Secondary uses and the governance of de-identified data: Lessons from the human genome diversity panel

por Fullerton, Stephanie M, Lee, Sandra S-J
Publicado 2011

Polygenic risk, population structure and ongoing difficulties with race in human genetics

por Kaplan, Jonathan Michael, Fullerton, Stephanie M.
Publicado 2022

Population genomic screening: Ethical considerations to guide age at implementation

por Spencer, Scott J., Fullerton, Stephanie M.
Publicado 2022

Patient safety in genomic medicine: an exploratory study

por Korngiebel, Diane M., Fullerton, Stephanie M., Burke, Wylie
Publicado 2016

Cloud-based biomedical data storage and analysis for genomic research: Landscape analysis of data governance in emerging NIH-supported platforms

por Dahlquist, Jacklyn M., Nelson, Sarah C., Fullerton, Stephanie M.
Publicado 2023

Factors Influencing Genetic Screening Enrollment among a Diverse, Community-Ascertained Cohort

por Rao, Nandana D., Kaganovsky, Jailanie, Fullerton, Stephanie M., Chen, Annie T., Shirts, Brian H.
Publicado 2023

Environmental scan of family chart linking for genetic cascade screening in a U.S. integrated health system

por Haas, Cameron B., Ralston, James, Fullerton, Stephanie M., Scrol, Aaron, Henrikson, Nora B.
Publicado 2022

Conflating race and ancestry: Tracing decision points about population descriptors over the precision medicine research life course

por Bentz, Michael, Saperstein, Aliya, Fullerton, Stephanie M., Shim, Janet K., Soo-Jin Lee, Sandra
Publicado 2023

Four misconceptions about investigative genetic genealogy

por Guerrini, Christi J, Wickenheiser, Ray A, Bettinger, Blaine, McGuire, Amy L, Fullerton, Stephanie M
Publicado 2021

Values in Translation: How Asking the Right Questions Can Move Translational Science Toward Greater Health Impact

por Kelley, Maureen, Edwards, Kelly, Starks, Helene, Fullerton, Stephanie M., James, Rosalina, Goering, Sara, Holland, Suzanne, Disis, Mary L., Burke, Wylie
Publicado 2012

Discordance in selected designee for return of genomic findings in the event of participant death and estate executor

por Goodman, Jessie L., Amendola, Laura M., Horike‐Pyne, Martha, Trinidad, Susan B., Fullerton, Stephanie M., Burke, Wylie, Jarvik, Gail P.
Publicado 2017

“It would be so much easier”: health system-led genetic risk notification—feasibility and acceptability of cascade screening in an integrated system

por Henrikson, Nora B., Blasi, Paula R., Fullerton, Stephanie M., Grafton, Jane, Leppig, Kathleen A., Jarvik, Gail P., Larson, Eric B.
Publicado 2019

Beyond inclusion: Enacting team equity in precision medicine research

por Jeske, Melanie, Vasquez, Emily, Fullerton, Stephanie M., Saperstein, Aliya, Bentz, Michael, Foti, Nicole, Shim, Janet K., Lee, Sandra Soo-Jin
Publicado 2022

Rethinking Benefit and Responsibility in the Context of Diversity: Perspectives from the Front Lines of Precision Medicine Research

por Vasquez, Emily E., Foti, Nicole, McMahon, Caitlin E., Jeske, Melanie, Bentz, Michael, Fullerton, Stephanie M., Shim, Janet K., Lee, Sandra Soo-Jin
Publicado 2023

Clinical verification of genetic results returned to research participants: findings from a Colon Cancer Family Registry

por Laurino, Mercy Y., Truitt, Anjali R., Tenney, Lederle, Fisher, Douglass, Lindor, Noralane M., Veenstra, David, Jarvik, Gail P., Newcomb, Polly A., Fullerton, Stephanie M.
Publicado 2017

Feasibility, acceptability, and limited efficacy of health system-led familial risk notification: protocol for a mixed-methods evaluation

por Blasi, Paula R., Scrol, Aaron, Anderson, Melissa L., Gray, Marlaine Figueroa, Tiffany, Brooks, Fullerton, Stephanie M., Ralston, James D., Leppig, Kathleen A., Henrikson, Nora B.
Publicado 2022

Patient and Family Preferences on Health System-Led Direct Contact for Cascade Screening

por Henrikson, Nora B., Blasi, Paula, Figueroa Gray, Marlaine, Tiffany, Brooks T., Scrol, Aaron, Ralston, James D., Fullerton, Stephanie M., Lim, Catherine Y., Ewing, John, Leppig, Kathleen A.
Publicado 2021

Targeting Representation: Interpreting Calls for Diversity in Precision Medicine Research

por Lee, Sandra Soo-Jin, Fullerton, Stephanie M., McMahon, Caitlin E., Bentz, Michael, Saperstein, Aliya, Jeske, Melanie, Vasquez, Emily, Foti, Nicole, Saco, Larissa, Shim, Janet K.
Publicado 2022

Diagnostic yield of genetic screening in a diverse, community-ascertained cohort

por Rao, Nandana D., Kaganovsky, Jailanie, Malouf, Emily A., Coe, Sandy, Huey, Jennifer, Tsinajinne, Darwin, Hassan, Sajida, King, Kristine M., Fullerton, Stephanie M., Chen, Annie T., Shirts, Brian H.
Publicado 2023

Studying the impact of translational genomic research: Lessons from eMERGE

por Clayton, Ellen Wright, Smith, Maureen E., Anderson, Katherine C., Chung, Wendy K., Connolly, John J., Fullerton, Stephanie M., McGowan, Michelle L., Peterson, Josh F., Prows, Cynthia A., Sabatello, Maya, Holm, Ingrid A.
Publicado 2023