Transcriptome analysis provides critical answers to the “variants of uncertain significance” conundrum

por Postel, Mackenzie D., Culver, Julie O., Ricker, Charité, Craig, David W.
Publicado 2022

Mind the gap: challenges in the clinical management of Lynch syndrome families

por Huizenga, Carin R, Martir-Negron, Arelis E, Blazer, Kathleen R, Culver, Julie O, MacDonald, Deborah J, Weitzel, Jeffrey N
Publicado 2011

Risk‐reducing mastectomy decisions among women with mutations in high‐ and moderate‐ penetrance breast cancer susceptibility genes

por Comeaux, Jacob G., Culver, Julie O., Lee, John E., Dondanville, Danielle, McArthur, Heather L., Quinn, Emily, Gorman, Nicholas, Ricker, Charité, Li, Ming, Lerman, Caryn
Publicado 2022

Clinical testing of BRCA1 and BRCA2: a worldwide snapshot of technological practices

por Toland, Amanda Ewart, Forman, Andrea, Couch, Fergus J., Culver, Julie O., Eccles, Diana M., Foulkes, William D., Hogervorst, Frans B. L., Houdayer, Claude, Levy-Lahad, Ephrat, Monteiro, Alvaro N., Neuhausen, Susan L., Plon, Sharon E., Sharan, Shyam K., Spurdle, Amanda B., Szabo, Csilla, Brody, Lawrence C.
Publicado 2018

Integration of Universal Germline Genetic Testing for All New Breast Cancer Patients

por Culver, Julie O., Freiberg, Yael, Ricker, Charité, Comeaux, Jacob G., Chang, Emmeline Y., Banerjee, Victoria, Sturgeon, Duveen, Solomon, Ilana, Kagey, Josie, Dobre, Mariana G., Carey, Joseph, Carr, Azadeh, Cho, Stephanie, Lu, Janice, Kang, Irene M., Patel, Ketan, Terando, Alicia, Ye, Jason C., Li, Ming, Lerman, Caryn, Spicer, Darcy, Nelson, Maria
Publicado 2022

Psychosocial outcomes following germline multigene panel testing in an ethnically and economically diverse cohort of patients

por Culver, Julie O., Ricker, Charité N., Bonner, Joseph, Kidd, John, Sturgeon, Duveen, Hodan, Rachel, Kingham, Kerry, Lowstuter, Katrina, Chun, Nicolette M., Lebensohn, Alexandra P., Rowe‐Teeter, Courtney, Levonian, Peter, Partynski, Katlyn, Lara‐Otero, Karlena, Hong, Christine, Morales Pichardo, Jennifer, Mills, Meredith A., Brown, Krystal, Lerman, Caryn, Ladabaum, Uri, McDonnell, Kevin J., Ford, James M., Gruber, Stephen B., Kurian, Allison W., Idos, Gregory E.
Publicado 2020

Multicenter Prospective Cohort Study of the Diagnostic Yield and Patient Experience of Multiplex Gene Panel Testing For Hereditary Cancer Risk

por Idos, Gregory E., Kurian, Allison W., Ricker, Charité, Sturgeon, Duveen, Culver, Julie O., Kingham, Kerry E., Koff, Rachel, Chun, Nicolette M., Rowe-Teeter, Courtney, Lebensohn, Alexandra P., Levonian, Peter, Lowstuter, Katrina, Partynski, Katlyn, Hong, Christine, Mills, Meredith A., Petrovchich, Iva, Ma, Cindy S., Hartman, Anne-Renee, Allen, Brian, Wenstrup, Richard J., Lancaster, Johnathan M., Brown, Krystal, Kidd, John, Evans, Brent, Mukherjee, Bhramar, McDonnell, Kevin J., Ladabaum, Uri, Ford, James M., Gruber, Stephen B.
Publicado 2019

Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D

por Yang, Xin, Song, Honglin, Leslie, Goska, Engel, Christoph, Hahnen, Eric, Auber, Bernd, Horváth, Judit, Kast, Karin, Niederacher, Dieter, Turnbull, Clare, Houlston, Richard, Hanson, Helen, Loveday, Chey, Dolinsky, Jill S, LaDuca, Holly, Ramus, Susan J, Menon, Usha, Rosenthal, Adam N, Jacobs, Ian, Gayther, Simon A, Dicks, Ed, Nevanlinna, Heli, Aittomäki, Kristiina, Pelttari, Liisa M, Ehrencrona, Hans, Borg, Åke, Kvist, Anders, Rivera, Barbara, Hansen, Thomas V O, Djursby, Malene, Lee, Andrew, Dennis, Joe, Bowtell, David D, Traficante, Nadia, Diez, Orland, Balmaña, Judith, Gruber, Stephen B, Chenevix-Trench, Georgia, Investigators, kConFab, Jensen, Allan, Kjær, Susanne K, Høgdall, Estrid, Castéra, Laurent, Garber, Judy, Janavicius, Ramunas, Osorio, Ana, Golmard, Lisa, Vega, Ana, Couch, Fergus J, Robson, Mark, Gronwald, Jacek, Domchek, Susan M, Culver, Julie O, de la Hoya, Miguel, Easton, Douglas F, Foulkes, William D, Tischkowitz, Marc, Meindl, Alfons, Schmutzler, Rita K, Pharoah, Paul D P, Antoniou, Antonis C
Publicado 2020