Substantial unexplained variation in cancer risks for MLH1 and MSH2 mutation carriers
Dowty, JG, Win, AK, Buchanan, D, Macinnis, RJ, Lindor, N, Thibodeau, SN, Casey, G, Gallinger, S, LeMarchand, L, Newcomb, P, Haile, R, Goldblatt, J, Parry, S, Macrae, FA, Hopper, JL, Jenkins, MA
Published in Hereditary cancer in clinical practice (12.04.2012)
Published in Hereditary cancer in clinical practice (12.04.2012)
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Metachronous colon cancer risk following surgery for first primary rectal cancer in Lynch syndrome
Parry, S, Win, AK, Parry, B, Kalady, M, Macrae, FA, Lindor, NM, Haile, RW, Newcomb, PA, Le Marchand, L, Gallinger, S, Hopper, JL, Jenkins, MA
Published in Hereditary cancer in clinical practice (12.04.2012)
Published in Hereditary cancer in clinical practice (12.04.2012)
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Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Michailidou, Kyriaki, Fachal, Laura, Lee, Andrew, Wang, Qin, Yang, Xin, Adank, Muriel A., Aittomäki, Kristiina, Andrulis, Irene L., Antonenkova, Natalia N., Arndt, Volker, Auer, Paul L., Auvinen, Päivi, Barrdahl, Myrto, Beane Freeman, Laura E., Beckmann, Matthias W., Benitez, Javier, Bermisheva, Marina, Bogdanova, Natalia V., Bonanni, Bernardo, Brauch, Hiltrud, Brooks-Wilson, Angela, Brucker, Sara Y., Brüning, Thomas, Campa, Daniele, Chlebowski, Rowan, Cordina-Duverger, Emilie, Daly, Mary B., dos-Santos-Silva, Isabel, Dumont, Martine, Dwek, Miriam, Eliassen, A. Heather, Ellberg, Carolina, Evans, D. Gareth, Försti, Asta, Gabrielson, Marike, Gago-Dominguez, Manuela, García-Sáenz, José A., Gaudet, Mia M., Giles, Graham G., Gilyazova, Irina R., Grenaker Alnæs, Grethe I., Grip, Mervi, Gronwald, Jacek, Grundy, Anne, Hahnen, Eric, Hart, Steven N., Heyworth, Jane, Hoover, Robert N., Jakubowska, Anna, Jones, Michael E., Kaaks, Rudolf, Kerin, Michael J., Kiiski, Johanna I., Knight, Julia A., Krüger, Ute, Kühl, Tabea, Lambrechts, Diether, Lee, Eunjung, Lejbkowicz, Flavio, Lissowska, Jolanta, MacInnis, Robert J., Makalic, Enes, Maleva Kostovska, Ivana, Manoukian, Siranoush, Martinez, Maria Elena, McLean, Catriona, Menon, Usha, Miller, Nicola, Mulligan, Anna Marie, Neven, Patrick, Pérez-Barrios, Clara, Polley, Eric C., Prokofyeva, Darya, Purrington, Kristen, Pylkäs, Katri, Rack, Brigitte, Rau-Murthy, Rohini, Schmidt, Daniel F., Schmutzler, Rita K., Scott, Rodney J., Shu, Xiao-Ou, Slager, Susan, Southey, Melissa C., Stegmaier, Christa, Stone, Jennifer, Tamimi, Rulla M., Tapper, William J., Taylor, Jack A., Terry, Mary Beth, Tollenaar, Rob A.E.M., Tzardi, Maria, van Veen, Elke M., Weinberg, Clarice R., Yang, Xiaohong R., Zhang, Yan, Dunning, Alison M., Chenevix-Trench, Georgia, Milne, Roger L., Chatterjee, Nilanjan, Kraft, Peter
Published in American journal of human genetics (2019)
Published in American journal of human genetics (2019)
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Association analysis identifies 65 new breast cancer risk loci
Lindström, Sara, Rostamianfar, Asha, Tyrer, Jonathan, Allen, Jamie, Keeman, Renske, Eilber, Ursula, Fachal, Laura, Finucane, Hilary, Adams, Marcia, Adank, Muriel A., Aittomäki, Kristiina, Antonenkova, Natalia N., Baynes, Caroline, Behrens, Sabine, Bernstein, Leslie, Blomqvist, Carl, Brenner, Hermann, Brock, Ian W., Brucker, Sara Y., Brüning, Thomas, Carracedo, Angel, Chan, Tsun L., Choi, Ji-Yeob, Christiansen, Hans, Conroy, Don M., Cordina-Duverger, Emilie, Cornelissen, Sten, Cunningham, Julie M., Czene, Kamila, Eccles, Diana M., Elvira, Mingajeva, Fasching, Peter A., García-Sáenz, José A., Grip, Mervi, Hankinson, Susan, Hartikainen, Jaana M., Hein, Alexander, Heyworth, Jane, Hicks, Belynda, Hillemanns, Peter, Hoover, Robert N., Hopper, John L., Hsiung, Chia-Ni, Huang, Guanmengqian, Janni, Wolfgang, Jones, Kristine, Kabisch, Maria, Kasuga, Yoshio, Kiiski, Johanna I., Krüger, Ute, Lambrechts, Diether, Lee, Min Hyuk, Lee, Jong Won, Neng Lee, Chuen, Lindblom, Annika, Lophatananon, Artitaya, Ma, Edmond S. K., MacInnis, Robert J., Maishman, Tom, Makalic, Enes, Malone, Kathleen E., Kostovska, Ivana Maleva, Mannermaa, Arto, Menon, Usha, Meyer, Jeffery, Taib, Nur Aishah Mohd, Nordestgaard, Børge G., Olson, Janet E., Olsson, Håkan, Peto, Julian, Phillips, Kelly-Anne, Prokofyeva, Darya, Pugh, Elizabeth, Rack, Brigitte, Radice, Paolo, Romero, Atocha, Ruddy, Kathryn J., Schmutzler, Rita K., Schoemaker, Minouk J., Scott, Rodney J., Scott, Christopher, Smeets, Ann, Stone, Jennifer, Surowy, Harald, Torres, Diana, Tseng, Chiu-Chen, Tsugane, Shoichiro, Untch, Michael, Vincent, Daniel, Vollenweider, Jason, Whittemore, Alice S., Har Yip, Cheng, Zhu, Bin, Antoniou, Antonis C., Couch, Fergus J., Hall, Per, Schmidt, Marjanka K., Dunning, Alison M., Edwards, Stacey L., Bader, Gary D.
Published in Nature (London) (02.11.2017)
Published in Nature (London) (02.11.2017)
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Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis
Papadimitriou, Nikos, Dimou, Niki, Tsilidis, Konstantinos K., Banbury, Barbara, Martin, Richard M., Lewis, Sarah J., Kazmi, Nabila, Robinson, Timothy M., Albanes, Demetrius, Aleksandrova, Krasimira, Berndt, Sonja I., Timothy Bishop, D., Brenner, Hermann, Buchanan, Daniel D., Bueno-de-Mesquita, Bas, Campbell, Peter T., Castellví-Bel, Sergi, Chan, Andrew T., Chang-Claude, Jenny, Ellingjord-Dale, Merete, Figueiredo, Jane C., Gallinger, Steven J., Giles, Graham G., Giovannucci, Edward, Gruber, Stephen B., Gsur, Andrea, Hampe, Jochen, Hampel, Heather, Harlid, Sophia, Harrison, Tabitha A., Hoffmeister, Michael, Hopper, John L., Hsu, Li, María Huerta, José, Huyghe, Jeroen R., Jenkins, Mark A., Keku, Temitope O., Kühn, Tilman, La Vecchia, Carlo, Le Marchand, Loic, Li, Christopher I., Li, Li, Lindblom, Annika, Lindor, Noralane M., Lynch, Brigid, Markowitz, Sanford D., Masala, Giovanna, May, Anne M., Milne, Roger, Monninkhof, Evelyn, Moreno, Lorena, Moreno, Victor, Newcomb, Polly A., Offit, Kenneth, Perduca, Vittorio, Pharoah, Paul D. P., Platz, Elizabeth A., Potter, John D., Rennert, Gad, Riboli, Elio, Sánchez, Maria-Jose, Schmit, Stephanie L., Schoen, Robert E., Severi, Gianluca, Sieri, Sabina, Slattery, Martha L., Song, Mingyang, Tangen, Catherine M., Thibodeau, Stephen N., Travis, Ruth C., Trichopoulou, Antonia, Ulrich, Cornelia M., van Duijnhoven, Franzel J. B., Van Guelpen, Bethany, Vodicka, Pavel, White, Emily, Wolk, Alicja, Woods, Michael O., Wu, Anna H., Peters, Ulrike, Gunter, Marc J., Murphy, Neil
Published in Nature communications (30.01.2020)
Published in Nature communications (30.01.2020)
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A study of cancer risks in relatives of patients with serrated polyposis
Win, AK, Walters, RJ, Buchanan, DD, Jenkins, MA, Sweet, K, McKeone, DM, Walsh, MD, Clendenning, M, Pearson, SA, Pavluk, E, Nagler, B, Hopper, JL, Walker, N, Rosty, C, Parry, S, Young, JP
Published in Hereditary cancer in clinical practice (12.04.2012)
Published in Hereditary cancer in clinical practice (12.04.2012)
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Expanded genetic analysis of a PALB2 c.3113G>A mutation carrying multiple-case breast cancer family via exome sequencing
Teo, ZL, Park, DJ, Odefrey, F, Hammet, F, Nguyen-Dumont, T, Tsimiklis, H, Pope, BJ, Lonie, A, Winship, I, Giles, GG, Hopper, JL, Southey, MC
Published in Hereditary cancer in clinical practice (12.04.2012)
Published in Hereditary cancer in clinical practice (12.04.2012)
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Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Zhang, Haoyu, Ahearn, Thomas U., Beesley, Jonathan, Jiang, Xia, Anton-Culver, Hoda, Aronson, Kristan J., Beckmann, Matthias W., Benitez, Javier, Bialkowska, Katarzyna, Blanco, Ana, Blomqvist, Carl, Borg, Ake, Briceno, Ignacio, Brucker, Sara Y., Burwinkel, Barbara, Buys, Saundra S., Byers, Helen, Caldés, Trinidad, Chang-Claude, Jenny, Clarke, Christine L., Cox, Angela, Cross, Simon S., Czene, Kamila, Domchek, Susan M., Ekici, Arif B., Figueroa, Jonine, Foretova, Lenka, Fostira, Florentia, Garber, Judy, Gaudet, Mia M., Goldgar, David E., Häberle, Lothar, Hake, Christopher R., Hamann, Ute, Hillemanns, Peter, Holleczek, Bernd, Hollestelle, Antoinette, Hooning, Maartje J., Hoover, Robert N., Imyanitov, Evgeny N., Isaacs, Claudine, Jager, Agnes, Janavicius, Ramunas, Kaaks, Rudolf, Keeman, Renske, Konstantopoulou, Irene, Lazarova, Emilija, Lejbkowicz, Flavio, Leslie, Goska, Lindblom, Annika, Lissowska, Jolanta, Loud, Jennifer T., Mannermaa, Arto, Matricardi, Laura, Meindl, Alfons, Menon, Usha, Muranen, Taru A., Newman, William G., Nikitina-Zake, Liene, Offit, Kenneth, Olah, Edith, Olopade, Olufunmilayo I., Orr, Nick, Park-Simon, Tjoung-Won, Parsons, Michael T., Phillips, Kelly-Anne, Rack, Brigitte, Rennert, Hedy S., Risch, Harvey A., Rookus, Matti A., Rübner, Matthias, Rüdiger, Thomas, Saloustros, Emmanouil, Sawyer, Elinor J., Schmutzler, Rita K., Schöttker, Ben, Sherman, Mark E., Shu, Xiao-Ou, Stoppa-Lyonnet, Dominique, Swerdlow, Anthony J., Szabo, Csilla I., Taylor, Jack A., Terry, MaryBeth, Thull, Darcy L., Toland, Amanda E., Tollenaar, Rob A. E. M., Tomlinson, Ian, Torres, Diana, Truong, Thérèse, Untch, Michael, Vachon, Celine M., van der Kolk, Lizet E., van Veen, Elke M., Vega, Ana, Wappenschmidt, Barbara, Weitzel, Jeffrey N., Winqvist, Robert, Yannoukakos, Drakoulis, Pharoah, Paul D. P., García-Closas, Montserrat
Published in Nature genetics (01.06.2020)
Published in Nature genetics (01.06.2020)
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Genetic insights into biological mechanisms governing human ovarian ageing
Hussain, Jazib, Abe, Hironori, Fontanillas, Pierre, Bakker, Olivier B., Sulem, Patrick, Terao, Chikashi, Horikoshi, Momoko, Shukla, Vallari, Borup, Rehannah, Olsen, Kristina W., Ferrer-Roda, Mònica, Timmers, Paul R. H. J., Ahearn, Thomas U., Naderi, Elnaz, Barbieri, Caterina M., Beaumont, Robin N., Becher, Heiko, Beckmann, Matthias W., Bochud, Murielle, Boomsma, Dorret I., Bowker, Nicholas, Campbell, Harry, Catamo, Eulalia, Chanock, Stephen J., Ciullo, Marina, Corre, Tanguy, Couch, Fergus J., Cox, Angela, Cross, Simon S., Cucca, Francesco, Czene, Kamila, Smith, George Davey, Faul, Jessica D., Ferrucci, Luigi, Franceschini, Nora, Gago-Dominguez, Manuela, Mezzavilla, Massimo, Grallert, Harald, Hayward, Caroline, Høffding, Miya K., Hu, Frank, Joaquim, Micaella D. R., John, Esther M., Joshi, Peter K., Kardia, Sharon L. R., Kartsonaki, Christiana, Kooperberg, Charles, Kurian, Allison W., Kutalik, Zoltan, LaChance, Genevieve, Langenberg, Claudia, Laven, Joop S. E., Lawlor, Deborah A., Le Marchand, Loic, Li, Jingmei, Lindblom, Annika, Mangino, Massimo, Mannermaa, Arto, Marten, Jonathan, McKnight, Barbara, Medland, Sarah E., Menni, Cristina, Milani, Lili, Mulas, Antonella, Mulligan, Anna M., Newman, Anne, Noordam, Raymond, Nutile, Teresa, Nyholt, Dale R., Pedersen, Nancy L., Porcu, Eleonora, Psaty, Bruce M., Rennert, Gad, Rennert, Hedy S., Ruggiero, Daniela, Sawyer, Elinor J., Schoemaker, Minouk J., Schraut, Katharina E., Smith, Albert V., Smith, Blair H., Sorice, Rossella, Spinelli, John J., van Meurs, Joyce B. J., Troester, Melissa A., Truong, Thérèse, Vachon, Celine M., Vitart, Veronique, Vollenweider, Peter, Wang, Qin, Weinberg, Clarice R., Franke, Lude, Burgess, Stephen, Pers, Tune H., Lopez-Contreras, Andres J., Visser, Jenny A., Namekawa, Satoshi H., Murabito, Joanne M., Ong, Ken K., Murray, Anna, Perry, John R. B.
Published in Nature (London) (19.08.2021)
Published in Nature (London) (19.08.2021)
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Discovery of common and rare genetic risk variants for colorectal cancer
Huyghe, Jeroen R., Chen, Sai, Schmit, Stephanie L., Conti, David V., Qu, Conghui, Edlund, Christopher K., Schumacher, Fredrick R., Levine, David M., Nelson, Sarah C., Sinnott-Armstrong, Nasa A., Albanes, Demetrius, Anderson, Kristin, Arnau-Collell, Coral, Banbury, Barbara L., Berndt, Sonja I., Boeing, Heiner, Buch, Stephan, Buchanan, Daniel D., Burnett-Hartman, Andrea, Butterbach, Katja, Campbell, Peter T., Carlson, Christopher S., Castellví-Bel, Sergi, Chan, Andrew T., Connolly, Charles M., Cross, Amanda J., de la Chapelle, Albert, Duggan, David, Easton, Douglas F., English, Dallas R., Feskens, Edith J. M., Forman, David, Gallinger, Steven, Gauderman, W. James, Giles, Graham G., Gong, Jian, Grove, John S., Haile, Robert W., Hampe, Jochen, Hampel, Heather, Harlid, Sophia, Hayes, Richard B., Hoffmeister, Michael, Hsu, Wan-Ling, Huang, Wen-Yi, Hunter, David J., Ibañez-Sanz, Gemma, Jenkins, Mark A., Joshi, Amit D., Joshu, Corinne E., Key, Timothy J., Kolonel, Laurence N., Küry, Sébastien, Kweon, Sun-Seog, Le Marchand, Loic, Lejbkowicz, Flavio, Li, Li, Lieb, Wolfgang, Lin, Yi, Ling, Hua, Louie, Tin L., Männistö, Satu, Martín, Vicente, Masala, Giovanna, McNeil, Caroline E., Melas, Marilena, Murphy, Neil, Myte, Robin, Newcomb, Polly A., Onland-Moret, N. Charlotte, Pearlman, Rachel, Pinchev, Mila, Pugh, Elizabeth, Raskin, Leon, Rodríguez-Barranco, Miguel, Sakoda, Lori C., Schoen, Robert E., Seminara, Daniela, Shah, Mitul, Shulman, Katerina, Stadler, Zsofia K., Thibodeau, Stephen N., Thomas, Sushma S., Toland, Amanda E., Trichopoulou, Antonia, Van Den Berg, David J., van Duijnhoven, Franzel J. B., Van Guelpen, Bethany, Vijai, Joseph, Visvanathan, Kala, Vodicka, Pavel, Vodickova, Ludmila, Vymetalkova, Veronika, Weigl, Korbinian, Weinstein, Stephanie J., Zaidi, Syed H., Zheng, Wei, Scacheri, Peter C., Casey, Graham, Hsu, Li
Published in Nature genetics (01.01.2019)
Published in Nature genetics (01.01.2019)
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Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
Dominguez-Valentin, Mev, Sampson, Julian R., Seppälä, Toni T., ten Broeke, Sanne W., Plazzer, John-Paul, Nakken, Sigve, Engel, Christoph, Aretz, Stefan, Jenkins, Mark A., Sunde, Lone, Bernstein, Inge, Capella, Gabriel, Balaguer, Francesc, Thomas, Huw, Evans, D. Gareth, Burn, John, Greenblatt, Marc, Hovig, Eivind, de Vos tot Nederveen Cappel, Wouter H., Sijmons, Rolf H., Bertario, Lucio, Tibiletti, Maria Grazia, Cavestro, Giulia Martina, Lindblom, Annika, Della Valle, Adriana, Lopez-Köstner, Francisco, Gluck, Nathan, Katz, Lior H., Heinimann, Karl, Vaccaro, Carlos A., Büttner, Reinhard, Görgens, Heike, Holinski-Feder, Elke, Morak, Monika, Holzapfel, Stefanie, Hüneburg, Robert, Knebel Doeberitz, Magnus von, Loeffler, Markus, Rahner, Nils, Schackert, Hans K., Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Hopper, John L., Win, Aung Ko, Haile, Robert W., Lindor, Noralane M., Gallinger, Steven, Le Marchand, Loïc, Newcomb, Polly A., Figueiredo, Jane C., Thibodeau, Stephen N., Wadt, Karin, Therkildsen, Christina, Okkels, Henrik, Ketabi, Zohreh, Moreira, Leticia, Sánchez, Ariadna, Serra-Burriel, Miquel, Pineda, Marta, Navarro, Matilde, Blanco, Ignacio, Green, Kate, Lalloo, Fiona, Crosbie, Emma J., Hill, James, Denton, Oliver G., Frayling, Ian M., Rødland, Einar Andreas, Vasen, Hans, Mints, Miriam, Neffa, Florencia, Esperon, Patricia, Alvarez, Karin, Kariv, Revital, Rosner, Guy, Pinero, Tamara Alejandra, Gonzalez, María Laura, Kalfayan, Pablo, Tjandra, Douglas, Winship, Ingrid M., Macrae, Finlay, Möslein, Gabriela, Mecklin, Jukka-Pekka, Nielsen, Maartje, Møller, Pål
Published in Genetics in medicine (01.01.2020)
Published in Genetics in medicine (01.01.2020)
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The relationship between the BRAF p.V600E mutation and a family history of CRC in the early-onset CRC cases from the Australasian Colon Cancer Family Study
Buchanan, DD, Win, AK, Walters, R, Walsh, MD, Clendenning, M, Nagler, B, Pavluk, E, Pearson, SA, Rosty, C, Maskiell, J, Hopper, JL, Jenkins, MA, Young, JP
Published in Hereditary cancer in clinical practice (01.01.2012)
Published in Hereditary cancer in clinical practice (01.01.2012)
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Journal Article
Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects
Howe, Laurence J., Nivard, Michel G., Morris, Tim T., Hansen, Ailin F., Rasheed, Humaira, Cho, Yoonsu, Chittoor, Geetha, Ahlskog, Rafael, Lind, Penelope A., Palviainen, Teemu, van der Zee, Matthijs D., Cheesman, Rosa, Mangino, Massimo, Wang, Yunzhang, Li, Shuai, Klaric, Lucija, Ratliff, Scott M., Bielak, Lawrence F., Nygaard, Marianne, Giannelis, Alexandros, Willoughby, Emily A., Reynolds, Chandra A., Balbona, Jared V., Andreassen, Ole A., Ask, Helga, Baras, Aris, Bauer, Christopher R., Boomsma, Dorret I., Campbell, Archie, Campbell, Harry, Chen, Zhengming, Christofidou, Paraskevi, Corfield, Elizabeth, Dahm, Christina C., Dokuru, Deepika R., Evans, Luke M., de Geus, Eco J. C., Giddaluru, Sudheer, Gordon, Scott D., Harden, K. Paige, Hill, W. David, Hughes, Amanda, Kerr, Shona M., Kim, Yongkang, Kweon, Hyeokmoon, Latvala, Antti, Lawlor, Deborah A., Li, Liming, Lin, Kuang, Magnus, Per, Magnusson, Patrik K. E., Mallard, Travis T., Martikainen, Pekka, Mills, Melinda C., Njølstad, Pål Rasmus, Overton, John D., Pedersen, Nancy L., Porteous, David J., Reid, Jeffrey, Silventoinen, Karri, Southey, Melissa C., Stoltenberg, Camilla, Tucker-Drob, Elliot M., Wright, Margaret J., Hewitt, John K., Keller, Matthew C., Stallings, Michael C., Lee, James J., Christensen, Kaare, Kardia, Sharon L. R., Peyser, Patricia A., Smith, Jennifer A., Wilson, James F., Hopper, John L., Hägg, Sara, Spector, Tim D., Pingault, Jean-Baptiste, Plomin, Robert, Havdahl, Alexandra, Bartels, Meike, Martin, Nicholas G., Oskarsson, Sven, Justice, Anne E., Millwood, Iona Y., Hveem, Kristian, Naess, Øyvind, Willer, Cristen J., Åsvold, Bjørn Olav, Koellinger, Philipp D., Kaprio, Jaakko, Medland, Sarah E., Walters, Robin G., Benjamin, Daniel J., Turley, Patrick, Evans, David M., Davey Smith, George, Hayward, Caroline, Brumpton, Ben, Hemani, Gibran, Davies, Neil M.
Published in Nature genetics (2022)
Published in Nature genetics (2022)
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Journal Article
Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants
Li, Shuai, Silvestri, Valentina, Leslie, Goska, Rebbeck, Timothy R, Neuhausen, Susan L, Hopper, John L, Nielsen, Henriette Roed, Lee, Andrew, Yang, Xin, McGuffog, Lesley, Parsons, Michael T, Andrulis, Irene L, Arnold, Norbert, Belotti, Muriel, Borg, Åke, Buecher, Bruno, Buys, Saundra S, Caputo, Sandrine M, Chung, Wendy K, Colas, Chrystelle, Colonna, Sarah V, Cook, Jackie, Daly, Mary B, de la Hoya, Miguel, de Pauw, Antoine, Delhomelle, Hélène, Eason, Jacqueline, Engel, Christoph, Evans, D Gareth, Faust, Ulrike, Fehm, Tanja N, Fostira, Florentia, Fountzilas, George, Frone, Megan, Garcia-Barberan, Vanesa, Garre, Pilar, Gauthier-Villars, Marion, Gehrig, Andrea, Glendon, Gord, Goldgar, David E, Golmard, Lisa, Greene, Mark H, Hahnen, Eric, Hamann, Ute, Hanson, Helen, Hassan, Tiara, Hentschel, Julia, Horvath, Judit, Izatt, Louise, Janavicius, Ramunas, Jiao, Yue, John, Esther M, Karlan, Beth Y, Kim, Sung-Won, Konstantopoulou, Irene, Kwong, Ava, Laugé, Anthony, Lee, Jong Won, Lesueur, Fabienne, Mebirouk, Noura, Meindl, Alfons, Mouret-Fourme, Emmanuelle, Musgrave, Hannah, Ngeow Yuen Yie, Joanne, Niederacher, Dieter, Park, Sue K, Pedersen, Inge Sokilde, Ramser, Juliane, Ramus, Susan J, Rantala, Johanna, Rashid, Muhammad U, Reichl, Florian, Ritter, Julia, Rump, Andreas, Santamariña, Marta, Saule, Claire, Schmidt, Gunnar, Schmutzler, Rita K, Senter, Leigha, Shariff, Saba, Singer, Christian F, Southey, Melissa C, Stoppa-Lyonnet, Dominique, Sutter, Christian, Tan, Yen, Teo, Soo Hwang, Terry, Mary Beth, Thomassen, Mads, Tischkowitz, Marc, Toland, Amanda E, Torres, Diana, Vega, Ana, Wagner, Sebastian A, Wang-Gohrke, Shan, Wappenschmidt, Barbara, Weber, Bernhard H F, Yannoukakos, Drakoulis, Spurdle, Amanda B, Easton, Douglas F, Chenevix-Trench, Georgia
Published in Journal of clinical oncology (10.05.2022)
Published in Journal of clinical oncology (10.05.2022)
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Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day, Felix R, Chasman, Daniel I, Sulem, Patrick, Sarkar, Abhishek K, Albrecht, Eva, Altmaier, Elisabeth, Amini, Marzyeh, Boutin, Thibaud, Demerath, Ellen, Giri, Ayush, Hottenga, Jouke J, Medland, Sarah E, Perjakova, Natalia, Porcu, Eleonora, Schraut, Katharina E, Smith, Albert V, Teumer, Alexander, Bandinelli, Stefania, Brauch, Hiltrud, Brenner, Hermann, Broer, Linda, Buring, Julie E, Catamo, Eulalia, Chanock, Stephen, Corre, Tanguy, Couch, Fergus J, Cousminer, Diana L, Crisponi, Laura, Czene, Kamila, Davey Smith, George, De Vivo, Immaculata, Devilee, Peter, Eriksson, Johan G, Fasching, Peter A, Fernández-Rhodes, Lindsay, Gandin, Ilaria, Hall, Per, Hallberg, Emily, Harris, Tamara B, Hartman, Catharina A, Hooning, Maartje J, Hopper, John L, Hu, Frank, Im, Hae Kyung, Järvelin, Marjo-Riitta, Joshi, Peter K, Karasik, David, Kellis, Manolis, LaChance, Genevieve, Langenberg, Claudia, Li, Jingmei, Lindstrom, Sara, Liu, YongMei, Mägi, Reedik, Mannermaa, Arto, Mbarek, Hamdi, Meisinger, Christa, Meitinger, Thomas, Metspalu, Andres, Michailidou, Kyriaki, Nalls, Mike A, Nyholt, Dale R, Padmanabhan, Sandosh, Pedersen, Nancy, Peters, Annette, Peto, Julian, Rahman, Iffat, Robino, Antonietta, Rosendaal, Frits R, Rudan, Igor, Schmidt, Marjanka K, Scott, Robert A, Sorice, Rossella, Sovio, Ulla, Stampfer, Meir, Traglia, Michela, Tyrer, Jonathan P, Völker, Uwe, Vollenweider, Peter, Winqvist, Robert, Wolffenbuttel, Bruce H R, Zygmunt, Marek, Alizadeh, Behrooz Z, Boomsma, Dorret I, Cucca, Francesco, Franceschini, Nora, Gieger, Christian, Gudnason, Vilmundur, Martin, Nicholas G, Nohr, Ellen A, Ridker, Paul M, Toniolo, Daniela, Ulivi, Sheila, Thorsteindottir, Unnur, Easton, Douglas F, Tung, Joyce Y, Chang-Claude, Jenny, Hinds, David, Ong, Ken K, Perry, John R B
Published in Nature genetics (01.06.2017)
Published in Nature genetics (01.06.2017)
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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
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