Publications and Presentations Database

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Book Chapter
Roberts, J. S. (2008).  Psychological issues in genetic testing. (Read, C., Smyer, M., Green, R. C., Ed.).Aging, Biotechnology, & the Future. 173-187.
Conference Presentation
LaRusse, S., Katzen, H., Brown, T., Barber, M., Whitehouse, P. J., Green, R. C., et al. (2002).  Participant recall of their own apolipoprotein E (APOE) genotype and risk estimate after six weeks: Results from the REVEAL Study.
Harvey, R., Emerson Lombardo, N., Nolen, V., & Roberts, J. S. (2004).  Partnerships to increase African American participation in Alzheimer’s disease research.
Roberts, J. S. (2016).  Patient understanding and satisfaction regarding clinical use of whole-genome sequencing.
Christensen, K. D., Roberts, J. S., Uhlmann, W. R., Whitehouse, P. J., Royal, C. D. M., Obisesan, T., et al. (2010).  Perceived personal utility of Alzheimer’s disease genetic susceptibility testing and its influence on post-test responses: Findings from the REVEAL Study.
Roberts, J. S., & et al (2008).  Psychological and behavioral impact of a condensed protocol for disclosing APOE genotype and risk information for Alzheimer’s disease: The REVEAL Study.
Christensen, K. D., Roberts, J. S., Uhlmann, W. R., Whitehouse, P. J., Obisesan, T., Bhatt, D. L., et al. (2010).  The psychological impact of learning APOE ε4 increases the risk for cardiovascular disease during genetic risk assessment for Alzheimer’s disease: Findings from the REVEAL Study.
Connell, C. M., Roberts, J. S., & McLaughlin, S. J. (2005).  Public knowledge about Alzheimer's disease and attitudes toward risk reduction: Results from a national survey.
Invited Presentation
Roberts, J. S. (2017).  Patient and provider perspectives on precision oncology.
Roberts, J. S. (2010).  Psychological and behavioral responses to genetic risk assessment for common, complex diseases.
Roberts, J. S. (2005).  Psychological issues in genetic testing.
Journal Article
Roberts, J. S., Robinson, J. O., Diamond, P. M., Bharadwaj, A., Christensen, K. D., Lee, K. B., et al. (2018).  Patient understanding of, satisfaction with, and perceived utility of whole genome sequencing: Findings from the MedSeq Project. Genetics in Medicine. Abstract
Hiraki, S., Chen, C. A., Roberts, J. S., Cupples, A. L., & Green, R. C. (2009).  Perceptions of familial risk in those seeking a genetic risk assessment for Alzheimer's disease. Journal of genetic counseling. 18(2), 130-6. 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
Weipert, C. M., Ryan, K. A., Everett, J. N., Yashar, B. M., Chinnaiyan, A. M., Roberts, J. S., et al. (2018).  Physician experiences and understanding of genomic sequencing in oncology. Journal of Genetic Counseling. 27(1), 187-196. Abstract
Marteau, T. M., Roberts, S., LaRusse, S., & Green, R. C. (2005).  Predictive genetic testing for Alzheimer's disease: impact upon risk perception.. Risk analysis : an official publication of the Society for Risk Analysis. 25(2), 397-404. Abstract
Wade, C. H., Shiloh, S., Roberts, J. S., Hensley Alford, S., Marteau, T. M., & Biesecker, B. B. (2012).  Preferences among diseases on a genetic susceptibility test for common health conditions: an ancillary study of the multiplex initiative. Public health genomics. 15(6), 322-6.
Carere, D. A., VanderWeele, T. J., Vassy, J. L., van der Wouden, C. H., Roberts, J. S., Kraft, P., et al. (2017).  Prescription medication changes following direct-to-consumer personal genomic testing: findings from the Impact of Personal Genomics (PGen) Study.. Genetics in medicine : official journal of the American College of Medical Genetics. 19(5), 537-545. Abstract
Harvey, E. K., Fogel, C. E., Peyrot, M., Christensen, K. D., Terry, S. F., & McInerney, J. D. (2007).  Providers' knowledge of genetics: a survey of 5915 individuals and families with genetic conditions. Genetics in medicine : official journal of the American College of Medical Genetics. 9(5), 259-67. Abstract
Roberts, J. S., McLaughlin, S. J., & Connell, C. M. (2014).  Public beliefs and knowledge about risk and protective factors for Alzheimer's disease. Alzheimer's & Dementia : the journal of the Alzheimer's Association. Abstract
Connell, C. M., Scott Roberts, J., & McLaughlin, S. J. (2007).  Public opinion about Alzheimer disease among blacks, hispanics, and whites: results from a national survey. Alzheimer disease and associated disorders. 21(3), 232-40. Abstract
Ryan, K. A., De Vries, R. G., Uhlmann, W. R., Roberts, J. S., & Gornick, M. C. (2017).  Public's Views toward Return of Secondary Results in Genomic Sequencing: It's (Almost) All about the Choice.. Journal of genetic counseling. Abstract
Ryan, K. A., De Vries, R. G., Uhlmann, W. R., Roberts, J. S., & Gornick, M. C. (2017).  Public's Views toward Return of Secondary Results in Genomic Sequencing: It's (Almost) All about the Choice.. Journal of genetic counseling. Abstract