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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Request full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text