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

Por O’Daniel, Julianne M., Berg, Jonathan S.
Publicado no Genome Med (2016)

Professional Perspectives About Pharmacogenetic Testing and Managing Ancillary Findings

Por Haga, Susanne B., Tindall, Genevieve, O'Daniel, Julianne M.
Publicado em 2012

Public Perspectives About Pharmacogenetic Testing and Managing Ancillary Findings

Por Haga, Susanne B., Tindall, Genevieve, O'Daniel, Julianne M.
Publicado em 2012

Parents’ perceptions of personal utility of exome sequencing results

Por Mollison, Lonna, O’Daniel, Julianne M., Henderson, Gail E., Berg, Jonathan S., Skinner, Debra
Publicado no Genet Med (2019)

Survey of U.S. Public Attitudes Towards Pharmacogenetic Testing

Por Haga, Susanne B., O’Daniel, Julianne M., Tindall, Genevieve M., Lipkus, Isaac R., Agans, Robert
Publicado em 2011

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

Por Haga, Susanne B., O’Daniel, Julianne M., Tindall, Genevieve M., Lipkus, Isaac R., Agans, Robert
Publicado em 2011

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

Por Haga, Susanne B., O’Daniel, Julianne M., Tindall, Genevieve M., Mills, Rachel, Lipkus, Isaac M., Agans, Robert
Publicado em 2012

Promoting Public Awareness and Engagement in Genome Sciences

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

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

Por Waltz, Margaret, Prince, Anya E. R., O’Daniel, Julianne M., Foreman, Ann Katherine M., Powell, Bradford C., Berg, Jonathan S.
Publicado no J Genet Couns (2020)

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

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

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

Por 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.
Publicado no Genet Med (2019)

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

Por 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
Publicado em 2012

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

Por 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.
Publicado no Public Health Genomics (2018)

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

Por 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
Publicado no Genet Med (2019)

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

Por 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.
Publicado no 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

Por 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.
Publicado no Genet Med (2017)

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

Por 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
Publicado no J Genet Couns (2018)

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

Por 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
Publicado no Genet Med (2018)

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

Por 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.
Publicado em 2013

Germline Analysis from Tumor-Germline Sequencing Dyads to identify clinically actionable secondary findings

Por Seifert, Bryce A., O'Daniel, Julianne M., Amin, Krunal, Marchuk, Daniel S., Patel, Nirali M., Parker, Joel S., Hoyle, Alan P., Mose, Lisle E., Marron, Andrew, Hayward, Michele C., Bizon, Christopher, Wilhelmsen, Kirk C., Evans, James P., Earp, H. Shelton, Sharpless, Norman E., Hayes, D. Neil, Berg, Jonathan S.
Publicado no Clin Cancer Res (2016)