Antineoplastic chemotherapy and immunosuppression in liver transplant recipients: Squaring the circle? von Coupier, Antoine, Gallien, Yves, Boillot, Olivier, Walter, Thomas, Guillaud, Olivier, Vallin, Mélanie, Thimonier, Elsa, Erard, Domitille, Dumortier, Jérôme

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An exceptional case of refractory variceal bleeding occurring during liver transplantation rescued with esophageal stent von Coupier, Antoine, Pioche, Mathieu, Steer, Nadia, Zoulim, Fabien, Mohkam, Kayvan, Lebossé, Fanny

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Liver involvement in patients with telomere-related genes mutations: prevalence, clinical, radiological, pathological features, outcome and risk factors von Sidali, Sabrina, Borie, Raphaël, Flore, Sicre, Lainey, Elodie, Rautou, Pierre-Emmanuel, Cadranel, Jacques, Naccache, Jean-marc, Cottin, Vincent, Dumortier, Jérôme, Jacquemin, Emmanuel, Baptiste, Nousbaum Jean, Hirschi, Sandrine, Bourdin, Arnaud, Meszaros, Magdalena, Dharancy, Sebastien, Hilaire, Sophie, Mallet, Vincent, Martine, Reynaud-Gaubert, Terriou, Louis, Gottrand, Frédéric, Chahla, Wadih Abou, Khan, Jean Emmanuel, Carrier, Paul, Saliba, Faouzi, Rubbia-Brandt, Laura, Elkrief, Laure, de Lédinghen, Victor, Abergel, Armand, Olivier, Tournilhac, Chouik, Yasmina, Coupier, Antoine, Leblanc, Thierry, Ollivier-Hourmand, Isabelle, Khac, Eric Nguyen, Morisse-Pradier, Hélène, El Husseini, Kinan, Goria, Odile, Ibrahima, Ba, Roulot, Dominique, Bureau, Christophe, Nunes, Hilario, Valla, Dominique, Paradis, Valérie, Caroline, Kannengiesser, Plessier, Aurélie

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GS03 - Liver involvement in patients with telomere-related genes mutations: prevalence, clinical, radiological, pathological features, outcome and risk factors von Sidali, Sabrina, Borie, Raphaël, Flore, Sicre, Lainey, Elodie, Rautou, Pierre-Emmanuel, Cadranel, Jacques, Naccache, Jean-marc, Cottin, Vincent, Dumortier, Jérôme, Jacquemin, Emmanuel, Baptiste, Nousbaum Jean, Hirschi, Sandrine, Bourdin, Arnaud, Meszaros, Magdalena, Dharancy, Sebastien, Hilaire, Sophie, Mallet, Vincent, Martine, Reynaud-Gaubert, Terriou, Louis, Gottrand, Frédéric, Chahla, Wadih Abou, Khan, Jean Emmanuel, Carrier, Paul, Saliba, Faouzi, Rubbia-Brandt, Laura, Elkrief, Laure, de Lédinghen, Victor, Abergel, Armand, Olivier, Tournilhac, Chouik, Yasmina, Coupier, Antoine, Leblanc, Thierry, Ollivier-Hourmand, Isabelle, Khac, Eric Nguyen, Morisse-Pradier, Hélène, El Husseini, Kinan, Goria, Odile, Ibrahima, Ba, Roulot, Dominique, Bureau, Christophe, Nunes, Hilario, Valla, Dominique, Paradis, Valérie, Caroline, Kannengiesser, Plessier, Aurélie

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An exceptional case of refractory variceal bleeding occurring during liver transplantation rescued with esophageal stent von Coupier, Antoine, Pioche, Mathieu, Steer, Nadia, Zoulim, Fabien, Mohkam, Kayvan, Lebossé, Fanny

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The Succinate Dehydrogenase Genetic Testing in a Large Prospective Series of Patients with Paragangliomas von Burnichon, Nelly, Rohmer, Vincent, Amar, Laurence, Herman, Philippe, Leboulleux, Sophie, Darrouzet, Vincent, Niccoli, Patricia, Gaillard, Dominique, Chabrier, Gérard, Chabolle, Frédéric, Coupier, Isabelle, Thieblot, Philippe, Lecomte, Pierre, Bertherat, Jérôme, Wion-Barbot, Nelly, Murat, Arnaud, Venisse, Annabelle, Plouin, Pierre-François, Jeunemaitre, Xavier, Gimenez-Roqueplo, Anne-Paule

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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Coignard, Juliette, Dennis, Joe, Tyrer, Jonathan P., McGuffog, Lesley, Bolla, Manjeet K., Adank, Muriel A., Ahearn, Thomas, Aittomäki, Kristiina, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Arun, Banu K., Baynes, Caroline, Becher, Heiko, Bernstein, Leslie, Białkowska, Katarzyna, Blomqvist, Carl, Bojesen, Stig E., Brenner, Hermann, Buys, Saundra S., Caligo, Maria A., Castelao, Jose E., Chang-Claude, Jenny, Chanock, Stephen J., Chung, Wendy K., Collée, J. Margriet, Czene, Kamila, Devilee, Peter, Dwek, Miriam, Evans, D. Gareth, Flyger, Henrik, Fostira, Florentia, García-Closas, Montserrat, García-Sáenz, José A., Gaudet, Mia M., Gehrig, Andrea, Giles, Graham G., Goldgar, David E., Guénel, Pascal, Haeberle, Lothar, Haiman, Christopher A., Hall, Per, Hamann, Ute, Harrington, Patricia A., Hart, Steven N., He, Wei, Hogervorst, Frans B. L., Hollestelle, Antoinette, Hulick, Peter J., Hunter, David J., Jager, Agnes, Jones, Michael E., Kaaks, Rudolf, Kapoor, Pooja Middha, Karlan, Beth Y., Keeman, Renske, Kiiski, Johanna I., Kraft, Peter, Lambrechts, Diether, Lesueur, Fabienne, Lindstrom, Tricia, Mannermaa, Arto, Meindl, Alfons, Montagna, Marco, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, O’Brien, Katie M., Olsson, Håkan, Ottini, Laura, Park-Simon, Tjoung-Won, Pedersen, Inge Sokilde, Peterlongo, Paolo, Peto, Julian, Pharoah, Paul D. P., Polley, Eric C., Pujana, Miquel Angel, Punie, Kevin, Rashid, Muhammad U., Rennert, Gad, Saloustros, Emmanouil, Santella, Regina, Scheuner, Maren T., Schmidt, Gunnar, Scott, Christopher, Swerdlow, Anthony, Tamimi, Rulla M., Taylor, Jack A., Thull, Darcy L., Tung, Nadine, Vachon, Celine M., Vega, Ana, Wang, Qin, Wendt, Camilla, Yang, Xiaohong R., Ziogas, Argyrios, Park, Sue K., Thomassen, Mads, Simard, Jacques, Chenevix-Trench, Georgia

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Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus von Li, Qiyuan, Andrulis, Irene L., Arndt, Volker, Arver, Brita, Bandera, Elisa V., Barkardottir, Rosa B., Barrowdale, Daniel, Beckmann, Matthias W., Benitez, Javier, Bisogna, Maria, Bogdanova, Natalia, Bonanni, Bernardo, Børresen-Dale, Anne-Lise, Brauch, Hiltrud, Bruinsma, Fiona, Buhari, Shaik Ahmad, Burwinkel, Barbara, Campbell, Ian, Chang-Claude, Jenny, Chiquette, Jocelyne, Choi, Ji-Yeob, Czene, Kamila, Diez, Orland, Doherty, Jennifer A., Domchek, Susan M., Dörk, Thilo, Dumont, Martine, Figueroa, Jonine, Flyger, Henrik, Fostira, Florentia, Foulkes, William D., Friedman, Eitan, Frost, Debra, Gambino, Gaetana, Ganz, Patricia A., Garber, Judy, Gentry-Maharaj, Aleksandra, Ghoussaini, Maya, Giles, Graham G., Glasspool, Rosalind, Goldgar, David E., González-Neira, Anna, Goodman, Marc T., Guénel, Pascal, Haiman, Christopher A., Hallberg, Emily, Hartman, Mikael, Healey, Sue, Heitz, Florian, Høgdall, Estrid, Hogervorst, Frans B. L., Huzarski, Tomasz, Imyanitov, Evgeny N., John, Esther M., Kapuscinski, Miroslav, Karlan, Beth Y., Knight, Julia A., Konstantopoulou, Irene, Kosma, Veli-Matti, Kupryjanczyk, Jolanta, de la Hoya, Miguel, Lambrechts, Diether, De Leeneer, Kim, Li, Jingmei, Lubinski, Jan, Margolin, Sara, McGuffog, Lesley, McNeish, Iain, Meindl, Alfons, Mulligan, Anna Marie, Ness, Roberta B., Neuhausen, Susan L., Odunsi, Kunle, Olah, Edith, Orr, Nick, Osorio, Ana, Park, Sue Kyung, Poole, Elizabeth M., Rantala, Johanna, Risch, Harvey A., Sangrajrang, Suleeporn, Schildkraut, Joellen M., Schmidt, Marjanka K., Shu, Xiao-Ou, Sieh, Weiva, Singer, Christian F., Sinilnikova, Olga M., Slager, Susan, Southey, Melissa C., Stenmark-Askmalm, Marie, Tihomirova, Laima, Tung, Nadine, van Doorn, Helena C., Van't Veer, Laura J., Wentzensen, Nicolas, Wildiers, Hans, Zheng, Wei, Simard, Jacques, Pharoah, Paul D., Chenevix-Trench, Georgia

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The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA... von Lakeman, Inge M. M., Vos, Juliën A. M., Barnes, Daniel R., Adlard, Julian, Andrulis, Irene L., Arason, Adalgeir, Arnold, Norbert, Arun, Banu K., Balmaña, Judith, Barrowdale, Daniel, Benitez, Javier, Borg, Ake, Caldés, Trinidad, Caligo, Maria A., Chung, Wendy K., Claes, Kathleen B. M., Collée, J. Margriet, Couch, Fergus J., Daly, Mary B., Dennis, Joe, Dhawan, Mallika, Domchek, Susan M., Eeles, Ros, Engel, Christoph, Evans, D. Gareth, Feliubadaló, Lidia, Foretova, Lenka, Friedman, Eitan, Frost, Debra, Ganz, Patricia A., Gayther, Simon A., Gerdes, Anne-Marie, Godwin, Andrew K., Goldgar, David E., Hahnen, Eric, Hake, Christopher R., Hamann, Ute, Hogervorst, Frans B. L., Hooning, Maartje J., Hopper, John L., Hulick, Peter J., Imyanitov, Evgeny N., Isaacs, Claudine, Izatt, Louise, Jakubowska, Anna, James, Paul A., Janavicius, Ramunas, Jensen, Uffe Birk, Jiao, Yue, John, Esther M., Karlan, Beth Y., Kets, Carolien M., Kwong, Ava, Legrand, Clémentine, Leslie, Goska, Lesueur, Fabienne, Loud, Jennifer T., Manoukian, Siranoush, McGuffog, Lesley, Miller, Austin, Gomes, Denise Molina, Montagna, Marco, Mouret-Fourme, Emmanuelle, Neuhausen, Susan L., Nevanlinna, Heli, Yie, Joanne Ngeow Yuen, Olah, Edith, Olopade, Olufunmilayo I., Park, Sue K., Parsons, Michael T., Peterlongo, Paolo, Radice, Paolo, Rantala, Johanna, Rennert, Gad, Schmutzler, Rita K., Sharma, Priyanka, Simard, Jacques, Singer, Christian F., Stadler, Zsofia, Stoppa-Lyonnet, Dominique, Sutter, Christian, Tan, Yen Yen, Teixeira, Manuel R., Teo, Soo Hwang, Teulé, Alex, Thomassen, Mads, Thull, Darcy L., Tischkowitz, Marc, Toland, Amanda E., Tung, Nadine, Vega, Ana, Wappenschmidt, Barbara, Devilee, Peter, van Asperen, Christi J., Bernstein, Jonine L., Offit, Kenneth, Easton, Douglas F., Rookus, Matti A., Chenevix-Trench, Georgia, Schmidt, Marjanka K.

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Morphology and genomic hallmarks of breast tumours developed by ATM deleterious variant carriers von Renault, Anne-Laure, Mebirouk, Noura, Fuhrmann, Laetitia, Bataillon, Guillaume, Cavaciuti, Eve, Le Gal, Dorothée, Girard, Elodie, Popova, Tatiana, La Rosa, Philippe, Beauvallet, Juana, Eon-Marchais, Séverine, Dondon, Marie-Gabrielle, d'Enghien, Catherine Dubois, Laugé, Anthony, Chemlali, Walid, Raynal, Virginie, Labbé, Martine, Bièche, Ivan, Baulande, Sylvain, Bay, Jacques-Olivier, Berthet, Pascaline, Caron, Olivier, Buecher, Bruno, Faivre, Laurence, Fresnay, Marc, Gauthier-Villars, Marion, Gesta, Paul, Janin, Nicolas, Lejeune, Sophie, Maugard, Christine, Moutton, Sébastien, Venat-Bouvet, Laurence, Zattara, Hélène, Fricker, Jean-Pierre, Gladieff, Laurence, Coupier, Isabelle, Chenevix-Trench, Georgia, Hall, Janet, Vincent-Salomon, Anne, Stoppa-Lyonnet, Dominique, Andrieu, Nadine, Lesueur, Fabienne

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Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Coignard, Juliette, Dennis, Joe, Tyrer, Jonathan P., McGuffog, Lesley, Bolla, Manjeet K., Adank, Muriel A., Ahearn, Thomas, Aittomäki, Kristiina, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Arun, Banu K., Baynes, Caroline, Bernstein, Leslie, Białkowska, Katarzyna, Blomqvist, Carl, Bojesen, Stig E., Brenner, Hermann, Buys, Saundra S., Caligo, Maria A., Castelao, Jose E., Chang-Claude, Jenny, Chanock, Stephen J., Chung, Wendy K., Collée, J. Margriet, Czene, Kamila, Devilee, Peter, Dwek, Miriam, Evans, D. Gareth, Flyger, Henrik, Fostira, Florentia, García-Closas, Montserrat, García-Sáenz, José A., Gaudet, Mia M., Gehrig, Andrea, Giles, Graham G., Goldgar, David E., Guénel, Pascal, Haeberle, Lothar, Haiman, Christopher A., Hall, Per, Hamann, Ute, Harrington, Patricia A., Hart, Steven N., He, Wei, Hogervorst, Frans B. L., Hollestelle, Antoinette, Hulick, Peter J., Hunter, David J., Jager, Agnes, Jones, Michael E., Kaaks, Rudolf, Kapoor, Pooja Middha, Karlan, Beth Y., Keeman, Renske, Kiiski, Johanna I., Kraft, Peter, Kurian, Allison W., Lambrechts, Diether, Lesueur, Fabienne, Lindstrom, Tricia, Mannermaa, Arto, Meindl, Alfons, Montagna, Marco, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, O’Brien, Katie M., Olsson, Håkan, Ottini, Laura, Park-Simon, Tjoung-Won, Pedersen, Inge Sokilde, Peterlongo, Paolo, Peto, Julian, Pharoah, Paul D. P., Polley, Eric C., Pujana, Miquel Angel, Punie, Kevin, Rashid, Muhammad U., Rennert, Gad, Saloustros, Emmanouil, Santella, Regina, Scheuner, Maren T., Schmidt, Gunnar, Scott, Christopher, Swerdlow, Anthony, Tamimi, Rulla M., Taylor, Jack A., Thull, Darcy L., Tung, Nadine, Vachon, Celine M., Vega, Ana, Wang, Qin, Wendt, Camilla, Yang, Xiaohong R., Ziogas, Argyrios, Park, Sue K., Thomassen, Mads, Simard, Jacques, Chenevix-Trench, Georgia

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Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers von Blanco, Ignacio, Kuchenbaecker, Karoline, Cuadras, Daniel, Wang, Xianshu, Barrowdale, Daniel, de Garibay, Gorka Ruiz, Librado, Pablo, Sánchez-Gracia, Alejandro, Rozas, Julio, Bonifaci, Núria, McGuffog, Lesley, Pankratz, Vernon S, Islam, Abul, Mateo, Francesca, Berenguer, Antoni, Petit, Anna, Català, Isabel, Brunet, Joan, Feliubadaló, Lidia, Tornero, Eva, Benítez, Javier, Osorio, Ana, Ramón y Cajal, Teresa, Nevanlinna, Heli, Aittomäki, Kristiina, Arun, Banu K, Toland, Amanda E, Karlan, Beth Y, Walsh, Christine, Lester, Jenny, Greene, Mark H, Mai, Phuong L, Nussbaum, Robert L, Andrulis, Irene L, Domchek, Susan M, Nathanson, Katherine L, Rebbeck, Timothy R, Barkardottir, Rosa B, Jakubowska, Anna, Lubinski, Jan, Durda, Katarzyna, Jaworska-Bieniek, Katarzyna, Claes, Kathleen, Van Maerken, Tom, Díez, Orland, Hansen, Thomas V, Jønson, Lars, Gerdes, Anne-Marie, Ejlertsen, Bent, de la Hoya, Miguel, Caldés, Trinidad, Dunning, Alison M, Oliver, Clare, Fineberg, Elena, Cook, Margaret, Peock, Susan, McCann, Emma, Murray, Alex, Jacobs, Chris, Pichert, Gabriella, Lalloo, Fiona, Chu, Carol, Dorkins, Huw, Paterson, Joan, Ong, Kai-Ren, Teixeira, Manuel R, Hogervorst, Frans B L, van der Hout, Annemarie H, Seynaeve, Caroline, van der Luijt, Rob B, Ligtenberg, Marjolijn J L, Devilee, Peter, Wijnen, Juul T, Rookus, Matti A, Meijers-Heijboer, Hanne E J, Blok, Marinus J, van den Ouweland, Ans M W, Aalfs, Cora M, Rodriguez, Gustavo C, Phillips, Kelly-Anne A, Piedmonte, Marion, Nerenstone, Stacy R, Bae-Jump, Victoria L, O'Malley, David M, Ratner, Elena S, Schmutzler, Rita K, Wappenschmidt, Barbara, Rhiem, Kerstin, Engel, Christoph, Meindl, Alfons, Ditsch, Nina, Arnold, Norbert, Plendl, Hansjoerg J, Niederacher, Dieter, Sutter, Christian, Wang-Gohrke, Shan, Steinemann, Doris, Preisler-Adams, Sabine, Kast, Karin, Varon-Mateeva, Raymonda

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Mutation analysis of PALB2 gene in French breast cancer families von Damiola, Francesca, Schultz, Inès, Barjhoux, Laure, Sornin, Valérie, Dondon, Marie-Gabrielle, Eon-Marchais, Séverine, Marcou, Morgane, Caron, Olivier, Gauthier-Villars, Marion, de Pauw, Antoine, Luporsi, Elisabeth, Berthet, Pascaline, Delnatte, Capucine, Bonadona, Valérie, Maugard, Christine, Pujol, Pascal, Lasset, Christine, Longy, Michel, Bignon, Yves-Jean, Fricker, Jean-Pierre, Andrieu, Nadine, Sinilnikova, Olga M., Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Muller, Danièle

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Telomere length, ATM mutation status and cancer risk in Ataxia-Telangiectasia families von Renault, Anne-Laure, Mebirouk, Noura, Cavaciuti, Eve, Le Gal, Dorothée, Lecarpentier, Julie, d'Enghien, Catherine Dubois, Laugé, Anthony, Dondon, Marie-Gabrielle, Labbé, Martine, Lesca, Gaetan, Leroux, Dominique, Gladieff, Laurence, Adenis, Claude, Faivre, Laurence, Gilbert-Dussardier, Brigitte, Lortholary, Alain, Fricker, Jean-Pierre, Dahan, Karin, Bay, Jacques-Olivier, Longy, Michel, Buecher, Bruno, Janin, Nicolas, Zattara, Hélène, Berthet, Pascaline, Combès, Audrey, Coupier, Isabelle, Hall, Janet, Stoppa-Lyonnet, Dominique, Andrieu, Nadine, Lesueur, Fabienne

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No Association of Early-Onset Breast or Ovarian Cancer with Early-Onset Cancer in Relatives in BRCA1 or BRCA2 Mutation Families von Imbert-Bouteille, Marion, Corsini, Carole, Picot, Marie-Christine, Mizrahy, Lucas, Akouete, Sandrine, Huguet, Helena, Thomas, Frédéric, Geneviève, David, Taourel, Patrice, Ychou, Marc, Galibert, Virginie, Rideau, Chloé, Baudry, Karen, Kogut Kubiak, Tatiana, Coupier, Isabelle, Hobeika, Rémy, Macary, Yvette, Toledano, Alain, Solassol, Jérôme, Maalouf, Antoine, Daures, Jean-Pierre, Pujol, Pascal

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The FANCM:p.Arg658 truncating variant is associated with risk of triple-negative breast cancer von Catucci, Irene, Caleca, Laura, Lasheras, Sandra Viz, Kiiski, Johanna I., Michailidou, Kyriaki, Bolla, Manjeet K., Cadoo, Karen, Arnold, Norbert, Aronson, Kristan J., Auvinen, Päivi, Barrowdale, Daniel, Barwell, Julian, Beane Freeman, Laura E., Behrens, Sabine, Blanco, Amie M., Blomqvist, Carl, Bojesen, Anders, Bojesen, Stig E., Bonanni, Bernardo, Buys, Saundra S., Caligo, Maria A., Castelao, Jose E., Chang-Claude, Jenny, Clarke, Christine L., Cybulski, Cezary, de la Hoya, Miguel, Dite, Gillian S., dos-Santos-Silva, Isabel, Eccles, Diana M., Eriksson, Mikael, Evans, D. Gareth, Figueroa, Jonine, Flyger, Henrik, Friebel, Tara M., Gago-Dominguez, Manuela, Garber, Judy, García-Closas, Montserrat, Gayther, Simon A., Giles, Graham G., Goldberg, Mark S., Guénel, Pascal, Gutierrez-Barrera, Angelica M., Haiman, Christopher A., Heyworth, Jane, Hollestelle, Antoinette, Howell, Anthony, Hu, Chunling, Jakimovska, Milena, James, Paul, John, Esther M., Jung, Audrey, Lambrechts, Diether, Lubinski, Jan, Manoochehri, Mehdi, Manoukian, Siranoush, Margolin, Sara, Maurer, Tabea, Mebirouk, Noura, Miller, Austin, Nathanson, Katherine L., Newman, William G., Offit, Kenneth, Olshan, Andrew F., Pocza, Timea, Rack, Brigitte, Rau-Murthy, Rohini, Rookus, Matti A., Ross, Eric A., Ruebner, Matthias, Scheuner, Maren T., Schmutzler, Rita K., Schneider, Michael, Scott, Christopher, Sharma, Priyanka, Simard, Jacques, Singer, Christian F., Thull, Darcy L., Tischkowitz, Marc, Torres, Diana, Troester, Melissa A., Truong, Thérèse, Untch, Michael, Vachon, Celine M., van Veen, Elke M., Vega, Ana, Viel, Alessandra, Wieme, Greet, Ziogas, Argyrios, McGuffog, Lesley, Pharoah, Paul D. P., Fostira, Florentia, Andrulis, Irene L., Ramus, Susan J., Greene, Mark H., Milne, Roger L., Chenevix-Trench, Georgia, Dörk, Thilo, Schmidt, Marjanka K., Easton, Douglas F., Couch, Fergus J.

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Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers von 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, Sinilnikova, Olga M., Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Houdayer, Claude, Hogervorst, Frans B.L., Hooning, Maartje J., Ligtenberg, Marjolijn J., Spurdle, Amanda, Chenevix-Trench, Georgia, 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.

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The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers von Garcia, Amandine I., Cox, David G., Barjhoux, Laure, Verny-Pierre, Carole, Barnes, Daniel, Antoniou, Antonis C., Stoppa-Lyonnet, Dominique, Sinilnikova, Olga M., Mazoyer, Sylvie

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Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers von 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

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Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers von SPURDLE, Amanda B, MARQUART, Louise, GSCHWANTLER-KAULICH, Daphne, BLUM, Joanne L, TUNG, Nadine, WEITZEL, Jeff, LYNCH, Henry, GARBER, Judy, EASTON, Douglas F, PEOCK, Susan, COOK, Margaret, OLIVER, Clare T, MCGUFFOG, Lesley, FROST, Debra, CONROY, Don, GARETH EVANS, D, LALLOO, Fiona, EELES, Ros, IZATT, Louise, DAVIDSON, Rosemarie, CHU, Carol, ECCLES, Diana, SELKIRK, Christina G, HEALEY, Sue, DALY, Mary, ISAACS, Claudine, STOPPA-LYONNET, Dominique, SINILNIKOVA, Olga M, BUECHER, Bruno, BELOTTI, Muriel, MAZOYER, Sylvie, BARJHOUX, Laure, VERNY-PIERRE, Carole, LASSET, Christine, SINILNIKOVA, Olga, DREYFUS, Hélène, PUJOL, Pascal, COLLONGE-RAME, Marie-Agnès, ROOKUS, Matti A, VERHOEF, Senno, KRIEGE, Mieke, HOOGERBRUGGE, Nicoline, AUSEMS, Margreet G. E. M, VAN OS, Theo A, WIJNEN, Juul, FEI WAN, DEVILEE, Peter, MEIJERS-HEIJBOER, Hanne E. J, BLOK, Marinus J, HEIKKINEN, Tuomas, NEVANLINNA, Heli, JAKUBOWSKA, Anna, LUBINSKI, Jan, HUZARSKI, Tomasz, BYRSKI, Tomasz, DUROCHER, Francine, XIAOQING CHEN, BEESLEY, Jonathan, SINGER, Christian F, DRESSLER, Anne-Catharine

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