Publications and Presentations Database

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Journal Article
Sturm, A. C., Hovick, S., Schmidlen, T., Scheinfeldt, L., Roberts, J. S., Morr, L., et al. (2018).  Operationalizing the reciprocal engagement model of genetic counseling practice: A framework for the scalable delivery of genomic counseling and testing. Journal of Genetic Counseling. Abstract
Sweet, K., Sturm, A. C., Schmidlen, T., McElroy, J., Scheinfeldt, L., Manickam, K., et al. (2017).  Outcomes of a Randomized Controlled Trial of Genomic Counseling for Patients Receiving Personalized and Actionable Complex Disease Reports.. Journal of genetic counseling. Abstract
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
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
Langford, A. T., Resnicow, K., Roberts, J. S., & Zikmund-Fisher, B. J. (2012).  Racial and ethnic differences in direct-to-consumer genetic tests awareness in HINTS 2007: sociodemographic and numeracy correlates. Journal of genetic counseling. 21(3), 440-7. Abstract
Connell, C. M., Scott Roberts, J., McLaughlin, S. J., & Akinleye, D. (2009).  Racial differences in knowledge and beliefs about Alzheimer disease. Alzheimer disease and associated disorders. 23(2), 110-6. Abstract
Christensen, K. D., Uhlmann, W. R., Roberts, J. S., Linnenbringer, E., Whitehouse, P. J., Royal, C. D. M., et al. (2018).  A randomized controlled trial of disclosing genetic risk information for Alzheimer disease via telephone.. Genetics in medicine : official journal of the American College of Medical Genetics. 20(1), 132-41. Abstract
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
Roberts, J. S., LaRusse, S. A., Katzen, H., Whitehouse, P. J., Barber, M., Post, S. G., et al. (2003).  Reasons for seeking genetic susceptibility testing among first-degree relatives of people with Alzheimer disease. Alzheimer disease and associated disorders. 17(2), 86-93. Abstract
Eckert, S. L. R., Katzen, H., Roberts, J. S., Barber, M., Ravdin, L. D., Relkin, N. R., et al. (2006).  Recall of disclosed apolipoprotein E genotype and lifetime risk estimate for Alzheimer's disease: the REVEAL Study. Genetics in medicine : official journal of the American College of Medical Genetics. 8(12), 746-51. 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
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
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