Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk von Wilcox, Naomi, Dumont, Martine, González-Neira, Anna, Carvalho, Sara, Joly Beauparlant, Charles, Crotti, Marco, Luccarini, Craig, Soucy, Penny, Dubois, Stéphane, Nuñez-Torres, Rocio, Pita, Guillermo, Gardner, Eugene J., Dennis, Joe, Alonso, M. Rosario, Álvarez, Nuria, Baynes, Caroline, Collin-Deschesnes, Annie Claude, Desjardins, Sylvie, Becher, Heiko, Behrens, Sabine, Bolla, Manjeet K., Castelao, Jose E., Chang-Claude, Jenny, Cornelissen, Sten, Dörk, Thilo, Engel, Christoph, Gago-Dominguez, Manuela, Guénel, Pascal, Hadjisavvas, Andreas, Hahnen, Eric, Hartman, Mikael, Herráez, Belén, Jung, Audrey, Keeman, Renske, Kiechle, Marion, Li, Jingmei, Loizidou, Maria A., Lush, Michael, Michailidou, Kyriaki, Panayiotidis, Mihalis I., Sim, Xueling, Teo, Soo Hwang, Tyrer, Jonathan P., van der Kolk, Lizet E., Wahlström, Cecilia, Wang, Qin, Perry, John R. B., Benitez, Javier, Schmidt, Marjanka K., Schmutzler, Rita K., Pharoah, Paul D. P., Droit, Arnaud, Dunning, Alison M., Kvist, Anders, Devilee, Peter, Easton, Douglas F., Simard, Jacques

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Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk von Wilcox, Naomi, Dumont, Martine, González-Neira, Anna, Carvalho, Sara, Joly Beauparlant, Charles, Crotti, Marco, Luccarini, Craig, Soucy, Penny, Dubois, Stéphane, Nuñez-Torres, Rocio, Pita, Guillermo, Gardner, Eugene J., Dennis, Joe, Alonso, M. Rosario, Álvarez, Nuria, Baynes, Caroline, Collin-Deschesnes, Annie Claude, Desjardins, Sylvie, Becher, Heiko, Behrens, Sabine, Bolla, Manjeet K., Castelao, Jose E., Chang-Claude, Jenny, Cornelissen, Sten, Dörk, Thilo, Engel, Christoph, Gago-Dominguez, Manuela, Guénel, Pascal, Hadjisavvas, Andreas, Hahnen, Eric, Hartman, Mikael, Herráez, Belén, Jung, Audrey, Keeman, Renske, Kiechle, Marion, Li, Jingmei, Loizidou, Maria A., Lush, Michael, Michailidou, Kyriaki, Panayiotidis, Mihalis I., Sim, Xueling, Teo, Soo Hwang, Tyrer, Jonathan P., van der Kolk, Lizet E., Wahlström, Cecilia, Wang, Qin, Perry, John R. B., Benitez, Javier, Schmidt, Marjanka K., Schmutzler, Rita K., Pharoah, Paul D. P., Droit, Arnaud, Dunning, Alison M., Kvist, Anders, Devilee, Peter, Easton, Douglas F., Simard, Jacques

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Epidemiological and ES cell‐based functional evaluation of BRCA2 variants identified in families with breast cancer von Sullivan, Teresa, Thirthagiri, Eswary, Chong, Chan‐Eng, Stauffer, Stacey, Reid, Susan, Southon, Eileen, Hassan, Tiara, Ravichandran, Aravind, Wijaya, Eldarina, Lim, Joanna, Taib, Nur Aishah Mohd, Fadzli, Farhana, Yip, Cheng Har, Hartman, Mikael, Li, Jingmei, Dam, Rob M., North, Susan L., Das, Ranabir, Easton, Douglas F., Biswas, Kajal, Teo, Soo‐Hwang, Sharan, Shyam K.

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Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants – an Asian study of 572 families von Ho, Weang-Kee, Hassan, Nur Tiara, Yoon, Sook-Yee, Yang, Xin, Lim, Joanna M.C., Binte Ishak, Nur Diana, Ho, Peh Joo, Wijaya, Eldarina A., Ng, Patsy Pei-Sze, Luccarini, Craig, Allen, Jamie, Tai, Mei-Chee, Chiang, Jianbang, Zhang, Zewen, See, Mee-Hoong, Thong, Meow-Keong, Woo, Yin-Ling, Dunning, Alison M., Hartman, Mikael, Yip, Cheng-Har, Mohd Taib, Nur Aishah, Easton, Douglas F., Li, Jingmei, Ngeow, Joanne, Antoniou, Antonis C., Teo, Soo-Hwang, Kiat-Tee Tan, Benita, Tan, Su-Ming, Mien Tan, Veronique Kiak, Tan, Ern Yu, Lim, Geok Hoon, Khng, Alexis, Ch’ng, Gaik-Siew, Omar, Jamil, Yong, Chee-Meng, Aliyas, Ismail, Malik, Rozita Abdul, Subramaniam, Suguna, Sim, Wee-Wee, Lim, Chun Sen, Lee, Saw-Joo, Lim, Keng-Joo, Shafiee, Mohamad Nasir, Ismail, Fuad Ismail, Ismail, Mohd Pazudin, Mohamed Jamli, Mohamad Faiz, Kumarasamy, Suresh, Low, John S.H., Ahmad Mustafa, Ahmad Muzamir, Makanjang, Mary J., Taib, Shahila, Cheah, Nellie, Fong, Chee-Kin, Ho, Kean-Fatt, Deniel, Azura, Ang, Soo Fan, Ahmad Badruddin, Ahmad Radzi, Tho, Lye-Mun

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Breast cancer risks associated with missense variants in breast cancer susceptibility genes von Dorling, Leila, Carvalho, Sara, Allen, Jamie, Parsons, Michael T, Fortuno, Cristina, González-Neira, Anna, Heijl, Stephan M, Adank, Muriel A, Ahearn, Thomas U, Andrulis, Irene L, Auvinen, Päivi, Becher, Heiko, Beckmann, Matthias W, Behrens, Sabine, Bermisheva, Marina, Bogdanova, Natalia V, Bojesen, Stig E, Bolla, Manjeet K, Bremer, Michael, Briceno, Ignacio, Camp, Nicola J, Campbell, Archie, Castelao, Jose E, Chang-Claude, Jenny, Chanock, Stephen J, Chenevix-Trench, Georgia, Collée, J Margriet, Czene, Kamila, Dennis, Joe, Dörk, Thilo, Eriksson, Mikael, Evans, D Gareth, Fasching, Peter A, Figueroa, Jonine, Flyger, Henrik, Gabrielson, Marike, Gago-Dominguez, Manuela, García-Closas, Montserrat, Giles, Graham G, Glendon, Gord, Guénel, Pascal, Gündert, Melanie, Hadjisavvas, Andreas, Hahnen, Eric, Hall, Per, Hamann, Ute, Harkness, Elaine F, Hartman, Mikael, Hogervorst, Frans B L, Hollestelle, Antoinette, Hoppe, Reiner, Howell, Anthony, Jakubowska, Anna, Jung, Audrey, Khusnutdinova, Elza, Kim, Sung-Won, Ko, Yon-Dschun, Kristensen, Vessela N, Lakeman, Inge M M, Li, Jingmei, Lindblom, Annika, Loizidou, Maria A, Lophatananon, Artitaya, Lubiński, Jan, Luccarini, Craig, Madsen, Michael J, Mannermaa, Arto, Manoochehri, Mehdi, Margolin, Sara, Mavroudis, Dimitrios, Milne, Roger L, Mohd Taib, Nur Aishah, Muir, Kenneth, Nevanlinna, Heli, Newman, William G, Oosterwijk, Jan C, Park, Sue K, Peterlongo, Paolo, Radice, Paolo, Saloustros, Emmanouil, Sawyer, Elinor J, Schmutzler, Rita K, Shah, Mitul, Sim, Xueling, Southey, Melissa C, Surowy, Harald, Suvanto, Maija, Tomlinson, Ian, Torres, Diana, Truong, Thérèse, van Asperen, Christi J, Waltes, Regina, Wang, Qin, Yang, Xiaohong R, Pharoah, Paul D P, Schmidt, Marjanka K, Benitez, Javier, Vroling, Bas, Dunning, Alison M, Teo, Soo Hwang

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Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk von Wilcox, N., Dumont, M., Gonzalez-Neira, A., Carvalho, S., Beauparlant, C.J., Crotti, M., Luccarini, C., Soucy, P., Dubois, S., Nunez-Torres, R., Pita, G., Gardner, E.J., Dennis, J., Alonso, M.R., Alvarez, N., Baynes, C., Collin-Deschesnes, A.C., Desjardins, S., Becher, H., Behrens, S., Bolla, M.K., Castelao, J.E., Chang-Claude, J., Cornelissen, S., Dork, T., Engel, C., Gago-Dominguez, M., Guenel, P., Hadjisavvas, A., Hahnen, E., Hartman, M., Herraez, B., Kiechle, M., Jung, A.D., Keeman, R., Li, J.M., Loizidou, M.A., Lush, M., Michailidou, K., Panayiotidis, M.I., Sim, X., Teo, S.H., Tyrer, J.P., Kolk, L.E. van der, Wahlstrom, C., Wang, Q., Perry, J.R.B., Benitez, J., Schmidt, M.K., Schmutzler, R.K., Pharoah, P.D.P., Droit, A., Dunning, A.M., Kvist, A., Devilee, P., Easton, D.F., Simard, J.

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Breast cancer risks associated with missense variants in breast cancer susceptibility genes von Dorling, L., Carvalho, S., Allen, J., Parsons, M.T., Fortuno, C., Gonzalez-Neira, A., Heijl, S.M., Adank, M.A., Ahearn, T.U., Auvinen, P., Becher, H., Beckmann, M.W., Behrens, S., Bermisheva, M., Bojesen, S.E., Bolla, M.K., Bremer, M., Briceno, I., Camp, N.J., Campbell, A., Castelao, J.E., Chang-Claude, J., Chanock, S.J., Chenevix-Trench, G., Collee, J.M., Czene, K., Dork, T., Eriksson, M., Evans, D.G., Fasching, P.A., Figueroa, J., Flyger, H., Gabrielson, M., Gago-Dominguez, M., Garcia-Closas, M., Giles, G.G., Glendon, G., Guenel, P., Gundert, M., Hadjisavvas, A., Hahnen, E., Hall, P., Hamann, U., Harkness, E.F., Hartman, M., Hogervorst, F.B.L., Hollestelle, A., Hoppe, R., Howell, A., Jakubowska, A., Jung, A., Khusnutdinova, E., Kim, S.W., Ko, Y.D., Kristensen, V.N., Lakeman, I.M.M., Li, J.M., Lindblom, A., Loizidou, M.A., Lophatananon, A., Luccarini, C., Madsen, M.J., Mannermaa, A., Manoochehri, M., Margolin, S., Mavroudis, D., Milne, R.L., Taib, N.A.M., Muir, K., Nevanlinna, H., Newman, W.G., Oosterwijk, J.C., Park, S.K., Peterlongo, P., Radice, P., Saloustros, E., Sawyer, E.J., Schmutzler, R.K., Shah, M.T., Sim, X., Southey, M.C., Surowy, H., Suvanto, M., Tomlinson, I., Torres, D., Truong, T., Asperen, C.J. van, Waltes, R., Yang, X.H.R., Pharoah, P.D.P., Schmidt, M.K., Benitez, J., Vroling, B., Dunning, A.M., Teo, S.H., Kvist, A., Hoya, M. de la, Spurdle, A.B., Vreeswijk, M.P.G., Easton, D.F.

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Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk von Wilcox, Naomi, Dumont, Martine, González-Neira, Anna, Carvalho, Sara, Joly Beauparlant, Charles, Crotti, Marco, Luccarini, Craig, Soucy, Penny, Dubois, Stéphane, Nuñez-Torres, Rocio, Pita, Guillermo, Gardner, Eugene J, Dennis, Joe, Alonso, M Rosario, Álvarez, Nuria, Baynes, Caroline, Collin-Deschesnes, Annie Claude, Desjardins, Sylvie, Becher, Heiko, Behrens, Sabine, Bolla, Manjeet K, Castelao, Jose E, Chang-Claude, Jenny, Cornelissen, Sten, Dörk, Thilo, Engel, Christoph, Gago-Dominguez, Manuela, Guénel, Pascal, Hadjisavvas, Andreas, Hahnen, Eric, Hartman, Mikael, Herráez, Belén, SGBCC Investigators, Jung, Audrey, Keeman, Renske, Kiechle, Marion, Li, Jingmei, Loizidou, Maria A, Lush, Michael, Michailidou, Kyriaki, Panayiotidis, Mihalis I, Sim, Xueling, Teo, Soo Hwang, Tyrer, Jonathan P, van der Kolk, Lizet E, Wahlström, Cecilia, Wang, Qin, Perry, John RB, Benitez, Javier, Schmidt, Marjanka K, Schmutzler, Rita K, Pharoah, Paul DP, Droit, Arnaud, Dunning, Alison M, Kvist, Anders, Devilee, Peter, Easton, Douglas F, Simard, Jacques

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Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk von Wilcox, Naomi, Dumont, Martine, González-Neira, Anna, Carvalho, Sara, Joly Beauparlant, Charles, Crotti, Marco, Luccarini, Craig, Soucy, Penny, Dubois, Stéphane, Nuñez-Torres, Rocio, Pita, Guillermo, Gardner, Eugene J, Dennis, Joe, Alonso, M Rosario, Álvarez, Nuria, Baynes, Caroline, Collin-Deschesnes, Annie Claude, Desjardins, Sylvie, Becher, Heiko, Behrens, Sabine, Bolla, Manjeet K, Castelao, Jose E, Chang-Claude, Jenny, Cornelissen, Sten, Dörk, Thilo, Engel, Christoph, Gago-Dominguez, Manuela, Guénel, Pascal, Hadjisavvas, Andreas, Hahnen, Eric, Hartman, Mikael, Herráez, Belén, SGBCC Investigators, Jung, Audrey, Keeman, Renske, Kiechle, Marion, Li, Jingmei, Loizidou, Maria A, Lush, Michael, Michailidou, Kyriaki, Panayiotidis, Mihalis I, Sim, Xueling, Teo, Soo Hwang, Tyrer, Jonathan P, van der Kolk, Lizet E, Wahlström, Cecilia, Wang, Qin, Perry, John RB, Benitez, Javier, Schmidt, Marjanka K, Schmutzler, Rita K, Pharoah, Paul DP, Droit, Arnaud, Dunning, Alison M, Kvist, Anders, Devilee, Peter, Easton, Douglas F, Simard, Jacques

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Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk von Wilcox, Naomi, Dumont, Martine, González-Neira, Anna, Carvalho, Sara, Joly Beauparlant, Charles, Crotti, Marco, Luccarini, Craig, Soucy, Penny, Dubois, Stéphane, Nuñez-Torres, Rocio, Pita, Guillermo, Gardner, Eugene J, Dennis, Joe, Alonso, M Rosario, Álvarez, Nuria, Baynes, Caroline, Collin-Deschesnes, Annie Claude, Desjardins, Sylvie, Becher, Heiko, Behrens, Sabine, Bolla, Manjeet K, Castelao, Jose E, Chang-Claude, Jenny, Cornelissen, Sten, Dörk, Thilo, Engel, Christoph, Gago-Dominguez, Manuela, Guénel, Pascal, Hadjisavvas, Andreas, Hahnen, Eric, Hartman, Mikael, Herráez, Belén, SGBCC Investigators, Jung, Audrey, Keeman, Renske, Kiechle, Marion, Li, Jingmei, Loizidou, Maria A, Lush, Michael, Michailidou, Kyriaki, Panayiotidis, Mihalis I, Sim, Xueling, Teo, Soo Hwang, Tyrer, Jonathan P, van der Kolk, Lizet E, Wahlström, Cecilia, Wang, Qin, Perry, John RB, Benitez, Javier, Schmidt, Marjanka K, Schmutzler, Rita K, Pharoah, Paul DP, Droit, Arnaud, Dunning, Alison M, Kvist, Anders, Devilee, Peter, Easton, Douglas F, Simard, Jacques

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Epidemiological and ES cell-based functional evaluation of BRCA2 variants identified in families with breast cancer von Sullivan, Teresa, Thirthagiri, Eswary, Chong, Chan-Eng, Stauffer, Stacey, Reid, Susan, Southon, Eileen, Hassan, Tiara, Ravichandran, Aravind, Wijaya, Eldarina, Lim, Joanna, Taib, Nur Aishah Mohd, Fadzli, Farhana, Yip, Cheng Har, Hartman, Mikael, Li, Jingmei, van Dam, Rob M, North, Susan L, Das, Ranabir, Easton, Douglas F, Biswas, Kajal, Teo, Soo-Hwang, Sharan, Shyam K, SGBCC Investigators, MYBRCA Investigators

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Breast cancer risks associated with missense variants in breast cancer susceptibility genes von Dorling, Leila, Carvalho, Sara, Allen, Jamie, Parsons, Michael T, Fortuno, Cristina, González-Neira, Anna, Heijl, Stephan M, Adank, Muriel A, Ahearn, Thomas U, Andrulis, Irene L, Auvinen, Päivi, Becher, Heiko, Beckmann, Matthias W, Behrens, Sabine, Bermisheva, Marina, Bogdanova, Natalia V, Bojesen, Stig E, Bolla, Manjeet K, Bremer, Michael, Briceno, Ignacio, Camp, Nicola J, Campbell, Archie, Castelao, Jose E, Chang-Claude, Jenny, Chanock, Stephen J, Chenevix-Trench, Georgia, NBCS Collaborators, Collée, J Margriet, Dennis, Joe, Dörk, Thilo, Eriksson, Mikael, Evans, D Gareth, Fasching, Peter A, Figueroa, Jonine, Flyger, Henrik, Gabrielson, Marike, Gago-Dominguez, Manuela, García-Closas, Montserrat, Giles, Graham G, Glendon, Gord, Guénel, Pascal, Gündert, Melanie, Hadjisavvas, Andreas, Hahnen, Eric, Hall, Per, Hamann, Ute, Harkness, Elaine F, Hartman, Mikael, Hogervorst, Frans BL, Hollestelle, Antoinette, Hoppe, Reiner, Howell, Anthony, SGBCC Investigators, Jakubowska, Anna, Jung, Audrey, Khusnutdinova, Elza, Kim, Sung-Won, Kristensen, Vessela N, Lakeman, Inge MM, Li, Jingmei, Lindblom, Annika, Loizidou, Maria A, Lophatananon, Artitaya, Lubiński, Jan, Luccarini, Craig, Mannermaa, Arto, Manoochehri, Mehdi, Margolin, Sara, Milne, Roger L, Muir, Kenneth, Nevanlinna, Heli, Newman, William G, Park, Sue K, Peterlongo, Paolo, Radice, Paolo, Saloustros, Emmanouil, Sawyer, Elinor J, Schmutzler, Rita K, Shah, Mitul, Southey, Melissa C, Surowy, Harald, Suvanto, Maija, Tomlinson, Ian, Torres, Diana, Truong, Thérèse, van Asperen, Christi J, Waltes, Regina, Wang, Qin, Yang, Xiaohong R, Pharoah, Paul DP, Schmidt, Marjanka K, Benitez, Javier, Vroling, Bas, Dunning, Alison M, Teo, Soo Hwang, Kvist, Anders, de la Hoya, Miguel, Devilee, Peter, Vreeswijk, Maaike PG, Easton, Douglas F

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Breast cancer risks associated with missense variants in breast cancer susceptibility genes von Dorling, Leila, Carvalho, Sara, Allen, Jamie, Parsons, Michael T, Fortuno, Cristina, González-Neira, Anna, Heijl, Stephan M, Adank, Muriel A, Ahearn, Thomas U, Andrulis, Irene L, Auvinen, Päivi, Becher, Heiko, Beckmann, Matthias W, Behrens, Sabine, Bermisheva, Marina, Bogdanova, Natalia V, Bojesen, Stig E, Bolla, Manjeet K, Bremer, Michael, Briceno, Ignacio, Camp, Nicola J, Campbell, Archie, Castelao, Jose E, Chang-Claude, Jenny, Chanock, Stephen J, Chenevix-Trench, Georgia, NBCS Collaborators, Collée, J Margriet, Dennis, Joe, Dörk, Thilo, Eriksson, Mikael, Evans, D Gareth, Fasching, Peter A, Figueroa, Jonine, Flyger, Henrik, Gabrielson, Marike, Gago-Dominguez, Manuela, García-Closas, Montserrat, Giles, Graham G, Glendon, Gord, Guénel, Pascal, Gündert, Melanie, Hadjisavvas, Andreas, Hahnen, Eric, Hall, Per, Hamann, Ute, Harkness, Elaine F, Hartman, Mikael, Hogervorst, Frans BL, Hollestelle, Antoinette, Hoppe, Reiner, Howell, Anthony, SGBCC Investigators, Jakubowska, Anna, Jung, Audrey, Khusnutdinova, Elza, Kim, Sung-Won, Kristensen, Vessela N, Lakeman, Inge MM, Li, Jingmei, Lindblom, Annika, Loizidou, Maria A, Lophatananon, Artitaya, Lubiński, Jan, Luccarini, Craig, Mannermaa, Arto, Manoochehri, Mehdi, Margolin, Sara, Milne, Roger L, Muir, Kenneth, Nevanlinna, Heli, Newman, William G, Park, Sue K, Peterlongo, Paolo, Radice, Paolo, Saloustros, Emmanouil, Sawyer, Elinor J, Schmutzler, Rita K, Shah, Mitul, Southey, Melissa C, Surowy, Harald, Suvanto, Maija, Tomlinson, Ian, Torres, Diana, Truong, Thérèse, van Asperen, Christi J, Waltes, Regina, Wang, Qin, Yang, Xiaohong R, Pharoah, Paul, Schmidt, Marjanka K, Benitez, Javier, Vroling, Bas, Dunning, Alison M, Teo, Soo Hwang, Kvist, Anders, de la Hoya, Miguel, Devilee, Peter, Vreeswijk, Maaike PG, Easton, Douglas

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Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk von Wilcox, Naomi, Dumont, Martine, González-Neira, Anna, Carvalho, Sara, Joly Beauparlant, Charles, Crotti, Marco, Luccarini, Craig, Soucy, Penny, Dubois, Stéphane, Nuñez-Torres, Rocio, Pita, Guillermo, Gardner, Eugene J, Dennis, Joe, Alonso, M Rosario, Álvarez, Nuria, Baynes, Caroline, Collin-Deschesnes, Annie Claude, Desjardins, Sylvie, Becher, Heiko, Behrens, Sabine, Bolla, Manjeet K, Castelao, Jose E, Chang-Claude, Jenny, Cornelissen, Sten, Dörk, Thilo, Engel, Christoph, Gago-Dominguez, Manuela, Guénel, Pascal, Hadjisavvas, Andreas, Hahnen, Eric, Hartman, Mikael, Herráez, Belén, SGBCC Investigators, Jung, Audrey, Keeman, Renske, Kiechle, Marion, Li, Jingmei, Loizidou, Maria A, Lush, Michael, Michailidou, Kyriaki, Panayiotidis, Mihalis I, Sim, Xueling, Teo, Soo Hwang, Tyrer, Jonathan P, van der Kolk, Lizet E, Wahlström, Cecilia, Wang, Qin, Perry, John RB, Benitez, Javier, Schmidt, Marjanka K, Schmutzler, Rita K, Pharoah, Paul DP, Droit, Arnaud, Dunning, Alison M, Kvist, Anders, Devilee, Peter, Easton, Douglas F, Simard, Jacques

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