Assessing the psychological impact of genetic susceptibility testing: Where have we been, where do we go from here?

von Roberts, J. Scott
Veröffentlicht in Hastings Cent Rep (2019)

Direct-to-Consumer Genetic Testing and Personal Genomics Services: A Review of Recent Empirical Studies

von Roberts, J. Scott, Ostergren, Jenny
Veröffentlicht 2013

Estimating and disclosing the risk of developing Alzheimer’s disease: challenges, controversies and future directions

von Roberts, J Scott, Tersegno, Sarah M
Veröffentlicht 2010

Genetic susceptibility testing for neurodegenerative diseases: Ethical and practice issues

von Roberts, J. Scott, Uhlmann, Wendy R.
Veröffentlicht 2013

Ethical Issues in Neurogenetics

von Uhlmann, Wendy R., Roberts, J. Scott
Veröffentlicht in Handb Clin Neurol (2018)

Emerging issues in public health genomics

von Roberts, J. Scott, Dolinoy, Dana, Tarini, Beth
Veröffentlicht in Annu Rev Genomics Hum Genet (2014)

Genetic testing for neurodegenerative diseases: Ethical and health communication challenges

von Roberts, J. Scott, Patterson, Anne, Uhlmann, Wendy
Veröffentlicht in Neurobiol Dis (2020)

Using Alzheimer’s disease as a model for genetic risk disclosure: Implications for personal genomics

von Roberts, J. Scott, Christensen, Kurt D., Green, Robert C.
Veröffentlicht 2011

Amyloid imaging, risk disclosure and Alzheimer’s disease: ethical and practical issues

von Roberts, J Scott, Dunn, Laura B, Rabinovici, Gil D
Veröffentlicht in Neurodegener Dis Manag (2013)

Public beliefs and knowledge about risk and protective factors for Alzheimer's disease

von Roberts, J. Scott, McLaughlin, Sara J., Connell, Cathleen M.
Veröffentlicht 2014

Changes to perceptions of the pros and cons of genetic susceptibility testing after APOE genotyping for Alzheimer disease risk

von Christensen, Kurt D., Roberts, J. Scott, Uhlmann, Wendy R., Green, Robert C.
Veröffentlicht 2011

Effectiveness of a condensed protocol for disclosing APOE genotype and providing risk education for Alzheimer disease

von Roberts, J. Scott, Chen, Clara A., Uhlmann, Wendy R., Green, Robert C.
Veröffentlicht 2012

Volunteering, polygenic risk for Alzheimer’s disease, and cognitive functioning among older adults

von Han, Sae Hwang, Roberts, J. Scott, Mutchler, Jan E., Burr, Jeffrey A.
Veröffentlicht in Soc Sci Med (2020)

Racial Differences in Knowledge and Beliefs About Alzheimer Disease

von Connell, Cathleen M, Roberts, J. Scott, McLaughlin, Sara J., Akinleye, Dapo
Veröffentlicht in Alzheimer Dis Assoc Disord (2009)

“I know what you told me, but this is what I think:” Perceived risk of Alzheimer disease among individuals who accurately recall their genetics-based risk estimate

von Linnenbringer, Erin, Roberts, J. Scott, Hiraki, Susan, Cupples, L. Adrienne, Green, Robert C.
Veröffentlicht 2010

Willingness to Pay for Genetic Testing for Alzheimer's Disease: A Measure of Personal Utility

von Kopits, Ilona M., Chen, Clara, Roberts, J. Scott, Uhlmann, Wendy, Green, Robert C.
Veröffentlicht 2011

Black and White Adult Family Members’ Attitudes Toward a Dementia Diagnosis

von Connell, Cathleen M, Roberts, J. Scott, McLaughlin, Sara J., Carpenter, Brian D.
Veröffentlicht in J Am Geriatr Soc (2009)

Genetic data partnerships: Academic publications with privately owned or generated genetic data

von Spector-Bagdady, Kayte, Fakih, Amanda, Krenz, Chris, Marsh, Erica E., Roberts, J. Scott
Veröffentlicht in Genet Med (2019)

Perceptions of Familial Risk in those Seeking a Genetic Risk Assessment for Alzheimer’s Disease

von Hiraki, Susan, Chen, Clara A., Roberts, J. Scott, Cupples, L. Adrienne, Green, Robert C.
Veröffentlicht 2008

Risk perceptions and worry about common diseases: A between- and within-subjects examination

von Shiloh, Shoshana, Wade, Christopher H., Roberts, J. Scott, Alford, Sharon Hensley, Biesecker, Barbara B.
Veröffentlicht 2012