Publications and Presentations Database

Sort by: [ Author (Asc)] Title Type Year
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
G
Green, R. C., Christensen, K. D., Cupples, A. L., Relkin, N. R., Whitehouse, P. J., Royal, C. D. M., et al. (2014).  A randomized noninferiority trial of condensed protocols for genetic risk disclosure of Alzheimer's disease.. Alzheimer's & dementia. Abstract
Green, R. C., Roberts, J. S., Cupples, A. L., Relkin, N. R., Whitehouse, P. J., Brown, T., et al. (2009).  Disclosure of APOE genotype for risk of Alzheimer's disease. The New England journal of medicine. 361(3), 245-54. Abstract
Green, R. C., Roberts, J. S., Hartz, S., & Kohane, I. (2013).  Return of results in genetics: Integration with clinical care.
Green, R. C., Roberts, J. S., Cupples, A. L., Relkin, N. R., Whitehouse, P. J., Brown, T., et al. (2009).  Disclosure of APOE genotype for risk of Alzheimer's disease. The New England journal of medicine. 361(3), 245-54. Abstract
Grill, J. D., Apostolova, L. G., Bullain, S., Burns, J. M., Cox, C. G., Dick, M., et al. (2017).  Communicating mild cognitive impairment diagnoses with and without amyloid imaging.. Alzheimer's research & therapy. 9(1), 35. Abstract
Grob, R., Roberts, S., & Timmermans, S. (2018).  Families’ Experiences with Newborn Screening: A Critical Source of Evidence. Hastings Center Report. Abstract
Guan, Y., Roter, D. L., Wolff, J. L., Gitlin, L. N., Christensen, K. D., Roberts, J. S., et al. (2017).  The impact of genetic counselors’ use of facilitative strategies on cognitive and emotional processing of genetic risk disclosure for Alzheimer’s disease. . Patient Education & Counseling. Abstract
Guan, Y., Roter, D. L., Wolff, J. L., Gitlin, L. N., Christensen, K. D., Roberts, J. S., et al. (2018).  The impact of genetic counselors’ use of facilitative strategies on cognitive and emotional processing of genetic risk disclosure for Alzheimer’s disease. Patient Education and Counseling. 101(5), 817-823. Abstract
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
H
Harvey, R., Emerson Lombardo, N., Nolen, V., & Roberts, J. S. (2004).  Partnerships to increase African American participation in Alzheimer’s disease research.
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
Hipps, Y. G., Roberts, J. S., Farrer, L. A., & Green, R. C. (2003).  Differences between African Americans and Whites in their attitudes toward genetic testing for Alzheimer's disease. Genetic testing. 7(1), 39-44. Abstract
Hipps, Y., Roberts, J. S., & Green, R. C. (2002).  African Americans and Whites differ in their interest in predictive testing for Alzheimer’s disease.
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
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
Hurley, A., & Roberts, J. S. (2005).  Developing and sustaining interdisciplinary and international partnerships: Lessons learned from the REVEAL project.
Hurley, A. C., Harvey, F. R., Roberts, J. S., Wilson-Chase, C., Lloyd, S., Prest, J., et al. (2005).  Genetic susceptibility for Alzheimer's disease: why did adult offspring seek testing?. American journal of Alzheimer's disease and other dementias. 20(6), 374-81. Abstract
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.
J
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.
Johnston, J., Lantos, J. D., Goldenberg, A., Chen, F., Parens, E., Koenig, B., et al. (2018).  Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies. The Hastings Center. 48(52),  Abstract
Jones, T., Lockhart, J. S., Mendelsohn-Victor, K. E., Duquette, D., Northouse, L. L., Duffy, S. A., et al. (2016).  Use of Cancer Genetics Services in African-American Young Breast Cancer Survivors.. American journal of preventive medicine. 51(4), 427-36. Abstract
K
Kales, H. C., Blow, F. C., Bingham, C. R., Roberts, J. S., Copeland, L. A., & Mellow, A. M. (2000).  Race, psychiatric diagnosis, and mental health care utilization in older patients. The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry. 8(4), 301-9. Abstract
Katapodi, M. C., Duquette, D., Yang, J. J., Mendelsohn-Victor, K., Anderson, B., Nikolaidis, C., et al. (2017).  Recruiting families at risk for hereditary breast and ovarian cancer from a statewide cancer registry: a methodological study.. Cancer causes & control : CCC. 28(3), 191-201. Abstract
Khan, C. M., Rini, C., Bernhardt, B. A., Roberts, J. S., Christensen, K. D., Evans, J. P., et al. (2015).  How can psychological science inform research about genetic counseling for clinical genomic sequencing?. Journal of genetic counseling. 24(2), 193-204. Abstract
Khoury, M. J., McBride, C. M., Schully, S. D., Ioannidis, J. P. A., Feero, G. W., Janssens, C. A. J. W., et al. (2009).  The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop. Genetics in medicine : official journal of the American College of Medical Genetics. 11(8), 559-67. Abstract