Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies by Denisova, Evgeniya, Westphal, Dana, Surowy, Harald M., Meier, Friedegund, Hutter, Barbara, Reifenberger, Julia, Rütten, Arno, Schulz, Alexander, Sergon, Mildred, Ziemer, Mirjana, Brors, Benedikt, Betz, Regina C., Redler, Silke

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Predisposition for TMPRSS2-ERG Fusion in Prostate Cancer by Variants in DNA Repair Genes by LUEDEKE, Manuel, LINNERT, Carmen M, HOFER, Matthias D, SUROWY, Harald M, RINCKLEB, Antje E, HOEGEL, Josef, KUEFER, Rainer, RUBIN, Mark A, VOGEL, Walther, MAIER, Christiane

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Gene expression profiling in porocarcinoma indicates heterogeneous tumor development and substantiates poromas as precursor lesions by Holst, Svenja, Weber, Anna K., Meier, Friedegund, Otte, Jörg, Petzsch, Patrick, Reifenberger, Julia, Wachtmeister, Thorsten, Westphal, Dana, Ziemer, Mirjana, Wruck, Wasco, Adjaye, James, Betz, Regina C., Rütten, Arno, Surowy, Harald M., Redler, Silke

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The GPRC5A frameshift variant c.183del is not associated with increased breast cancer risk in BRCA1 mutation carriers by Klaschik, Kristina, Hauke, Jan, Neidhardt, Guido, Tränkle, Christian, Surowy, Harald M., Heilmann‐Heimbach, Stefanie, Rappl, Gunter, Mangold, Elisabeth, Arnold, Norbert, Niederacher, Dieter, Sutter, Christian, Burwinkel, Barbara, Engel, Christoph, Wappenschmidt, Barbara, Meindl, Alfons, Ernst, Corinna, Weber‐Lassalle, Konstantin, Weber‐Lassalle, Nana, Schmidt, Sandra, Borde, Julika, Schmutzler, Rita K., Hahnen, Eric, Pohl‐Rescigno, Esther

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Genexpressionsprofile beim Porokarzinom deuten auf heterogene Tumorentwicklung hin und untermauern Porome als Vorläuferläsionen by Holst, Svenja, Weber, Anna K., Meier, Friedegund, Otte, Jörg, Petzsch, Patrick, Reifenberger, Julia, Wachtmeister, Thorsten, Westphal, Dana, Ziemer, Mirjana, Wruck, Wasco, Adjaye, James, Betz, Regina C., Rütten, Arno, Surowy, Harald M., Redler, Silke

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The prostate cancer risk locus at 10q11 is associated with DNA repair capacity by Rinckleb, Antje E., Surowy, Harald M., Luedeke, Manuel, Varga, Dominic, Schrader, Mark, Hoegel, Josef, Vogel, Walther, Maier, Christiane

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Germline mutations of the MSR1 gene in prostate cancer families from Germany by Maier, Christiane, Vesovic, Zorica, Bachmann, Natascha, Herkommer, Kathleen, Braun, Anja K., Surowy, Harald M., Assum, Guenter, Paiss, Thomas, Vogel, Walther

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Genexpressionsprofile beim Porokarzinom deuten auf heterogene Tumorentwicklung hin und untermauern Porome als Vorläuferläsionen by Holst, Svenja, Weber, Anna K., Meier, Friedegund, Otte, Jörg, Petzsch, Patrick, Reifenberger, Julia, Wachtmeister, Thorsten, Westphal, Dana, Ziemer, Mirjana, Wruck, Wasco, Adjaye, James, Betz, Regina C., Rütten, Arno, Surowy, Harald M., Redler, Silke

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Gene expression profiling in porocarcinoma indicates heterogeneous tumor development and substantiates poromas as precursor lesions by Holst, Svenja, Weber, Anna K., Meier, Friedegund, Otte, Jörg, Petzsch, Patrick, Reifenberger, Julia, Wachtmeister, Thorsten, Westphal, Dana, Ziemer, Mirjana, Wruck, Wasco, Adjaye, James, Betz, Regina C., Rütten, Arno, Surowy, Harald M., Redler, Silke

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Germline mutations of theMSR1 gene in prostate cancer families from Germany by Maier, Christiane, Vesovic, Zorica, Bachmann, Natascha, Herkommer, Kathleen, Braun, Anja K., Surowy, Harald M., Assum, Guenter, Paiss, Thomas, Vogel, Walther

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Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis by Shu, Xiang, Wu, Lang, Khankari, Nikhil K, Shu, Xiao-Ou, Wang, Thomas J, Michailidou, Kyriaki, Bolla, Manjeet K, Wang, Qin, Dennis, Joe, Milne, Roger L, Schmidt, Marjanka K, Pharoah, Paul D P, Andrulis, Irene L, Hunter, David J, Simard, Jacques, Easton, Douglas F, Zheng, Wei

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Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study by Lewis, Sarah J, Martin, Richard M, Boyle, Terry, Giles, Graham G, Michailidou, Kyriaki, Bolla, Manjeet K, Dennis, Joe, Lush, Michael, Investigators, ABCTB, Ahearn, Thomas U, Ambrosone, Christine B, Andrulis, Irene L, Arndt, Volker, Augustinsson, Annelie, Auvinen, Päivi, Beane Freeman, Laura E, Behrens, Sabine, Bermisheva, Marina, Bojesen, Stig E, Bonanni, Bernardo, Brüning, Thomas, Buys, Saundra S, Cessna, Melissa H, Chang-Claude, Jenny, Clarke, Christine L, Cox, Angela, Cross, Simon S, Daly, Mary B, Dörk, Thilo, Eriksson, Mikael, Evans, D. Gareth, Fasching, Peter A, Fletcher, Olivia, Fritschi, Lin, Gabrielson, Marike, Gago-Dominguez, Manuela, García-Sáenz, José A, Goldberg, Mark S, Guénel, Pascal, Hahnen, Eric, Haiman, Christopher A, Håkansson, Niclas, Hall, Per, Hollestelle, Antoinette, Hooning, Maartje J, Hoppe, Reiner, Hopper, John, Howell, Anthony, Jakubowska, Anna, Janni, Wolfgang, Jung, Audrey, Kaaks, Rudolf, Keeman, Renske, Kitahara, Cari M, Koutros, Stella, Kubelka-Sabit, Katerina, Kurian, Allison W, Lambrechts, Diether, Le Marchand, Loic, Lindblom, Annika, Loibl, Sibylle, Lubiński, Jan, Mannermaa, Arto, Martinez, Maria Elena, Mavroudis, Dimitrios, Menon, Usha, Murphy, Rachel A, Collaborators, NBCS, Nevelsteen, Ines, Newman, William G, Olshan, Andrew F, Orr, Nick, Patel, Alpa, Rack, Brigitte, Radice, Paolo, Rees-Punia, Erika, Rennert, Hedy S, Romero, Atocha, Saloustros, Emmanouil, Sandler, Dale P, Schmidt, Marjanka K, Schwentner, Lukas, Scott, Christopher, Shah, Mitul, Shu, Xiao-Ou, Simard, Jacques, Southey, Melissa C, Stone, Jennifer, Surowy, Harald, Tamimi, Rulla M, Tapper, William J, Tollenaar, Rob A E M, Troester, Melissa A, Untch, Michael, Vachon, Celine M, Yannoukakos, Drakoulis, Zheng, Wei, Ziogas, Argyrios, Easton, Douglas F, Milne, Roger L

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Delineation of the adult phenotype of Coffin–Siris syndrome in 35 individuals by Schmetz, Ariane, Lüdecke, Hermann-Josef, Surowy, Harald, Sivalingam, Sugirtahn, Bruel, Ange-Line, Caumes, Roseline, Charles, Perrine, Chatron, Nicolas, Chrzanowska, Krystyna, Codina-Solà, Marta, Colson, Cindy, Cuscó, Ivon, Denommé-Pichon, Anne-Sophie, Edery, Patrick, Faivre, Laurence, Green, Andrew, Heide, Solveig, Hsieh, Tzung-Chien, Hustinx, Alexander, Kleinendorst, Lotte, Knopp, Cordula, Kraft, Florian, Krawitz, Peter M., Lasa-Aranzasti, Amaia, Lesca, Gaetan, López-González, Vanesa, Maraval, Julien, Mignot, Cyril, Neuhann, Teresa, Netzer, Christian, Oehl-Jaschkowitz, Barbara, Petit, Florence, Philippe, Christophe, Posmyk, Renata, Putoux, Audrey, Reis, André, Sánchez-Soler, María José, Suh, Julia, Tkemaladze, Tinatin, Tran Mau Them, Frédéric, Travessa, André, Trujillano, Laura, Valenzuela, Irene, van Haelst, Mieke M., Vasileiou, Georgia, Vincent-Delorme, Catherine, Walther, Mona, Verde, Pablo, Bramswig, Nuria C., Wieczorek, Dagmar

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Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classi... by de la Hoya, Miguel, Soukarieh, Omar, López-Perolio, Irene, Vega, Ana, Walker, Logan C, van Ierland, Yvette, Baralle, Diana, Santamariña, Marta, Lattimore, Vanessa, Wijnen, Juul, Whiley, Philip, Blanco, Ana, Raponi, Michela, Hauke, Jan, Wappenschmidt, Barbara, Becker, Alexandra, Hansen, Thomas V O, Behar, Raquel, Investigators, KConFaB, Niederacher, Diether, Arnold, Norbert, Dworniczak, Bernd, Steinemann, Doris, Faust, Ulrike, Rubinstein, Wendy, Hulick, Peter J, Houdayer, Claude, Caputo, Sandrine M, Castera, Laurent, Pesaran, Tina, Chao, Elizabeth, Brewer, Carole, Southey, Melissa C, van Asperen, Christi J, Singer, Christian F, Sullivan, Jan, Poplawski, Nicola, Mai, Phuong, Peto, Julian, Johnson, Nichola, Burwinkel, Barbara, Surowy, Harald, Bojesen, Stig E, Flyger, Henrik, Lindblom, Annika, Margolin, Sara, Chang-Claude, Jenny, Rudolph, Anja, Radice, Paolo, Galastri, Laura, Olson, Janet E, Hallberg, Emily, Giles, Graham G, Milne, Roger L, Andrulis, Irene L, Glendon, Gord, Hall, Per, Czene, Kamila, Blows, Fiona, Shah, Mitul, Wang, Qin, Dennis, Joe, Michailidou, Kyriaki, McGuffog, Lesley, Bolla, Manjeet K, Antoniou, Antonis C, Easton, Douglas F, Couch, Fergus J, Tavtigian, Sean, Vreeswijk, Maaike P, Parsons, Michael, Meeks, Huong D, Martins, Alexandra, Goldgar, David E, Spurdle, Amanda B

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FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor by Peterlongo, Paolo, Catucci, Irene, Colombo, Mara, Caleca, Laura, Mucaki, Eliseos, Bogliolo, Massimo, Marin, Maria, Damiola, Francesca, Bernard, Loris, Pensotti, Valeria, Volorio, Sara, Dall'Olio, Valentina, Meindl, Alfons, Bartram, Claus, Sutter, Christian, Surowy, Harald, Sornin, Valérie, Dondon, Marie-Gabrielle, Eon-Marchais, Séverine, Stoppa-Lyonnet, Dominique, Andrieu, Nadine, Sinilnikova, Olga M, Mitchell, Gillian, James, Paul A, Thompson, Ella, Marchetti, Marina, Verzeroli, Cristina, Tartari, Carmen, Capone, Gabriele Lorenzo, Putignano, Anna Laura, Genuardi, Maurizio, Medici, Veronica, Marchi, Isabella, Federico, Massimo, Tognazzo, Silvia, Matricardi, Laura, Agata, Simona, Dolcetti, Riccardo, Della Puppa, Lara, Cini, Giulia, Gismondi, Viviana, Viassolo, Valeria, Perfumo, Chiara, Mencarelli, Maria Antonietta, Baldassarri, Margherita, Peissel, Bernard, Roversi, Gaia, Silvestri, Valentina, Rizzolo, Piera, Spina, Francesca, Vivanet, Caterina, Tibiletti, Maria Grazia, Caligo, Maria Adelaide, Gambino, Gaetana, Tommasi, Stefania, Pilato, Brunella, Tondini, Carlo, Corna, Chiara, Bonanni, Bernardo, Barile, Monica, Osorio, Ana, Benitez, Javier, Balestrino, Luisa, Ottini, Laura, Manoukian, Siranoush, Pierotti, Marco A, Renieri, Alessandra, Varesco, Liliana, Couch, Fergus J, Wang, Xianshu, Devilee, Peter, Hilbers, Florentine S, van Asperen, Christi J, Viel, Alessandra, Montagna, Marco, Cortesi, Laura, Diez, Orland, Balmaña, Judith, Hauke, Jan, Schmutzler, Rita K, Papi, Laura, Pujana, Miguel Angel, Lázaro, Conxi, Falanga, Anna, Offit, Kenneth, Vijai, Joseph, Campbell, Ian, Burwinkel, Barbara, Kvist, Anders, Ehrencrona, Hans, Mazoyer, Sylvie, Pizzamiglio, Sara, Verderio, Paolo, Surralles, Jordi, Rogan, Peter K, Radice, Paolo

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Heritability of baseline and induced micronucleus frequencies by Surowy, Harald, Rinckleb, Antje, Luedeke, Manuel, Stuber, Madeleine, Wecker, Anna, Varga, Dominic, Maier, Christiane, Hoegel, Josef, Vogel, Walther

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Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of sys... by Morra, Anna, Escala-Garcia, Maria, Beesley, Jonathan, Keeman, Renske, Canisius, Sander, Ahearn, Thomas U, Andrulis, Irene L, Anton-Culver, Hoda, Arndt, Volker, Auer, Paul L, Augustinsson, Annelie, Beane Freeman, Laura E, Becher, Heiko, Beckmann, Matthias W, Behrens, Sabine, Bojesen, Stig E, Bolla, Manjeet K, Brenner, Hermann, Brüning, Thomas, Buys, Saundra S, Caan, Bette, Campa, Daniele, Canzian, Federico, Castelao, Jose E, Chang-Claude, Jenny, Chanock, Stephen J, Cheng, Ting-Yuan David, Clarke, Christine L, Colonna, Sarah V, Couch, Fergus J, Cox, Angela, Cross, Simon S, Czene, Kamila, Daly, Mary B, Dennis, Joe, Dörk, Thilo, Dossus, Laure, Dunning, Alison M, Dwek, Miriam, Eccles, Diana M, Ekici, Arif B, Eliassen, A Heather, Eriksson, Mikael, Evans, D Gareth, Fasching, Peter A, Flyger, Henrik, Fritschi, Lin, Gago-Dominguez, Manuela, García-Sáenz, José A, Giles, Graham G, Grip, Mervi, Guénel, Pascal, Gündert, Melanie, Hahnen, Eric, Haiman, Christopher A, Håkansson, Niclas, Hall, Per, Hamann, Ute, Hart, Steven N, Hartikainen, Jaana M, Hartmann, Arndt, He, Wei, Hooning, Maartje J, Hoppe, Reiner, Hopper, John L, Howell, Anthony, Hunter, David J, Jager, Agnes, Jakubowska, Anna, Janni, Wolfgang, John, Esther M, Jung, Audrey Y, Kaaks, Rudolf, Keupers, Machteld, Kitahara, Cari M, Koutros, Stella, Kraft, Peter, Kristensen, Vessela N, Kurian, Allison W, Lacey, James V, Lambrechts, Diether, Le Marchand, Loic, Lindblom, Annika, Linet, Martha, Luben, Robert N, Lubiński, Jan, Lush, Michael, Mannermaa, Arto, Manoochehri, Mehdi, Margolin, Sara, Martens, John W M, Martinez, Maria Elena, Mavroudis, Dimitrios, Michailidou, Kyriaki, Milne, Roger L, Mulligan, Anna Marie, Muranen, Taru A, Nevanlinna, Heli, Newman, William G, Nielsen, Sune F

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Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element by Baxter, Joseph S., Gillespie, Andrea, Maguire, Sarah, Bolla, Manjeet K., Wang, Qin, Dennis, Joe, Andrulis, Irene L., Arndt, Volker, Aronson, Kristan J., Augustinsson, Annelie, Behrens, Sabine, Bogdanova, Natalia V., Brucker, Sara Y., Cai, Qiuyin, Campa, Daniele, Couch, Fergus J., Cox, Angela, Dörk, Thilo, Dwek, Miriam, Eccles, Diana M., Ekici, Arif B., Eliassen, A. Heather, Engel, Christoph, Figueroa, Jonine, Flyger, Henrik, Gao, Chi, García-Closas, Montserrat, García-Sáenz, José A., Giles, Graham G., Goldberg, Mark S., Guénel, Pascal, Gündert, Melanie, Haeberle, Lothar, Haiman, Christopher A., Hamann, Ute, Hatse, Sigrid, Ito, Hidemi, Jager, Agnes, Jakubowska, Anna, Janni, Wolfgang, John, Esther M., Jung, Audrey, Kaaks, Rudolf, Khusnutdinova, Elza, Kosma, Veli-Matti, Kraft, Peter, Kurian, Allison W., Kwong, Ava, Lambrechts, Diether, Larson, Nicole L., Lejbkowicz, Flavio, Li, Jingmei, Mannermaa, Arto, Matsuo, Keitaro, Mavroudis, Dimitrios, Mayes, Rebecca, Milne, Roger L., Mohd Taib, Nur Aishah, Muir, Kenneth, Murphy, Rachel A., Nevanlinna, Heli, Offit, Kenneth, Olson, Janet E., Olsson, Håkan, Park, Sue K., Peterlongo, Paolo, Plaseska-Karanfilska, Dijana, Presneau, Nadege, Pylkäs, Katri, Rennert, Gad, Romero, Atocha, Ruebner, Matthias, Rüdiger, Thomas, Saloustros, Emmanouil, Sandler, Dale P., Sawyer, Elinor J., Schmidt, Marjanka K., Schoemaker, Minouk J., Shah, Mitul, Shen, Chen-Yang, Shu, Xiao-Ou, Simard, Jacques, Southey, Melissa C., Stone, Jennifer, Surowy, Harald, Teras, Lauren R., Toland, Amanda E., Tomlinson, Ian, Tseng, Chiu-Chen, Vachon, Celine M., Weinberg, Clarice R., Wendt, Camilla, Yamaji, Taiki, Zheng, Wei, Pharoah, Paul D.P., Dunning, Alison M., Easton, Douglas F., Lord, Christopher J., Haider, Syed, Orr, Nick

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Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis by Escala-Garcia, Maria, Canisius, Sander, Keeman, Renske, Beesley, Jonathan, Anton-Culver, Hoda, Arndt, Volker, Augustinsson, Annelie, Becher, Heiko, Beckmann, Matthias W., Behrens, Sabine, Bermisheva, Marina, Bojesen, Stig E., Bolla, Manjeet K., Brenner, Hermann, Canzian, Federico, Castelao, Jose E., Chang-Claude, Jenny, Chanock, Stephen J., Couch, Fergus J., Czene, Kamila, Daly, Mary B., Dennis, Joe, Devilee, Peter, Dunning, Alison M., Easton, Douglas F., Ekici, Arif B., Eliassen, A. Heather, Fasching, Peter A., Flyger, Henrik, Gago-Dominguez, Manuela, García-Closas, Montserrat, García-Sáenz, José A., Geisler, Jürgen, Giles, Graham G., Grip, Mervi, Gündert, Melanie, Hahnen, Eric, Haiman, Christopher A., Håkansson, Niclas, Hall, Per, Hamann, Ute, Hartikainen, Jaana M., Hollestelle, Antoinette, Hoppe, Reiner, Hopper, John L., Hunter, David J., Jacot, William, Jakubowska, Anna, John, Esther M., Jung, Audrey Y., Kaaks, Rudolf, Khusnutdinova, Elza, Koppert, Linetta B., Kraft, Peter, Kristensen, Vessela N., Kurian, Allison W., Lambrechts, Diether, Lindblom, Annika, Luben, Robert N., Lubiński, Jan, Mannermaa, Arto, Manoochehri, Mehdi, Margolin, Sara, Mavroudis, Dimitrios, Muranen, Taru A., Nevanlinna, Heli, Olshan, Andrew F., Olsson, Håkan, Park-Simon, Tjoung-Won, Patel, Alpa V., Peterlongo, Paolo, Pharoah, Paul D. P., Punie, Kevin, Radice, Paolo, Rennert, Gad, Rennert, Hedy S., Romero, Atocha, Roylance, Rebecca, Ruebner, Matthias, Saloustros, Emmanouil, Sawyer, Elinor J., Schmutzler, Rita K., Schoemaker, Minouk J., Scott, Christopher, Southey, Melissa C., Surowy, Harald, Swerdlow, Anthony J., Tamimi, Rulla M., Teras, Lauren R., Thomas, Emilie, Tomlinson, Ian, Troester, Melissa A., Vachon, Celine M., Winqvist, Robert, Wolk, Alicja, Ziogas, Argyrios, Michailidou, Kyriaki, Chenevix-Trench, Georgia, Bachelot, Thomas, Schmidt, Marjanka K.

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Two truncating variants in FANCC and breast cancer risk by Dörk, Thilo, Peterlongo, Paolo, Mannermaa, Arto, Wang, Qin, Anton-Culver, Hoda, Arndt, Volker, Augustinsson, Annelie, Beeghly-Fadiel, Alicia, Bermisheva, Marina, Brenner, Hermann, Burwinkel, Barbara, Canzian, Federico, Chang-Claude, Jenny, Chanock, Stephen J., Christiansen, Hans, Czene, Kamila, dos-Santos-Silva, Isabel, Dwek, Miriam, Figueroa, Jonine, Gabrielson, Marike, Gao, Chi, García-Sáenz, José A., Giles, Graham G., Goldberg, Mark S., Goldgar, David E., Haeberle, Lothar, Haiman, Christopher A., Håkansson, Niclas, Hall, Per, Hartman, Mikael, Hauke, Jan, Hillemanns, Peter, Hogervorst, Frans B. L., Hooning, Maartje J., Hopper, John L., Howell, Tony, Huo, Dezheng, Ito, Hidemi, Iwasaki, Motoki, Jakubowska, Anna, Janni, Wolfgang, John, Esther M., Jung, Audrey, Kang, Daehee, Kapoor, Pooja Middha, Khusnutdinova, Elza, Kitahara, Cari M., Koutros, Stella, Kraft, Peter, Kristensen, Vessela N., Marchand, Loic Le, Li, Jingmei, Lindström, Sara, Lo, Wing-Yee, Long, Jirong, Lubiński, Jan, Martinez, Elena, Matsuo, Keitaro, Menon, Usha, Milne, Roger L., Muir, Kenneth, Mulligan, Anna Marie, Neuhausen, Susan L., Nevanlinna, Heli, Neven, Patrick, Olson, Janet E., Park, Sue K., Park-Simon, Tjoung-Won, Peto, Julian, Presneau, Nadege, Rashid, Muhammad U., Rennert, Gad, Rennert, Hedy S., Romero, Atocha, Ruebner, Matthias, Saloustros, Emmanouil, Schneider, Michael O., Shen, Chen-Yang, Shu, Xiao-Ou, Simard, Jacques, Southey, Melissa C., Spinelli, John J., Tamimi, Rulla M., Tapper, William J., Teo, Soo H., Terry, Mary Beth, Tollenaar, Rob A. E. M., Torres, Diana, Troester, Melissa A., Truong, Thérèse, Tsugane, Shoichiro, Untch, Michael, Vachon, Celine M., Veen, Elke M. van, Vijai, Joseph, Wolk, Alicja, Yu, Jyh-Cherng, Ziogas, Argyrios, Schindler, Detlev, Devilee, Peter

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