TP53 Testing and Li-Fraumeni Syndrome: Current Status of Clinical Applications and Future Directions

von Sorrell, April D., Espenschied, Carin R., Culver, Julie O., Weitzel, Jeffrey N.
Veröffentlicht 2013

Why should primary care physicians know about breast cancer genetics?

von Pinsky, Linda E, Culver, Julie Bars, Hull, Judith, Levy-Lahad, Ephrat, Daly, Mary, Burke, Wylie
Veröffentlicht 2001

Genetic Assessment of Breast Cancer Risk in Primary Care Practice

von Burke, Wylie, Culver, Julie, Pinsky, Linda, Hall, Sarah, Reynolds, Susan E, Yasui, Yutaka, Press, Nancy
Veröffentlicht 2009

Genetics, Genomics and Cancer Risk Assessment: State of the art and future directions in the era of personalized medicine

von Weitzel, Jeffrey N., Blazer, Kathleen R., MacDonald, Deborah J., Culver, Julie O., Offit, Kenneth
Veröffentlicht 2011

Next-Generation Testing for Cancer Risk: Perceptions, Experiences, and Needs Among Early Adopters in Community Healthcare Settings

von Blazer, Kathleen R., Nehoray, Bita, Solomon, Ilana, Niell-Swiller, Mariana, Culver, Julie O., Uman, Gwen C., Weitzel, Jeffrey N.
Veröffentlicht in Genet Test Mol Biomarkers (2015)

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

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

Personalized Cancer Genetics Training for Personalized Medicine: Improving community-based health care through a genetically literate workforce

von Blazer, Kathleen R., MacDonald, Deborah J., Culver, Julie O., Huizenga, Carin R., Morgan, Robert J., Uman, Gwen C., Weitzel, Jeffrey N.
Veröffentlicht 2011

Closing the Loop: Action research in a multimodal hereditary cancer patient conference is an effective tool to assess and address patient needs

von Espenschied, Carin R., MacDonald, Deborah J., Culver, Julie O., Sand, Sharon, Hurley, Karen, Banks, Kimberly C., Weitzel, Jeffrey N., Blazer, Kathleen R.
Veröffentlicht 2012

Increased Yield of Actionable Mutations Using Multi-Gene Panels to Assess Hereditary Cancer Susceptibility in an Ethnically Diverse Clinical Cohort

von Ricker, Charité, Culver, Julie O., Lowstuter, Katrina, Sturgeon, Duveen, Sturgeon, Julia D., Chanock, Christopher R., Gauderman, William J., McDonnell, Kevin, Idos, Gregory, Gruber, Stephen B.
Veröffentlicht in Cancer Genet (2016)

A novel BAP1 mutation is associated with melanocytic neoplasms and thyroid cancer

von McDonnell, Kevin J., Gallanis, Gregory T., Heller, Kathleen A., Melas, Marilena, Idos, Gregory E., Culver, Julie O., Martin, Sue-Ellen, Peng, David H., Gruber, Stephen B.
Veröffentlicht in Cancer Genet (2015)

Development and Evaluation of a Decision Aid for BRCA Carriers with Breast Cancer

von Culver, Julie O., MacDonald, Deborah J., Thornton, Andrea A., Sand, Sharon R., Grant, Marcia, Bowen, Deborah J., Burke, Harry, Garcia, Nellie, Metcalfe, Kelly A., Weitzel, Jeffrey N.
Veröffentlicht 2011

Health literacy, numeracy, and interpretation of graphical breast cancer risk estimates

von Brown, Sandra M., Culver, Julie O., Osann, Kathryn E., MacDonald, Deborah J., Sand, Sharon, Thornton, Andrea A., Grant, Marcia, Bowen, Deborah J., Metcalfe, Kelly A., Burke, Harry B., Robson, Mark E., Friedman, Susan, Weitzel, Jeffrey N.
Veröffentlicht 2011

Prospective Study of Cancer Genetic Variants: Variation in Rate of Reclassification by Ancestry

von Slavin, Thomas P, Van Tongeren, Lily R, Behrendt, Carolyn E, Solomon, Ilana, Rybak, Christina, Nehoray, Bita, Kuzmich, Lili, Niell-Swiller, Mariana, Blazer, Kathleen R, Tao, Shu, Yang, Kai, Culver, Julie O, Sand, Sharon, Castillo, Danielle, Herzog, Josef, Gray, Stacy W, Weitzel, Jeffrey N
Veröffentlicht in J Natl Cancer Inst (2018)

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

von 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.
Veröffentlicht in NPJ Genom Med (2018)

Patient communication of cancer genetic test results in a diverse population

von Ricker, Charité N, Koff, Rachel B, Qu, Chenxu, Culver, Julie, Sturgeon, Duveen, Kingham, Kerry E, Lowstuter, Katrina, Chun, Nicolette M, Rowe-Teeter, Courtney, Lebensohn, Alexandra, Levonian, Peter, Partynski, Katlyn, Lara-Otero, Karlena, Hong, Christine, Petrovchich, Iva M, Mills, Meredith A, Hartman, Anne-Renee, Allen, Brian, Ladabaum, Uri, McDonnell, Kevin, Ford, James M, Gruber, Stephen B, Kurian, Allison W, Idos, Gregory E
Veröffentlicht in Transl Behav Med (2018)

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

von 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.
Veröffentlicht in Cancer (2020)

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

von 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.
Veröffentlicht in JCO Precis Oncol (2019)

HIGH COLORECTAL AND LOW ENDOMETRIAL CANCER RISK IN EPCAM DELETION-POSITIVE LYNCH SYNDROME: A COHORT STUDY

von Kempers, Marlies JE, Kuiper, Roland P, Ockeloen, Charlotte W, Chappuis, Pierre O, Hutter, Pierre, Rahner, Nils, Schackert, Hans K, Steinke, Verena, Holinski-Feder, Elke, Morak, Monika, Kloor, Matthias, Büttner, Reinhard, Verwiel, Eugene TP, van Krieken, J. Han, Nagtegaal, Iris D, Goossens, Monique, van der Post, Rachel S., Niessen, Renée C, Sijmons, Rolf H, Kluijt, Irma, Hogervorst, Frans BL, Leter, Edward M, Gille, Johan JP, Aalfs, Cora M, Redeker, Egbert JW, Hes, Frederik J, Tops, Carli MJ, van Nesselrooij, Bernadette PM, van Gijn, Marielle E, García, Encarna B Gómez, Eccles, Diana M, Bunyan, David J, Syngal, Sapna, Stoffel, Elena M, Culver, Julie O, Palomares, Melanie R, Graham, Tracy, Velsher, Lea, Papp, Janos, Oláh, Edith, Chan, Tsun L, Leung, Suet Y, van Kessel, Ad Geurts, Kiemeney, Lambertus ALM, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn JL
Veröffentlicht 2010

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

von 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
Veröffentlicht in J Natl Cancer Inst (2020)

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

von Yang, Xin, Leslie, Goska, Doroszuk, Alicja, Schneider, Sandra, Allen, Jamie, Decker, Brennan, Dunning, Alison M., Redman, James, Scarth, James, Plaskocinska, Inga, Luccarini, Craig, Shah, Mitul, Pooley, Karen, Dorling, Leila, Lee, Andrew, Adank, Muriel A., Adlard, Julian, Aittomäki, Kristiina, Andrulis, Irene L., Ang, Peter, Barwell, Julian, Bernstein, Jonine L., Bobolis, Kristie, Borg, Åke, Blomqvist, Carl, Claes, Kathleen B.M., Concannon, Patrick, Cuggia, Adeline, Culver, Julie O., Damiola, Francesca, de Pauw, Antoine, Diez, Orland, Dolinsky, Jill S., Domchek, Susan M., Engel, Christoph, Evans, D. Gareth, Fostira, Florentia, Garber, Judy, Golmard, Lisa, Goode, Ellen L., Gruber, Stephen B., Hahnen, Eric, Hake, Christopher, Heikkinen, Tuomas, Hurley, Judith E., Janavicius, Ramunas, Kleibl, Zdenek, Kleiblova, Petra, Konstantopoulou, Irene, Kvist, Anders, Laduca, Holly, Lee, Ann S.G., Lesueur, Fabienne, Maher, Eamonn R., Mannermaa, Arto, Manoukian, Siranoush, McFarland, Rachel, McKinnon, Wendy, Meindl, Alfons, Metcalfe, Kelly, Mohd Taib, Nur Aishah, Moilanen, Jukka, Nathanson, Katherine L., Neuhausen, Susan, Ng, Pei Sze, Nguyen-Dumont, Tu, Nielsen, Sarah M., Obermair, Florian, Offit, Kenneth, Olopade, Olufunmilayo I., Ottini, Laura, Penkert, Judith, Pylkäs, Katri, Radice, Paolo, Ramus, Susan J., Rudaitis, Vilius, Side, Lucy, Silva-Smith, Rachel, Silvestri, Valentina, Skytte, Anne-Bine, Slavin, Thomas, Soukupova, Jana, Tondini, Carlo, Trainer, Alison H., Unzeitig, Gary, Usha, Lydia, van Overeem Hansen, Thomas, Whitworth, James, Wood, Marie, Yip, Cheng Har, Yoon, Sook-Yee, Yussuf, Amal, Zogopoulos, George, Goldgar, David, Hopper, John L., Chenevix-Trench, Georgia, Pharoah, Paul, George, Sophia H.L., Balmaña, Judith, Houdayer, Claude, James, Paul, El-Haffaf, Zaki, Ehrencrona, Hans, Janatova, Marketa, Peterlongo, Paolo, Nevanlinna, Heli, Schmutzler, Rita, Teo, Soo-Hwang, Robson, Mark, Pal, Tuya, Couch, Fergus, Weitzel, Jeffrey N., Elliott, Aaron, Southey, Melissa, Winqvist, Robert, Easton, Douglas F., Foulkes, William D., Antoniou, Antonis C., Tischkowitz, Marc
Veröffentlicht in J Clin Oncol (2020)