patient preferences on the cost-effectiveness of screening for Lynch syndrome." Am J Manag Care 18(5): e179-185. http://www.ncbi.nlm.nih.gov/pubmed/22694112
  46. Wang, G., M. Kuppermann, B. Kim, K. A. Phillips and U. Ladabaum (2012). "Influence of patient preferences on the cost-effectiveness of screening for lynch syndrome." J Oncol Pract 8(3 Suppl): e24s-30s. PMCID: 3348599. http://www.ncbi.nlm.nih.gov/pubmed/22942831
  47. Walsh, J., M. Arora, C. Hosenfeld, U. Ladabaum, M. Kuppermann and S. J. Knight (2012). "Preferences for genetic testing to identify hereditary colorectal cancer: perspectives of high-risk patients, community members, and clinicians." J Cancer Educ 27(1): 112-119. http://www.ncbi.nlm.nih.gov/pubmed/22131063
  48. Ponce, N. A., J. Tsui, S. J. Knight, A. Afable-Munsuz, U. Ladabaum, R. A. Hiatt and J. S. Haas (2012). "Disparities in cancer screening in individuals with a family history of breast or colorectal cancer." Cancer 118(6): 1656-1663. PMCID: 3262934. http://www.ncbi.nlm.nih.gov/pubmed/22009719
  49. Ladabaum, U. and J. M. Ford (2012). "Lynch syndrome in patients with colorectal cancer: finding the needle in the haystack." JAMA 308(15): 1581-1583. http://www.ncbi.nlm.nih.gov/pubmed/23073955
  50. Kelley, R. K., C. Atreya, A. P. Venook and P. G. Febbo (2012). "Predictive biomarkers in advance of a companion drug: ahead of their time?" J Natl Compr Canc Netw 10(3): 303-309. http://www.ncbi.nlm.nih.gov/pubmed/22393192
  51. Beattie, M. S., G. Wang and K. A. Phillips (2012). "Differences in US healthcare coverage policies in BRCA testing and potential implications." Personalized Medicine. 9(1): 5-8. http://www.futuremedicine.com/doi/full/10.2217/pme.11.85
  52. Wang, G., M. S. Beattie, N. A. Ponce and K. A. Phillips (2011). "Eligibility criteria in private and public coverage policies for BRCA genetic testing and genetic counseling." Genet Med 13(12): 1045-1050. http://www.ncbi.nlm.nih.gov/pubmed/21844812
  53. Trosman, J. R., S. L. Van Bebber and K. A. Phillips (2011). "Health technology assessment and private payers's coverage of personalized medicine." Am J Manag Care 17 Suppl 5 Developing: SP53-60. http://www.ncbi.nlm.nih.gov/pubmed/21711078
  54. Trosman, J. R., S. L. Van Bebber and K. A. Phillips (2011). "Health technology assessment and private payers' coverage of personalized medicine." J Oncol Pract 7(3 Suppl): 18s-24s. PMCID: 3092460. http://www.ncbi.nlm.nih.gov/pubmed/21886515
  55. Pletcher, M. J. and M. Pignone (2011). "Evaluating the clinical utility of a biomarker: a review of methods for estimating health impact." Circulation 123(10): 1116-1124. PMCID: 3138723. http://www.ncbi.nlm.nih.gov/pubmed/21403122
  56. Odierna, D. H., A. Afable-Munsuz, O. Ikediobi, M. Beattie, S. Knight, M. Ko, A. Wilson and N. A. Ponce (2011). "Early developments in gene-expression profiling of breast tumors: potential for increasing black-white patient disparities in breast cancer outcomes?" Per Med 8(6): 669-679. PMCID: 3242007. http://www.ncbi.nlm.nih.gov/pubmed/22190978
  57. Lorizio, W., H. Rugo, M. S. Beattie, S. Tchu, T. Melese, M. Melisko, A. H. Wu, H. J. Lawrence, M. Nikoloff and E. Ziv (2011). "Pharmacogenetic testing affects choice of therapy among women considering tamoxifen treatment." Genome Med 3(10): 64. PMCID: 3239226. http://www.ncbi.nlm.nih.gov/pubmed/21970596
  58. Liang, S. Y., K. A. Phillips, G. Wang, C. Keohane, J. Armstrong, W. M. Morris and J. S. Haas (2011). "Tradeoffs of using administrative claims and medical records to identify the use of personalized medicine for patients with breast cancer." Med Care 49(6): e1-8. PMCID: 3383782. http://www.ncbi.nlm.nih.gov/pubmed/21422962
  59. Ladabaum, U., G. Wang, J. Terdiman, A. Blanco, M. Kuppermann, C. R. Boland, J. Ford, E. Elkin and K. A. Phillips (2011). "Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis." Ann Intern Med 155(2): 69-79. PMCID: 3793257. http://www.ncbi.nlm.nih.gov/pubmed/21768580
  60. Kelley, R. K., G. Wang and A. P. Venook (2011). "Biomarker use in colorectal cancer therapy." J Natl Compr Canc Netw 9(11): 1293-1302. PMCID: 3696980. http://www.ncbi.nlm.nih.gov/pubmed/22056657
  61. Kelley, R. K. and A. P. Venook (2011). "Prognostic and predictive markers in stage II colon cancer: is there a role for gene expression profiling?" Clin Colorectal Cancer 10(2): 73-80. PMCID: 3561586. http://www.ncbi.nlm.nih.gov/pubmed/21859557
  62. Kelley, R. K., S. L. Van Bebber, K. A. Phillips and A. P. Venook (2011). "Personalized medicine and oncology practice guidelines: a case study of contemporary biomarkers in colorectal cancer." J Natl Compr Canc Netw 9(1): 13-25. PMCID: 3695822. http://www.ncbi.nlm.nih.gov/pubmed/21233242
  63. Johnson, F. R., A. F. Mohamed, S. Ozdemir, D. A. Marshall and K. A. Phillips (2011). "How does cost matter in health-care discrete-choice experiments?" Health Econ 20(3): 323-330. PMCID: 3918954. http://www.ncbi.nlm.nih.gov/pubmed/20217834
  64. Haas, J. S., K. A. Phillips, S. Y. Liang, M. J. Hassett, C. Keohane, E. B. Elkin, J. Armstrong and M. Toscano (2011). "Genomic testing and therapies for breast cancer in clinical practice." Am J Manag Care 17(5 Spec No): e174-181. http://www.ncbi.nlm.nih.gov/pubmed/21711068
  65. Haas, J. S., K. A. Phillips, S. Y. Liang, M. J. Hassett, C. Keohane, E. B. Elkin, J. Armstrong and M. Toscano (2011). "Genomic testing and therapies for breast cancer in clinical practice." J Oncol Pract 7(3 Suppl): e1s-7s. PMCID: 3092459. http://www.ncbi.nlm.nih.gov/pubmed/21886507
  66. Haas, J. S., S. Y. Liang, M. J. Hassett, S. Shiboski, E. B. Elkin and K. A. Phillips (2011). "Gene expression profile testing for breast cancer and the use of chemotherapy, serious adverse effects, and costs of care." Breast Cancer Res Treat 130(2): 619-626. PMCID: 3590013. http://www.ncbi.nlm.nih.gov/pubmed/21681446
  67. Ferrusi, I. L., N. B. Leighl, N. A. Kulin and D. A. Marshall (2011). "Do economic evaluations of targeted therapy provide support for decision makers?" Am J Manag Care 17 Suppl 5 Developing: SP61-70. PMCID: 3918963. http://www.ncbi.nlm.nih.gov/pubmed/21711079
  68. Ferrusi, I. L., N. B. Leighl, N. A. Kulin and D. A. Marshall (2011). "Do economic evaluations of targeted therapy provide support for decision makers?" J Oncol Pract 7(3 Suppl): 36s-45s. PMCID: 3092467. http://www.ncbi.nlm.nih.gov/pubmed/21886518
  69. Ferrusi, I. L., N. B. Leighl, N. A. Kulin and D. A. Marshall (2011). "Do economic evaluations of targeted therapy provide support for decision makers?" J Oncol Pract 7(3 Suppl): 36s-45s. PMCID: 3092467. http://www.ncbi.nlm.nih.gov/pubmed/21886518
  70. Elkin, E. B., D. A. Marshall, N. A. Kulin, I. L. Ferrusi, M. J. Hassett, U. Ladabaum and K. A. Phillips (2011). "Economic evaluation of targeted cancer interventions: critical review and recommendations." Genet Med 13(10): 853-860. PMCID: 3774033. http://www.ncbi.nlm.nih.gov/pubmed/21637102
  71. Arar, N., S. J. Knight, S. M. Modell and A. M. Issa (2011). "The Genome-based Knowledge Management in Cycles model: a complex adaptive systems framework for implementation of genomic applications." Personalized Medicine. 8(2): 191-205. http://www.futuremedicine.com/doi/full/10.2217/pme.11.5
  72. Wang, G., R. K. Kelley and Gappnet (2010). "KRAS mutational analysis for colorectal cancer. Application: pharmacogenomic." PLoS Curr 2. PMCID: 2940138. http://www.ncbi.nlm.nih.gov/pubmed/20877448
  73. Van Bebber, S. L., J. R. Trosman, S. Y. Liang, G. Wang, D. A. Marshall, S. Knight and K. A. Phillips (2010). "Capacity building for assessing new technologies: approaches to examining personalized medicine in practice." Per Med 7(4): 427-439. PMCID: 3157083. http://www.ncbi.nlm.nih.gov/pubmed/21857867
  74. Trosman, J. R., S. L. Van Bebber and K. A. Phillips (2010). "Coverage policy development for personalized medicine: private payer perspectives on developing policy for the 21-gene assay." J Oncol Pract 6(5): 238-242. PMCID: 2936466. http://www.ncbi.nlm.nih.gov/pubmed/21197187
  75. Marshall, D., S. E. McGregor and G. Currie (2010). "Measuring Preferences for Colorectal Cancer Screening: What are the Implications for Moving Forward?" Patient 3(2): 79-89. http://www.ncbi.nlm.nih.gov/pubmed/22273359
  76. Ladabaum, U., A. Ferrandez and A. Lanas (2010). "Cost-effectiveness of colorectal cancer screening in high-risk Spanish patients: use of a validated model to inform public policy." Cancer Epidemiol Biomarkers Prev 19(11): 2765-2776. PMCID: 3159034. http://www.ncbi.nlm.nih.gov/pubmed/20810603
  77. Kelley, R. K. and A. P. Venook (2010). "Nonadherence to imatinib during an economic downturn." N Engl J Med 363(6): 596-598. http://www.ncbi.nlm.nih.gov/pubmed/20818898
  78. Kelley, R. K. (2010). "What clinicians need to know about molecular markers in solid tumors. MedscapeCME Oncology. ." Retrieved 1/12/2015, 2015, from http://www.medscape.org/viewarticle/725989.
  79. Johnson, F. R., S. Ozdemir and K. A. Phillips (2010). "Effects of simplifying choice tasks on estimates of taste heterogeneity in stated-choice surveys." Soc Sci Med 70(2): 183-190. PMCID: 3152257. http://www.ncbi.nlm.nih.gov/pubmed/19880234
  80. Elkin, E. B. and P. B. Bach (2010). "Cancer's next frontier: addressing high and increasing costs." JAMA 303(11): 1086-1087. PMCID: 3647336. http://www.ncbi.nlm.nih.gov/pubmed/20233828
  81. Cheung, E. L., A. D. Olson, T. M. Yu, P. Z. Han and M. S. Beattie (2010). "Communication of BRCA results and family testing in 1,103 high-risk women." Cancer Epidemiol Biomarkers Prev 19(9): 2211-2219. PMCID: 3207738. http://www.ncbi.nlm.nih.gov/pubmed/20699375
  82. Bowen, D. J., J. Harris, C. M. Jorgensen, M. F. Myers and A. Kuniyuki (2010). "Socioeconomic influences on the effects of a genetic testing direct-to-consumer marketing campaign." Public Health Genomics 13(3): 131-142. http://www.ncbi.nlm.nih.gov/pubmed/19641293
  83. Wideroff, L., K. A. Phillips, G. Randhawa, A. Ambs, K. Armstrong, C. L. Bennett, M. L. Brown, M. S. Donaldson, M. Follen, S. J. Goldie, R. A. Hiatt, M. J. Khoury, G. Lewis, H. L. McLeod, M. Piper, I. Powell, D. Schrag, K. A. Schulman and J. Scott (2009). "A health services research agenda for cellular, molecular and genomic technologies in cancer care." Public Health Genomics 12(4): 233-244. PMCID: 2844634. http://www.ncbi.nlm.nih.gov/pubmed/19367091
  84. Shaukat, A., M. Parekh, J. Lipscomb and U. Ladabaum (2009). "Can calcium chemoprevention of adenoma recurrence substitute or serve as an adjunct for colonoscopic surveillance?" Int J Technol Assess Health Care 25(2): 222-231. PMCID: 2972652. http://www.ncbi.nlm.nih.gov/pubmed/19331713
  85. Phillips, K. A., D. A. Marshall, J. S. Haas, E. B. Elkin, S. Y. Liang, M. J. Hassett, I. Ferrusi, J. E. Brock and S. L. Van Bebber (2009). "Clinical practice patterns and cost effectiveness of human epidermal growth receptor 2 testing strategies in breast cancer patients." Cancer 115(22): 5166-5174. PMCID: 2783254. http://www.ncbi.nlm.nih.gov/pubmed/19753618
  86. Marshall, D. A., F. R. Johnson, N. A. Kulin, S. Ozdemir, J. M. Walsh, J. K. Marshall, S. Van Bebber and K. A. Phillips (2009). "How do physician assessments of patient preferences for colorectal cancer screening tests differ from actual preferences? A comparison in Canada and the United States using a stated-choice survey." Health Econ 18(12): 1420-1439. PMCID: 3964796. http://www.ncbi.nlm.nih.gov/pubmed/19191268
  87. Marshall, D. A. and M. Hux (2009). "Design and analysis issues for economic analysis alongside clinical trials." Med Care 47(7 Suppl 1): S14-20. http://www.ncbi.nlm.nih.gov/pubmed/19536012
  88. Liang, S. Y., J. S. Haas and K. A. Phillips (2009). "Medicare formulary coverage for top-selling biologics." Nat Biotechnol 27(12): 1082-1084. PMCID: 2845541. http://www.ncbi.nlm.nih.gov/pubmed/20010576
  89. Ikediobi, O. N., J. Shin, R. L. Nussbaum, K. A. Phillips, J. M. Walsh, U. Ladabaum and D. Marshall (2009). "Addressing the challenges of the clinical application of pharmacogenetic testing." Clin Pharmacol Ther 86(1): 28-31. PMCID: 2910521. http://www.ncbi.nlm.nih.gov/pubmed/19536122
  90. Hay, J., J. N. Harris, E. A. Waters, M. F. Clayton, L. Ellington, A. D. Abernethy and H. Prayor-Patterson (2009). "Personal communication in primary and secondary cancer prevention: evolving discussions, emerging challenges." J Health Commun 14 Suppl 1: 18-29. http://www.ncbi.nlm.nih.gov/pubmed/19449265
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