Impact of returning unsolicited genomic results to nongenetic health care providers in the eMERGE III Network von Madden, Jill A., Brothers, Kyle K., Williams, Janet L., Myers, Melanie F., Leppig, Kathleen A., Clayton, Ellen Wright, Wiesner, Georgia L., Holm, Ingrid A.

Volltext

Taking an antiracist posture in scientific publications in human genetics and genomics von Brothers, Kyle B., Bennett, Robin L., Cho, Mildred K.

Volltext

ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG) von Miller, David T., Lee, Kristy, Abul-Husn, Noura S., Amendola, Laura M., Brothers, Kyle, Chung, Wendy K., Gollob, Michael H., Gordon, Adam S., Harrison, Steven M., Hershberger, Ray E., Klein, Teri E., Richards, Carolyn Sue, Stewart, Douglas R., Martin, Christa Lese

Volltext

ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG) von Miller, David T., Lee, Kristy, Abul-Husn, Noura S., Amendola, Laura M., Brothers, Kyle, Chung, Wendy K., Gollob, Michael H., Gordon, Adam S., Harrison, Steven M., Hershberger, Ray E., Klein, Teri E., Richards, C. Sue, Stewart, Douglas R., Martin, Christa Lese

Volltext

Data sharing and community-engaged research von Sabatello, Maya, Martschenko, Daphne O, Cho, Mildred K, Brothers, Kyle B

Volltext

Fostering Responsible Research on Ancient DNA von Wagner, Jennifer K., Colwell, Chip, Claw, Katrina G., Stone, Anne C., Bolnick, Deborah A., Hawks, John, Brothers, Kyle B., Garrison, Nanibaa’ A.

Volltext

The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results von Bombard, Yvonne, Brothers, Kyle B., Fitzgerald-Butt, Sara, Garrison, Nanibaa’ A., Jamal, Leila, James, Cynthia A., Jarvik, Gail P., McCormick, Jennifer B., Nelson, Tanya N., Ormond, Kelly E., Rehm, Heidi L., Richer, Julie, Souzeau, Emmanuelle, Vassy, Jason L., Wagner, Jennifer K., Levy, Howard P.

Volltext

Operational Implementation of Prospective Genotyping for Personalized Medicine: The Design of the Vanderbilt PREDICT Project von Pulley, J M, Denny, J C, Peterson, J F, Bernard, G R, Vnencak-Jones, C L, Ramirez, A H, Delaney, J T, Bowton, E, Brothers, K, Johnson, K, Crawford, D C, Schildcrout, J, Masys, D R, Dilks, H H, Wilke, R A, Clayton, E W, Shultz, E, Laposata, M, McPherson, J, Jirjis, J N, Roden, D M

Volltext

Words matter: The language of difference in human genetics von Cho, Mildred K., Duque Lasio, Maria Laura, Amarillo, Ina, Mintz, Kevin Todd, Bennett, Robin L., Brothers, Kyle B.

Volltext

PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing von Biesecker, B.B., Woolford, S.W., Klein, W.M.P., Brothers, K.B., Umstead, K.L., Lewis, K.L., Biesecker, L.G., Han, P.K.J.

Volltext

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study von Hart, M. Ragan, Biesecker, Barbara B., Blout, Carrie L., Christensen, Kurt D., Amendola, Laura M., Bergstrom, Katie L., Biswas, Sawona, Bowling, Kevin M., Brothers, Kyle B., Conlin, Laura K., Cooper, Greg M., Dulik, Matthew C., East, Kelly M., Everett, Jessica N., Finnila, Candice R., Ghazani, Arezou A., Gilmore, Marian J., Goddard, Katrina A. B, Jarvik, Gail P., Johnston, Jennifer J., Kauffman, Tia L., Kelley, Whitley V., Krier, Joel B., Lewis, Katie L., McGuire, Amy L., McMullen, Carmit, Ou, Jeffrey, Plon, Sharon E., Rehm, Heidi L., Richards, C. Sue, Romasko, Edward J., Miren Sagardia, Ane, Spinner, Nancy B., Thompson, Michelle L., Turbitt, Erin, Vassy, Jason L., Wilfond, Benjamin S., Veenstra, David L., Berg, Jonathan S., Green, Robert C., Biesecker, Leslie G., Hindorff, Lucia A.

Volltext

Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies von Robinson, Jill O., Wynn, Julia, Biesecker, Barbara, Biesecker, Leslie G., Bernhardt, Barbara, Brothers, Kyle B., Chung, Wendy K., Christensen, Kurt D., Green, Robert C., McGuire, Amy L., Hart, M. Ragan, Griesemer, Ida, Patrick, Donald L., Rini, Christine, Veenstra, David, Cronin, Angel M., Gray, Stacy W.

Volltext

Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background von Ormond, Kelly E., Hallquist, Miranda L. G., Buchanan, Adam H., Dondanville, Danielle, Cho, Mildred K., Smith, Maureen, Roche, Myra, Brothers, Kyle B., Coughlin, Curtis R., Hercher, Laura, Hudgins, Louanne, Jamal, Seema, Levy, Howard P., Raskin, Misha, Stosic, Melissa, Uhlmann, Wendy, Wain, Karen E., Currey, Erin, Faucett, W. Andrew

Volltext

Professionally Responsible Disclosure of Genomic Sequencing Results in Pediatric Practice von McCullough, Laurence B, Brothers, Kyle B, Chung, Wendy K, Joffe, Steven, Koenig, Barbara A, Wilfond, Benjamin, Yu, Joon-Ho

Volltext

Systematic reanalysis of genomic data improves quality of variant interpretation von Hiatt, S.M., Amaral, M.D., Bowling, K.M., Finnila, C.R., Thompson, M.L., Gray, D.E., Lawlor, J.M.J., Cochran, J.N., Bebin, E.M., Brothers, K.B., East, K.M., Kelley, W.V., Lamb, N.E., Levy, S.E., Lose, E.J., Neu, M.B., Rich, C.A., Simmons, S., Myers, R.M., Barsh, G.S., Cooper, G.M.

Volltext

Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network von Fullerton, Stephanie M., Wolf, Wendy A., Brothers, Kyle B., Clayton, Ellen Wright, Crawford, Dana C., Denny, Joshua C., Greenland, Philip, Koenig, Barbara A., Leppig, Kathleen A., Lindor, Noralane M., McCarty, Catherine A., McGuire, Amy L., McPeek Hinz, Eugenia R., Mirel, Daniel B., Ramos, Erin M., Ritchie, Marylyn D., Smith, Maureen E., Waudby, Carol J., Burke, Wylie, Jarvik, Gail P.

Volltext

Rethinking the “open future” argument against predictive genetic testing of children von Garrett, Jeremy R., Lantos, John D., Biesecker, Leslie G., Childerhose, Janet E., Chung, Wendy K., Holm, Ingrid A., Koenig, Barbara A., McEwen, Jean E., Wilfond, Benjamin S., Brothers, Kyle

Volltext

Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG) von Gordon, Adam S., Lee, Kristy, Abul-Husn, Noura S., Amendola, Laura M., Brothers, Kyle, Chung, Wendy K., Gollob, Michael H., Harrison, Steven M., Hershberger, Ray E., Richards, C. Sue, Stewart, Douglas R., Martin, Christa Lese, Miller, David T.

Volltext

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine von Goddard, Katrina A.B., Bernhardt, Barbara A., Biswas, Sawona, Bowling, Kevin M., Caga-anan, Charlisse F., Chinnaiyan, Arul M., Clayton, Ellen W., East, Kelly, Garraway, Levi A., Garrett, Jeremy R., Gray, Stacy W., Hindorff, Lucia A., Lewis, Michelle Huckaby, Hutter, Carolyn M., Janne, Pasi A., Knoppers, Bartha M., Krantz, Ian D., Manolio, Teri A., Nickerson, Deborah A., Ou, Jeffrey, Parsons, Donald W., Petersen, Gloria M., Plon, Sharon E., Rehm, Heidi L., Robinson, Dan, Salama, Joseph S., Scollon, Sarah, Shirts, Brian, Tabor, Holly K., Tarczy-Hornoch, Peter, Appelbaum, Paul S., Arora, Shubhangi, Brothers, Kyle B., Brown, Brian L., Caga-anan, Charlisse F., Calikoglu, Muge G., Christensen, Kurt D., Cirino, Allison L., Conlin, Laura K., Crosslin, David R., Davis, James V., Dorschner, Michael O., Dugan, Noreen P., Exe, Nicole, Fishler, Kristen, Ghrundmeier, Bob, Gordon, Adam S., Gray, David E., Gray, Stacy W., Gutierrez, Amanda M., Hensman, Naomi, Hiatt, Susan M., Himes, Patricia, Horike-Pyne, Martha J., Hull, Sara, Jensen, Brian C., Joffe, Steve, Kaufman, Dave, Kim, Jerry H., Klein, William, Lambert, Michele P., Leo, Michael C., Lewis, Katie, Lonigro, Bob, Machini, Kalotina, Manolio, Teri A., McCullough, Laurence, McMullen, Carmit, Mooney, Sean D., Moore, Elizabeth G., Muzny, Donna, Ng, David, Nickerson, Deborah A., Oliver, Nelly M., Parsons, Will, Plon, Sharon, Powell, Bradford C., Raesz-Martinez, Robin A., Raskind, Wendy H., Rehm, Heidi L., Reiss, Jacob A., Robertson, Peggy D., Robinson, Dan, Salama, Joseph, Scarano, Maria I., Sholl, Lynette M., Silverman, Elian, Simmons, Shirley, Spinner, Nancy B., Stoffel, Elena, Tilley, Christian R., Trinidad, Susan, Ubel, Peter, Vassy, Jason L., Vries, Raymond D., Weck, Karen, Wolf, Susan M., Wynn, Julia, Yu, Joon-Ho, Zikmund-Fisher, Brian J.

Volltext

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study von Hart, M. Ragan, Biesecker, Barbara B., Blout, Carrie L., Christensen, Kurt D., Amendola, Laura M., Bergstrom, Katie L., Biswas, Sawona, Bowling, Kevin M., Brothers, Kyle B., Conlin, Laura K., Cooper, Greg M., Dulik, Matthew C., East, Kelly M., Everett, Jessica N., Finnila, Candice R., Ghazani, Arezou A., Gilmore, Marian J., Goddard, Katrina A. B, Jarvik, Gail P., Johnston, Jennifer J., Kauffman, Tia L., Kelley, Whitley V., Krier, Joel B., Lewis, Katie L., McGuire, Amy L., McMullen, Carmit, Ou, Jeffrey, Plon, Sharon E., Rehm, Heidi L., Richards, C. Sue, Romasko, Edward J., Miren Sagardia, Ane, Spinner, Nancy B., Thompson, Michelle L., Turbitt, Erin, Vassy, Jason L., Wilfond, Benjamin S., Veenstra, David L., Berg, Jonathan S., Green, Robert C., Biesecker, Leslie G., Hindorff, Lucia A.

Volltext