Publications and Presentations Database

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Roberts, J. S. (2010).  Disclosure of genetic research results: Practical and ethical issues.
Roberts, J. S., Milliron, K., Hoskins, K., & Merajver, S. (2010).  Development and evaluation of a personalized, web-based decision aid for women considering genetic testing for risk of breast cancer.
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
Roberts, J. S., Lock, M., Prest, J., Barber, M., Whitehouse, P., LaRusse, S., et al. (2004).  How does genetic testing affect anxiety about developing Alzheimer’s disease? .
Roberts, J. S. (2008).  Ethical and Practice Issues Raised by Emerging Cancer Genetics Technologies.
Roberts, J. S. (2015).  Genetics, biomarkers and predictive testing.
Roberts, J. S. (2011).  The impact of disclosing genetic risk information for Alzheimer’s disease: Findings from the REVEAL Study.
Roberts, J. S. (2018).  Assessing the Impact of Genetic Susceptibility Testing: Where Do We Go from Here?.
Roberts, J. S. (2007).  Genetic susceptibility testing for adult-onset disorders.
Roberts, J. S., & Silverio, E. (2005).  Education and support in Alzheimer's early stages.
Roberts, J. S. (2010).  Psychological and behavioral responses to genetic risk assessment for common, complex diseases.
Roberts, J. S. (2016).  Emerging approaches in treatment and prevention of Alzheimer’s disease: Ethical and practical challenges.
Roberts, J. S. (2014).  Current research trends in Alzheimer’s disease.
Roberts, J. S. (2015).  Genetic testing: Implications for health, illness and society.
Roberts, J. S. (2011).  Examining the benefits and harms of direct-to-consumer genetic testing.
Roberts, J. S., Connell, C. M., Cisewski, D., Hipps, Y. G., Demissie, S., & Green, R. C. (2003).  Differences between African Americans and whites in their perceptions of Alzheimer disease. Alzheimer disease and associated disorders. 17(1), 19-26. Abstract
Roberts, J. S. (2007).  Understanding the psychological and behavioral impact of genetic susceptibility testing for Alzheimer’s disease.
Roberts, J. S. (2008).  Methodological challenges in assessing the process and impact of genetic susceptibility testing.
Roberts, J. S., & Ostergren, J. (2013).  Direct-to-consumer genetic testing and personal genomics services: a review of recent empirical studies. Current genetic medicine reports. 1(3), 182-200. Abstract
Roberts, J. S., & Green, R. C. (2005).  Genetic research in dementia: Risk evaluation and education for Alzheimer’s disease.
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
Roberts, J. S. (2004).  Genetic risk assessment for individuals at risk for Alzheimer’s disease.
Roberts, J. S. (2017).  Alzheimer’s disease from a public health perspective.
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
Roberts, J. S. (2015).  Ethical considerations in using biomarkers as an enrichment strategy.