Public willingness to participate in personalized health research and biobanking: A large-scale Swiss survey von Brall, Caroline, Berlin, Claudia, Zwahlen, Marcel, Ormond, Kelly E., Egger, Matthias, Vayena, Effy

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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genet... von Kalia, Sarah S., Adelman, Kathy, Bale, Sherri J., Chung, Wendy K., Eng, Christine, Evans, James P., Herman, Gail E., Hufnagel, Sophia B., Klein, Teri E., Korf, Bruce R., McKelvey, Kent D., Ormond, Kelly E., Richards, C. Sue, Vlangos, Christopher N., Watson, Michael, Martin, Christa L., Miller, David T.

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Expectations and attitudes towards medical artificial intelligence: A qualitative study in the field of stroke von Amann, Julia, Vayena, Effy, Ormond, Kelly E, Frey, Dietmar, Madai, Vince I, Blasimme, Alessandro

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Improving reporting standards for polygenic scores in risk prediction studies von Wand, Hannah, Lambert, Samuel A., Tamburro, Cecelia, Iacocca, Michael A., O’Sullivan, Jack W., Sillari, Catherine, Kullo, Iftikhar J., Rowley, Robb, Dron, Jacqueline S., Brockman, Deanna, Venner, Eric, McCarthy, Mark I., Antoniou, Antonis C., Easton, Douglas F., Hegele, Robert A., Khera, Amit V., Chatterjee, Nilanjan, Kooperberg, Charles, Edwards, Karen, Vlessis, Katherine, Kinnear, Kim, Danesh, John N., Parkinson, Helen, Ramos, Erin M., Roberts, Megan C., Ormond, Kelly E., Khoury, Muin J., Janssens, A. Cecile J. W., Goddard, Katrina A. B., Kraft, Peter, MacArthur, Jaqueline A. L., Inouye, Michael, Wojcik, Genevieve L.

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Ethical considerations in prenatal testing: Genomic testing and medical uncertainty von Richardson, Anastasia, Ormond, Kelly E.

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Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents von Botkin, Jeffrey R., Belmont, John W., Berg, Jonathan S., Berkman, Benjamin E., Bombard, Yvonne, Holm, Ingrid A., Levy, Howard P., Ormond, Kelly E., Saal, Howard M., Spinner, Nancy B., Wilfond, Benjamin S., McInerney, Joseph D.

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ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing von Green, Robert C., Berg, Jonathan S., Grody, Wayne W., Kalia, Sarah S., Korf, Bruce R., Martin, Christa L., McGuire, Amy L., Nussbaum, Robert L., O’Daniel, Julianne M., Ormond, Kelly E., Rehm, Heidi L., Watson, Michael S., Williams, Marc S., Biesecker, Leslie G.

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Clinical Interpretation and Implications of Whole-Genome Sequencing von Dewey, Frederick E, Grove, Megan E, Pan, Cuiping, Goldstein, Benjamin A, Bernstein, Jonathan A, Chaib, Hassan, Merker, Jason D, Goldfeder, Rachel L, Enns, Gregory M, David, Sean P, Pakdaman, Neda, Ormond, Kelly E, Caleshu, Colleen, Kingham, Kerry, Klein, Teri E, Whirl-Carrillo, Michelle, Sakamoto, Kenneth, Wheeler, Matthew T, Butte, Atul J, Ford, James M, Boxer, Linda, Ioannidis, John P. A, Yeung, Alan C, Altman, Russ B, Assimes, Themistocles L, Snyder, Michael, Ashley, Euan A, Quertermous, Thomas

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Assessing women's preferences towards tests that may reveal uncertain results from prenatal genomic testing: Development of attributes for a discrete choice experiment, using a mix... von Hammond, Jennifer, Klapwijk, Jasmijn E, Riedijk, Sam, Lou, Stina, Ormond, Kelly E, Vogel, Ida, Hui, Lisa, Sziepe, Emma-Jane, Buchanan, James, Ingvoldstad-Malmgren, Charlotta, Soller, Maria Johansson, Harding, Eleanor, Hill, Melissa, Lewis, Celine

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Challenges in the clinical application of whole-genome sequencing von Ormond, Kelly E, MSc, Wheeler, Matthew T, MD, Hudgins, Louanne, Prof, Klein, Teri E, PhD, Butte, Atul J, MD, Altman, Russ B, Prof, Ashley, Euan A, MRCP, Greely, Henry T, Prof

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Evidence that personal genome testing enhances student learning in a course on genomics and personalized medicine von Salari, Keyan, Karczewski, Konrad J, Hudgins, Louanne, Ormond, Kelly E

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Perspectives of Rare Disease Social Media Group Participants on Engaging With Genetic Counselors: Mixed Methods Study von Yabumoto, Megan, Miller, Emily, Rao, Anoushka, Tabor, Holly K, Ormond, Kelly E, Halley, Meghan C

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Noninvasive Prenatal Testing/Noninvasive Prenatal Diagnosis: the Position of the National Society of Genetic Counselors von Devers, Patricia L., Cronister, Amy, Ormond, Kelly E., Facio, Flavia, Brasington, Campbell K., Flodman, Pamela

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Evidence-based recommendations for delivering the diagnosis of X & Y chromosome multisomies in children, adolescents, and young adults: an integrative review von Riggan, Kirsten A, Ormond, Kelly E, Allyse, Megan A, Close, Sharron

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Noninvasive prenatal diagnosis: pregnant women's interest and expected uptake von Tischler, Reana, Hudgins, Louanne, Blumenfeld, Yair J., Greely, Henry T., Ormond, Kelly E.

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Defining critical educational components of informed consent for genetic testing: views of US-based genetic counselors and medical geneticists von Hallquist, Miranda L G, Borensztein, Maia J, Coughlin, 2nd, Curtis R, Buchanan, Adam H, Andrew Faucett, W, Peay, Holly L, Smith, Maureen E, Tricou, Eric P, Uhlmann, Wendy R, Wain, Karen E, Ormond, Kelly E

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Phased whole-genome genetic risk in a family quartet using a major allele reference sequence von Dewey, Frederick E, Chen, Rong, Cordero, Sergio P, Ormond, Kelly E, Caleshu, Colleen, Karczewski, Konrad J, Whirl-Carrillo, Michelle, Wheeler, Matthew T, Dudley, Joel T, Byrnes, Jake K, Cornejo, Omar E, Knowles, Joshua W, Woon, Mark, Sangkuhl, Katrin, Gong, Li, Thorn, Caroline F, Hebert, Joan M, Capriotti, Emidio, David, Sean P, Pavlovic, Aleksandra, West, Anne, Thakuria, Joseph V, Ball, Madeleine P, Zaranek, Alexander W, Rehm, Heidi L, Church, George M, West, John S, Bustamante, Carlos D, Snyder, Michael, Altman, Russ B, Klein, Teri E, Butte, Atul J, Ashley, Euan A

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Public preferences towards data management and governance in Swiss biobanks: results from a nationwide survey von Brall, Caroline, Berlin, Claudia, Zwahlen, Marcel, Vayena, Effy, Egger, Matthias, Ormond, Kelly E

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What are the bottlenecks to health data sharing in Switzerland? An interview study von Ormond, Kelly E, Bavamian, Sabine, Becherer, Claudia, Currat, Christine, Joerger, Francisca, Geiger, Thomas R, Hiendlmeyer, Elke, Maurer, Julia, Staub, Timo, Vayena, Effy

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Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study von Haverfield, Eden V., Esplin, Edward D., Aguilar, Sienna J., Hatchell, Kathryn E., Ormond, Kelly E., Hanson-Kahn, Andrea, Atwal, Paldeep S., Macklin-Mantia, Sarah, Hines, Stephanie, Sak, Caron W. -M., Tucker, Steven, Bleyl, Steven B., Hulick, Peter J., Gordon, Ora K., Velsher, Lea, Gu, Jessica Y. J., Weissman, Scott M., Kruisselbrink, Teresa, Abel, Christopher, Kettles, Michele, Slavotinek, Anne, Mendelsohn, Bryce A., Green, Robert C., Aradhya, Swaroop, Nussbaum, Robert L.

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