Search Results - Oosterwijk, Melissa A.

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    BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer by Mesman, Romy L S, Martin, Charlotte, Calléja, Fabienne M G R, Meeks, Huong, Hallberg, Emily, Hinton, Jamie, Lilyquist, Jenna, Hu, Chunling, Aalfs, Cora M, Aittomäki, Kristiina, Andrulis, Irene, Anton-Culver, Hoda, Arndt, Volker, Beckmann, Matthias W, Benitez, Javier, Bogdanova, Natalia V, Bojesen, Stig E, Bolla, Manjeet K, Borresen-Dale, Anne-Lise, Brauch, Hiltrud, Brennan, Paul, Brenner, Hermann, Brüning, Thomas, Burwinkel, Barbara, Chang-Claude, Jenny, Chenevix-Trench, Georgia, Choi, Ji-Yeob, Collée, J Margriet, Cross, Simon S, Czene, Kamila, Darabi, Hatef, Dennis, Joe, Dörk, Thilo, Dos-Santos-Silva, Isabel, Dunning, Alison M, Fasching, Peter A, Figueroa, Jonine, Flyger, Henrik, García-Closas, Montserrat, Giles, Graham G, Glendon, Gord, Guénel, Pascal, Haiman, Christopher A, Hamann, Ute, Hartman, Mikael, Hogervorst, Frans B, Hollestelle, Antoinette, Hopper, John L, Ito, Hidemi, Kang, Daehee, Lambrechts, Diether, Li, Jingmei, Lindblom, Annika, Lophatananon, Artitaya, Lubinski, Jan, Machackova, Eva, Mannermaa, Arto, Margolin, Sara, Matsuo, Keitaro, Miao, Hui, Milne, Roger L, Nevanlinna, Heli, Olson, Janet E, Olswold, Curtis, Oosterwijk, Jan J C, Osorio, Ana, Peterlongo, Paolo, Pharoah, Paul D P, Pylkäs, Katri, Radice, Paolo, Rhenius, Valerie, Rudolph, Anja, Sawyer, Elinor J, Schmidt, Marjanka K, Schoemaker, Minouk J, Shah, Mitul, Shen, Chen-Yang, Shrubsole, Martha, Southey, Melissa C, Swerdlow, Anthony, Tomlinson, Ian, Torres, Diana, Truong, Thérèse, van Asperen, Christi J, Wang, Qin, Winqvist, Robert, Wu, Anna H, Yu, Jyh-Cherng, Zheng, Wei, Zheng, Ying, Foretova, Lenka, Varesco, Liliana, Moghadasi, Setareh, Spurdle, Amanda, Devilee, Peter, Vrieling, Harry, Monteiro, Alvaro N A, Goldgar, David E, Carreira, Aura, Vreeswijk, Maaike P G

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  8. 8

    Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 by Silvestri, Valentina, Barrowdale, Daniel, Mulligan, Anna Marie, Neuhausen, Susan L, Fox, Stephen, Karlan, Beth Y, Carter, Natalie J, Nathanson, Katherine L, Domchek, Susan M, Nussbaum, Robert L, Rantala, Johanna, Yoon, Sook-Yee, Caligo, Maria A, Spugnesi, Laura, Bojesen, Anders, Pedersen, Inge Sokilde, Jensen, Uffe Birk, Senter, Leigha, Andrulis, Irene L, Hulick, Peter J, Imyanitov, Evgeny N, Greene, Mark H, Mai, Phuong L, Rappaport-Fuerhauser, Christine, Kramer, Gero, Vijai, Joseph, Offit, Kenneth, Robson, Mark, Machackova, Eva, Foretova, Lenka, Navratilova, Marie, Vasickova, Petra, Hallberg, Emily, Ruddy, Kathryn J, Sharma, Priyanka, Teixeira, Manuel R, Pinto, Pedro, Arason, Adalgeir, Johannsson, Oskar Th, Barkardottir, Rosa B, Izquierdo, Angel, Pujana, Miguel Angel, Balmaña, Judith, Ivady, Gabriella, Papp, Janos, Olah, Edith, Kwong, Ava, Perez Segura, Pedro, Caldes, Trinidad, Van Maerken, Tom, Isaacs, Claudine, Elan, Camille, Lasset, Christine, Stoppa-Lyonnet, Dominique, Barjhoux, Laure, Belotti, Muriel, Gehrig, Andrea, Sutter, Christian, Hahnen, Eric, Kast, Karin, Wand, Dorothea, Godwin, Andrew K, Evans, D Gareth, Frost, Debra, Perkins, Jo, Adlard, Julian, Platte, Radka, Eeles, Ros, Ellis, Steve, Hamann, Ute, Fostira, Florentia, Fountzilas, George, Pasini, Barbara, Rizzolo, Piera, Cortesi, Laura, Papi, Laura, Varesco, Liliana, Zanna, Ines, Savarese, Antonella, Manoukian, Siranoush, Barile, Monica, Bonanni, Bernardo, Viel, Alessandra, Pensotti, Valeria, Tommasi, Stefania, Peterlongo, Paolo, Weitzel, Jeffrey N, Osorio, Ana, Benitez, Javier, McGuffog, Lesley, Gerdes, Anne-Marie, Ejlertsen, Bent, Hansen, Thomas V O, Ding, Yuan Chun, Goldgar, David E, Buys, Saundra S, Terry, Mary Beth, John, Esther M, Southey, Melissa, Antoniou, Antonis C

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    Breast cancer risks associated with missense variants in breast cancer susceptibility genes by Dorling, Leila, Carvalho, Sara, Allen, Jamie, Parsons, Michael T, Fortuno, Cristina, González-Neira, Anna, Heijl, Stephan M, Adank, Muriel A, Ahearn, Thomas U, Andrulis, Irene L, Becher, Heiko, Beckmann, Matthias W, Behrens, Sabine, Bermisheva, Marina, Bojesen, Stig E, Bolla, Manjeet K, Bremer, Michael, Briceno, Ignacio, Camp, Nicola J, Campbell, Archie, Castelao, Jose E, Chang-Claude, Jenny, Chanock, Stephen J, Chenevix-Trench, Georgia, Czene, Kamila, Dennis, Joe, Dörk, Thilo, Eriksson, Mikael, Evans, D Gareth, Fasching, Peter A, Figueroa, Jonine, Flyger, Henrik, Gabrielson, Marike, Gago-Dominguez, Manuela, García-Closas, Montserrat, Giles, Graham G, Glendon, Gord, Guénel, Pascal, Hadjisavvas, Andreas, Hahnen, Eric, Hall, Per, Hamann, Ute, Harkness, Elaine F, Hogervorst, Frans B L, Hollestelle, Antoinette, Hoppe, Reiner, Howell, Anthony, Jakubowska, Anna, Jung, Audrey, Khusnutdinova, Elza, Kim, Sung-Won, Ko, Yon-Dschun, Kristensen, Vessela N, Lakeman, Inge M M, Li, Jingmei, Lindblom, Annika, Loizidou, Maria A, Lophatananon, Artitaya, Lubiński, Jan, Luccarini, Craig, Madsen, Michael J, Mannermaa, Arto, Manoochehri, Mehdi, Margolin, Sara, Mavroudis, Dimitrios, Milne, Roger L, Mohd Taib, Nur Aishah, Muir, Kenneth, Nevanlinna, Heli, Newman, William G, Oosterwijk, Jan C, Park, Sue K, Peterlongo, Paolo, Radice, Paolo, Saloustros, Emmanouil, Sawyer, Elinor J, Schmutzler, Rita K, Shah, Mitul, Sim, Xueling, Southey, Melissa C, Surowy, Harald, Suvanto, Maija, Tomlinson, Ian, Torres, Diana, Truong, Thérèse, van Asperen, Christi J, Waltes, Regina, Wang, Qin, Yang, Xiaohong R, Pharoah, Paul D P, Schmidt, Marjanka K, Benitez, Javier, Dunning, Alison M, Teo, Soo Hwang, Kvist, Anders, de la Hoya, Miguel, Devilee, Peter, Spurdle, Amanda B, Vreeswijk, Maaike P G, Easton, Douglas F

    Published in Genome medicine
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    Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers by Robson, Mark, Andrulis, Irene L, Spurdle, Amanda B, Schmidt, Marjanka K, Engel, Christoph, Wappenschmidt, Barbara, Southey, Melissa, Radice, Paolo, Lee, Andrew, Rebbeck, Timothy R, James, Paul, Lester, Jenny, Daly, Mary B, Goldgar, David E, Tihomirova, Laima, van Rensburg, Elizabeth J, v O Hansen, Thomas, Gerdes, Anne-Marie, Nielsen, Finn C, Hart, Steven, Slager, Susan, Benitez, Javier, Tafur, Isaac, Hander, Mary, Scuvera, Giulietta, Mariani, Paolo, Volorio, Sara, Varesco, Liliana, Papi, Laura, Tibiletti, Maria Grazia, Giannini, Giuseppe, Fostira, Florentia, Konstantopoulou, Irene, Garber, Judy, Brewer, Carole, Foo, Claire, Douglas, Fiona, Tischkowitz, Marc, Barwell, Julian, Ong, Kai-ren, Side, Lucy E, Rogers, Mark T, Morrison, Patrick J, Eeles, Ros, Hodgson, Shirley, Ellis, Steve, Godwin, Andrew K, Rhiem, Kerstin, Meindl, Alfons, Arnold, Norbert, Plendl, Hansjoerg, Niederacher, Dieter, Steinemann, Doris, Varon-Mateeva, Raymonda, Wang-Gohrke, Shan, Buecher, Bruno, Rouleau, Etienne, Damiola, Francesca, Faivre, Laurence, Longy, Michel, Sinilnikova, Olga M, Mazoyer, Sylvie, Caux-Moncoutier, Virginie, Isaacs, Claudine, Khan, Sofia, Meijers-Heijboer, Hanne E J, van der Hout, Annemarie H, Wijnen, Juul T, van Roozendaal, K E P, Mensenkamp, Arjen R, van der Luijt, Rob B, Teulé, Alex, Menendez, Mireia, Cybulski, Cezary, Gronwald, Jacek, Durda, Katarzyna, Arason, Adalgeir, Maugard, Christine, Montagna, Marco, Agata, Simona, Vijai, Joseph, Jacobs, Lauren, Fink-Retter, Anneliese, Rappaport, Christine, Kaulich, Daphne Gschwantler, Pfeiler, Georg, Tea, Muy-Kheng, Greene, Mark H, Imyanitov, Evgeny N, Toland, Amanda Ewart, Pedersen, Inge Sokilde, Berger, Raanan, Laitman, Yael, Rantala, Johanna, Arver, Brita, Loman, Niklas, Ehrencrona, Hans, Olopade, Olufunmilayo I, Easton, Douglas F, Offit, Kenneth

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    Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer by Kirchhoff, Tomas, Green, Todd, Vijai, Joseph, Korn, Joshua M, Guiducci, Candace, Segrè, Ayellet V, McGee, Kate, McGuffog, Lesley, Healey, Sue, Sinilnikova, Olga M, Stoppa-Lyonnet, Dominique, Gauthier-Villars, Marion, Sobol, Hagay, Longy, Michel, GEMO Study Collaborators, Hogervorst, Frans B L, Rookus, Matti A, Hoogerbrugge, Nicoline, van Roozendaal, Kees E P, Piedmonte, Marion, Rubinstein, Wendy, Nerenstone, Stacy, Van Le, Linda, Blank, Stephanie V, de la Hoya, Miguel, Nevanlinna, Heli, Aittomäki, Kristiina, Blanco, Ignacio, Arason, Adalgeir, Johannsson, Oskar T, Barkardottir, Rosa B, Devilee, Peter, Olopade, Olofunmilayo I, Neuhausen, Susan L, Wang, Xianshu, Fredericksen, Zachary S, Manoukian, Siranoush, Barile, Monica, Viel, Alessandra, Radice, Paolo, Phelan, Catherine M, Narod, Steven, Lejbkowicz, Flavio, Flugelman, Anath, Andrulis, Irene L, Glendon, Gord, Ozcelik, Hilmi, Toland, Amanda E, Montagna, Marco, D'Andrea, Emma, Friedman, Eitan, Laitman, Yael, Ramus, Susan J, Domchek, Susan M, Nathanson, Katherine L, Rebbeck, Tim, Spurdle, Amanda B, Chen, Xiaoqing, Holland, Helene, John, Esther M, Buys, Saundra S, Daly, Mary B, Southey, Melissa C, Terry, Mary Beth, Tung, Nadine, Overeem Hansen, Thomas V, Nielsen, Finn C, Greene, Mark H, Greene, Mark I, Osorio, Ana, Durán, Mercedes, Benítez, Javier, Weitzel, Jeffrey N, Garber, Judy, Hamann, Ute, Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Platte, Radka, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Walker, Lisa, Eason, Jacqueline, Barwell, Julian, Godwin, Andrew K, Schmutzler, Rita K, Wappenschmidt, Barbara, Engert, Stefanie, Arnold, Norbert, Dean, Michael, Gold, Bert, Klein, Robert J, Couch, Fergus J, Chenevix-Trench, Georgia, Easton, Douglas F, Daly, Mark J, Antoniou, Antonis C, Altshuler, David M

    Published in PLoS genetics
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    Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers by Ramus, Susan J., Kuchenbaecker, Karoline B., Beesley, Jonathan, Healey, Sue, Thomassen, Mads, Jensen, Uffe Birk, Skytte, Anne-Bine, Lindblom, Annika, Olsson, Håkan, Melin, Beatrice, Domchek, Susan M., Nathanson, Katherine L., Jakubowska, Anna, Lubinski, Jan, Jaworska, Katarzyna, Durda, Katarzyna, Złowocka, Elżbieta, Gronwald, Jacek, Huzarski, Tomasz, Byrski, Tomasz, Benitez, Javier, Tejada, Maria-Isabel, Aalfs, Cora M., Meijers-Heijboer, Hanne E.J., van Asperen, Christi J., van Roozendaal, K.E.P., Collée, J. Margriet, van der Luijt, Rob B., Frost, Debra, Platte, Radka, Fineberg, Elena, Evans, D. Gareth, Lalloo, Fiona, Jacobs, Chris, Adlard, Julian, Davidson, Rosemarie, Cook, Jackie, Paterson, Joan, Morrison, Patrick J., Kennedy, M. John, Godwin, Andrew K., Caux-Moncoutier, Virginie, Gauthier-Villars, Marion, Mazoyer, Sylvie, Lasset, Christine, Hardouin, Agnès, Berthet, Pascaline, Faivre, Laurence, Buys, Saundra, Beth Terry, Mary, Chung, Wendy K., John, Esther M, Tea, Muy-Kheng, Pfeiler, Georg, Fink-Retter, Anneliese, Hansen, Thomas v. O., Ejlertsen, Bent, Offit, Kenneth, Gaudet, Mia M., Vijai, Joseph, Robson, Mark, Phillips, Kelly-Anne, Hoffman, James S, Montagna, Marco, Tognazzo, Silvia, Isaacs, Claudine, Janavicius, Ramunas, Blanco, Ignacio, Navarro, Matilde, Karlan, Beth Y., Olah, Edith, Vaszko, Tibor, Teo, Soo-Hwang, Ganz, Patricia A., Diez, Orland, Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Meindl, Alfons, Arnold, Norbert, Niederacher, Dieter, Deissler, Helmut, Fiebig, Britta, Nevanlinna, Heli, Aittomäki, Kristiina, Plante, Marie, Spurdle, Amanda B., Ding, Yuan Chun, Lindor, Noralane, Fredericksen, Zachary, Pankratz, V. Shane, Peissel, Bernard, Bernard, Loris, Dolcetti, Riccardo, Radice, Paolo, Greene, Mark H., Mai, Phuong L., Ozcelik, Hilmi, Couch, Fergus J., Chenevix-Trench, Georgia

    Published in Human mutation
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    Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers by Im, Kate M., Kirchhoff, Tomas, Wang, Xianshu, Green, Todd, Chow, Clement Y., Korn, Joshua, Gaudet, Mia M., Fredericksen, Zachary, Shane Pankratz, V., Guiducci, Candace, Crenshaw, Andrew, McGuffog, Lesley, Kartsonaki, Christiana, Morrison, Jonathan, Healey, Sue, Sinilnikova, Olga M., Mai, Phuong L., Greene, Mark H., Piedmonte, Marion, Rubinstein, Wendy S., Hogervorst, Frans B., Rookus, Matti A., Collée, J. Margriet, Hoogerbrugge, Nicoline, Meijers-Heijboer, Hanne E. J., Van Roozendaal, Cees E., Perez-Segura, Pedro, Jakubowska, Anna, Huzarski, Tomasz, Blecharz, Paweł, Nevanlinna, Heli, Aittomäki, Kristiina, Lazaro, Conxi, Blanco, Ignacio, Barkardottir, Rosa B., D’Andrea, Emma, Devilee, Peter, Olopade, Olufunmilayo I., Peissel, Bernard, Bonanni, Bernardo, Peterlongo, Paolo, Singer, Christian F., Rennert, Gad, Lejbkowicz, Flavio, Andrulis, Irene L., Ozcelik, Hilmi, Toland, Amanda Ewart, Caligo, Maria Adelaide, Beattie, Mary S., Chan, Salina, Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Timothy R., Phelan, Catherine, Narod, Steven, John, Esther M., Hopper, John L., Buys, Saundra S., Southey, Melissa C., Terry, Mary-Beth, Tung, Nadine, Hansen, Thomas v. O., Benitez, Javier, Weitzel, Jeffrey N., Garber, Judy, Hamann, Ute, Peock, Susan, Cook, Margaret, Oliver, Clare T., Frost, Debra, Eeles, Ros, Izatt, Louise, Paterson, Joan, Brewer, Carole, Hodgson, Shirley, Porteous, Mary, Walker, Lisa, Rogers, Mark T., Side, Lucy E., Godwin, Andrew K., Wappenschmidt, Barbara, Laitman, Yael, Deissler, Helmut, Varon-Mateeva, Raymonda, Preisler-Adams, Sabine, Kast, Karin, Venat-Bouvet, Laurence, Stoppa-Lyonnet, Dominique, Chenevix-Trench, Georgia, Easton, Douglas F., Klein, Robert J., Daly, Mark J., Friedman, Eitan, Dean, Michael, Clark, Andrew G., Altshuler, David M., Antoniou, Antonis C., Couch, Fergus J., Offit, Kenneth, Gold, Bert

    Published in Human genetics
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