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Submitted

Gornick, M. C., Ryan, K. A., Scherer, A. M., Roberts, J. S., De Vries, R. G., & Uhlmann, W. R. (Submitted).  Interpretations of the term "actionable" when discussing genetic test results: What you mean is not what I heard. Journal of Genetic Counseling. Abstract

2019

Roberts, J. S., Gornick, M. C., Le, L. Q., Bartnik, N. J., Zikmund-Fisher, B. J., Chinnaiyan, A. M., et al. (2019).  Next‐generation sequencing in precision oncology: Patient understanding and expectations. Cancer Medicine. Abstract

2018

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
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
Lingler, J. H., Roberts, J. S., Kim, H., Morris, J. L., Hu, L., Mattos, M., et al. (2018).  Amyloid PET candidates may focus more on benefits than risks of results disclosure. Alzheimers Dement (Amst). 10, 413-420. 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. (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
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
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
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
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
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
Spector-Bagdady, K., De Vries, R. G., Gornick, M. C., Shuman, A. G., Kardia, S., & Platt, J. (2018).  Encouraging Participation and Transparency In Biobank Research. Health Affairs. 37, 1313-1320. Abstract
Gornick, M., Cobain, E., Le, L. Q., Bartnik, N., Stoffel, E., Schuetze, S., et al. (2018).  Oncologists’ use of clinical sequencing data to inform clinical management. JCO Precision Oncology. Abstract
Sturm, A. C., Schmidlen, T., Scheinfeldt, L., Hovick, S., McElroy, J. P., Toland, A. E., et al. (2018).  Early Outcome Data Assessing Utility of a Post-Test Genomic Counseling Framework for the Scalable Delivery of Precision Health.. Journal of Personalized Medicine. 8(3),  Abstract

2017

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
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
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
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
Sweet, K., Sturm, A. C., Schmidlen, T., Hovick, S., Peng, J., Manickam, K., et al. (2017).  EMR documentation of physician-patient communication following genomic counseling for actionable complex disease and pharmacogenomic results.. Clinical genetics. 91(4), 545-556. Abstract