Utilization of Religious Coping Strategies Among African American Women at Increased Risk for Hereditary Breast and Ovarian Cancer

gan Weathers, Benita, Kessler, Lisa, Collier, Aliya, Stopfer, Jill E., Domchek, Susan, Halbert, Chanita Hughes
Cyhoeddwyd 2009

Long-Term Reactions to Genetic Testing for BRCA1 and BRCA2 Mutations: Does Time Heal Women's Concerns?

gan Halbert, Chanita Hughes, Stopfer, Jill E., McDonald, Jasmine, Weathers, Benita, Collier, Aliya, Troxel, Andrea B., Domchek, Susan
Cyhoeddwyd 2011

Factors Determining Dissemination of Results and Uptake of Genetic Testing in Families with Known BRCA1/2 Mutations

gan Finlay, Esme, Stopfer, Jill E., Burlingame, Eric, Evans, Katherine Goldfeder, Nathanson, Katherine L., Weber, Barbara L., Armstrong, Katrina, Rebbeck, Timothy R., Domchek, Susan M.
Cyhoeddwyd 2008

Preliminary validation of a consumer-oriented colorectal cancer risk assessment tool compatible with the U.S. Surgeon General’s My Family Health Portrait

gan Feero, W. Gregory, Facio, Flavia M., Glogowski, Emily A., Hampel, Heather L., Stopfer, Jill E., Eidem, Haley, Pizzino, Amy M., Barton, David K., Biesecker, Leslie G.
Cyhoeddwyd yn Genet Med (2014)

Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2 negative patients with early onset breast cancer

gan Maxwell, Kara N., Wubbenhorst, Bradley, D’Andrea, Kurt, Garman, Bradley, Long, Jessica M., Powers, Jacquelyn, Rathbun, Katherine, Stopfer, Jill E., Zhu, Jiajun, Bradbury, Angela R., Simon, Michael S., DeMichele, Angela, Domchek, Susan M., Nathanson, Katherine L.
Cyhoeddwyd yn Genet Med (2014)

Activating mutation in MET oncogene in familial colorectal cancer

gan Neklason, Deborah W, Done, Michelle W, Sargent, Nykole R, Schwartz, Ann G, Anton-Culver, Hoda, Griffin, Constance A, Ahnen, Dennis J, Schildkraut, Joellen M, Tomlinson, Gail E, Strong, Louise C, Miller, Alexander R, Stopfer, Jill E, Burt, Randall W
Cyhoeddwyd 2011

Returning Individual Genetic Research Results to Research Participants: Uptake and Outcomes Among Patients With Breast Cancer

gan Bradbury, Angela R., Patrick-Miller, Linda, Egleston, Brian L., Maxwell, Kara N., DiGiovanni, Laura, Brower, Jamie, Fetzer, Dominique, Gaieski, Jill Bennett, Brandt, Amanda, McKenna, Danielle, Long, Jessica, Powers, Jacquelyn, Stopfer, Jill E., Nathanson, Katherine L., Domchek, Susan M.
Cyhoeddwyd yn JCO Precis Oncol (2018)

Research participants’ experiences with return of genetic research results and preferences for web‐based alternatives

gan Gaieski, Jill B., Patrick‐Miller, Linda, Egleston, Brian L., Maxwell, Kara N., Walser, Sarah, DiGiovanni, Laura, Brower, Jamie, Fetzer, Dominique, Ganzak, Amanda, McKenna, Danielle, Long, Jessica M., Powers, Jacquelyn, Stopfer, Jill E., Nathanson, Katherine L., Domchek, Susan M., Bradbury, Angela R.
Cyhoeddwyd yn Mol Genet Genomic Med (2019)

Common Familial Colorectal Cancer Linked to Chromosome 7q31: a genome-wide analysis

gan Neklason, Deborah W., Kerber, Richard A., Nilson, David B., Anton-Culver, Hoda, Schwartz, Ann G., Griffin, Constance A., Lowery, Jan T., Schildkraut, Joellen M., Evans, James P., Tomlinson, Gail E., Strong, Louise C., Miller, Alexander R., Stopfer, Jill E., Finkelstein, Dianne M., Nadkarni, Prakash M., Kasten, Carol H., Mineau, Geraldine P., Burt, Randall W.
Cyhoeddwyd 2008

Randomized Noninferiority Trial of Telephone vs In-Person Disclosure of Germline Cancer Genetic Test Results

gan Bradbury, Angela R, Patrick-Miller, Linda J, Egleston, Brian L, Hall, Michael J, Domchek, Susan M, Daly, Mary B, Ganschow, Pamela, Grana, Generosa, Olopade, Olufunmilayo I, Fetzer, Dominique, Brandt, Amanda, Chambers, Rachelle, Clark, Dana F, Forman, Andrea, Gaber, Rikki, Gulden, Cassandra, Horte, Janice, Long, Jessica M, Lucas, Terra, Madaan, Shreshtha, Mattie, Kristin, McKenna, Danielle, Montgomery, Susan, Nielsen, Sarah, Powers, Jacquelyn, Rainey, Kim, Rybak, Christina, Savage, Michelle, Seelaus, Christina, Stoll, Jessica, Stopfer, Jill E, Yao, Xinxin (Shirley)
Cyhoeddwyd yn J Natl Cancer Inst (2018)

Preferences for in-person disclosure: Patients declining telephone disclosure characteristics and outcomes in the multicenter Communication Of GENetic Test Results by Telephone stu...

gan Beri, Nina, Patrick-Miller, Linda J., Egleston, Brian L., Hall, Michael J., Domchek, Susan M., Daly, Mary B., Ganschow, Pamela, Grana, Generosa, Olopade, Olufunmilayo I., Fetzer, Dominique, Brandt, Amanda, Chambers, Rachelle, Clark, Dana F., Forman, Andrea, Gaber, Rikki, Gulden, Cassandra, Horte, Janice, Long, Jessica, Lucas, Terra, Madaan, Shreshtha, Mattie, Kristin, McKenna, Danielle, Montgomery, Susan, Nielsen, Sarah, Powers, Jacquelyn, Rainey, Kim, Rybak, Christina, Savage, Michelle, Seelaus, Christina, Stoll, Jessica, Stopfer, Jill E, Yao, Xinxin (Shirley), Bradbury, Angela R.
Cyhoeddwyd yn Clin Genet (2018)

Use and Patient-Reported Outcomes of Clinical Multigene Panel Testing for Cancer Susceptibility in the Multicenter Communication of Genetic Test Results by Telephone Study

gan Hall, Michael J., Patrick-Miller, Linda J., Egleston, Brian L., Domchek, Susan M., Daly, Mary B., Ganschow, Pamela, Grana, Generosa, Olopade, Olufunmilayo I., Fetzer, Dominique, Brandt, Amanda, Chambers, Rachelle, Clark, Dana F., Forman, Andrea, Gaber, Rikki, Gulden, Cassandra, Horte, Janice, Long, Jessica M., Lucas, Terra, Madaan, Shreshtha, Mattie, Kristin, McKenna, Danielle, Montgomery, Susan, Nielsen, Sarah, Powers, Jacquelyn, Rainey, Kim, Rybak, Christina, Savage, Michelle, Seelaus, Christina, Stoll, Jessica, Stopfer, Jill E., Yao, Xinxin (Shirley), Bradbury, Angela R.
Cyhoeddwyd yn JCO Precis Oncol (2018)

Longitudinal follow-up after telephone disclosure in the randomized COGENT Study

gan Kilbride, Madison K., Egleston, Brian L., Hall, Michael J., Patrick-Miller, Linda J., Daly, Mary B., Ganschow, Pamela, Grana, Generosa, Olopade, Olufunmilayo I., Fetzer, Dominique, Brandt, Amanda, Chambers, Rachelle, Clark, Dana F., Forman, Andrea, Gaber, Rikki, Gulden, Cassandra, Horte, Janice, Long, Jessica M., Lucas, Terra, Madaan, Shreshtha, Mattie, Kristin, McKenna, Danielle, Montgomery, Susan, Nielsen, Sarah, Powers, Jacquelyn, Rainey, Kim, Rybak, Christina, Savage, Michelle, Seelaus, Christina, Stoll, Jessica, Stopfer, Jill E., Yao, Xinxin (Shirley), Domchek, Susan M., Bradbury, Angela R.
Cyhoeddwyd yn Genet Med (2020)

A rare TP53 mutation predominant in Ashkenazi Jews confers risk of multiple cancers

gan Powers, Jacquelyn, Pinto, Emilia M., Barnoud, Thibaut, Leung, Jessica C., Martynyuk, Tetyana, Kossenkov, Andrew V., Philips, Aaron H., Desai, Heena, Hausler, Ryan, Kelly, Gregory, Le, Anh N., Li, Marilyn M., MacFarland, Suzanne P., Pyle, Louise C., Zelley, Kristin, Nathanson, Katherine L., Domchek, Susan M., Slavin, Thomas P., Weitzel, Jeffrey N., Stopfer, Jill E., Garber, Judy E., Joseph, Vijai, Offit, Kenneth, Dolinsky, Jill S., Gutierrez, Stephanie, McGoldrick, Kelly, Couch, Fergus J., Levin, Brooke, Edelman, Morris C., Levy, Carolyn Fein, Spunt, Sheri L., Kriwacki, Richard W., Zambetti, Gerard P., Ribeiro, Raul C., Murphy, Maureen E., Maxwell, Kara N.
Cyhoeddwyd yn Cancer Res (2020)