Clinical implications of CTNNA1 germline mutations in asymptomatic carriers von Benusiglio, Patrick R., Colas, Chrystelle, Guillerm, Erell, Canard, Axelle, Delhomelle, Hélène, Warcoin, Mathilde, Bellanger, Jérôme, Eyries, Mélanie, Zizi, Mohamed, Netter, Jeanne, Soubrier, Florent, Parc, Yann, Mourregot, Anne, Maran Gonzalez, Aurélie, Cusin, Veronica, Denis, Jérôme A., Coupier, Isabelle, Svrcek, Magali, Coulet, Florence

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Is BRCA1/BRCA2‐related breast carcinogenesis estrogen dependent? von Noruzinia, Mehadad, Coupier, Isabelle, Pujol, Pascal

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Deletion of chromosomes 13q and 14q is a common feature of tumors with BRCA2 mutations von Rouault, Audrey, Banneau, Guillaume, Macgrogan, Gaëtan, Jones, Natalie, Elarouci, Nabila, Barouk-Simonet, Emmanuelle, Venat, Laurence, Coupier, Isabelle, Letouzé, Eric, de Reyniès, Aurélien, Bonnet, Françoise, Iggo, Richard, Sévenet, Nicolas, Longy, Michel

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Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families von GAD, Sophie, CAUX-MONCOUTIER, Virginie, CHEVRIER, Annie, ROSSI, Annick, FRICKER, Jean-Pierre, TAN DAT NGUYEN, DEMANGE, Liliane, AURIAS, Alain, BENSIMON, Aaron, STOPPA-LYONNET, Dominique, PAGES-BERHOUET, Sabine, GAUTHIER-VILLARS, Marion, COUPIER, Isabelle, PUJOL, Pascal, FRENAY, Marc, GILBERT, Brigitte, MAUGARD, Christine, BIGNON, Yves-Jean

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Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome von Bonadona, Valérie, Bonaïti, Bernard, Olschwang, Sylviane, Grandjouan, Sophie, Huiart, Laetitia, Longy, Michel, Guimbaud, Rosine, Buecher, Bruno, Bignon, Yves-Jean, Caron, Olivier, Colas, Chrystelle, Noguès, Catherine, Lejeune-Dumoulin, Sophie, Olivier-Faivre, Laurence, Polycarpe-Osaer, Florence, Nguyen, Tan Dat, Desseigne, Françoise, Saurin, Jean-Christophe, Berthet, Pascaline, Leroux, Dominique, Duffour, Jacqueline, Manouvrier, Sylvie, Frébourg, Thierry, Sobol, Hagay, Lasset, Christine, Bonaïti-Pellié, Catherine, French Cancer Genetics Network, for the

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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes von Fachal, Laura, Kar, Siddhartha, Moradi Marjaneh, Mahdi, Alonso, M. Rosario, Anton-Culver, Hoda, Arason, Adalgeir, Arun, Banu K., Auer, Paul L., Barrowdale, Daniel, Białkowska, Katarzyna, Bolla, Manjeet K., Brooks-Wilson, Angela, Caldés, Trinidad, Campbell, Ian, Carter, Brian D., Christiansen, Hans, Collée, J. Margriet, Couch, Fergus J., Cox, Angela, Cross, Simon S., de la Hoya, Miguel, Ding, Yuan Chun, Dite, Gillian S., Domchek, Susan M., Dwek, Miriam, Eriksson, Mikael, Evans, D. Gareth, Floris, Giuseppe, Gambino, Gaetana, Gapstur, Susan M., García-Sáenz, José A., Gaudet, Mia M., Giles, Graham G., Glendon, Gord, Goldgar, David E., Greene, Mark H., Grip, Mervi, Guénel, Pascal, Håkansson, Niclas, Hall, Per, Harrington, Patricia A., Heyworth, Jane, Hogervorst, Frans B. L., Howell, Anthony, Huang, Guanmengqian, Hulick, Peter J., Jakimovska, Milena, Jakubowska, Anna, Janavicius, Ramunas, Johnson, Nichola, Kaaks, Rudolf, Kapoor, Pooja Middha, Ko, Yon-Dschun, Konstantopoulou, Irene, Laitman, Yael, Lee, Eunjung, Lindblom, Annika, Lo, Wing-Yee, Lophatananon, Artitaya, Manoukian, Siranoush, Margolin, Sara, Martinez, Maria Elena, Mayes, Rebecca, McLean, Catriona, Mebirouk, Noura, Miller, Austin, Moreno, Fernando, Mulligan, Anna Marie, Narod, Steven A., Nassir, Rami, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, Osorio, Ana, Pankratz, V. Shane, Park, Sue K., Parsons, Michael T., Paul, James, Pedersen, Inge Sokilde, Prokofyeva, Darya, Ramus, Susan J., Rantala, Johanna, Risch, Harvey A., Saloustros, Emmanouil, Schoemaker, Minouk J., Scott, Rodney J., Shah, Mitul, Shen, Chen-Yang, Smichkoska, Snezhana, Tamimi, Rulla M., Thomassen, Mads, Toland, Amanda E., Tollenaar, Rob A. E. M., Troester, Melissa A., Vachon, Celine M., van Asperen, Christi J., Vega, Ana, Viel, Alessandra, Wildiers, Hans, Zhang, Yan

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A family with two cases of melanocytic tumors and fragile X syndrome von Lesage, Candice, Coupier, Isabelle, Guillot, Bernard

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Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study von Dowty, James G., Lee, Grant, Templeton, Allyson S., Alvarez, Karin, Ankathil, Ravindran, Austin, Rachel, Barca-Tierno, Verónica, Berthet, Pascaline, Boisjoli, Talya, Briollais, Laurent, Brunet, Joan, Bucksch, Karolin, Buettner, Reinhard, Burn, John, Caldés, Trinidad, Casey, Graham, Chew, Min H., Choi, Yun-hee, Church, James, Clendenning, Mark, Colas, Chrystelle, Coupier, Isabelle, de la Chapelle, Albert, Dębniak, Tadeusz, Della Valle, Adriana, Dominguez-Valentin, Mev, Engel, Christoph, Esperon, Patricia, Foulkes, William, Frebourg, Thierry, Gallinger, Steven, Garre, Pilar, Genuardi, Maurizio, Giraud, Sophie, Goodwin, Annabel, Green, Kate, Guindalini, Rodrigo S.C., Half, Elizabeth E., Hampel, Heather, Ho, Judy W.C., Hoogerbrugge, Nicoline, Hüneburg, Robert, Huntley, Vanessa, Jensen, Uffe B, Juhari, Wan K.W., Kloor, Matthias, Kupfer, Sonia S., Lagerstedt-Robinson, Kristina, Lalloo, Fiona, Lautrup, Charlotte K., Leggett, Barbara A., Lejeune, Sophie, Lindor, Noralane, Loeffler, Markus, Lucassen, Anneke M, Lynch, Patrick M., Møller, Pål, Navarro, Matilde, Neffa, Florencia, Neklason, Deborah, Nixon, Dawn M., Palmero, Edenir I., Pande, Mala, Parry, Susan, Pineda, Marta, Qiu, Jay, Ramesar, Raj, Rasmussen, Lene J., Redler, Silke, Ricciardiello, Luigi, Schulmann, Karsten, Schuster, Helène, Senter, Leigha, Seppälä, Toni T, Shtoyerman, Rakefet, Sijmons, Rolf H., Soto, Jose Luis, Spigelman, Allan, Steinke-Lange, Verena, Stoffel, Elena M., Strassburg, Christian P., Sunde, Lone, Therkildsen, Christina, Thibodeau, Steve, Tucker, Katherine M., Tunca, Berrin, Uhrhammer, Nancy, Vaccaro, Carlos, van Duijnhoven, Fränzel J.B., van Wanzeele, Meghan J., Vasen, Hans F.A., von Knebel Doeberitz, Magnus, von Salomé, Jenny, Ward, Robyn L., Wise, Paul E., Yamaguchi, Tatsuro, Zahary, Mohd N., Hopper, John L., Haile, Robert W., Jenkins, Mark A.

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ETMR-like infantile cerebellar embryonal tumors in the extended morphologic spectrum of DICER1-related tumors von Uro-Coste, Emmanuelle, Masliah-Planchon, Julien, Siegfried, Aurore, Blanluet, Maud, Lambo, Sander, Kool, Marcel, Roujeau, Thomas, Boetto, Sergio, Palenzuela, Gilles, Bertozzi, Anne-Isabelle, Gambart, Marion, Coupier, Isabelle, Oliver-Petit, Isabelle, Golmard, Lisa, Julia, Sophie, Savagner, Fréderique, Mohand-Oumoussa, Badreddine, Tauziede-Espariat, Arnault, Delisle, Marie-Bernadette, Figarella-Branger, Dominique, Bourdeaut, Franck, Rigau, Valérie

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Psychological and ethical issues raised by genomic in paediatric care pathway, a qualitative analysis with parents and childhood cancer patients von Droin-Mollard, Marion, de Montgolfier, Sandrine, Gimenez-Roqueplo, Anne-Paule, Flahault, Cécile, Petit, Arnaud, Bourdeaut, Franck, Julia, Sophie, Rial-Sebbag, Emmanuelle, Coupier, Isabelle, Simaga, Fatoumata, Brugières, Laurence, Guerrini-Rousseau, Léa, Claret, Béatrice, Cavé, Hélène, Strullu, Marion, Hervouet, Lucile, Lahlou-Laforêt, Khadija

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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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Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers von Mavaddat, Nasim, Antoniou, Antonis C., Mooij, Thea M., Hooning, Maartje J., Heemskerk-Gerritsen, Bernadette A., Nogues, Catherine, Laborde, Lilian, Breysse, Emmanuel, Stoppa-Lyonnet, Dominique, Gauthier-Villars, Marion, Buecher, Bruno, Caron, Olivier, Fourme-Mouret, Emmanuelle, Fricker, Jean-Pierre, Lasset, Christine, Bonadona, Valerie, Berthet, Pascaline, Faivre, Laurence, Luporsi, Elisabeth, Mari, Veronique, Gladieff, Laurence, Gesta, Paul, Sobol, Hagay, Eisinger, Francois, Nogues, Catherine, Longy, Michel, Dugast, Catherine, Colas, Chrystelle, Coupier, Isabelle, Pujol, Pascal, Corsini, Carole, Lortholary, Alain, Vennin, Philippe, Adenis, Claude, Nguyen, Tan Dat, Delnatte, Capucine, Tinat, Julie, Tennevet, Isabelle, Limacher, Jean-Marc, Maugard, Christine, Bignon, Yves-Jean, Demange, Liliane, Penet, Clotilde, Dreyfus, Helene, Cohen-Haguenauer, Odile, Venat-Bouvet, Laurence, Leroux, Dominique, Zattara-Cannoni, Helene, Fert-Ferrer, Sandra, Bera, Odile, Nogues, Catherine, Gauthier-Villars, Marion, Caron, Olivier, Gesta, Paul, Pujol, Pascal, Lortholary, Alain, Ellis, Steve, Ellis, Steve, Barrowdale, Daniel, Frost, Debra, Evans, D. Gareth, Izatt, Louise, Adlard, Julian, Eeles, Ros, Brewer, Carole, Tischkowitz, Marc, Henderson, Alex, Cook, Jackie, Eccles, Diana, Hogervorst, F. B. L., Hogervorst, F. B. L., Collee, J. M., van Asperen, C. J., Mensenkamp, A. R., Ausems, M. G. E. M., Meijers-Heijboer, H. E. J., van Engelen, K., Blok, M. J., Oosterwijk, J. C., Verloop, J., van den Broek, E., van Engelen, Klaartje, Mourits, Marian J. E., Ausems, Margreet G. E. M., Koppert, Linetta B., Hopper, John L., John, Esther M., Chung, Wendy K., Andrulis, Irene L., Daly, Mary B., Buys, Saundra S., Benitez, Javier, Caldes, Trinidad, Jakubowska, Anna, Simard, Jacques, Singer, Christian F., Tan, Yen, Olah, Edith, Navratilova, Marie, Foretova, Lenka

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Imaging Work-Up for Screening of Paraganglioma and Pheochromocytoma in SDHx Mutation Carriers: A Multicenter Prospective Study from the PGL.EVA Investigators von Gimenez-Roqueplo, Anne-Paule, Caumont-Prim, Aurore, Houzard, Claire, Hignette, Chantal, Hernigou, Anne, Halimi, Philippe, Niccoli, Patricia, Leboulleux, Sophie, Amar, Laurence, Borson-Chazot, Françoise, Cardot-Bauters, Catherine, Delemer, Brigitte, Chabolle, Frédéric, Coupier, Isabelle, Libé, Rossella, Peitzsch, Mirko, Peyrard, Séverine, Tenenbaum, Florence, Plouin, Pierre-François, Chatellier, Gilles, Rohmer, Vincent

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Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study von Schrijver, Lieske H., Antoniou, Antonis C., Olsson, Håkan, Mooij, Thea M., Roos-Blom, Marie-José, Azarang, Leyla, Adlard, Julian, Ahmed, Munaza, Barrowdale, Daniel, Davidson, Rosemarie, Donaldson, Alan, Eeles, Ros, Henderson, Alex, Izatt, Louise, Ong, Kai-Ren, Bonadona, Valérie, van Engelen, Klaartje, Menko, Fred H., Mourits, Marian J.E., Singer, Christian F., Tan, Yen Y., Schmutzler, Rita K., Gerdes, Anne-Marie, Simard, Jacques, Rantala, Johanna, Osorio, Ana, Hopper, John L., Beth Terry, Mary, Noguès, Catherine, Engel, Christoph, Kast, Karin, Goldgar, David E., van Leeuwen, Flora E., Easton, Douglas F., Andrieu, Nadine, Rookus, Matti A., Noguès, Catherine, Laborde, Lilian, Pontois, Pauline, Breysse, Emanuelle, Berline, Margot, Stoppa-Lyonnet, Dominique, Buecher, Bruno, Caron, Olivier, Mouret-Fourme, Emmanuelle, Saule, Claire, Fricker, Jean-Pierre, Lasset, Christine, Berthet, Pascaline, Faivre, Laurence, Luporsi, Elisabeth, Gladieff, Laurence, Chieze-Valéro, Stéphanie, Moretta, Jessica, Popovici, Cornel, Longy, Michel, Soubrier, Florent, Coupier, Isabelle, Corsini, Carole, Morin-Meschin, Marie-Emmanuelle, Lortholary, Alain, Adenis, Claude, Maillez, Audrey, Nguyen, Tan Dat, Tennevet, Isabelle, Maugard, Christine, Bignon, Yves-Jean, Gay Bellile, Mathilde, Penet, Clotilde, Dreyfus, Hélène, Cohen-Haguenauer, Odile, Venat-Bouvet, Laurence, Leroux, Dominique, Layet, Valérie, Lacaze, Elodie, Fert-Ferrer, Sandra, Bera, Odile, Tougeron, David, Lallaoui, Hakima, van Leeuwen, F.E., Schmidt, M.K., Jenner, D.J., Collée, J.M., van den Ouweland, A.M.W., Hooning, M.J., Boere, I.A., van Cronenburg, T.C.T.E.F., Wevers, M.R., Mensenkamp, A.R., Ausems, M.G.E.M., van de Beek, I., Gille, J.J.P., Gómez García, E.B., Blok, M.J., de Boer, M., Berger, L.P.V., de Bock, G.H., Siesling, S., Verloop, J., van den Broek, E.C.

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High Prevalence of Somatic Oncogenic Driver Alterations in Patients With NSCLC and Li-Fraumeni Syndrome von Mezquita, Laura, Jové, Maria, Nadal, Ernest, Kfoury, Maria, Morán, Teresa, Ricordel, Charles, Dhooge, Marion, Tlemsani, Camille, Léna, Hervé, Teulé, Alex, Álvarez, Jose-Valero, Raimbourg, Judith, Hiret, Sandrine, Lacroix, Ludovic, Menéndez, Mireia, Saldaña, Juana, Brunet, Joan, Lianes, Pilar, Coupier, Isabelle, Auclin, Edouard, Recondo, Gonzalo, Friboulet, Luc, Adam, Julien, Green, Emma, Planchard, David, Frébourg, Thierry, Capellà, Gabriel, Rouleau, Etienne, Lázaro, Conxi, Caron, Olivier, Besse, Benjamin

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Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing von Girard, Elodie, Eon‐Marchais, Séverine, Olaso, Robert, Renault, Anne‐Laure, Damiola, Francesca, Dondon, Marie‐Gabrielle, Barjhoux, Laure, Goidin, Didier, Meyer, Vincent, Le Gal, Dorothée, Beauvallet, Juana, Mebirouk, Noura, Lonjou, Christine, Coignard, Juliette, Marcou, Morgane, Cavaciuti, Eve, Baulard, Céline, Bihoreau, Marie‐Thérèse, Cohen‐Haguenauer, Odile, Leroux, Dominique, Penet, Clotilde, Fert‐Ferrer, Sandra, Colas, Chrystelle, Frebourg, Thierry, Eisinger, François, Adenis, Claude, Fajac, Anne, Gladieff, Laurence, Tinat, Julie, Floquet, Anne, Chiesa, Jean, Giraud, Sophie, Mortemousque, Isabelle, Soubrier, Florent, Audebert‐Bellanger, Séverine, Limacher, Jean‐Marc, Lasset, Christine, Lejeune‐Dumoulin, Sophie, Dreyfus, Hélène, Bignon, Yves‐Jean, Longy, Michel, Pujol, Pascal, Venat‐Bouvet, Laurence, Bonadona, Valérie, Berthet, Pascaline, Luporsi, Elisabeth, Maugard, Christine M., Noguès, Catherine, Delnatte, Capucine, Fricker, Jean‐Pierre, Gesta, Paul, Faivre, Laurence, Lortholary, Alain, Buecher, Bruno, Caron, Olivier, Gauthier‐Villars, Marion, Coupier, Isabelle, Servant, Nicolas, Boland, Anne, Mazoyer, Sylvie, Deleuze, Jean‐François, Stoppa‐Lyonnet, Dominique, Andrieu, Nadine, Lesueur, Fabienne

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Postzygotic mosaicism of SMARCB1 variants in patients with rhabdoid tumors: A not-so-rare condition exposing to successive tumors von Thomson, Grégory, Filser, Mathilde, Guerrini-Rousseau, Léa, Tauziede-Espariat, Arnault, Bourneix, Christine, Gauthier-Villars, Marion, Simaga, Fatoumata, Beccaria, Kévin, Faure-Conter, Cécile, Maureille, Aurélien, Zattara-Cannoni, Hélène, Andre, Nicolas, Entz-Werle, Natacha, Brugieres, Laurence, Mansuy, Ludovic, Denizeau, Philippe, Julia, Sophie, Ingster, Olivier, Lejeune, Sophie, Brahimi, Afane, Coupier, Isabelle, Bonadona, Valérie, Delattre, Olivier, Masliah-Planchon, Julien, Bourdeaut, Franck

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Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations von Pujol, Pascal, Vande Perre, Pierre, Faivre, Laurence, Sanlaville, Damien, Corsini, Carole, Baertschi, Bernard, Anahory, Michèle, Vaur, Dominique, Olschwang, Sylviane, Soufir, Nadem, Bastide, Noëlle, Amar, Sarah, Vintraud, Michèle, Ingster, Olivier, Richard, Stéphane, Le Coz, Pierre, Spano, Jean-Philippe, Caron, Olivier, Hammel, Pascal, Luporsi, Elisabeth, Toledano, Alain, Rebillard, Xavier, Cambon-Thomsen, Anne, Putois, Olivier, Rey, Jean-Marc, Hervé, Christian, Zorn, Caroline, Baudry, Karen, Galibert, Virginie, Gligorov, Joseph, Azria, David, Bressac-de Paillerets, Brigitte, Burnichon, Nelly, Spielmann, Marc, Zarca, Daniel, Coupier, Isabelle, Cussenot, Olivier, Gimenez-Roqueplo, Anne-Paule, Giraud, Sophie, Lapointe, Anne-Sophie, Niccoli, Patricia, Raingeard, Isabelle, Le Bidan, Muriel, Frebourg, Thierry, Rafii, Arash, Geneviève, David

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Contralateral breast cancer risk in patients with breast cancer and a germline-BRCA1/2 pathogenic variant undergoing radiation von van Barele, Mark, Akdeniz, Delal, Heemskerk-Gerritsen, Bernadette A M, Andrieu, Nadine, Noguès, Catherine, van Asperen, Christi J, Wevers, Marijke, Ausems, Margreet G E M, de Bock, Geertruida H, Dommering, Charlotte J, Gómez-García, Encarnacion B, van Leeuwen, Flora E, Mooij, Thea M, Easton, Douglas F, Antoniou, Antonis C, Evans, D Gareth, Izatt, Louise, Tischkowitz, Marc, Frost, Debra, Brewer, Carole, Olah, Edit, Simard, Jacques, Singer, Christian F, Thomassen, Mads, Kast, Karin, Rhiem, Kerstin, Engel, Christoph, de la Hoya, Miguel, Foretová, Lenka, Jakubowska, Anna, Jager, Agnes, Sattler, Margriet G A, Schmidt, Marjanka K, Hooning, Maartje J

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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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