Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Butterbach, Katja"'
Autor:
Schmit, Stephanie L, Edlund, Christopher K, Schumacher, Fredrick R, Gong, Jian, Harrison, Tabitha A, Huyghe, Jeroen R, Qu, Chenxu, Melas, Marilena, Van Den Berg, David J, Wang, Hansong, Tring, Stephanie, Plummer, Sarah J, Albanes, Demetrius, Alonso, M Henar, Amos, Christopher I, Anton, Kristen, Aragaki, Aaron K, Arndt, Volker, Barry, Elizabeth L, Berndt, Sonja I, Bezieau, Stéphane, Bien, Stephanie, Bloomer, Amanda, Boehm, Juergen, Boutron-Ruault, Marie-Christine, Brenner, Hermann, Brezina, Stefanie, Buchanan, Daniel D, Butterbach, Katja, Caan, Bette J, Campbell, Peter T, Carlson, Christopher S, Castelao, Jose E, Chan, Andrew T, Chang-Claude, Jenny, Chanock, Stephen J, Cheng, Iona, Cheng, Ya-Wen, Chin, Lee Soo, Church, James M, Church, Timothy, Coetzee, Gerhard A, Cotterchio, Michelle, Cruz Correa, Marcia, Curtis, Keith R, Duggan, David, Easton, Douglas F, English, Dallas, Feskens, Edith JM, Fischer, Rocky, FitzGerald, Liesel M, Fortini, Barbara K, Fritsche, Lars G, Fuchs, Charles S, Gago-Dominguez, Manuela, Gala, Manish, Gallinger, Steven J, Gauderman, W James, Giles, Graham G, Giovannucci, Edward L, Gogarten, Stephanie M, Gonzalez-Villalpando, Clicerio, Gonzalez-Villalpando, Elena M, Grady, William M, Greenson, Joel K, Gsur, Andrea, Gunter, Marc, Haiman, Christopher A, Hampe, Jochen, Harlid, Sophia, Harju, John F, Hayes, Richard B, Hofer, Philipp, Hoffmeister, Michael, Hopper, John L, Huang, Shu-Chen, Huerta, Jose Maria, Hudson, Thomas J, Hunter, David J, Idos, Gregory E, Iwasaki, Motoki, Jackson, Rebecca D, Jacobs, Eric J, Jee, Sun Ha, Jenkins, Mark A, Jia, Wei-Hua, Jiao, Shuo, Joshi, Amit D, Kolonel, Laurence N, Kono, Suminori, Kooperberg, Charles, Krogh, Vittorio, Kuehn, Tilman, Küry, Sébastien, LaCroix, Andrea, Laurie, Cecelia A, Lejbkowicz, Flavio, Lemire, Mathieu, Lenz, Heinz-Josef, Levine, David
Publikováno v:
Journal of the National Cancer Institute, vol 111, iss 2
BackgroundPrevious genome-wide association studies (GWAS) have identified 42 loci (P < 5 × 10-8) associated with risk of colorectal cancer (CRC). Expanded consortium efforts facilitating the discovery of additional susceptibility loci may capture un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7197cc0364738b8aed8ca475b72f2dec
https://escholarship.org/uc/item/3bk0g2vk
https://escholarship.org/uc/item/3bk0g2vk
Autor:
Southey, Melissa C, Goldgar, David E, Winqvist, Robert, Pylkäs, Katri, Couch, Fergus, Tischkowitz, Marc, Foulkes, William D, Dennis, Joe, Michailidou, Kyriaki, van Rensburg, Elizabeth J, Heikkinen, Tuomas, Nevanlinna, Heli, Hopper, John L, Dörk, Thilo, Claes, Kathleen Bm, Reis-Filho, Jorge, Teo, Zhi Ling, Radice, Paolo, Catucci, Irene, Peterlongo, Paolo, Tsimiklis, Helen, Odefrey, Fabrice A, Dowty, James G, Schmidt, Marjanka K, Broeks, Annegien, Hogervorst, Frans B, Verhoef, Senno, Carpenter, Jane, Clarke, Christine, Scott, Rodney J, Fasching, Peter A, Haeberle, Lothar, Ekici, Arif B, Beckmann, Matthias W, Peto, Julian, Dos-Santos-Silva, Isabel, Fletcher, Olivia, Johnson, Nichola, Bolla, Manjeet K, Sawyer, Elinor J, Tomlinson, Ian, Kerin, Michael J, Miller, Nicola, Marme, Federik, Burwinkel, Barbara, Yang, Rongxi, Guénel, Pascal, Truong, Thérèse, Menegaux, Florence, Sanchez, Marie, Bojesen, Stig, Nielsen, Sune F, Flyger, Henrik, Benitez, Javier, Zamora, M Pilar, Perez, Jose Ignacio Arias, Menéndez, Primitiva, Anton-Culver, Hoda, Neuhausen, Susan, Ziogas, Argyrios, Clarke, Christina A, Brenner, Hermann, Arndt, Volker, Stegmaier, Christa, Brauch, Hiltrud, Brüning, Thomas, Ko, Yon-Dschun, Muranen, Taru A, Aittomäki, Kristiina, Blomqvist, Carl, Bogdanova, Natalia V, Antonenkova, Natalia N, Lindblom, Annika, Margolin, Sara, Mannermaa, Arto, Kataja, Vesa, Kosma, Veli-Matti, Hartikainen, Jaana M, Spurdle, Amanda B, Investigators, kConFab, Australian Ovarian Cancer Study Group, Wauters, Els, Smeets, Dominiek, Beuselinck, Benoit, Floris, Giuseppe, Chang-Claude, Jenny, Rudolph, Anja, Seibold, Petra, Flesch-Janys, Dieter, Olson, Janet E, Vachon, Celine, Pankratz, Vernon S, McLean, Catriona, Haiman, Christopher A, Henderson, Brian E, Schumacher, Fredrick, Le Marchand, Loic, Kristensen, Vessela, Alnæs, Grethe Grenaker, Zheng, Wei, Hunter, David J, Lindstrom, Sara, Hankinson, Susan E, Kraft, Peter, Andrulis, Irene, Knight, Julia A, Glendon, Gord, Mulligan, Anna Marie, Jukkola-Vuorinen, Arja, Grip, Mervi, Kauppila, Saila, Devilee, Peter, Tollenaar, Robert AEM, Seynaeve, Caroline, Hollestelle, Antoinette, Garcia-Closas, Montserrat, Figueroa, Jonine, Chanock, Stephen J, Lissowska, Jolanta, Czene, Kamila, Darabi, Hatef, Eriksson, Mikael, Eccles, Diana M, Rafiq, Sajjad, Tapper, William J, Gerty, Sue M, Hooning, Maartje J, Martens, John WM, Collée, J Margriet, Tilanus-Linthorst, Madeleine, Hall, Per, Li, Jingmei, Brand, Judith S, Humphreys, Keith, Cox, Angela, Reed, Malcolm WR, Luccarini, Craig, Baynes, Caroline, Dunning, Alison M, Hamann, Ute, Torres, Diana, Ulmer, Hans Ulrich, Rüdiger, Thomas, Jakubowska, Anna, Lubinski, Jan, Jaworska, Katarzyna, Durda, Katarzyna, Slager, Susan, Toland, Amanda E, Ambrosone, Christine B, Yannoukakos, Drakoulis, Swerdlow, Anthony, Ashworth, Alan, Orr, Nick, Jones, Michael, González-Neira, Anna, Pita, Guillermo, Alonso, M Rosario, Álvarez, Nuria, Herrero, Daniel, Tessier, Daniel C, Vincent, Daniel, Bacot, Francois, Simard, Jacques, Dumont, Martine, Soucy, Penny, Eeles, Rosalind, Muir, Kenneth, Wiklund, Fredrik, Gronberg, Henrik, Schleutker, Johanna, Nordestgaard, Børge G, Weischer, Maren, Travis, Ruth C, Neal, David, Donovan, Jenny L, Hamdy, Freddie C, Khaw, Kay-Tee, Stanford, Janet L, Blot, William J, Thibodeau, Stephen, Schaid, Daniel J, Kelley, Joseph L, Maier, Christiane, Kibel, Adam S, Cybulski, Cezary, Cannon-Albright, Lisa, Butterbach, Katja, Park, Jong, Kaneva, Radka, Batra, Jyotsna, Teixeira, Manuel R, Kote-Jarai, Zsofia, Olama, Ali Amin Al, Benlloch, Sara, Renner, Stefan P, Hartmann, Arndt, Hein, Alexander, Ruebner, Matthias, Lambrechts, Diether, Van Nieuwenhuysen, Els, Vergote, Ignace, Lambretchs, Sandrina, Doherty, Jennifer A, Rossing, Mary Anne, Nickels, Stefan, Eilber, Ursula, Wang-Gohrke, Shan, Odunsi, Kunle, Sucheston-Campbell, Lara E, Friel, Grace, Lurie, Galina, Killeen, Jeffrey L, Wilkens, Lynne R, Goodman, Marc T, Runnebaum, Ingo, Hillemanns, Peter A, Pelttari, Liisa M, Butzow, Ralf, Modugno, Francesmary, Edwards, Robert P, Ness, Roberta B, Moysich, Kirsten B, du Bois, Andreas, Heitz, Florian, Harter, Philipp, Kommoss, Stefan, Karlan, Beth Y, Walsh, Christine, Lester, Jenny, Jensen, Allan, Kjaer, Susanne Krüger, Høgdall, Estrid, Peissel, Bernard, Bonanni, Bernardo, Bernard, Loris, Goode, Ellen L, Fridley, Brooke L, Vierkant, Robert A, Cunningham, Julie M, Larson, Melissa C, Fogarty, Zachary C, Kalli, Kimberly R, Liang, Dong, Lu, Karen H, Hildebrandt, Michelle AT, Wu, Xifeng, Levine, Douglas A, Dao, Fanny, Bisogna, Maria, Berchuck, Andrew, Iversen, Edwin S, Marks, Jeffrey R, Akushevich, Lucy, Cramer, Daniel W, Schildkraut, Joellen, Terry, Kathryn L, Poole, Elizabeth M, Stampfer, Meir, Tworoger, Shelley S, Bandera, Elisa V, Orlow, Irene, Olson, Sara H, Bjorge, Line, Salvesen, Helga B, van Altena, Anne M, Aben, Katja KH, Kiemeney, Lambertus A, Massuger, Leon FAG, Pejovic, Tanja, Bean, Yukie, Brooks-Wilson, Angela, Kelemen, Linda E, Cook, Linda S, Le, Nhu D, Górski, Bohdan, Gronwald, Jacek, Menkiszak, Janusz, Høgdall, Claus K, Lundvall, Lene, Nedergaard, Lotte, Engelholm, Svend Aage, Dicks, Ed, Tyrer, Jonathan, Campbell, Ian, McNeish, Iain, Paul, James, Siddiqui, Nadeem, Glasspool, Rosalind, Whittemore, Alice S, Rothstein, Joseph H, McGuire, Valerie, Sieh, Weiva, Cai, Hui, Shu, Xiao-Ou, Teten, Rachel T, Sutphen, Rebecca, McLaughlin, John R, Narod, Steven A, Phelan, Catherine M, Monteiro, Alvaro N, Fenstermacher, David, Lin, Hui-Yi, Permuth, Jennifer B, Sellers, Thomas A, Chen, Y Ann, Tsai, Ya-Yu, Chen, Zhihua, Gentry-Maharaj, Aleksandra, Gayther, Simon A, Ramus, Susan J, Menon, Usha, Wu, Anna H, Pearce, Celeste L, Van Den Berg, David, Pike, Malcolm C, Dansonka-Mieszkowska, Agnieszka, Plisiecka-Halasa, Joanna, Moes-Sosnowska, Joanna, Kupryjanczyk, Jolanta, Pharoah, Paul Dp, Song, Honglin, Winship, Ingrid, Chenevix-Trench, Georgia, Giles, Graham G, Tavtigian, Sean V, Easton, Doug F, Milne, Roger L
Publikováno v:
Journal of Medical Genetics, 53(12), 800-811. BMJ Publishing Group
Southey, M C, Goldgar, D E, Winqvist, R, Pylkäs, K, Couch, F, Tischkowitz, M, Foulkes, W D, Dennis, J, Michailidou, K, van Rensburg, E J, Heikkinen, T, Nevanlinna, H, Hopper, J L, Dörk, T, Claes, K B, Reis-Filho, J, Teo, Z L, Radice, P, Catucci, I, Peterlongo, P, Tsimiklis, H, Odefrey, F A, Dowty, J G, Schmidt, M K, Broeks, A, Hogervorst, F B, Verhoef, S, Carpenter, J, Clarke, C, Scott, R J, Fasching, P A, Haeberle, L, Ekici, A B, Beckmann, M W, Peto, J, Dos-Santos-Silva, I, Fletcher, O, Johnson, N, Bolla, M K, Sawyer, E J, Tomlinson, I, Kerin, M J, Miller, N, Marme, F, Bojesen, S, Nordestgaard, B G, Kjaer, S K, Høgdall, E, Høgdall, C K, Engelholm, S A & Australian Ovarian Cancer Study Group 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk : data from COGS ', Journal of Medical Genetics, vol. 53, no. 12, pp. 800-811 . https://doi.org/10.1136/jmedgenet-2016-103839
Journal of Medical Genetics, 53(12), 800-811
Southey, M C, Goldgar, D E, Winqvist, R, Pylkäs, K, Couch, F, Tischkowitz, M, Foulkes, W D, Dennis, J, Michailidou, K, van Rensburg, E J, Heikkinen, T, Nevanlinna, H, Hopper, J L, Dörk, T, Claes, K B, Reis-Filho, J, Teo, Z L, Radice, P, Catucci, I, Peterlongo, P, Tsimiklis, H, Odefrey, F A, Dowty, J G, Schmidt, M K, Broeks, A, Hogervorst, F B, Verhoef, S, Carpenter, J, Clarke, C, Scott, R J, Fasching, P A, Haeberle, L, Ekici, A B, Beckmann, M W, Peto, J, Dos-Santos-Silva, I, Fletcher, O, Johnson, N, Bolla, M K, Sawyer, E J, Tomlinson, I, Kerin, M J, Miller, N, Marme, F, Burwinkel, B, Yang, R, Guénel, P, Truong, T, Menegaux, F, Muir, K & Australian Ovarian Cancer Study Group 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk : data from COGS ', Journal of Medical Genetics, vol. 53, no. 12, pp. 800-811 . https://doi.org/10.1136/jmedgenet-2016-103839
Southey, M C, Goldgar, D, Winqvist, R, et al. & Donovan, J 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk : data from COGS ', Journal of Medical Genetics, vol. 53, no. 12, pp. 800-811 . https://doi.org/10.1136/jmedgenet-2016-103839
Journal of Medical Genetics
JOURNAL OF MEDICAL GENETICS
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Southey, M C, Goldgar, D E, Winqvist, R, Pylkäs, K, Couch, F, Tischkowitz, M, Foulkes, W D, Dennis, J, Michailidou, K, Van Rensburg, E J, Heikkinen, T, Nevanlinna, H, Hopper, J L, Dörk, T, Claes, K B, Reis-filho, J, Teo, Z L, Radice, P, Catucci, I, Peterlongo, P, Tsimiklis, H, Odefrey, F A, Dowty, J G, Schmidt, M K, Broeks, A, Hogervorst, F B, Verhoef, S, Carpenter, J, Clarke, C, Scott, R J, Fasching, P A, Haeberle, L, Ekici, A B, Beckmann, M W, Peto, J, Dos-santos-silva, I, Fletcher, O, Johnson, N, Bolla, M K, Sawyer, E J, Tomlinson, I, Kerin, M J, Miller, N, Marme, F, Burwinkel, B, Yang, R, Guénel, P, Truong, T, Menegaux, F, Sanchez, M, Bojesen, S, Nielsen, S F, Flyger, H, Benitez, J, Zamora, M P, Perez, J I A, Menéndez, P, Anton-culver, H, Neuhausen, S, Ziogas, A, Clarke, C A, Brenner, H, Arndt, V, Stegmaier, C, Brauch, H, Brüning, T, Ko, Y, Muranen, T A, Aittomäki, K, Blomqvist, C, Bogdanova, N V, Antonenkova, N N, Lindblom, A, Margolin, S, Mannermaa, A, Kataja, V, Kosma, V, Hartikainen, J M, Spurdle, A B, Investigators, K, Wauters, E, Smeets, D, Beuselinck, B, Floris, G, Chang-claude, J, Rudolph, A, Seibold, P, Flesch-janys, D, Olson, J E, Vachon, C, Pankratz, V S, Mclean, C, Haiman, C A, Henderson, B E, Schumacher, F, Le Marchand, L, Kristensen, V, Alnæs, G G, Zheng, W, Hunter, D J, Lindstrom, S, Hankinson, S E, Kraft, P, Andrulis, I, Knight, J A, Glendon, G, Mulligan, A M, Jukkola-vuorinen, A, Grip, M, Kauppila, S, Devilee, P, Tollenaar, R A E M, Seynaeve, C, Hollestelle, A, Garcia-closas, M, Figueroa, J, Chanock, S J, Lissowska, J, Czene, K, Darabi, H, Eriksson, M, Eccles, D M, Rafiq, S, Tapper, W J, Gerty, S M, Hooning, M J, Martens, J W M, Collée, J M, Tilanus-linthorst, M, Hall, P, Li, J, Brand, J S, Humphreys, K, Cox, A, Reed, M W R, Luccarini, C, Baynes, C, Dunning, A M, Hamann, U, Torres, D, Ulmer, H U, Rüdiger, T, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Slager, S, Toland, A E, Ambrosone, C B, Yannoukakos, D, Swerdlow, A, Ashworth, A, Orr, N, Jones, M, González-neira, A, Pita, G, Alonso, M R, Álvarez, N, Herrero, D, Tessier, D C, Vincent, D, Bacot, F, Simard, J, Dumont, M, Soucy, P, Eeles, R, Muir, K, Wiklund, F, Gronberg, H, Schleutker, J, Nordestgaard, B G, Weischer, M, Travis, R C, Neal, D, Donovan, J L, Hamdy, F C, Khaw, K, Stanford, J L, Blot, W J, Thibodeau, S, Schaid, D J, Kelley, J L, Maier, C, Kibel, A S, Cybulski, C, Cannon-albright, L, Butterbach, K, Park, J, Kaneva, R, Batra, J, Teixeira, M R, Kote-jarai, Z, Olama, A A A, Benlloch, S, Renner, S P, Hartmann, A, Hein, A, Ruebner, M, Lambrechts, D, Van Nieuwenhuysen, E, Vergote, I, Lambretchs, S, Doherty, J A, Rossing, M A, Nickels, S, Eilber, U, Wang-gohrke, S, Odunsi, K, Sucheston-campbell, L E, Friel, G, Lurie, G, Killeen, J L, Wilkens, L R, Goodman, M T, Runnebaum, I, Hillemanns, P A, Pelttari, L M, Butzow, R, Modugno, F, Edwards, R P, Ness, R B, Moysich, K B, Du Bois, A, Heitz, F, Harter, P, Kommoss, S, Karlan, B Y, Walsh, C, Lester, J, Jensen, A, Kjaer, S K, Høgdall, E, Peissel, B, Bonanni, B, Bernard, L, Goode, E L, Fridley, B L, Vierkant, R A, Cunningham, J M, Larson, M C, Fogarty, Z C, Kalli, K R, Liang, D, Lu, K H, Hildebrandt, M A T, Wu, X, Levine, D A, Dao, F, Bisogna, M, Berchuck, A, Iversen, E S, Marks, J R, Akushevich, L, Cramer, D W, Schildkraut, J, Terry, K L, Poole, E M, Stampfer, M, Tworoger, S S, Bandera, E V, Orlow, I, Olson, S H, Bjorge, L, Salvesen, H B, Van Altena, A M, Aben, K K H, Kiemeney, L A, Massuger, L F A G, Pejovic, T, Bean, Y, Brooks-wilson, A, Kelemen, L E, Cook, L S, Le, N D, Górski, B, Gronwald, J, Menkiszak, J, Høgdall, C K, Lundvall, L, Nedergaard, L, Engelholm, S A, Dicks, E, Tyrer, J, Campbell, I, Mcneish, I, Paul, J, Siddiqui, N, Glasspool, R, Whittemore, A S, Rothstein, J H, Mcguire, V, Sieh, W, Cai, H, Shu, X, Teten, R T, Sutphen, R, Mclaughlin, J R, Narod, S A, Phelan, C M, Monteiro, A N, Fenstermacher, D, Lin, H, Permuth, J B, Sellers, T A, Chen, Y A, Tsai, Y, Chen, Z, Gentry-maharaj, A, Gayther, S A, Ramus, S J, Menon, U, Wu, A H, Pearce, C L, Van Den Berg, D, Pike, M C, Dansonka-mieszkowska, A, Plisiecka-halasa, J, Moes-sosnowska, J, Kupryjanczyk, J, Pharoah, P D, Song, H, Winship, I, Chenevix-trench, G, Giles, G G, Tavtigian, S V, Easton, D F & Milne, R L 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS ', Journal of Medical Genetics, pp. jmedgenet-2016-103839 . https://doi.org/10.1136/jmedgenet-2016-103839
Southey, M C, Goldgar, D E, Winqvist, R, Pylkäs, K, Couch, F J, Tischkowitz, M, Foulkes, W D, Dennis, J, Michailidou, K & Orr, N 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS ', Journal of Medical Genetics, vol. 53, no. 12, pp. 800-811 . https://doi.org/10.1136/jmedgenet-2016-103839
Journal of Medical Genetics, 53, 800-811
Journal of Medical Genetics, 53, 12, pp. 800-811
Southey, M C, Goldgar, D E, Winqvist, R, Pylkäs, K, Couch, F, Tischkowitz, M, Foulkes, W D, Dennis, J, Michailidou, K, van Rensburg, E J, Heikkinen, T, Nevanlinna, H, Hopper, J L, Dörk, T, Claes, K B, Reis-Filho, J, Teo, Z L, Radice, P, Catucci, I, Peterlongo, P, Tsimiklis, H, Odefrey, F A, Dowty, J G, Schmidt, M K, Broeks, A, Hogervorst, F B, Verhoef, S, Carpenter, J, Clarke, C, Scott, R J, Fasching, P A, Haeberle, L, Ekici, A B, Beckmann, M W, Peto, J, Dos-Santos-Silva, I, Fletcher, O, Johnson, N, Bolla, M K, Sawyer, E J, Tomlinson, I, Kerin, M J, Miller, N, Marme, F, Bojesen, S, Nordestgaard, B G, Kjaer, S K, Høgdall, E, Høgdall, C K, Engelholm, S A & Australian Ovarian Cancer Study Group 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk : data from COGS ', Journal of Medical Genetics, vol. 53, no. 12, pp. 800-811 . https://doi.org/10.1136/jmedgenet-2016-103839
Journal of Medical Genetics, 53(12), 800-811
Southey, M C, Goldgar, D E, Winqvist, R, Pylkäs, K, Couch, F, Tischkowitz, M, Foulkes, W D, Dennis, J, Michailidou, K, van Rensburg, E J, Heikkinen, T, Nevanlinna, H, Hopper, J L, Dörk, T, Claes, K B, Reis-Filho, J, Teo, Z L, Radice, P, Catucci, I, Peterlongo, P, Tsimiklis, H, Odefrey, F A, Dowty, J G, Schmidt, M K, Broeks, A, Hogervorst, F B, Verhoef, S, Carpenter, J, Clarke, C, Scott, R J, Fasching, P A, Haeberle, L, Ekici, A B, Beckmann, M W, Peto, J, Dos-Santos-Silva, I, Fletcher, O, Johnson, N, Bolla, M K, Sawyer, E J, Tomlinson, I, Kerin, M J, Miller, N, Marme, F, Burwinkel, B, Yang, R, Guénel, P, Truong, T, Menegaux, F, Muir, K & Australian Ovarian Cancer Study Group 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk : data from COGS ', Journal of Medical Genetics, vol. 53, no. 12, pp. 800-811 . https://doi.org/10.1136/jmedgenet-2016-103839
Southey, M C, Goldgar, D, Winqvist, R, et al. & Donovan, J 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk : data from COGS ', Journal of Medical Genetics, vol. 53, no. 12, pp. 800-811 . https://doi.org/10.1136/jmedgenet-2016-103839
Journal of Medical Genetics
JOURNAL OF MEDICAL GENETICS
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Southey, M C, Goldgar, D E, Winqvist, R, Pylkäs, K, Couch, F, Tischkowitz, M, Foulkes, W D, Dennis, J, Michailidou, K, Van Rensburg, E J, Heikkinen, T, Nevanlinna, H, Hopper, J L, Dörk, T, Claes, K B, Reis-filho, J, Teo, Z L, Radice, P, Catucci, I, Peterlongo, P, Tsimiklis, H, Odefrey, F A, Dowty, J G, Schmidt, M K, Broeks, A, Hogervorst, F B, Verhoef, S, Carpenter, J, Clarke, C, Scott, R J, Fasching, P A, Haeberle, L, Ekici, A B, Beckmann, M W, Peto, J, Dos-santos-silva, I, Fletcher, O, Johnson, N, Bolla, M K, Sawyer, E J, Tomlinson, I, Kerin, M J, Miller, N, Marme, F, Burwinkel, B, Yang, R, Guénel, P, Truong, T, Menegaux, F, Sanchez, M, Bojesen, S, Nielsen, S F, Flyger, H, Benitez, J, Zamora, M P, Perez, J I A, Menéndez, P, Anton-culver, H, Neuhausen, S, Ziogas, A, Clarke, C A, Brenner, H, Arndt, V, Stegmaier, C, Brauch, H, Brüning, T, Ko, Y, Muranen, T A, Aittomäki, K, Blomqvist, C, Bogdanova, N V, Antonenkova, N N, Lindblom, A, Margolin, S, Mannermaa, A, Kataja, V, Kosma, V, Hartikainen, J M, Spurdle, A B, Investigators, K, Wauters, E, Smeets, D, Beuselinck, B, Floris, G, Chang-claude, J, Rudolph, A, Seibold, P, Flesch-janys, D, Olson, J E, Vachon, C, Pankratz, V S, Mclean, C, Haiman, C A, Henderson, B E, Schumacher, F, Le Marchand, L, Kristensen, V, Alnæs, G G, Zheng, W, Hunter, D J, Lindstrom, S, Hankinson, S E, Kraft, P, Andrulis, I, Knight, J A, Glendon, G, Mulligan, A M, Jukkola-vuorinen, A, Grip, M, Kauppila, S, Devilee, P, Tollenaar, R A E M, Seynaeve, C, Hollestelle, A, Garcia-closas, M, Figueroa, J, Chanock, S J, Lissowska, J, Czene, K, Darabi, H, Eriksson, M, Eccles, D M, Rafiq, S, Tapper, W J, Gerty, S M, Hooning, M J, Martens, J W M, Collée, J M, Tilanus-linthorst, M, Hall, P, Li, J, Brand, J S, Humphreys, K, Cox, A, Reed, M W R, Luccarini, C, Baynes, C, Dunning, A M, Hamann, U, Torres, D, Ulmer, H U, Rüdiger, T, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Slager, S, Toland, A E, Ambrosone, C B, Yannoukakos, D, Swerdlow, A, Ashworth, A, Orr, N, Jones, M, González-neira, A, Pita, G, Alonso, M R, Álvarez, N, Herrero, D, Tessier, D C, Vincent, D, Bacot, F, Simard, J, Dumont, M, Soucy, P, Eeles, R, Muir, K, Wiklund, F, Gronberg, H, Schleutker, J, Nordestgaard, B G, Weischer, M, Travis, R C, Neal, D, Donovan, J L, Hamdy, F C, Khaw, K, Stanford, J L, Blot, W J, Thibodeau, S, Schaid, D J, Kelley, J L, Maier, C, Kibel, A S, Cybulski, C, Cannon-albright, L, Butterbach, K, Park, J, Kaneva, R, Batra, J, Teixeira, M R, Kote-jarai, Z, Olama, A A A, Benlloch, S, Renner, S P, Hartmann, A, Hein, A, Ruebner, M, Lambrechts, D, Van Nieuwenhuysen, E, Vergote, I, Lambretchs, S, Doherty, J A, Rossing, M A, Nickels, S, Eilber, U, Wang-gohrke, S, Odunsi, K, Sucheston-campbell, L E, Friel, G, Lurie, G, Killeen, J L, Wilkens, L R, Goodman, M T, Runnebaum, I, Hillemanns, P A, Pelttari, L M, Butzow, R, Modugno, F, Edwards, R P, Ness, R B, Moysich, K B, Du Bois, A, Heitz, F, Harter, P, Kommoss, S, Karlan, B Y, Walsh, C, Lester, J, Jensen, A, Kjaer, S K, Høgdall, E, Peissel, B, Bonanni, B, Bernard, L, Goode, E L, Fridley, B L, Vierkant, R A, Cunningham, J M, Larson, M C, Fogarty, Z C, Kalli, K R, Liang, D, Lu, K H, Hildebrandt, M A T, Wu, X, Levine, D A, Dao, F, Bisogna, M, Berchuck, A, Iversen, E S, Marks, J R, Akushevich, L, Cramer, D W, Schildkraut, J, Terry, K L, Poole, E M, Stampfer, M, Tworoger, S S, Bandera, E V, Orlow, I, Olson, S H, Bjorge, L, Salvesen, H B, Van Altena, A M, Aben, K K H, Kiemeney, L A, Massuger, L F A G, Pejovic, T, Bean, Y, Brooks-wilson, A, Kelemen, L E, Cook, L S, Le, N D, Górski, B, Gronwald, J, Menkiszak, J, Høgdall, C K, Lundvall, L, Nedergaard, L, Engelholm, S A, Dicks, E, Tyrer, J, Campbell, I, Mcneish, I, Paul, J, Siddiqui, N, Glasspool, R, Whittemore, A S, Rothstein, J H, Mcguire, V, Sieh, W, Cai, H, Shu, X, Teten, R T, Sutphen, R, Mclaughlin, J R, Narod, S A, Phelan, C M, Monteiro, A N, Fenstermacher, D, Lin, H, Permuth, J B, Sellers, T A, Chen, Y A, Tsai, Y, Chen, Z, Gentry-maharaj, A, Gayther, S A, Ramus, S J, Menon, U, Wu, A H, Pearce, C L, Van Den Berg, D, Pike, M C, Dansonka-mieszkowska, A, Plisiecka-halasa, J, Moes-sosnowska, J, Kupryjanczyk, J, Pharoah, P D, Song, H, Winship, I, Chenevix-trench, G, Giles, G G, Tavtigian, S V, Easton, D F & Milne, R L 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS ', Journal of Medical Genetics, pp. jmedgenet-2016-103839 . https://doi.org/10.1136/jmedgenet-2016-103839
Southey, M C, Goldgar, D E, Winqvist, R, Pylkäs, K, Couch, F J, Tischkowitz, M, Foulkes, W D, Dennis, J, Michailidou, K & Orr, N 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS ', Journal of Medical Genetics, vol. 53, no. 12, pp. 800-811 . https://doi.org/10.1136/jmedgenet-2016-103839
Journal of Medical Genetics, 53, 800-811
Journal of Medical Genetics, 53, 12, pp. 800-811
Background: The rarity of mutations in PALB2, CHEK2 and ATM make it difficult to estimate precisely associated cancer risks. Population-based family studies have provided evidence that at least some of these mutations are associated with breast cance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bec638ffb29848a933253363bb733127
https://opus4.kobv.de/opus4-fau/frontdoor/index/index/docId/9798
https://opus4.kobv.de/opus4-fau/frontdoor/index/index/docId/9798
Autor:
Schumacher, Fredrick R, Schmit, Stephanie L, Jiao, Shuo, Edlund, Christopher K, Wang, Hansong, Zhang, Ben, Hsu, Li, Huang, Shu-Chen, Fischer, Christopher P, Harju, John F, Idos, Gregory E, Lejbkowicz, Flavio, Manion, Frank J, McDonnell, Kevin, McNeil, Caroline E, Melas, Marilena, Rennert, Hedy S, Shi, Wei, Thomas, Duncan C, Van Den Berg, David J, Hutter, Carolyn M, Aragaki, Aaron K, Butterbach, Katja, Caan, Bette J, Carlson, Christopher S, Chanock, Stephen J, Curtis, Keith R, Fuchs, Charles S, Gala, Manish, Giovannucci, Edward L, Gogarten, Stephanie M, Hayes, Richard B, Henderson, Brian, Hunter, David J, Jackson, Rebecca D, Kolonel, Laurence N, Kooperberg, Charles, Küry, Sébastien, LaCroix, Andrea, Laurie, Cathy C, Laurie, Cecelia A, Lemire, Mathieu, Levine, David, Ma, Jing, Makar, Karen W, Qu, Conghui, Taverna, Darin, Ulrich, Cornelia M, Wu, Kana, Kono, Suminori, West, Dee W, Berndt, Sonja I, Bezieau, Stephane, Brenner, Hermann, Campbell, Peter T, Chan, Andrew T, Chang-Claude, Jenny, Coetzee, Gerhard A, Conti, David V, Duggan, David, Figueiredo, Jane C, Fortini, Barbara K, Gallinger, Steven J, Gauderman, W James, Giles, Graham, Green, Roger, Haile, Robert, Harrison, Tabitha A, Hoffmeister, Michael, Hopper, John L, Hudson, Thomas J, Jacobs, Eric, Iwasaki, Motoki, Jee, Sun Ha, Jenkins, Mark, Jia, Wei-Hua, Joshi, Amit, Li, Li, Lindor, Noralene M, Matsuo, Keitaro, Moreno, Victor, Mukherjee, Bhramar, Newcomb, Polly A, Potter, John D, Raskin, Leon, Rennert, Gad, Rosse, Stephanie, Severi, Gianluca, Schoen, Robert E, Seminara, Daniela, Shu, Xiao-Ou, Slattery, Martha L, Tsugane, Shoichiro, White, Emily, Xiang, Yong-Bing, Zanke, Brent W, Zheng, Wei, Le Marchand, Loic, Casey, Graham, Gruber, Stephen B
Publikováno v:
Nature communications, vol 6, iss 1
Schumacher, FR; Schmidt, SL; Jiao, S; Edlund, CK; Wang, H; Zhang, B; et al.(2019). Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci. Nature Communications. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/3p66z8vz
Schumacher, FR; Schmidt, SL; Jiao, S; Edlund, CK; Wang, H; Zhang, B; et al.(2019). Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci. Nature Communications. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/3p66z8vz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c05ea3272d734b72f3c8f517bcc31698
https://escholarship.org/uc/item/3p66z8vz
https://escholarship.org/uc/item/3p66z8vz
Autor:
Schumacher, Fredrick R, Schmit, Stephanie L, Jiao, Shuo, Edlund, Christopher K, Wang, Hansong, Zhang, Ben, Hsu, Li, Huang, Shu-Chen, Fischer, Christopher P, Harju, John F, Idos, Gregory E, Lejbkowicz, Flavio, Manion, Frank J, McDonnell, Kevin, McNeil, Caroline E, Melas, Marilena, Rennert, Hedy S, Shi, Wei, Thomas, Duncan C, Van Den Berg, David J, Hutter, Carolyn M, Aragaki, Aaron K, Butterbach, Katja, Caan, Bette J, Carlson, Christopher S, Chanock, Stephen J, Curtis, Keith R, Fuchs, Charles S, Gala, Manish, Giovannucci, Edward L, Gogarten, Stephanie M, Hayes, Richard B, Henderson, Brian, Hunter, David J, Jackson, Rebecca D, Kolonel, Laurence N, Kooperberg, Charles, Küry, Sébastien, LaCroix, Andrea, Laurie, Cathy C, Laurie, Cecelia A, Lemire, Mathieu, Levine, David, Ma, Jing, Makar, Karen W, Qu, Conghui, Taverna, Darin, Ulrich, Cornelia M, Wu, Kana, Kono, Suminori, West, Dee W, Berndt, Sonja I, Bezieau, Stéphane, Brenner, Hermann, Campbell, Peter T, Chan, Andrew T, Chang-Claude, Jenny, Coetzee, Gerhard A, Conti, David V, Duggan, David, Figueiredo, Jane C, Fortini, Barbara K, Gallinger, Steven J, Gauderman, W James, Giles, Graham, Green, Roger, Haile, Robert, Harrison, Tabitha A, Hoffmeister, Michael, Hopper, John L, Hudson, Thomas J, Jacobs, Eric, Iwasaki, Motoki, Jee, Sun Ha, Jenkins, Mark, Jia, Wei-Hua, Joshi, Amit, Li, Li, Lindor, Noralene M, Matsuo, Keitaro, Moreno, Victor, Mukherjee, Bhramar, Newcomb, Polly A, Potter, John D, Raskin, Leon, Rennert, Gad, Rosse, Stephanie, Severi, Gianluca, Schoen, Robert E, Seminara, Daniela, Shu, Xiao-Ou, Slattery, Martha L, Tsugane, Shoichiro, White, Emily, Xiang, Yong-Bing, Zanke, Brent W, Zheng, Wei
Publikováno v:
Nature communications, vol 6, iss 1
Genetic susceptibility to colorectal cancer is caused by rare pathogenic mutations and common genetic variants that contribute to familial risk. Here we report the results of a two-stage association study with 18,299 cases of colorectal cancer and 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::0f945cd019749b4861ff426ede2e71c8
https://escholarship.org/uc/item/49b704wg
https://escholarship.org/uc/item/49b704wg
Autor:
Peters, Ulrike, Jiao, Shuo, Schumacher, Fredrick R, Hutter, Carolyn M, Aragaki, Aaron K, Baron, John A, Berndt, Sonja I, Bézieau, Stéphane, Brenner, Hermann, Butterbach, Katja, Caan, Bette J, Campbell, Peter T, Carlson, Christopher S, Casey, Graham, Chan, Andrew T, Chang-Claude, Jenny, Chanock, Stephen J, Chen, Lin S, Coetzee, Gerhard A, Coetzee, Simon G, Conti, David V, Curtis, Keith R, Duggan, David, Edwards, Todd, Fuchs, Charles S, Gallinger, Steven, Giovannucci, Edward L, Gogarten, Stephanie M, Gruber, Stephen B, Haile, Robert W, Harrison, Tabitha A, Hayes, Richard B, Henderson, Brian E, Hoffmeister, Michael, Hopper, John L, Hudson, Thomas J, Hunter, David J, Jackson, Rebecca D, Jee, Sun Ha, Jenkins, Mark A, Jia, Wei-Hua, Kolonel, Laurence N, Kooperberg, Charles, Küry, Sébastien, Lacroix, Andrea Z, Laurie, Cathy C, Laurie, Cecelia A, Le Marchand, Loic, Lemire, Mathieu, Levine, David, Lindor, Noralane M, Liu, Yan, Ma, Jing, Makar, Karen W, Matsuo, Keitaro, Newcomb, Polly A, Potter, John D, Prentice, Ross L, Qu, Conghui, Rohan, Thomas, Rosse, Stephanie A, Schoen, Robert E, Seminara, Daniela, Shrubsole, Martha, Shu, Xiao-Ou, Slattery, Martha L, Taverna, Darin, Thibodeau, Stephen N, Ulrich, Cornelia M, White, Emily, Xiang, Yongbing, Zanke, Brent W, Zeng, Yi-Xin, Zhang, Ben, Zheng, Wei, Hsu, Li, Colon Cancer Family Registry and the Genetics and Epidemiology of Colorectal Cancer Consortium
Publikováno v:
Gastroenterology, vol 144, iss 4
Background & aimsHeritable factors contribute to the development of colorectal cancer. Identifying the genetic loci associated with colorectal tumor formation could elucidate the mechanisms of pathogenesis.MethodsWe conducted a genome-wide associatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5871a5264d2666fc3be4e83a6677b441
https://escholarship.org/uc/item/7bv9p9qq
https://escholarship.org/uc/item/7bv9p9qq
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Autor:
Conde, Lucia, Halperin, Eran, Akers, Nicholas K, Brown, Kevin M, Smedby, Karin E, Rothman, Nathaniel, Nieters, Alexandra, Slager, Susan L, Brooks-Wilson, Angela, Agana, Luz, Riby, Jacques, Liu, Jianjun, Adami, Hans-Olov, Darabi, Hatef, Hjalgrim, Henrik, Low, Hui-Qi, Humphreys, Keith, Melbye, Mads, Chang, Ellen T, Glimelius, Bengt, Cozen, Wendy, Davis, Scott, Hartge, Patricia, Morton, Lindsay M, Schenk, Maryjean, Wang, Sophia S, Armstrong, Bruce, Kricker, Anne, Milliken, Sam, Purdue, Mark P, Vajdic, Claire M, Boyle, Peter, Lan, Qing, Zahm, Shelia H, Zhang, Yawei, Zheng, Tongzhang, Becker, Nikolaus, Benavente, Yolanda, Boffetta, Paolo, Brennan, Paul, Butterbach, Katja, Cocco, Pierluigi, Foretova, Lenka, Maynadié, Marc, de Sanjosé, Silvia, Staines, Anthony, Spinelli, John J, Achenbach, Sara J, Call, Timothy G, Camp, Nicola J, Glenn, Martha, Caporaso, Neil E, Cerhan, James R, Cunningham, Julie M, Goldin, Lynn R, Hanson, Curtis A, Kay, Neil E, Lanasa, Mark C, Leis, Jose F, Marti, Gerald E, Rabe, Kari G, Rassenti, Laura Z, Spector, Logan G, Strom, Sara S, Vachon, Celine M, Weinberg, J Brice, Holly, Elizabeth A, Chanock, Stephen, Smith, Martyn T, Bracci, Paige M, Skibola, Christine F
Publikováno v:
Nature genetics, vol 42, iss 8
To identify susceptibility loci for non-Hodgkin lymphoma subtypes, we conducted a three-stage genome-wide association study. We identified two variants associated with follicular lymphoma at 6p21.32 (rs10484561, combined P = 1.12 x 10(-29) and rs7755
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https://explore.openaire.eu/search/publication?articleId=od_______325::cfb86f094e2d2fe93489b54dd5f64777
https://escholarship.org/uc/item/2z5643ch
https://escholarship.org/uc/item/2z5643ch
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