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

Por Sorrell, April D., Espenschied, Carin R., Culver, Julie O., Weitzel, Jeffrey N.
Publicado em 2013

Why should primary care physicians know about breast cancer genetics?

Por Pinsky, Linda E, Culver, Julie Bars, Hull, Judith, Levy-Lahad, Ephrat, Daly, Mary, Burke, Wylie
Publicado em 2001

Genetic Assessment of Breast Cancer Risk in Primary Care Practice

Por Burke, Wylie, Culver, Julie, Pinsky, Linda, Hall, Sarah, Reynolds, Susan E, Yasui, Yutaka, Press, Nancy
Publicado em 2009

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

Por Weitzel, Jeffrey N., Blazer, Kathleen R., MacDonald, Deborah J., Culver, Julie O., Offit, Kenneth
Publicado em 2011

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

Por Blazer, Kathleen R., Nehoray, Bita, Solomon, Ilana, Niell-Swiller, Mariana, Culver, Julie O., Uman, Gwen C., Weitzel, Jeffrey N.
Publicado no Genet Test Mol Biomarkers (2015)

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 em 2011

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

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

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

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

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

Por 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.
Publicado no Cancer Genet (2016)

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

Por 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.
Publicado no Cancer Genet (2015)

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

Por 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.
Publicado em 2011

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

Por 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.
Publicado em 2011

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

Por 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
Publicado no J Natl Cancer Inst (2018)

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 no NPJ Genom Med (2018)

Patient communication of cancer genetic test results in a diverse population

Por 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
Publicado no Transl Behav Med (2018)

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

Por 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
Publicado em 2010

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 no J Natl Cancer Inst (2020)

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

Por 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
Publicado no J Clin Oncol (2020)