BRCA Mutations Increase Fertility in Families at Hereditary Breast/Ovarian Cancer Risk by Kwiatkowski, Fabrice, Arbre, Marie, Bidet, Yannick, Laquet, Claire, Uhrhammer, Nancy, Bignon, Yves-Jean

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The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer by OLIVIER, Magali, LANGERØD, Anita, VARLEY, Jennifer, BIGNON, Yves, UHRHAMMER, Nancy, WINQVIST, Robert, JUKKOLA-VUORINEN, Arja, NIEDERACHER, Dieter, KATO, Shunsuke, ISHIOKA, Chikashi, HAINAUT, Pierre, BØRRESEN-DALE, Anne-Lise, CARRIERI, Patrizia, BERGH, Jonas, KLAAR, Sigrid, EYFJORD, Jorunn, THEILLET, Charles, RODRIGUEZ, Carmen, LIDEREAU, Rosette, BIECHE, Ivan

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Diagnosis of PTEN mosaicism: the relevance of additional tumor DNA sequencing. A case report and review of the literature by Cavaillé, Mathias, Crampon, Delphine, Achim, Viorel, Bubien, Virginie, Uhrhammer, Nancy, Privat, Maud, Ponelle-Chachuat, Flora, Gay-Bellile, Mathilde, Lepage, Mathis, Ouedraogo, Zangbéwendé Guy, Jones, Natalie, Bidet, Yannick, Sevenet, Nicolas, Bignon, Yves-Jean

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Involvement of IL17A, IL17F and IL23R Polymorphisms in Colorectal Cancer Therapy by Omrane, Inés, Medimegh, Imen, Baroudi, Olfa, Ayari, Hager, Bedhiafi, Walid, Stambouli, Nejla, Ferchichi, Marwa, Kourda, Nadia, Bignon, Yves-Jean, Uhrhammer, Nancy, Mezlini, Amel, Bougatef, Karim, Benammar-Elgaaied, Amel

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Association between hereditary predisposition to common cancers and congenital multimalformations by Kwiatkowski, Fabrice, Perthus, Isabelle, Uhrhammer, Nancy, Francannet, Christine, Arbre, Marie, Bidet, Yannick, Bignon, Yves‐Jean

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Abstract 5224: Next-generation sequencing of a panel of genes contributing to breast cancer risk by Uhrhammer, Nancy A., El Saghir, Nagi, Bidet, Yannick, Delahaye-Sourdeix, Manon, Ponelle, Flora, Ollier, Marie, Viala, Sandrine, Kreidieh, Firas, Khoueiry-Zgheib, Nathalie, Bignon, Yves-Jean

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Early Onset Multiple Primary Tumors in Atypical Presentation of Cowden Syndrome Identified by Whole-Exome-Sequencing by Cavaillé, Mathias, Ponelle-Chachuat, Flora, Uhrhammer, Nancy, Viala, Sandrine, Gay-Bellile, Mathilde, Privat, Maud, Bidet, Yannick, Bignon, Yves-Jean

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Rare duplication of the CDC73 gene and atypical hyperparathyroidism‐jaw tumor syndrome: A case report and review of the literature by Garrigues, Guilhaume, Batisse‐Lignier, Marie, Uhrhammer, Nancy, Privat, Maud, Ponelle‐Chachuat, Flora, Kelly, Antony, Gay‐Bellile, Mathilde, Viala, Sandrine, Bidet, Yannick, Bignon, Yves‐Jean, Cavaillé, Mathias

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Rad50 c.687delT Does Not Contribute Significantly to Familial Breast Cancer in a French Population by UHRHAMMER, Nancy, DELORT, Laetitia, BIGNON, Yves-Jean

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Werner syndrome and mutations of the WRN and LMNA genes in France by Uhrhammer, Nancy A., Lafarge, Laurence, Santos, Laetitia Dos, Domaszewska, Anna, Lange, Magdalena, Yang, Yong, Aractingi, Selim, Bessis, Didier, Bignon, Yves-Jean

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Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome by 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 by Fachal, Laura, Aschard, Hugues, Beesley, Jonathan, Barnes, Daniel R, Allen, Jamie, Kristensen, Vessela N, Kar, Siddhartha, Pooley, Karen A, Dennis, Joe, Michailidou, Kyriaki

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RNA Panel Sequencing Is an Effective Tool to Help Classify Splice Variants for Clinical Oncogenetic Diagnosis by Privat, Maud, Ponelle-Chachuat, Flora, Viala, Sandrine, Uhrhammer, Nancy, Lepage, Mathis, Cayre, Anne, Bidet, Yannick, Bignon, Yves-Jean, Gay-Bellile, Mathilde, Cavaillé, Mathias

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CHEK2 contribution to hereditary breast cancer in non-BRCA families by Desrichard, Alexis, Bidet, Yannick, Uhrhammer, Nancy, Bignon, Yves-Jean

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Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach by Caputo, Sandrine M., Damiola, Francesca, Revillion, Françoise, Derive, Nicolas, Buisson, Adrien, Basset, Noémie, Schwartz, Mathias, Vilquin, Paul, Garrec, Celine, Privat, Maud, Gay-Bellile, Mathilde, Allary, Anne-Sophie, Belotti, Muriel, Benigni, Charlotte, Benusiglio, Patrick R., Berthet, Pascaline, Bézieau, Stéphane, Bidart, Marie, Bignon, Yves-Jean, Blanluet, Maud, Bloucard, Amelie, Bonnet, Françoise, Boulaire, Manon, Bouras, Ahmed, Brahimi, Afane, Bubien, Virginie, Chieze-Valéro, Stephanie, Cohen-Haguenauer, Odile, Collonge-Rame, Marie-Agnès, Coupier, Isabelle, Crivelli, Louise, Cusin, Véronica, De Pauw, Antoine, Delhomelle, Hélène, Demontety, Sophie, Denizeau, Philippe, Dreyfus, Helene, d’Enghein, Catherine Dubois, Dupré, Anaïs, Durlach, Anne, Dussart, Sophie, Fajac, Anne, Fert-Ferrer, Sandra, Fiévet, Alice, Fouillet, Robin, Mouret-Fourme, Emmanuelle, Gauthier-Villars, Marion, Gesta, Paul, Giraud, Sophie, Gladieff, Laurence, Goussot, Vincent, Guibert, Virginie, Guillerm, Erell, Guy, Christophe, Hardouin, Agnès, Ingster, Olivier, Jacquot-Sawka, Caroline, Jones, Natalie, Krieger, Sophie, Lacoste, Sofiane, Lallaoui, Hakima, Larbre, Helene, Laugé, Anthony, Le Mentec, Marine, Lecerf, Caroline, Le Gall, Jessica, Legros, Angélina, Lignon, Norbert, Doriane Livon, Lortholary, Alain, Mailliez, Audrey, Malsa, Sarah, Maugard, Christine, Menjard, Julie, Molière, Diane, Moncoutier, Virginie, Moretta-Serra, Jessica, Muller, Etienne, Nguyen Minh Tuan, Thien-vu, Noguchi, Tetsuro, Oca, Florine, Popovici, Cornel, Prieur, Fabienne, Raad, Sabine, Ricou, Agathe, Salle, Lucie, Saule, Claire, Sevenet, Nicolas, Suybeng, Voreak, Tennevet, Isabelle, Tenreiro, Henrique, Tinat, Julie, Toulas, Christine, Vande Perre, Pierre, Vaur, Dominique, Villy, Marie-Charlotte, Yvard, Alice, Zattara, Helene, Caron, Olivier, Boutry-Kryza, Nadia

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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers by 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 by 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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Case Series of 11 ICDH1/I Families Including Incidental Findings, Signet Ring Cell Colon Cancer and Review of the Literature by Lepage, Mathis, Uhrhammer, Nancy, Privat, Maud, Ponelle-Chachuat, Flora, Kossai, Myriam, Scanzi, Julien, Ouedraogo, Zangbéwendé Guy, Gay-Bellile, Mathilde, Bidet, Yannick, Cavaillé, Mathias

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Analysis of 11 candidate genes in 849 adult patients with suspected hereditary cancer predisposition by Cavaillé, Mathias, Uhrhammer, Nancy, Privat, Maud, Ponelle‐Chachuat, Flora, Gay‐Bellile, Mathilde, Lepage, Mathis, Molnar, Ioana, Viala, Sandrine, Bidet, Yannick, Bignon, Yves‐Jean

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Mutation screening of the BRCA1 gene in early onset and familial breast/ovarian cancer in Moroccan population by Laraqui, Abdelilah, Uhrhammer, Nancy, Lahlou-Amine, Idriss, El Rhaffouli, Hicham, El Baghdadi, Jamila, Dehayni, Mohamed, Moussaoui, Rahali Driss, Ichou, Mohamed, Sbitti, Yassir, Al Bouzidi, Abderrahman, Amzazi, Said, Bignon, Yves-Jean

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