Treffer 1 - 20 von 84 für Suche 'Colley, James P.', Suchdauer: 2,19s Treffer weiter einschränken
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    Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer von Lindstrom, Sara, Dennis, Joe, Maranian, Mel J, Brand, Judith S, Nordestgaard, Børge G, Flyger, Henrik, Rahman, Nazneen, Fletcher, Olivia, Nevanlinna, Heli, Muranen, Taru A, Aaltonen, Kirsimari, Ahsan, Habibul, John, Esther M, Gammon, Marilie D, Ursin, Giske, Schmidt, Daniel F, Gapstur, Susan M, Gaudet, Mia M, Diver, W Ryan, Schumacher, Fredrick, Hoover, Robert N, Lambrechts, Diether, Wildiers, Hans, van Limbergen, Erik, Broeks, Annegien, Cornelissen, Sten, Couch, Fergus J, Olson, Janet E, Hallberg, Emily, Meijers-Heijboer, Hanne, Ito, Hidemi, Iwata, Hiroji, Guénel, Pascal, Sanchez, Marie, Marme, Frederik, Surowy, Harald, Sohn, Christof, Van Den Berg, David, Benitez, Javier, Lu, Wei, Gao, Yu-Tang, Andrulis, Irene L, Knight, Julia A, Mulligan, Anna Marie, Sawyer, Elinor J, Tomlinson, Ian, Kerin, Michael J, Lindblom, Annika, Hollestelle, Antoinette, Collée, J Margriet, Blot, William, Signorello, Lisa B, Cai, Qiuyin, Hou, Ming-Feng, Kristensen, Vessela N, Milne, Roger L, McLean, Catriona, Peeters, Petra, Khaw, Kay-Tee, Palli, Domenico, Mortensen, Lotte Maxild, Dossus, Laure, Meindl, Alfons, Sutter, Christian, Yang, Rongxi, Muir, Kenneth, Siriwanarangsan, Pornthep, Miao, Hui, Chia, Kee Seng, Chan, Ching Wan, Fasching, Peter A, Beckmann, Matthias W, Haeberle, Lothar, Brenner, Hermann, Stegmaier, Christa, Ashworth, Alan, Schoemaker, Minouk J, Brinton, Louise, Zheng, Wei, Grip, Mervi, Brauch, Hiltrud, Radice, Paolo, Manoukian, Siranoush, Bernard, Loris, Dörk, Thilo, Hartikainen, Jaana M, Tollenaar, Robert A E M, Seynaeve, Caroline, Van Asperen, Christi J, Brennan, Paul, McKay, James, Neuhausen, Susan L, Baynes, Caroline, Ahmed, Shahana, Healey, Catherine S, Herrero, Daniel, Simard, Jacques, Chenevix-Trench, Georgia, Hall, Per, Easton, Douglas F

    Veröffentlicht in Nature genetics

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    The impact of coding germline variants on contralateral breast cancer risk and survival von Morra, Anna, Mavaddat, Nasim, Muranen, Taru A., Allen, Jamie, Andrulis, Irene L., Auvinen, Päivi, Behrens, Sabine, Bolla, Manjeet K., Brauch, Hiltrud, Camp, Nicola J., Geisler, Jürgen, Grenaker Alnæs, Grethe I., Czene, Kamila, Decker, Brennan, Dorling, Leila, Ekici, Arif B., Fasching, Peter A., Gago-Dominguez, Manuela, García-Closas, Montserrat, Giles, Graham G., Guénel, Pascal, Gündert, Melanie, Hamann, Ute, Harrington, Patricia A., He, Wei, Hooning, Maartje J., Hoppe, Reiner, Howell, Anthony, Amor, David, Andrews, Lesley, Balleine, Rosemary, Bennett, Ian, Bogwitz, Michael, Botes, Leon, Caldon, Liz, Cao, Michelle, Chakrabarti, Anannya, Chauhan, Deepa, Cohen, Paul, Cui, James, DeFazio, Anna, Delatycki, Martin, Dixon, Joanne, Edkins, Ted, Farshid, Gelareh, Fellows, Andrew, Flanagan, James, Fox, Stephen, French, Juliet, Gaff, Clara, George, Peter, Hunt, Clare, Kidd, Alexa, Koehler, Jessica, Kollias, James, Li, Shuai, Lipton, Lara, Loi, Sherene, Mann, Graham, Marsh, Deborah, McLachlan, Sue Anne, Milne, Roger, Nightingale, Sophie, O'Sullivan, Sarah, Ortega, David Gallego, Pachter, Nick, Patterson, Briony, Phillips, Kelly, Ramus, Susan, Rickard, Edwina, Robinson, Bridget, Saleh, Mona, Skandarajah, Anita, Saunders, Christobel, Scott, Rodney, Sexton, Adrienne, Shelling, Andrew, Taylor, Jessica, Thorne, Heather, Visvader, Jane, Young, Mary Ann, Zaheed, Milita, Jakubowska, Anna, Keeman, Renske, Kristensen, Vessela N., Milne, Roger L., Mulligan, Anna Marie, Park-Simon, Tjoung-Won, Peterlongo, Paolo, Pharoah, Paul D.P., Rhenius, Valerie, Sawyer, Elinor J., Schmutzler, Rita K., Shah, Mitul, Tomlinson, Ian, Vreeswijk, Maaike P.G., Wendt, Camilla, Yang, Xiaohong R., Devilee, Peter, Easton, Douglas F.


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    CYP3A71C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers von Johnson, Nichola, Maguire, Sarah, Morra, Anna, Tomczyk, Katarzyna, Bolla, Manjeet K., Wang, Qin, Dennis, Joe, Ahearn, Thomas U., Andrulis, Irene L., Anton-Culver, Hoda, Antonenkova, Natalia N., Aronson, Kristan J., Baynes, Caroline, Freeman, Laura E. Beane, Beckmann, Matthias W., Benitez, Javier, Bermisheva, Marina, Blomqvist, Carl, Boeckx, Bram, Brauch, Hiltrud, Brenner, Hermann, Burwinkel, Barbara, Canzian, Federico, Castelao, Jose E., Chanock, Stephen J., Chenevix-Trench, Georgia, Conroy, Don M., Couch, Fergus J., Cox, Angela, Cross, Simon S., Dörk, Thilo, Engel, Christoph, Figueroa, Jonine, Flyger, Henrik, Gapstur, Susan M., Giles, Graham G., Goldberg, Mark S., González-Neira, Anna, Guénel, Pascal, Hahnen, Eric, Hamann, Ute, Harrington, Patricia A., Hopper, John L., Howell, Anthony, Jakubowska, Anna, John, Esther M., Keeman, Renske, Kitahara, Cari M., Koutros, Stella, Kristensen, Vessela N., Kurian, Allison W., Le Marchand, Loic, Linet, Martha, Lubiński, Jan, Mannermaa, Arto, Manoukian, Siranoush, Mavroudis, Dimitrios, Mayes, Rebecca, Milne, Roger L., Neuhausen, Susan L., Nevanlinna, Heli, Nielsen, Sune F., Nordestgaard, Børge G., Obi, Nadia, Olson, Janet E., Olsson, Håkan, Park-Simon, Tjoung-Won, Plaseska-Karanfilska, Dijana, Rennert, Gad, Rennert, Hedy S., Ruddy, Kathryn J., Saloustros, Emmanouil, Sawyer, Elinor J., Scott, Christopher, Shu, Xiao-Ou, Simard, Jacques, Smichkoska, Snezhana, Sohn, Christof, Southey, Melissa C., Spinelli, John J., Stone, Jennifer, Tamimi, Rulla M., Tollenaar, Rob A. E. M., Tomlinson, Ian, Troester, Melissa A., van Veen, Elke M., Wang, Sophia S., Wendt, Camilla, Wildiers, Hans, Wolk, Alicja, Zheng, Wei, Dunning, Alison M., Pharoah, Paul D. P., Howie, A. Forbes, Peto, Julian, dos-Santos-Silva, Isabel, Swerdlow, Anthony J., Chang-Claude, Jenny, Orr, Nick, Fletcher, Olivia

    Veröffentlicht in British journal of cancer

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    Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset von Davidson, Aimee L., Parsons, Michael T., Bolla, Manjeet K., Wang, Qin, Dennis, Joe, Andrulis, Irene L., Antoniou, Antonis C., Behrens, Sabine, Bogdanova, Natalia V., Brüning, Thomas, Castelao, Jose E., Sahlberg, Kristine K., Børresen-Dale, Anne-Lise, Olsen, Karina Standahl, Engebråten, Olav, Grenaker Alnæs, Grethe I., Collée, J. Margriet, Eriksson, Mikael, Fasching, Peter A., Gago-Dominguez, Manuela, Glendon, Gord, Grassmann, Felix, Gronwald, Jacek, Guénel, Pascal, Hadjisavvas, Andreas, Haeberle, Lothar, Hamann, Ute, Ho, Peh Joo, Hoppe, Reiner, Antill, Yoland, Bogwitz, Michael, Brennan, Meagan, Caldon, Liz, Cao, Michelle, Chakrabarti, Anannya, Chauhan, Deepa, Colley, Alison, Crook, Ashley, Cui, James, Courtney, Eliza, Dawson, Sarah-Jane, deFazio, Anna, Delatycki, Martin, Dixon, Joanne, Edwards, Stacey, French, Juliet, Gattas, Mike, Greening, Sian, Hart, Stewart, Hayward, Nick, Hopper, John, Jenkins, Mark, Kirk, Judy, Koehler, Jessica, Lakhani, Sunil, Lawrence, Mitchell, Lippey, Jocelyn, Loi, Sherene, McLachlan, Sue Anne, O'Sullivan, Sarah, Pang, Jia-Min, Pathak, Gargi, Pearn, Amy, Phillips, Kelly, Pieper, Ellen, Ragunathan, Abi, Robinson, Bridget, Saleh, Mona, Salisbury, Elizabeth, Saunders, Christobel, Saunus, Jodi, Sexton, Adrienne, Shelling, Andrew, Visvader, Jane, Young, Mary Ann, Jakubowska, Anna, Khusnutdinova, Elza K., Kristensen, Vessela N., Lim, Joanna, Liu, Jenny, Lophatananon, Artitaya, Mannermaa, Arto, Mavroudis, Dimitrios A., Mensenkamp, Arjen R., Milne, Roger L., Newman, William G., Panayiotidis, Mihalis I., Park, Sue K., Park-Simon, Tjoung-Won, Rhenius, Valerie, Saloustros, Emmanouil, Sawyer, Elinor J., Schmidt, Marjanka K., Shah, Mitul, Teo, Soo Hwang, Torres, Diana, Truong, Thérèse, van de Beek, Irma, Wendt, Camilla C., Dunning, Alison M.


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    Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer‐specific survival von Morra, Anna, Schreurs, Maartje A. C., Anton‐Culver, Hoda, Augustinsson, Annelie, Bojesen, Stig E., Brauch, Hiltrud, Buys, Saundra S., Castelao, Jose E., Cessna, Melissa H., Chung, Wendy K., Gram, Inger Torhild, Naume, Bjørn, Geisler, Jürgen, Cross, Simon S., Easton, Douglas F., Eccles, Diana M., Eriksson, Mikael, Evans, D. Gareth, Fehm, Tanja N., Flyger, Henrik, Gabrielson, Marike, García‐Sáenz, José A., Gündert, Melanie, Hahnen, Eric, Hartikainen, Jaana M., Hoppe, Reiner, Clarke, Christine, Marsh, Deborah, Carpenter, Jane, Pathmanathan, Nirmala, Graham, J. Dinny, Sachchithananthan, Mythily, Amor, David, Balleine, Rosemary, Beesley, Jonathan, Bennett, Ian, Burke, Jo, Butow, Phyllis, Campbell, Ian, Chenevix‐Trench, Georgia, Cohen, Paul, Crook, Ashley, Cui, James, Dawson, Sarah‐Jane, Dixon, Joanne, Edwards, Stacey, Fong, Peter, Gattas, Mike, George, Peter, Kollias, James, Lakhani, Sunil, Lee, Jason, Lindeman, Geoff, Lipton, Lara, Lobb, Liz, Marsh, Deborah, O’Connell, Shona, Pachter, Nick, Phillips, Kelly, Pieper, Ellen, Ramus, Susan, Rickard, Edwina, Saunus, Jodi, Scott, Rodney, Scott, Clare, Shelling, Andrew, Taylor, Jessica, Taylor, Renea, Thorne, Heather, Trainer, Alison, Tucker, Kathy, Walker, Logan, Winship, Ingrid, Zaheed, Milita, Jakubowska, Anna, Jernström, Helena, John, Esther M., Kristensen, Vessela N., Lambrechts, Diether, Lindblom, Annika, Lubiński, Jan, Lux, Michael P., Mulligan, Anna Marie, Muranen, Taru A., Newman, William G., Obi, Nadia, Patel, Alpa V., Phillips, Kelly‐Anne, Plaseska‐Karanfilska, Dijana, Presneau, Nadege, Pylkäs, Katri, Rashid, Muhammad U., Sawyer, Elinor J., Schuetze, Sabine, Tapper, William J., Troester, Melissa A., Veen, Elke M., Wang, Qin, Winqvist, Robert, Ziogas, Argyrios

    Veröffentlicht in Cancer medicine (Malden, MA)

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    Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities von Atala, Kristhen, Dutta, Debdeep, Khanshour, Anas, Balasubramanyam, Ashok, Burrage, Lindsay C., Clark, Gary D., Ketkar, Shamika, Posey, Jennifer E., Rosenfeld, Jill A., Seto, Elaine, Scott, Daryl A., Tran, Alyssa A., Hubshman, Monika Weisz, Kanca, Oguz, Eng, Christine M., Falk, Marni, Hassey, Kelly, Zhang, Zhe, Mikati, Mohamad, Beggs, Alan H., Berry, Gerard T., Coggins, Matthew, Fieg, Elizabeth L., High, Frances, Holm, Ingrid A., Maas, Richard L., MacRae, Calum A., Pallais, J. Carl, Rao, Deepak A., Silverman, Edwin K., Sweetser, David A., Glanton, Emily, Maghiro, Audrey Stephannie C., McCray, Alexa T., Tan, Amelia L.M., Dasari, Surendra, Bademci, Guney, Barbouth, Deborah, Bivona, Stephanie, Borja, Nicholas, Gonzalez, Joanna M., Latchman, Kumarie, Tekin, Mustafa, Zuchner, Stephan, Gropman, Andrea, Macnamara, Ellen F., Maduro, Valerie V., Novacic, Donna, Toro, Camilo, Wahl, Colleen E., Adams, David R., Afzali, Ben, Burke, Elizabeth A., Fu, Jiayu, Wood, Heidi, Allworth, Aimee, Blue, Elizabeth, Chanprasert, Sirisak, Glass, Ian, Lam, Christina, Mirzaa, Ghayda, Raskind, Wendy, Alvarez, Raquel L., Bejerano, Gill, Bonner, Devon, Fisher, Paul G., Kohler, Jennefer N., Kravets, Elijah, Marwaha, Shruti, Ruzhnikov, Maura, Sutton, Shirley, Ungar, Rachel A., Crouse, Andrew B., Whitlock, Jordan, Butte, Manish J., Corona, Rosario, Dell'Angelica, Esteban C., Dorrani, Naghmeh, Fogel, Brent L., McGee, Elisabeth, Nieves-Rodriguez, Shirley, Alvey, Justin, Bohnsack, John, Moretti, Paolo, Quinlan, Aaron, Marth, Gabor, Bican, Anna, Cassini, Thomas, Corner, Brian, Hamid, Rizwan, Rives, Lynette, Robertson, Amy K., Ezell, Kimberly, Cogan, Joy D., Hayes, Nichole, Wegner, Daniel, Cole, F. Sessions, Schedl, Timothy, Wangler, Michael F., Bellen, Hugo J.

    Veröffentlicht in Genetics in medicine

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