Rezultati - Roberts, J Scott

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

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Direct-to-Consumer Genetic Testing and Personal Genomics Services: A Review of Recent Empirical Studies od Roberts, J. Scott, Ostergren, Jenny

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Estimating and disclosing the risk of developing Alzheimer’s disease: challenges, controversies and future directions od Roberts, J Scott, Tersegno, Sarah M

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Genetic susceptibility testing for neurodegenerative diseases: Ethical and practice issues od Roberts, J. Scott, Uhlmann, Wendy R.

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Ethical Issues in Neurogenetics od Uhlmann, Wendy R., Roberts, J. Scott

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Emerging issues in public health genomics od Roberts, J. Scott, Dolinoy, Dana, Tarini, Beth

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Genetic testing for neurodegenerative diseases: Ethical and health communication challenges od Roberts, J. Scott, Patterson, Anne, Uhlmann, Wendy

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Using Alzheimer’s disease as a model for genetic risk disclosure: Implications for personal genomics od Roberts, J. Scott, Christensen, Kurt D., Green, Robert C.

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Amyloid imaging, risk disclosure and Alzheimer’s disease: ethical and practical issues od Roberts, J Scott, Dunn, Laura B, Rabinovici, Gil D

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Public beliefs and knowledge about risk and protective factors for Alzheimer's disease od Roberts, J. Scott, McLaughlin, Sara J., Connell, Cathleen M.

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Changes to perceptions of the pros and cons of genetic susceptibility testing after APOE genotyping for Alzheimer disease risk od Christensen, Kurt D., Roberts, J. Scott, Uhlmann, Wendy R., Green, Robert C.

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Effectiveness of a condensed protocol for disclosing APOE genotype and providing risk education for Alzheimer disease od Roberts, J. Scott, Chen, Clara A., Uhlmann, Wendy R., Green, Robert C.

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Volunteering, polygenic risk for Alzheimer’s disease, and cognitive functioning among older adults od Han, Sae Hwang, Roberts, J. Scott, Mutchler, Jan E., Burr, Jeffrey A.

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Racial Differences in Knowledge and Beliefs About Alzheimer Disease od Connell, Cathleen M, Roberts, J. Scott, McLaughlin, Sara J., Akinleye, Dapo

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Disclosure of individual research results at federally funded Alzheimer's Disease Research Centers od Roberts, J. Scott, Ferber, Rebecca, Blacker, Deborah, Rumbaugh, Malia, Grill, Joshua D.

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“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 od Linnenbringer, Erin, Roberts, J. Scott, Hiraki, Susan, Cupples, L. Adrienne, Green, Robert C.

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Willingness to Pay for Genetic Testing for Alzheimer's Disease: A Measure of Personal Utility od Kopits, Ilona M., Chen, Clara, Roberts, J. Scott, Uhlmann, Wendy, Green, Robert C.

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Black and White Adult Family Members’ Attitudes Toward a Dementia Diagnosis od Connell, Cathleen M, Roberts, J. Scott, McLaughlin, Sara J., Carpenter, Brian D.

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Genetic data partnerships: Academic publications with privately owned or generated genetic data od Spector-Bagdady, Kayte, Fakih, Amanda, Krenz, Chris, Marsh, Erica E., Roberts, J. Scott

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Perceptions of Familial Risk in those Seeking a Genetic Risk Assessment for Alzheimer’s Disease od Hiraki, Susan, Chen, Clara A., Roberts, J. Scott, Cupples, L. Adrienne, Green, Robert C.

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