A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinoma von Kientz, Caroline, Joly, Marie-Odile, Faivre, Laurence, Clemenson, Alix, Dalac, Sophie, Lepage, Côme, Chapusot, Caroline, Jacquot, Caroline, Schiappa, Renaud, Lebrun, Marine

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Hereditary Colorectal Cancer and Polyposis Syndromes Caused by Variants in Uncommon Genes von Bouras, Ahmed, Fabre, Aurélie, Zattara, Hélène, Handallou, Sandrine, Desseigne, Françoise, Kientz, Caroline, Prieur, Fabienne, Peysselon, Magalie, Legrand, Clémentine, Calavas, Laura, Saurin, Jean‐Christophe, Wang, Qing

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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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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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A novel POLD1 pathogenic variant identified in two families with a cancer spectrum mimicking Lynch syndrome von Legrand, Clémentine, Lebrun, Marine, Naïbo, Pierre, Peysselon, Magalie, Prieur, Fabienne, Kientz, Caroline, Desseigne, Françoise, Handallou, Sandrine, Rey, Jean-Marc, Nambot, Sophie, Goussot, Vincent, Hamzaoui, Nadim, Wang, Qing

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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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A new hybrid record linkage process to make epidemiological databases interoperable: application to the GEMO and GENEPSO studies involving BRCA1 and BRCA2 mutation carriers von Jiao, Yue, Lesueur, Fabienne, Azencott, Chloe-Agathe, Laurent, Maite, Mebirouk, Noura, Laborde, Lilian, Beauvallet, Juana, Dondon, Marie-Gabrielle, Eon-Marchais, Severine, Lauge, Anthony, Nogues, Catherine, Andrieu, Nadine, Stoppa-Lyonnet, Dominique, Caputo, Sandrine M.

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A new hybrid record linkage process to make epidemiological databases interoperable: application to the GEMO and GENEPSO studies involving BRCA1 and BRCA2 mutation carriers von Jiao, Yue, Lesueur, Fabienne, Azencott, Chloé-Agathe, Laurent, Maïté, Mebirouk, Noura, Laborde, Lilian, Beauvallet, Juana, Dondon, Marie-Gabrielle, Eon-Marchais, Séverine, Laugé, Anthony, Noguès, Catherine C., Andrieu, Nadine, Stoppa-Lyonnet, Dominique, Caputo, Sandrine M, Boutry-Kryza, Nadia, Calender, Alain, Giraud, Sophie, Léone, Mélanie, Bressac- de Paillerets, Brigitte, Caron, Olivier, Guillaud-Bataille, Marine, Bignon, Yves-Jean, Uhrhammer, Nancy, Bonadona, Valérie, Lasset, Christine, Berthet, Pascaline, Castera, Laurent, Vaur, Dominique, Bourdon, Violaine, Noguchi, Tetsuro, Popovici, Cornel, Remenieras, Audrey, Sobol, Hagay, Coupier, Isabelle, Harmand, Pierre-Olivier, Pujol, Pascal, Vilquin, Paul, Dumont, Aurélie, Révillion, Françoise, Muller, Danièle, Barouk-Simonet, Emmanuelle, Bonnet, Françoise, Bubien, Virginie, Longy, Michel, Sevenet, Nicolas, Gladieff, Laurence, Guimbaud, Rosine, Feillel, Viviane, Toulas, Christine, Dreyfus, Hélène, Leroux, Dominique, Peysselon, Magalie, Rebischung, Christine, Baurand, Amandine, Bertolone, Geoffrey, Coron, Fanny, Faivre, Laurence, Goussot, Vincent, Jacquot, Caroline, Sawka, Caroline, Kientz, Caroline, Lebrun, Marine, Prieur, Fabienne, Fert-Ferrer, Sandra, Mari, Véronique, Venat-Bouvet, Laurence, Bézieau, Stéphane, Delnatte, Capucine, Mortemousque, Isabelle, Coulet, Florence, Soubrier, Florent, Warcoin, Mathilde, Bronner, Myriam, Lizard, Sarab, Sokolowska, Johanna, Collonge-Rame, Marie-Agnès, Damette, Alexandre, Gesta, Paul, Lallaoui, Hakima, Chiesa, Jean, Molina-Gomes, Denise, Ingster, Olivier, Manouvrier-Hanu, Sylvie, Lejeune, Sophie, Pontois, Pauline, Lyonnet, Dominique Stoppa, Gauthier-Villars, Marion, Buecher, Bruno, Mouret-Fourme, Emmanuelle, Fricker, Jean-Pierre, Luporsi, Elisabeth, Frenay, Marc, Eisinger, Francois, Moretta, Jessica, Dugast, Catherine, Colas, Chrystelle, Lortholary, Alain, Vennin, Philippe, Adenis, Claude, Nguyen, Tan Dat

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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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MLH1 promoter hypermethylation: are you absolutely sure about the absence of MLH1 germline mutation? About a new case von Kientz, Caroline, Prieur, Fabienne, Clemenson, Alix, Joly, Marie-Odile, Stachowicz, Marie-Laure, Auclair, Jessie, Attignon, Valéry, Schiappa, Renaud, Wang, Qing

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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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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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L'analyse des changements sociaux au Rwanda. L'expérience de Frères des Hommes von Van Ongevalle, Jan

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Rapport évaluation externe et capitalisation du programme de promotion de la participation des ménages paysans aux politiques de développement agricole et de lutte contre la malnut... von Van Ongevalle, Jan

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A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinoma von Kientz, Caroline, Joly, Marie-Odile, Faivre, Laurence, Clemenson, Alix, Dalac, Sophie, Lepage, Côme, Chapusot, Caroline, Jacquot, Caroline, Schiappa, Renaud, Lebrun, Marine

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Quantitative Airborne Inventories in Dense Tropical Forest Using Imaging Spectroscopy von Laybros, Anthony, Aubry-Kientz, Melaine, Feret, Jean-Baptiste, Bedeau, Caroline, Brunaux, Olivier, Derroire, Geraldine, Vincent, Gregoire

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Comparative Toxigenicity and Associated Mutagenicity of Aspergillus fumigatus and Aspergillus flavus Group Isolates Collected from the Agricultural Environment von Lanier, Caroline, Garon, David, Heutte, Natacha, Kientz, Valérie, André, Véronique

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Comparative Toxigenicity and Associated Mutagenicity ofAspergillus fumigatusandAspergillus flavusGroup Isolates Collected from the Agricultural Environment von Lanier, Caroline, Garon, David, Heutte, Natacha, Kientz, Valerie, Andre, Veronique

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Comparative Toxigenicity and Associated Mutagenicity of Aspergillus fumigatus and Aspergillus flavus Group Isolates Collected from the Agricultural Environment von Lanier, Caroline, Garon, David, Heutte, Natacha, Kientz, Valérie, André, Véronique

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Transfusion of platelet components prepared with photochemical pathogen inactivation treatment during a Chikungunya virus epidemic in Ile de La Réunion von Rasonglès, Patrice, Angelini-Tibert, Marie France, Simon, Philip, Currie, Caroline, Isola, Herve, Kientz, Daniel, Slaedts, Marc, Jacquet, Michele, Sundin, David, Lin, Lily, Corash, Laurence, Cazenave, Jean Pierre

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