The impact of variant classification on the clinical management of hereditary cancer syndromes

by Turner, Scott A, Rao, Smita K, Morgan, R Hayes, Vnencak-Jones, Cindy L, Wiesner, Georgia L
Published in Genetics in medicine

Impact of returning unsolicited genomic results to nongenetic health care providers in the eMERGE III Network

by Madden, Jill A., Brothers, Kyle K., Williams, Janet L., Myers, Melanie F., Leppig, Kathleen A., Clayton, Ellen Wright, Wiesner, Georgia L., Holm, Ingrid A.
Published in Genetics in medicine

Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of results

by Sherafati, Alborz, Elsekaily, Omar, Saadatagah, Seyedmohammad, Kochan, David C., Lee, Christopher, Wiesner, Georgia L., Liu, Cong, Dellefave-Castillo, Lisa, Namjou, Bahram, Perez, Emma F., Salvati, Zachary M., Connolly, John J., Hakonarson, Hakon, Williams, Marc S., Jarvik, Gail P., Chung, Wendy K., McNally, Elizabeth M., Manolio, Teri A., Kullo, Iftikhar J.
Published in Genetics in medicine

Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis

by Edwards, Karen L, Lemke, Amy A, Trinidad, Susan B, Lewis, Susan M, Starks, Helene, Snapinn, Katherine W, Griffin, Mary Quinn, Wiesner, Georgia L, Burke, Wylie
Published in Genetics in medicine

Stakeholder perspectives on implementing a universal Lynch syndrome screening program: a qualitative study of early barriers and facilitators

by Schneider, Jennifer L, Davis, James, Kauffman, Tia L, Reiss, Jacob A, McGinley, Cheryl, Arnold, Kathleen, Zepp, Jamilyn, Gilmore, Marian, Muessig, Kristin R, Syngal, Sapna, Acheson, Louise, Wiesner, Georgia L, Peterson, Susan K, Goddard, Katrina A B
Published in Genetics in medicine

Frequency of genomic secondary findings among 21,915 eMERGE network participants

by Gordon, Adam S, Zouk Hana, Venner, Eric, Eng, Christine M, Funke, Birgit H, Amendola, Laura M, Carrell, David S, Chisholm, Rex L, Chung, Wendy K, Denny, Joshua C, Fedotov, Alexander, Hakonarson Hakon, Kullo, Iftikhar J, Larson, Eric B, Leduc, Magalie S, Leppig, Kathleen A, Lennon, Niall J, Linder, Jodell E, Muzny, Donna M, Prows, Cynthia A, Rasmussen-Torvik, Laura J, Rasouly Hila Milo, Roden, Dan M, Rosenthal, Elisabeth A, Smith, Maureen E, Stanaway, Ian B, Van Driest Sara L, Walker, Kimberly, Wiesner, Georgia L, Williams, Marc S, Witkowski Leora, Crosslin David R, Gibbs, Richard A, Rehm, Heidi L, Jarvik, Gail P
Published in Genetics in medicine

Returning integrated genomic risk and clinical recommendations: The eMERGE study

by Chisholm, Rex L., Clayton, Ellen Wright, DiVietro, Alanna, Green, Richard, Harden, Maegan V., Limdi, Nita A., Rasmussen, Luke V., Schmidlen, Tara, Cimino, James J., Guiducci, Candace, Harr, Margaret, Larkin, Katie, Mooney, Sean D., Mutai, Brenda, Namjou, Bahram, Perez, Emma F., Saadatagah, Seyedmohammad, Seabolt, Lynn, Shaibi, Gabriel Q., Sharp, Richard R., Sterling, Rene, Tiwari, Hemant K., Allworth, Aimee, DiVietro, Alanna, Khera, Amit, Kontorovich, Amy, Prince, Anya, Iverson, Ayuko, Khales, Bahram Namjou, Benoit, Barbara, Satterfield, Benjamin, Devine, Beth, Grundmeier, Bob, Piening, Brian, Korf, Bruce, Hammack, Catherine, Gascoigne, Caytie, Lange, Christoph, Liu, Cong, Shimbo, Daichi, Singh, Davinder, Edwards, Digna Velez, Morales, Eduardo, Cohn, Elizabeth, Karlson, Elizabeth, DeFranco, Emily, Perez, Emma, Cash, Erin, Berner, Eta, Wang, Fei, Mentch, Frank, Wiesner, Georgia, Belbin, Gillian, Hakonarson, Hakon, Tiwari, Hemant, Thomas, Hope, Hellwege, Jacklyn, Snyder, James, Olson, Janet, Glessner, Joe, Alsip, Jorge, Kannry, Joseph, Peterson, Josh, Galasso, Julia, Starren, Justin, Mittendorf, Kate, Anderson, Katherine, Bonini, Katherine, Rasmussen-Torvik, Laura, Gomez, Lizbeth, Petukhova, Lynn, Beasley, Mark, Horike, Martha, Hamed, Marwan, Davis, Matthew, Preuss, Michael, Shi, Mingjian, Perera, Minoli, Elkind, Mitch, Saadatagah, Mohammad, Netherly, Neil, Lennon, Niall, Limdi, Nita, Robinson, Nora, Elsekaily, Omar, Kovatch, Patricia, O’Reilly, Paul, Murali, Priyanka, Sharp, Richard, Peters, Riki, Rowley, Robb, Freimuth, Robert, Green, Robert, Winter, Robert, Irvin, Ryan, Knerr, Sarah, Bland, S.T., Booth, Stuart James, Desai, Vimi, Luo, Yuan
Published in Genetics in medicine

Family history-taking in community family practice: implications for genetic screening

by Acheson, L S, Wiesner, G L, Zyzanski, S J, Goodwin, M A, Stange, K C
Published in Genetics in medicine

Frequency of genomic incidental findings among 21,915 eMERGE network participants

by Gordon, Adam S., Zouk, Hana, Venner, Eric, Eng, Christine M., Funke, Birgit H., Amendola, Laura M., Carrell, David S., Chisholm, Rex L., Chung, Wendy K., Denny, Joshua C., Fedotov, Alexander, Hakonarson, Hakon, Kullo, Iftikhar J., Larson, Eric B., Leduc, Magalie S., Leppig, Kathleen A., Lennon, Niall J., Linder, Jodell E., Muzny, Donna M., Prows, Cynthia A., Rasmussen-Torvik, Laura J., Rasouly, Hila Milo, Roden, Dan M., Rosenthal, Elisabeth A., Smith, Maureen E., Stanaway, Ian B., Van Driest, Sara L., Walker, Kimberly, Wiesner, Georgia L., Williams, Marc S., Witkowski, Leora, Crosslin, David R., Gibbs, Richard A., Rehm, Heidi L., Jarvik, Gail P.
Published in Genetics in medicine