Publications and Presentations Database

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A
Roberts, J. S. (2008).  Advances in Alzheimer’s research.
Hipps, Y., Roberts, J. S., & Green, R. C. (2002).  African Americans and Whites differ in their interest in predictive testing for Alzheimer’s disease.
Roberts, J. S., & et al (2007).  Age group differences in response to genetic risk assessment for Alzheimer’s disease.
Roberts, J. S., & et al (2006).  Age group differences in response to genetic risk assessment for Alzheimer’s disease.
Roberts, J. S. (2017).  Alzheimer’s disease from a public health perspective.
Hurley, A., Harvey, R., Roberts, J. S., & Hovarth, K. J. (2008).  Alzheimer’s disease genetic susceptibility in an aging society. (Read, C., Smyer, M., Green, R. C., Ed.).Aging, Biotechnology, & the Future. 157-172.
Lingler, J. H., Roberts, J. S., Kim, H., Morris, J. L., Hu, L., Mattos, M., et al. (2018).  Amyloid PET candidates may focus more on benefits than risks of results disclosure. Alzheimers Dement (Amst). 10, 413-420. Abstract
Roberts, J. S. (2015).  Applying lessons learned from the REVEAL Study to genetic testing and counseling in Alzheimer’s prevention research.
Bartnik, N. J., Roberts, J. S., Gornick, M. C., Le, L. Q., & Study, M. I. - O. N. C. O. S. E. Q. (2015).  Are oncologists using genome sequencing results to inform patient care?.
Roberts, J. S., Welsh-Bohmer, K., Green, R. C., & Karlawish, J. (2017).  Assessing the impact of disclosing amyloid imaging results to cognitively normal older adults: The REVEAL-SCAN study.
B
Roberts, J. S., Akinleye, D., Hipps, Y. G., & Green, R. C. (2005).  Beliefs about prevention and treatment of Alzheimer's disease among African Americans.
Christensen, K. D., Jayaratne, T. E., Roberts, J. S., Kardia, S. L. R., & Petty, E. M. (2009).  Black and White Americans’ Understandings of Genetics.
Roberts, J. S. (2015).  Bring your genes to Cal: How an educational program was drawn into the public debate over genetic testing.
C
Roberts, J. S. (2015).  Challenges and controversies in direct-to-consumer genetic testing.
Jarvik, L., & Roberts, J. S. (2008).  Children of persons with Alzheimer’s disease: what does the future hold?. Alzheimer disease and associated disorders. 22, 6-20.
Roberts, J. S., Uhlmann, W. R., Petersen, R., Karlawish, J., & Green, R. C. (2009).  Clinical practices regarding Mild Cognitive Impairment (MCI) among neurology service providers.
Guan, Y., Roter, D. L., Erby, L. H., Wolff, J. L., Gitlin, L. N., Roberts, J. S., et al. (2018).  Communication predictors of patient and companion satisfaction with Alzheimer’s disease genetic risk disclosure. Journal of Health Communication. 23(8), 807-814. Abstract
Szymaniak, J. M., Christensen, K. D., Uhlmann, W. R., Green, R. C., & Roberts, J. S. (2009).  A Condensed Genetic Counseling Approach for Alzheimer's Diseases Susceptibility Testing: What is the Psychological Impact? .
Roberts, J. S. (2016).  Consumer perspectives on receiving personal genomic services.
Roberts, J. S. (2015).  A conversation on the genomic revolution / evolution.
Sweet, K., Hovick, S., Sturm, A. C., Schmidlen, T., Gordon, E., Bernhardt, B., et al. (2016).  Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study.. Journal of genetic counseling. Abstract
Roberts, J. S., Akinleye, D., & Hipps, Y. G. (2004).  Cultural differences in perceptions of Alzheimer’s disease.
Roberts, J. S. (2005).  Cultural differences in perceptions of dementia.
Roberts, J. S. (2014).  Current research in Alzheimer’s disease.
Roberts, J. S. (2012).  Current topics in Alzheimer’s disease.