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2011

Goldman, J. S., Hahn, S. E., Catania, J. W., LaRusse-Eckert, S., Butson, M. B., Rumbaugh, M., et al. (2011).  Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors. Genetics in medicine : official journal of the American College of Medical Genetics. 13(6), 597-605. Abstract
Akinleye, I., Roberts, J.S., Royal, C.D.M., Linnenbringer, E., Obisesan, T. O., Fasaye, G-A., et al. (2011).  Differences between African American and White research volunteers in their attitudes, beliefs and knowledge regarding genetic testing for Alzheimer's disease. Journal of genetic counseling. Abstract
Roychowdhury, S., Iyer, M. K., Robinson, D. R., Lonigro, R. J., Wu, Y. - M., Cao, X., et al. (2011).  Personalized oncology through integrative high-throughput sequencing: a pilot study. Science translational medicine. 3(111), 111ra121. Abstract
Christensen, K. D., Roberts, J. S., Uhlmann, W. R., & Green, R. C. (2011).  Changes to perceptions of the pros and cons of genetic susceptibility testing after APOE genotyping for Alzheimer disease risk. Genetics in medicine : official journal of the American College of Medical Genetics. Abstract
Wade, C. H., Shiloh, S., Woolford, S. W., Roberts, J. S., Alford, S. H., Marteau, T. M., et al. (2011).  Modeling decisions to undergo genetic testing for susceptibility to common health conditions: an ancillary study of the Multiplex Initiative. Psychology & Health. 27(4), 430-44. Abstract
Hock, K. T., Christensen, K. D., Yashar, B. M., Roberts, J. S., Gollust, S. E., & Uhlmann, W. R. (2011).  Direct-to-consumer genetic testing: an assessment of genetic counselors' knowledge and beliefs. Genetics in medicine : official journal of the American College of Medical Genetics. 13(4), 325-32. Abstract
Christensen, K. D., Roberts, J. S., Shalowitz, D. I., Everett, J. N., Kim, S. Y. H., Raskin, L., et al. (2011).  Disclosing individual CDKN2A research results to melanoma survivors: interest, impact, and demands on researchers. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. Abstract
Kopits, I. M., Chen, C., Roberts, J. S., Uhlmann, W., & Green, R. C. (2011).  Willingness to pay for genetic testing for Alzheimer's disease: a measure of personal utility. Genetic testing and molecular biomarkers. 15(12), 871-5. Abstract
Roberts, J. S., Christensen, K. D., & Green, R. C. (2011).  Using Alzheimer's disease as a model for genetic risk disclosure: implications for personal genomics. Clinical genetics. Abstract

2010

Roberts, J. S., Karlawish, J. H., Uhlmann, W. R., Petersen, R. C., & Green, R. C. (2010).  Mild cognitive impairment in clinical care: a survey of American Academy of Neurology members. Neurology. 75(5), 425-31. Abstract
Taylor, D. H., Cook-Deegan, R. M., Hiraki, S., Roberts, J. S., Blazer, D. G., & Green, R. C. (2010).  Genetic testing for Alzheimer's and long-term care insurance. Health affairs (Project Hope). 29(1), 102-8. Abstract
Vernarelli, J. A., Roberts, J. S., Hiraki, S., Chen, C. A., Cupples, A. L., & Green, R. C. (2010).  Effect of Alzheimer disease genetic risk disclosure on dietary supplement use. The American journal of clinical nutrition. 91(5), 1402-7. Abstract
McLaughlin, S. J., Connell, C. M., Heeringa, S. G., Li, L. W., & Roberts, J. S. (2010).  Successful aging in the United States: prevalence estimates from a national sample of older adults.. The journals of gerontology. Series B, Psychological sciences and social sciences. 65B(2), 216-26. Abstract
Roberts, J. S., & Tersegno, S. M. (2010).  Estimating and disclosing the risk of developing Alzheimer's disease: challenges, controversies and future directions.. Future neurology. 5(4), 501-517. Abstract
Roberts, J. S., Shalowitz, D. I., Christensen, K. D., Everett, J. N., Kim, S. Y. H., Raskin, L., et al. (2010).  Returning individual research results: development of a cancer genetics education and risk communication protocol. Journal of empirical research on human research ethics : JERHRE. 5(3), 17-30. Abstract
Ashida, S., Koehly, L. M., Roberts, J. S., Chen, C. A., Hiraki, S., & Green, R. C. (2010).  The role of disease perceptions and results sharing in psychological adaptation after genetic susceptibility testing: the REVEAL Study. European journal of human genetics : EJHG. 18(12), 1296-301. Abstract
Linnenbringer, E., Roberts, J. S., Hiraki, S., Cupples, A. L., & Green, R. C. (2010).  "I know what you told me, but this is what I think:" perceived risk of Alzheimer disease among individuals who accurately recall their genetics-based risk estimate. Genetics in medicine : official journal of the American College of Medical Genetics. 12(4), 219-27. Abstract  Download: PDF (310.84 KB)
Christensen, K. D., Jayaratne, T. E., Roberts, J. S., Kardia, S. L. R., & Petty, E. M. (2010).  Understandings of basic genetics in the United States: results from a national survey of black and white men and women. Public health genomics. 13(7-8), 467-76. Abstract

2009

Chung, W. W., Chen, C. A., Cupples, A. L., Roberts, J. S., Hiraki, S. C., Nair, A. K., et al. (2009).  A new scale measuring psychologic impact of genetic susceptibility testing for Alzheimer disease. Alzheimer disease and associated disorders. 23(1), 50-6. Abstract
Ashida, S., Koehly, L. M., Roberts, J. S., Chen, C. A., Hiraki, S., & Green, R. C. (2009).  Disclosing the disclosure: factors associated with communicating the results of genetic susceptibility testing for Alzheimer's disease. Journal of health communication. 14(8), 768-84. Abstract