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 
T
Tarini, B. A., Gornick, M. C., Zikmund-Fisher, B. J., Saal, H. M., Edmondson, L., & Uhlmann, W. (2018).  Family History Collection Practices: National Survey of Pediatric Primary Care Providers. Clinical Pediatrics. 57(5), 537-546. Abstract
Taylor, D. H., Cook-Deegan, R. M., Hiraki, S., Roberts, J. S., Blazer, D. G., & Green, R. C. (2010).  Genetic testing for Alzheimer's and long-term care insurance. Health affairs (Project Hope). 29(1), 102-8. Abstract
U
Uhlmann, W. R. (2005).  Genetic Counseling and Ethical Issues.
Uhlmann, W. (2011).  “The Swinging Gate: Genetic Testing and Ethical Issues”.
Uhlmann, W. R. (2012).  “The Swinging Gate: Genetic Testing and Ethical Issues,” .
Uhlmann, W. R. (2013).  Bioethics Grand Rounds: "The Swinging Gate: Genetic Testing and Ethical Issues".
Uhlmann, W. (2011).  “Genetic Susceptibility Testing for Alzheimer’s Disease: What Does the REVEAL Study Reveal?”.
Uhlmann, W. R. (2014).  Bioethics Grand Rounds: "Genetic Testing of Children for Adult-Onset Conditions: Ethical Considerations".
V
Vassy, J. L., Lautenbach, D. M., McLaughlin, H. M., Kong, S. W., Christensen, K. D., Krier, J., et al. (2014).  The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine. Trials. 15, 85. Abstract
Vernarelli, J. A., Roberts, J. S., Hiraki, S., Chen, C. A., Cupples, A. L., & Green, R. C. (2010).  Effect of Alzheimer disease genetic risk disclosure on dietary supplement use. The American journal of clinical nutrition. 91(5), 1402-7. Abstract
W
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.
Wade, C. H., Shiloh, S., Woolford, S. W., Roberts, J. S., Alford, S. H., Marteau, T. M., et al. (2011).  Modeling decisions to undergo genetic testing for susceptibility to common health conditions: an ancillary study of the Multiplex Initiative. Psychology & Health. 27(4), 430-44. Abstract
Wain, K. E., Uhlmann, W. R., Heidebrink, J., & Roberts, J. S. (2009).  Living at risk: the sibling's perspective of early-onset Alzheimer's disease. Journal of genetic counseling. 18(3), 239-51. 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
van der Wouden, C. H., Carere, D. A., Maitland-van der Zee, A. H., Ruffin, M. T., Roberts, J. S., & Green, R. C. (2016).  Consumer Perceptions of Interactions With Primary Care Providers After Direct-to-Consumer Personal Genomic Testing.. Annals of internal medicine. 164(8), 513-22. Abstract
Z
Zick, C. D., Mathews, C. J., Roberts, J. S., Cook-Deegan, R., Pokorski, R. J., & Green, R. C. (2005).  Genetic testing for Alzheimer's disease and its impact on insurance purchasing behavior.. Health affairs (Project Hope). 24(2), 483-90. Abstract