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Lim, Elgene, Vaillant, Francois, Wu, Di, Forrest, Natalie C., Pal, Bhupinder, Hart, Adam H., Asselin-Labat, Marie-Liesse, Gyorki, David E., Ward, Teresa, Partanen, Audrey, Feleppa, Frank, Huschtscha, Lily I., Thorne, Heather J., kConFab, Fox, Stephen B., Yan, Max, French, Juliet D., Brown, Melissa A., Smyth, Gordon K., Visvader, Jane E. and Lindemann, G. J. (2009) Aberrant luminal progenitors as the candidate target population for basal tumor development in BRCA1 mutation carriers. Nature Medicine, 15 8: 907-913. doi:10.1038/nm.2000 304   480 Cited 495 times in Scopus495 1
Verderio, Paolo, Pizzamiglio, Sara, Southey, Melissa C., Spurdle, Amanda B., Hopper, John L., Chen, Xiaoqing, Beesley, Jonathan, Australian Ovarian Cancer Study Group, kConFab, Schmutzler, Rita K., Engel, Christoph, Burwinkel, Barbara, Bugert, Peter, Ficarazzi, Filomena, Manoukian, Siranoush, Barile, Monica, Wappenschmidt, Barbara, Chenevix-Trench, Georgia, Radice, Paolo and Peterlongo, Paolo (2010) A BRCA1 promoter variant (rs11655505) and breast cancer risk. Journal of Medical Genetics, 47 4: 268-270. doi:10.1136/jmg.2009.073544 132   3 Cited 4 times in Scopus4 0
Antoniou, Antonis C., Wang, Xianshu, Fredericksen, Zachary S., McGuffog, Lesley, Tarrell, Robert, Sinilnikova, Olga M., Healey, Sue, Morrison, Jonathan, Kartsonaki,Christiana, Lesnick, Timothy, Ghoussaini, Maya, Barrowdale, Daniel, Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Eccles, Diana, Evans, D. Gareth, Eeles, Ros, Izatt, Louise, Chu, Carol, Douglas, Fiona, Paterson, Joan, Stoppa-Lyonnet, Dominique, Houdayer, Claude, Mazoyer, Sylvie, Giraud, Sophie, Lasset, Christine, Remenieras, Audrey, Caron, Olivier, Hardouin, Agnes, Berthet, Pascaline, Hogervorst, Frans B. L., Rookus, Matti A., Jager, Agnes, van den Ouweland, Ans, Hoogerbrugge, Nicoline, van der Luijt, Rob B., Meijers-Heijboer, Rob B., Gomez Garcia, Encarna B., Devilee, Peter, Vreeswijk, Maaike P. G., Lubinski, Jan, Jakubowska, Anna, Gronwald, Jacek, Huzarski, Tomasz, Byrski, Tomasz, Gorski, Bohdan, Cybulski, Cezary, Spurdle, Amanda B., Holland, Helene, Goldgar, David E., John, Esther M., Hopper, John L., Southey, Melissa, Buys,Saundra S., Daly,Mary B., Terry, Mary-Beth, Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Meindl, Alfons, Preisler-Adams, Sabine, Arnold, Norbert, Niederacher, Dieter, Sutter, Christian, Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Timothy, Blum, Joanne L., Piedmonte, Marion, Rodriguez, Gustavo C., Wakeley, Katie, Boggess, John F., Basil, Jack, Blank, Stephanie V., Friedman, Eitan, Kaufman, Bella, Laitman, Yael, Milgrom, Roni, Andrulism, Irene L., Glendon, Gord, Ozcelik, Hilmi, Kirchhoff, Tomas, Vijai, Joseph, Gaudet, Mia M., Altshuler, David, Guiducci, Candace, Loman, Niklas, Harbst, Katja, Rantala, Johanna, Ehrencrona, Hans, Gerdes, Anne-Marie, Thomassen, Mads, Sunde, Lone, Peterlongo, Paolo, Manoukian, Siranoush, Bonanni, Bernardo, Viel, Alessandra, Radice, Paolo, Caldes, Trinidad, de la Hoya, Miguel, Singer, Christian F., Fink-Retter, Anneliese, Greene,Mark H., L. Mai, Phuong, Loud, Jennifer T., Guidugli, Lucia, Lindor, Noralane M., Hansen, Thomas V. O., Nielsen, Finn C., Blanco, Ignacio, Lazaro,Conxi, Garber, Judy, Ramus, Susan J., Gayther, Simon A., Phelan, Catherine, Narod, Stephen, Szabo, Csilla I ., Benitez, Javier, Osorio, Ana, Nevanlinna,Heli, Heikkinen, Tuomas, Caligo, Maria A., Beattie,Mary S., Hamann,Ute, Godwin, Andrew K., Montagna, Marco, Casella, Cinzie, Neuhausen, Susan L., Karlan, Beth Y., Tung, Nadine, Toland, Amanda E ., Weitzel, Jeffrey, Olopade, Olofunmilayo, Simard, Jacques, Soucy, Penny, Rubinstein, Wendy S., Arason, Adalgeir, Rennert, Gad, Martin, Nicholas G., Montgomery, Grant W., Chang-Claude,Jenny, Flesch-Janys, Dieter, Brauch, Hiltrud, Severi, Gianluca, Baglietto, Laura, Cox, Angela, Cross, Simon S., Miron, Penelope, Gerty, Sue M, Tapper, William, Yannoukakos, Drakoulis, Fountzilas, George, Fasching, Peter A., Beckmann, Matthias W., dos Santos Silva, Isabel, Peto, Julian, Lambrechts, Diether, Paridaens, Robert, Rudiger, Thomas, Forsti, Asta, Winqvist, Robert, Pylkas, Katri, Diasio, Robert B., Lee, Adam M., Eckel-Passow, Jeanette, Vachon, Celine, Blows, Fiona, Driver, Kristy, Dunning, Alison, Pharoah, Paul P. D., Offit, Kenneth, Pankratz, V. Shane, Hakonarson, Hakon, Chenevix-Trench, Georgia, Easton,Douglas F., Couch, Fergus J., EMBRACE, GEMO Study Collaborators, HEBON, kConFab, SWE-BRCA, MOD SQUAD, GENICA, Brown, Melissa, Cummings, Margaret and Lakhani, Sunil (2010) A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population. Nature Genetics, 42 10: 885-892. doi:10.1038/ng.669 236 5 134 Cited 131 times in Scopus131 24
Thompson, Ella R., Boyle, Samantha E., Johnson, Julie, Ryland, Georgina L., Sawyer, Sarah, Choong, David Y.H., kConFab, Chenevix-Trench, Georgia, Trainer, Alison H., Lindeman, Geoffrey J., Mitchell, Gillian, James, Paul A. and Campbell, Ian G. (2012) Analysis of RAD51C Germline Mutations in High-Risk Breast and Ovarian Cancer Families and Ovarian Cancer Patients. Human Mutation, 33 1: 95-99. doi:10.1002/humu.21625 68   21 Cited 25 times in Scopus25 0
Milne, Roger L., Gaudet, Mia M., Spurdle, Amanda B., Fasching, Peter A., Couch, Fergus J., Benitez, Javier, Arias Perez, Jose Ignacio, Zamora, M. Pilar, Malats, Nuria, dos Santos Silva, Isabel, Gibson, Lorna J., Fletcher, Olivia, Johnson, Nichola, Anton-Culver, Hoda, Ziogas, Argyrios, Figueroa, Jonine, Brinton, Louise, Sherman, Mark E., Lissowska, Jolanta, Hopper, John L., Dite, Gillian S., Apicella, Carmel, Southey, Melissa C., Sigurdson, Alice J., Linet, Martha S., Schonfeld, Sara J., Freedman, D. Michal, Mannermaa, Arto, Kosma, Veli-Matti, Kataja, Vesa, Auvinen, Paivi, Andrulis, Irene L., Glendon, Gord, Knight, Julia A., Weerasooriya, Nayana, Cox, Angela, Reed, Malcolm W. R., Cross, Simon S., Dunning, Alison M., Ahmed, Shahana, Shah, Mitul, Brauch, Hiltrud, Ko, Yon-Dschun, Bruning, Thomas, GENICA Network, Lambrechts, Diether, Reumers, Joke, Smeets, Ann, Wang-Gohrke, Shan, Hall, Per, Dzene, Kamila, Liu, Jianjun, Irwanto, Astrid K., Chenevix-Trench, Georgia, Holland, Helene, kConFab, AOCS, Giles, Graham G., Baglietto, Laura, Severi, Gianluca, Bojensen, Stig E., Nordestgaard, Borge G., Flyger, Henrik, John, Esther M., West, Dee W., Whittemore, Alice S., Vachon, Celine, Olson, Janet E., Fredericksen, Zachary, Kosel, Matthew, Hein, Rebecca, Vrieling, Alina, Flesch-Janys, Dieter, Heinz, Judith, Beckmann, Matthias W., Heusinger, Katharina, Ekici, Arif B., Haeberle, Lothar, Humphreys, Manjeet K., Morrison, Jonathan, Easton, Doug F., Pharoah, Paul D., Garcia-Closas, Montserrat, Goode, Ellen L., Chang-Claude, Jenny, Brown, Melissa, Cummings, Margaret and Lakhani, Sunil (2010) Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study. Breast Cancer Research, 12 6: R110.1-R110.11. doi:10.1186/bcr2797 269 69 43 Cited 38 times in Scopus38 0
Bolton, Kelly L., Chenevix-Trench, Georgia, Goh, Cindy, Sadetzki, Siegal, Ramus, Susan J., Karlan, Beth Y., Lambrechts, Diether, Despierre, Evelyn, Barrowdale, Daniel, McGuffog, Lesley, Healey, Sue, Easton, Douglas F., Sinilnikova, Olga, Benitez, Javier, Garcia, María J., Neuhausen, Susan, Gail, Mitchell H., Hartge, Patricia, Peock, Susan, Frost, Debra, Evans, Gareth, Eeles, Rosalind, Godwin, Andrew K., Daly, Mary B., Kwong, Ava, Ma, Edmond S. K., Lazaro, Conxi, Blanco, Ignacio, Montagna, Marco, D'Andrea, Emma, Nicoletto, Maria Ornella, Johnatty, Sharon E., Kruger, Susanne, Jensen, Allan, Hogdall, Estrid, Goode, Ellen L., Fridley, Brooke L., Loud, Jennifer T., Greene, Mark H., Mai, Phuong L., Chetrit, Angela, Lubin, Flora, Hirsh-Yechezkel, Galit, Glendon, Gord, Andrulis, Irene L., Toland, Amanda E., Senter, Leigha, Gore, Martin E., Gourley, Charlie, Michie, Caroline O., Song, Honglin, Tyrer, Jonathan, Whittemore, Alice S., McGuire, Valerie, Sieh, Weiva, Kristoffersson, Ulf, Olsson, Håkan, Borg, Åke, Levine, Douglas A., Steele, Linda, Beattie, Mary S., Chan, Salina, Nussbaum, Robert L., Moysich, Kirsten B., Gross, Jenny, Cass, Ilana, Walsh, Christine, Li, Andrew J., Leuchter, Ronald, Gordon, Ora, Garcia-Closas, Montserrat, Gayther, Simon A., Chanock, Stephen J., Antoniou, Antonis C., Pharoah, Paul D. P., EMBRACE, kConFab Investigators and Cancer Genome Atlas Research Network (2012) Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer. Jama-Journal of the American Medical Association, 307 4: 382-390. doi:10.1001/jama.2012.20 179   87 Cited 93 times in Scopus93 10
Spurdle, Amanda B., Lakhani, Sunil R., Da Silva, Leonard M., Balleine, Rosemary L., kConFab Investigators and Goldgar, David E. (2010) Bayes analysis provides evidence of pathogenicity for the BRCA1 c.135-1G>T (IVS3-1) and BRCA2 c.7977-1G>C (IVS17-1) variants displaying in vitro splicing results of equivocal clinical significance.. Human Mutation, 31 2: E1141-E1145. doi:10.1002/humu.21181 100   7 Cited 6 times in Scopus6 0
Waddell, N, Ten Haaf, A, Marsh, A, Johnson, J, Walker, LC, Gongora, M, Brown, M, Grover, P, Girolami, M, Grimmond, S, Chenevix-Trench, G, Spurdle, AB and kConFab Investigators (2008) BRCA1 and BRCA2 missense variants of high and low clinical significance influence lymphoblastoid cell line post-irradiation gene expression. PLoS Genetics, 4 5: Article Number: e1000080. doi:10.1371/journal.pgen.1000080 74   5 Cited 4 times in Scopus4 0
Spurdle, Amanda B., Whiley, Phillip J., Thompson, Bryony, Feng, Bingjian, Healey, Sue, Brown, Melissa A., Pettigrew, Christopher, kConFab, Van Asperen, Christi J., Ausems, Margreet G. E. M., Kattentidt-Mouravieva, Anna A., Pigg, Maritta H., Schmutzler, Rita K., Engel, Christoph, Meindl, Alfons, German Consortium of Hereditary Breast and Ovarian Cancer, Caputo, Sandrine, Sinilnikova, Olga M., Lidereau, Rosette, French COVAR group collaborators, Couch, Fergus J., Guidugli, Lucia, van Overeem Hansen, Thomas, Thomassen, Mads, Eccles, Diana M., Tucker, Kathy, Benitez, Javier, Domchek, Susan M., Toland, Amanda E., Van Rensburg, Elizabeth J., Wappenschmidt, Barbara, Borg, Åke, Vreeswijk, Maaike P. G ., Goldgar, David E. and ENIGMA Consortium (2012) BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk. Journal of Medical Genetics, 49 8: 525-532. doi:10.1136/jmedgenet-2012-101037 103 1 15 Cited 16 times in Scopus16 1
Waddell, Nic, Jonnalagadda, Jyoti, Marsh, Anna, Grist, Scott, Jenkins, Mark, Hobson, Karen, Taylor, Malcolm, Lindeman, Geoff J., Tavtigian, Sean V., Suthers, Graeme, Goldgar, David, Oefner, Peter J., kConFab Investigators, Taylor, Darrin, Grimmond, Sean, Khanna, Kum Kum and Chenevix-Trench, Georgia (2006) Characterization of the breast cancer associated ATM 7271T>G (V2424G) mutation by gene expression profiling. Genes Chromosomes and Cancer, 45 12: 1169-1181. doi:10.1002/gcc.20381 111   7 Cited 5 times in Scopus5 0
Mia M. Gaudet, Tomas Kirchhoff, Todd Green, Joseph Vijai, Joshua M. Korn, Candace Guiducci, Ayellet V. Segre, Kate McGee, Lesley McGuffog, Christiana Kartsonaki, Jonathan Morrison, Sue Healey, Olga M. Sinilnikova, Dominique Stoppa-Lyonnet, Sylvie Mazoyer, Marion Gauthier-Villars, Hagay Sobol, Michel Longy, Marc Frenay, GEMO Study Collaborators, Frans B. L. Hogervorst, Matti a. Rookus, J. Margriet Collee, Nicoline Hoogerbrugge, Kees E. P. van Roozendaal, HEBON Study Collaborators, Marion Piedmonte, Wendy Rubinstein, Stacy Nerenstone, Linda Van Le, Stephanie V. Blank, Trinidad Caldes, Miguel de la Hoya, Heli Nevanlinna, Kristiina Aittomaki, Conxi Lazaro, Ignacio Blanco, Adalgeir Arason, Oskar T. Johannsson, Rosa B. Barkardottir, Peter Devilee, Olofunmilayo I. Olopade, Susan L. Neuhausen, Xianshu Wang, Zachary S. Fredericksen, Paolo Peterlongo, Siranoush Manoukian, Monica Barile, Alessandra Viel, Paolo Radice, Catherine M. Phelan, Steven Narod, Gad Rennert, Flavio Lejbkowicz, Anath Flugelman, Irene L. Andrulis, Gord Glendon, Hilmi Ozcelik, OCGN, Amanda E. Toland, Marco Montagna, Emma D'Andrea, Eitan Friedman, Yael Laitman, Ake Borg, Mary Beattie, Susan J. Ramus, Susan M. Domchek, Katherine L. Nathanson, Tim Rebbeck, Spurdle, Amanda B., Chen, Xiaoqing, Helene Holland, kConFab, Esther M. John, John L. Hopper, Saundra s. Buys, Mary B. Daly, Melissa C. Southey, Mary Beth Terry, Nadine Tung, Thomas V. Overeem Hansen, Finn C. Nielsen, Mark H. Greene, Phuong L. Mai, Ana Osorio, Mercedes Duran, Rauel Andres, Javier Benitez, Jeffrey N. Weitzel, Judy Garber, Susan Peock, EMBRACE, Ute Hamann, Margaret Cook, Clare Oliver, Debra Frost, Radka Platte, D. Gareth Evans, Fiona Lalloo, Ros Eeles, Louise Izatt, Lisa Walker, Jacqueline Eason, Rita K. Schmutzler, Julian Barwell, Andrew K. Godwin, Barbara Wappenschmidt, Stefanie Engert, Norbert Arnold, Bert Gold, Michael Dean, Robert J. Klein, Dorothea Gadzicki, Fergus J. Couch, Chenevix-Trench, Georgia, Douglas F. Easton, Mark J. Daly, Antonis C. Antoniou, David M. Altshuler, Kenneth Offit, Brown, Melissa, Cummings, Margaret and Lakhani, Sunil (2010) Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. PLoS Genetics, 6 10: e1001183-1-e1001183-12. doi:10.1371/journal.pgen.1001183 255 1 45 Cited 3 times in Scopus3 1
Wang, Xianshu, Pankratz, V. Shane, Fredericksen, Zachary, Tarrell, Robert, Karaus, Mary, McGuffog, Lesley, Pharaoh, Paul D.P., Ponder, Bruce A.J., Dunning, Alison M., Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, EMBRACE, Sinilnikova, Olga M., Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Houdayer, Claude, GEMO, Hogervorst, Frans B.L., Hooning, Maartje J., Ligtenberg, Marjolijn J., HEBON, Spurdle, Amanda, Chenevix-Trench, Georgia, kConFab, Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Meindl, Alfons, Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Timothy R., Singer, Christian F., Gschwantler-Kaulich, Daphne, Dressler, Catherina, Fink, Anneliese, Szabo, Csilla I., Zikan, Michal, Foretova, Lenka, Claes, Kathleen, Thomas, Gilles, Hoover, Robert N., Hunter, David J., Chanock, Stephen J., Easton, Douglas F., Antoniou, Antonis C., Couch, Fergus J., Brown, Melissa, Cummings, Margaret and Lakhani, Sunil (2010) Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers. Human Molecular Genetics, 19 14: 2886-2897. doi:10.1093/hmg/ddq174 154 3 31 Cited 33 times in Scopus33 0
Flanagan, James M., Cocciardi, Sibylle, Waddell, Nic, Johnstone, Cameron N., Marsh, Anna, Henderson, Stephen, Simpson, Peter, da Silva, Leonard, kConFab Investigators, Khanna, Kumkum, Lakhani, Sunil, Boshoff, Chris, Chenevix-Trench, Georgia, Brown, Melissa, Cummings, Margaret and Edwards, Stacey (2010) DNA methylome of familial breast cancer identifies distinct profiles defined by mutation status. American Journal of Human Genetics, 86 3: 420-433. doi:10.1016/j.ajhg.2010.02.008 150 7 40 Cited 47 times in Scopus47 0
Perry, John R. B., Hsu, Yi-Hsiang, Chasman, Daniel I., Johnson, Andrew D., Elks, Cathy, Albrecht, Eva, Andrulis, Irene L., Beesley, Jonathan, Berenson, Gerald S., Bergmann, Sven, Bojesen, Stig E., Bolla, Manjeet K., Brown, Judith, Buring, Julie E., Campbell, Harry, Chang-Claude, Jenny, Chenevix-Trench, Georgia, Corre, Tanguy, Couch, Fergus J., Cox, Angela, Czene, Kamila, D'adamo, Adamo Pio, Davies, Gail, Deary, Ian J., Dennis, Joe, Easton, Douglas F., Engelhardt, Ellen G., Eriksson, Johan G., Esko, Tonu, Fasching, Peter A., Figueroa, Jonine D., Flyger, Henrik, Fraser, Abigail, Garcia-Closas, Montse, Gasparini, Paolo, Gieger, Christian, Giles, Graham, Guenel, Pascal, Haegg, Sara, Hall, Per, Hayward, Caroline, Hopper, John, Ingelsson, Erik, kConFab investigators, Kardia, Sharon L. R., Kasiman, Katherine, Knight, Julia A., Lahti, Jari, Lawlor, Debbie A., Magnusson, Patrik K. E., Margolin, Sara, Marsh, Julie A., Metspalu, Andres, Olson, Janet E., Pennell, Craig E., Polasek, Ozren, Rahman, Iffat, Ridker, Paul M., Robino, Antonietta, Rudan, Igor, Rudolph, Anja, Salumets, Andres, Schmidt, Marjanka K., Schoemaker, Minouk J., Smith, Erin N., Smith, Jennifer A., Southey, Melissa, Stoeckl, Doris, Swerdlow, Anthony J., Thompson, Deborah J., Truong, Therese, Ulivi, Sheila, Waldenberger, Melanie, Wang, Qin, Wild, Sarah, Wilson, James F., Wright, Alan F., Zgaga, Lina, Ong, Ken K., ReproGen Consortium, Murabito, Joanne M., Karasik, David and Murray, Anna (2014) DNA mismatch repair gene MSH6 implicated in determining age at natural menopause. Human Molecular Genetics, 23 9: 2490-2497. doi:10.1093/hmg/ddt620 25   Cited 1 times in Scopus1 4
Stevens, K.N., Garcia-Closas, M., Fredericksen, Z., Kosel, M., Pankratz, V.S., Hopper, J.L., Dite, G.S., Apicella, C., Southey, M.C., Schmidt, M.K., Broeks, A., Van 't Veer, L.J., Tollenaar, R.A.E.M., Fasching, P.A., Beckmann, M.W., Hein, A., Ekici, A.B., Johnson, N., Peto, J., dos Santos Silva, I., Gibson, L., Sawyer, E., Tomlinson, I., Kerin, M.J., Chanock, S., Lissowska, J., Hunter, D.J., Hoover, R.N., Thomas, G.D., Milne, R.L., Pérez, J.A., González-Neira, A., Benítez, J., Burwinkel, B., Meindl, A., Schmutzler, R.K., Bartrar, C.R., Hamann, U., Ko, Y.D., Brüning, T., Chang-Claude, J., Hein, R., Wang-Gohrke, S., Dörk, T., Schürmann, P., Bremer, M., Hillemanns, P., Bogdanova, N., Zalutsky, J.V., Rogov, Y.I., Antonenkova, N., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, V.-M., Hartikainen, J., Chenevix-Trench, G., Chen, X., Peterlongo, P., Bonanni, B., Bernard, L., Manoukian, S., Wang, X., Cerhan, J., Vachon, C.M., Olson, J., Giles, G.G., Baglietto, L., McLean, C.A., Severi, G., John, E.M., Miron, A., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Grip, M., Andrulis, I., Knight, J.A., Glendon, G., Mulligan, A.M., Cox, A., Brock, I.W., Elliott, G., Cross, S.S., Pharoah, P.P., Dunning, A.M., Pooley, K.A., Humphreys, M.K., Wang, J., Kang, D., Yoo, K.-Y., Noh, D.-Y., Sangrajrang, S., Gabrieau, V., Brennan, P., McKay, J., Anton-Culver, H., Ziogas, A., Couch, F.J., Easton, D.F., the GENICA Network, kConFab Investigators and Australian Ovarian Cancer Study Group (2011) Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk. British Journal of Cancer, 105 12: 1934-1939. doi:10.1038/bjc.2011.448 62 1 1 Cited 1 times in Scopus1 0
Walker, Logan C., Fredericksen, Zachary S., Wang, Xianshu, Tarrell, Robert, Pankratz, Vernon S., Lindor, Noralane M., Beesley, Jonathan, Healey, Sue, Chen, Xiaoqing, kConFab, Stoppa-Lyonnet, Dominique, Tirapo, Carole, Mazoyer, Sylvie, Giraud, Sophie, Frickeer, Jean-Pierre, Muller, Daniele, Delnatte, Capucine, GEMO Study Collaborators, Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Schonbuchner, Ines, Deissler, Helmut, Meindl, Alfons, Hogervorst, Frans B., Verheus, Martijn, Hooning, Maartje J., van den Ouweland, Ans M. W., Nelen, Marcel R., Ausems, Margreet G. E. M., Aalfs, Cora M., van Asperen, Christi J., Devilee, Peter, Gerrits, Monique M., Waisfisz, Quinten f, Szabo, Csilla I., ModSQuaD2, Easton, Douglas F., Peock, Susan, Cook, Margaret, Oliver, Clare T., Frost, Debra, Harrington, Patricia, Evans, D. Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Chu, Carol, Davidson, Rosemarie, Eccles, Diana, Ong, Kai-Ren, Cook, Jackie, EMBRACE, Rebbeck, Tim, Nathanson, Katherine L., Domchek, Susan M., Singer, Christian F., Gschwantler-Kaulich, Daphne, Dressler, Anne-Catharina, Pfeiler, Georg, Godwin, Andrew K., Heikkinen, Tuomas, Nevanlinna, Heli, Agnarsson, Bjarni A., Caligo, Maria Adelaide, Olsson, Hakan, Kristoffersson, Ulf, Liljegren, Annelie, Arver, Brita, Karlsson, Per, Melin, Beatrice, SWE-BRCA47, Sinilnikova, Olga M., McGuffog, Lesley, Antoniou, Antonis C., Chenevix-Trench, Georgia, Spurdle, Amanda B. and Couch, Fergus J. (2010) Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers. Breast Cancer Research, 12 6: R1020-1-R102-10. doi:10.1186/bcr2785 157 2 14 Cited 14 times in Scopus14 0
Arnold, Jeremy M., Choong, David Y. H., Thompson, Ella R., kConFab, Waddell, Nic, Lindeman, Geoffrey J., Visvader, Jane E., Campbell, Ian G., Chenevix-Trench, Georgia, Brown, Melissa, Cummings, Margaret and Edwards, Stacey (2010) Frequent somatic mutations of GATA3 in non-BRCA1/BRCA2 familial breast tumors, but not in BRCA1-, BRCA2- or sporadic breast tumors. Breast Cancer Research And Treatment, 119 2: 491-496. doi:10.1007/s10549-008-0269-x 100 1 13 Cited 15 times in Scopus15 0
Beesley, Jonathan, Pickett, Hilda A., Johnatty,Sharon E., Dunning, Alison M., Chen, Xiaoqing, Li, Jun, Michailidou, Kyriaki, Lu, Yi, Rider, David N., Palmieri, Rachel T., Stutz, Michael D., Lambrechts, Diether, Despierre, Evelyn, Lambrechts, Sandrina, Vergote, Ignace, Chang-Claude, Jenny, Nickels, Stefan, Vrieling, Alina, Flesch-Janys, Dieter, Wang-Gohrke, Shan, Eilber, Ursula, Bogdanova, Natalia, Antonenkova, Natalia, Runnebaum, Ingo B., Dörk, Thilo, Goodman, Marc T., Lurie, Galina, Wilkens, Lynne R., Matsuno, Rayna K., Kiemeney, Lambertus A., Aben, Katja K.H., Marees, Tamara, Massuger, Leon F. A. G., Fridley, Brooke L., Vierkant, Robert A., Bandera, Elisa V., Olson, Sara H., Orlow, Irene, Rodriguez-Rodriguez, Lorna, Cook, Linda S., Le, Nhu D., Brooks-Wilson, Angela, Kelemen, Linda E., Campbell, Ian, Gayther, Simon A., Ramus, Susan J., Gentry-Maharaj, Aleksandra, Menon, Usha, Ahmed, Shahana, Baynes, Caroline, Pharoah, Paul D., kConFab Investigators, Australian Ovarian Cancer Study Group, ABCTB Investigators, Muir, Kenneth, Lophatananon, Artitaya, Chaiwerawattana, Arkom, Wiangnon, Surapon, Macgregor, Stuart, Easton, Douglas F., Reddel, Roger R., Goode, Ellen L., Chenevix-Trench, Georgia and on behalf of the Ovarian Cancer Association Consortium (2011) Functional polymorphisms in the TERT promoter are associated with risk of serous epithelial ovarian and breast cancers. PLoS One, 6 9: e24987 .1-e24987 .6. doi:10.1371/journal.pone.0024987 78   14 Cited 13 times in Scopus13 1
Chenevix-Trench, Georgia, Healey, Sue, Lakhani, Sunil, Waring, Paul, Cummings, Margaret, Brinkworth, Ross, Deffenbaugh, Amie M., Burbidge, Lynn Anne, Pruss, Dmitry, Judkins, Thad, Scholl, Tom, Bekessy, Anna, Marsh, Anna, Lovelock, Paul, Wong, Ming, Tesoriero, Andrea, Renard, Helene, Southey, Melissa, Hopper, John L., Yannoukakos, Koulis, Brown, Melissa, kConFab Investigators, Easton, Douglas, Tavtigian, Sean V., Goldgar, David and Spurdle, Amanda B. (2006) Genetic and Histopathologic Evaluation of BRCA1 and BRCA2 DNA Sequence Variance of Unknown Clinical Significance. Cancer Research, 66 4: 2019-2027. doi:10.1158/0008-5472.CAN-05-3546 222   104 Cited 104 times in Scopus104 0
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