A missing link in the bench-to-bedside paradigm: engaging regulatory stakeholders in clinical genomics research

由 O’Daniel, Julianne M., Berg, Jonathan S.
發表在 Genome Med (2016)

Professional Perspectives About Pharmacogenetic Testing and Managing Ancillary Findings

由 Haga, Susanne B., Tindall, Genevieve, O'Daniel, Julianne M.
出版 2012

Public Perspectives About Pharmacogenetic Testing and Managing Ancillary Findings

由 Haga, Susanne B., Tindall, Genevieve, O'Daniel, Julianne M.
出版 2012

Parents’ perceptions of personal utility of exome sequencing results

由 Mollison, Lonna, O’Daniel, Julianne M., Henderson, Gail E., Berg, Jonathan S., Skinner, Debra
發表在 Genet Med (2019)

Survey of U.S. Public Attitudes Towards Pharmacogenetic Testing

由 Haga, Susanne B., O’Daniel, Julianne M., Tindall, Genevieve M., Lipkus, Isaac R., Agans, Robert
出版 2011

Public Attitudes Towards Ancillary Information Revealed by Pharmacogenetic Testing Under Limited Information Conditions

由 Haga, Susanne B., O’Daniel, Julianne M., Tindall, Genevieve M., Lipkus, Isaac R., Agans, Robert
出版 2011

Survey of Genetic Counselors and Clinical Geneticists’ Use and Attitudes Towards Pharmacogenetic Testing

由 Haga, Susanne B., O’Daniel, Julianne M., Tindall, Genevieve M., Mills, Rachel, Lipkus, Isaac M., Agans, Robert
出版 2012

Promoting Public Awareness and Engagement in Genome Sciences

由 Haga, Susanne B., Rosanbalm, Katie D., Boles, Larry, Tindall, Genevieve M., Livingston, Troy M., O'Daniel, Julianne M.
出版 2013

Referencing BRCA in hereditary cancer risk discussions: In search of an anchor in a sea of uncertainty

由 Waltz, Margaret, Prince, Anya E. R., O’Daniel, Julianne M., Foreman, Ann Katherine M., Powell, Bradford C., Berg, Jonathan S.
發表在 J Genet Couns (2020)

Genomic Risk Profiling: Attitudes and Use in Personal and Clinical Care of Primary Care Physicians Who Offer Risk Profiling

由 Haga, Susanne B., Carrig, Madeline M., O’Daniel, Julianne M., Orlando, Lori A., Killeya-Jones, Ley A., Ginsburg, Geoffrey S., Cho, Alex
出版 2011

Genomic Knowledge in the Context of Diagnostic Exome Sequencing: Changes over Time, Persistent Subgroup Differences, and Associations with Psychological Sequencing Outcomes

由 Rini, Christine, Henderson, Gail E., Evans, James P., Berg, Jonathan S., Foreman, Ann Katherine M., Griesemer, Ida, Waltz, Margaret, O’Daniel, Julianne M., Roche, Myra I.
發表在 Genet Med (2019)

Actionability of commercial laboratory sequencing panels for newborn screening and the importance of transparency for parental decision-making

由 DeCristo, Daniela M., Milko, Laura V., O’Daniel, Julianne M., Foreman, Ann Katherine M., Mollison, Lonna F., Powell, Bradford C., Powell, Cynthia M., Berg, Jonathan S.
發表在 Genome Med (2021)

Effect of genetic testing for risk of type 2 diabetes mellitus on health behaviors and outcomes: study rationale, development and design

由 Cho, Alex H, Killeya-Jones, Ley A, O'Daniel, Julianne M, Kawamoto, Kensaku, Gallagher, Patrick, Haga, Susanne, Lucas, Joseph E, Trujillo, Gloria M, Joy, Scott V, Ginsburg, Geoffrey S
出版 2012

Examining the cascade of participant attrition in a genomic medicine research study: barriers and facilitators to achieving diversity

由 Moore, Elizabeth G., Roche, Myra, Rini, Christine, Corty, Edward W., Girnary, Zahra, O’Daniel, Julianne M., Lin, Feng-Chang, Corbie-Smith, Giselle, Evans, James P., Henderson, Gail, Berg, Jonathan S.
發表在 Public Health Genomics (2018)

Variant Interpretation is a Component of Clinical Practice Among Genetic Counselors in Multiple Specialties

由 Wain, Karen E., Azzariti, Danielle R., Goldstein, Jennifer L., Johnson, Amy Knight, Krautscheid, Patti, Lepore, Brianna, O’Daniel, Julianne M., Ritter, Deborah, Savatt, Juliann M., Riggs, Erin Rooney, Martin, Christa Lese
發表在 Genet Med (2019)

Is Incidental Finding the Best Term? A Study of Patients’ Preferences

由 Tan, Nina, Amendola, Laura M, O’Daniel, Julianne M., Burt, Amber, Horike-Pyne, Martha J., Boshe, Lacey, Henderson, Gail E., Rini, Christine, Roche M.S., Myra I., Hisama, Fuki M., Burke, Wylie, Wilfond, Benjamin, Jarvik, Gail P.
發表在 Genet Med (2016)

The who, what and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study

由 Rini, Christine, Khan, Cynthia M., Moore, Elizabeth, Roche, Myra I., Evans, James P., Berg, Jonathan S., Powell, Bradford C., Corbie-Smith, Giselle, Foreman, Ann Katherine M., Griesemer, Ida, Lee, Kristy, O’Daniel, Julianne M., Henderson, Gail E.
發表在 Genet Med (2017)

Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: A Framework for the Scalable Delivery of Genomic Counseling and Testing

由 Schmidlen, Tara, Sturm, Amy C., Hovick, Shelly, Scheinfeldt, Laura, Roberts, J. Scott, Morr, Lindsey, McElroy, Joseph, Toland, Amanda E., Christman, Michael, O’Daniel, Julianne M., Gordon, Erynn S., Bernhardt, Barbara A., Ormond, Kelly E., Sweet, Kevin
發表在 J Genet Couns (2018)

Factors influencing NCGENES research participants’ requests for non-medically actionable secondary findings

由 Roche, Myra I., Griesemer, Ida, Khan, Cynthia M., Moore, Elizabeth, Lin, Feng-Chang, O’Daniel, Julianne M., Foreman, Ann Katherine M., Lee, Kristy, Powell, Bradford C., Berg, Jonathan S., Evans, James P., Henderson, Gail E., Rini, Christine
發表在 Genet Med (2018)

ACMG Recommendations for Reporting of Incidental Findings in Clinical Exome and Genome Sequencing

由 Green, Robert C., Berg, Jonathan S., Grody, Wayne W., Kalia, Sarah S., Korf, Bruce R., Martin, Christa L., McGuire, Amy, Nussbaum, Robert L., O’Daniel, Julianne M., Ormond, Kelly E., Rehm, Heidi L., Watson, Michael S., Williams, Marc S., Biesecker, Leslie G.
出版 2013