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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 8
2022
Moller, Pal; Seppala, Toni; Dowty, James G.; Haupt, Saskia; Dominguez-Valentin, Mev; Sunde, Lone; Bernstein, Inge; Engel, Christoph; Aretz, Stefan; Nielsen, Maartje; Capella, Gabriel; Evans, Dafydd Gareth; Burn, John; Holinski-Feder, Elke; Bertario, Lucio; Bonanni, Bernardo; Lindblom, Annika; Levi, Zohar; Macrae, Finlay; Winship, Ingrid; Plazzer, John-Paul; Sijmons, Rolf; Laghi, Luigi; Della Valle, Adriana; Heinimann, Karl; Half, Elizabeth; Lopez-Koestner, Francisco; Alvarez-Valenzuela, Karin; Scott, Rodney J.; Katz, Lior; Laish, Ido; Vainer, Elez; Vaccaro, Carlos Alberto; Carraro, Dirce Maria; Gluck, Nathan; Abu-Freha, Naim; Stakelum, Aine; Kennelly, Rory; Winter, Des; Rossi, Benedito Mauro; Greenblatt, Marc; Bohorquez, Mabel; Sheth, Harsh; Tibiletti, Maria Grazia; Lino-Silva, Leonardo S.; Horisberger, Karoline; Portenkirchner, Carmen; Nascimento, Ivana; Rossi, Norma Teresa; da Silva, Leandro Apolinario; Thomas, Huw; Zarand, Attila; Mecklin, Jukka-Pekka; Pylvanainen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Peltomaki, Paivi; Therkildsen, Christina; Lindberg, Lars Joachim; Thorlacius-Ussing, Ole; Knebel Doeberitz, Magnus von; Loeffler, Markus; Rahner, Nils; Steinke-Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Hueneburg, Robert; de Vargas, Aida Falcon; Latchford, Andrew; Gerdes, Anne-Marie; Backman, Ann-Sofie; Guillen-Ponce, Carmen; Snyder, Carrie; Lautrup, Charlotte K.; Amor, David; Palmero, Edenir; Stoffel, Elena; Duijkers, Floor; Hall, Michael J.; Hampel, Heather; Williams, Heinric; Okkels, Henrik; Lubinski, Jan; Reece, Jeanette; Ngeow, Joanne; Guillem, Jose G.; Arnold, Julie; Wadt, Karin; Monahan, Kevin; Senter, Leigha; Rasmussen, Lene J.; Hest, Liselotte P. van; Ricciardiello, Luigi; Kohonen-Corish, Maija R. J.; Ligtenberg, Marjolijn J. L.; Southey, Melissa; Aronson, Melyssa; Zahary, Mohd N.; Samadder, N. Jewel; Poplawski, Nicola; Hoogerbrugge, Nicoline; Morrison, Patrick J.; James, Paul; Lee, Grant; Chen-Shtoyerman, Rakefet; Ankathil, Ravindran; Pai, Rish; Ward, Robyn; Parry, Susan; Debniak, Tadeusz; John, Thomas; Overeem Hansen, Thomas van; Caldes, Trinidad; Yamaguchi, Tatsuro; Barca-Tierno, Veronica; Garre, Pilar; Cavestro, Giulia Martina; Weitz, Juergen; Redler, Silke; Buettner, Reinhard; Heuveline, VincentZ; Hopper, John L.; Win, Aung Ko; Lindor, Noralane; Gallinger, Steven; Le Marchand, Loic; Newcomb, Polly A.; Figueiredo, Jane; Buchanan, Daniel D.; Thibodeau, Stephen N.; ten Broeke, Sanne W.; Hovig, Eivind; Nakken, Sigve; Pineda, Marta; Duenas, Nuria; Brunet, Joan; Green, Kate; Lalloo, Fiona; Newton, Katie; Crosbie, Emma J.; Mints, Miriam; Tjandra, Douglas; Neffa, Florencia; Esperon, Patricia; Kariv, Revital; Rosner, Guy; Pavicic, Walter Hernan; Kalfayan, Pablo; Torrezan, Giovana Tardin; Bassaneze, Thiago; Martin, Claudia; Moslein, Gabriela; Ahadova, Aysel; Kloor, Matthias; Sampson, Julian R. und Jenkins, Mark A.
(2022):
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.
In: Hereditary Cancer in Clinical Practice, Bd. 20, Nr. 1, 36
2021
Dominguez-Valentin, Mev; Plazzer, John-Paul; Sampson, Julian R.; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capella, Gabriel; Balaguer, Francesc; Macrae, Finlay; Winship, Ingrid M.; Thomas, Huw; Evans, Dafydd Gareth; Burn, John; Greenblatt, Marc; Vos Tot Nederveen Cappel, Wouter H. de; Sijmons, Rolf H.; Nielsen, Maartje; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Della Valle, Adriana; Lopez-Kostner, Francisco; Alvarez, Karin; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Nakken, Sigve; Hovig, Eivind; Green, Kate; Lalloo, Fiona; Hill, James; Vasen, Hans F. A.; Perne, Claudia; Büttner, Reinhard; Görgens, Heike; Holinski-Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; Knebel Doeberitz, Magnus von; Loeffler, Markus; Rahner, Nils; Weitz, Jürgen; Steinke-Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Crosbie, Emma J.; Pineda, Marta; Navarro, Matilde; Brunet, Joan; Moreira, Leticia; Sanchez, Ariadna; Serra-Burriel, Miquel; Mints, Miriam; Kariv, Revital; Rosner, Guy; Pinero, Tamara Alejandra; Pavicic, Walter Hernan; Kalfayan, Pablo; Broeke, Sanne W. ten; Mecklin, Jukka-Pekka; Pylvänäinen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Peltomäki, Päivi; Hopper, John L.; Win, Aung Ko; Buchanan, Daniel D.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loic; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Hansen, Thomas V. O.; Lindberg, Lars; Rodland, Einar Andreas; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Seppälä, Toni T. und Moller, Pal
(2021):
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study.
In: Journal of Clinical Medicine, Bd. 10, Nr. 13, 2856
Seppälä, Toni T.; Dominguez-Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capella, Gabriel; Thomas, Huw; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria G.; Cavestro, Giulia M.; Mints, Miriam; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Green, Kate; Lalloo, Fiona; Hill, James; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Strauss, Hans-Georg; Tecklenburg, Johanna; Holinski-Feder, Elke; Steinke-Lange, Verena; Mecklin, Jukka-Pekka; Plazzer, John-Paul; Pineda, Marta; Navarro, Matilde; Vida, Joan B.; Kariv, Revital; Rosner, Guy; Pinero, Tamara A.; Pavicic, Walter; Kalfayan, Pablo; Ten Broeke, Sanne W.; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Burn, John; Greenblatt, Marc; Cappel, Wouter H. de Vos Tot Nederveen; Della Valle, Adriana; Lopez-Koestner, Francisco; Alvarez, Karin; Büttner, Reinhard; Goergens, Heike; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; Knebel Doeberitz, Magnus von; Loeffler, Markus; Redler, Silke; Weitz, Jürgen; Pylvaenaeinen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Hopper, John L.; Win, Aung K.; Lindor, Noralane M.; Gallinger, Steven; Marchand, Loic Le; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Wadt, Karin A. W.; Mourits, Marian J. E.; Ketabi, Zohreh; Denton, Oliver G.; Rodland, Einar A.; Vasen, Hans; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Rokkones, Erik; Sampson, Julian R.; Evans, D. G. und Moller, Pal
(2021):
Uptake of hysterectomy and bilateral salpingooophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.
In: European Journal of Cancer, Bd. 148: S. 124-133
2020
Dominguez-Valentin, Mev; Sampson, Julian R.; Seppala, 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; Vos Tot Nederveen Cappel, Wouter H. de; Sijmons, Rolf H.; Bertario, Lucio; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Della Valle, Adriana; Lopez-Kostner, Francisco; Gluck, Nathan; Katz, Lior H.; Heinimann, Karl; Vaccaro, Carlos A.; Buettner, Reinhard; Goergens, Heike; Holinski-Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hueneburg, Robert; Knebel Doeberitz, Magnus von; Loeffler, Markus; Rahner, Nils; Schackert, Hans K.; Steinke-Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Pylvanainen, Kirsi; Renkonen-Sinisalo, Laura; Hopper, John L.; Win, Aung Ko; Haile, Robert W.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loic; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Wadt, Karin; Therkildsen, Christina; Okkels, Henrik; Ketabi, Zohreh; Moreira, Leticia; Sanchez, 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.; Rodland, Einar Andreas; Vasen, Hans; Mints, Miriam; Neffa, Florencia; Esperon, Patricia; Alvarez, Karin; Kariv, Revital; Rosner, Guy; Pinero, Tamara Alejandra; Gonzalez, Maria Laura; Kalfayan, Pablo; Tjandra, Douglas; Winship, Ingrid M.; Macrae, Finlay; Möslein, Gabriela; Mecklin, Jukka-Pekka; Nielsen, Maartje und Moller, Pal
(2020):
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.
In: Genetics in Medicine, Bd. 22, Nr. 1: S. 15-25
Dominguez-Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capella, Gabriel; Thomas, Huw; Nakken, Sigve; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Mints, Miriam; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Green, Kate; Lalloo, Fiona; Hill, James; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Strauss, Hans-Georg; Tecklenburg, Johanna; Holinski-Feder, Elke; Steinke-Lange, Verena; Mecklin, Jukka-Pekka; Plazzer, John-Paul; Pineda, Marta; Navarro, Matilde; Brunet Vidal, Joan; Kariv, Revital; Rosner, Guy; Alejandra Pinero, Tamara; Laura Gonzalez, Maria; Kalfayan, Pablo; Ryan, Neil; Ten Broeke, Sanne W.; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Burn, John; Greenblatt, Marc; Vos tot Nederveen Cappel, Wouter H. de; Della Valle, Adriana; Lopez-Koestner, Francisco; Alvarez, Karin; Buettner, Reinhard; Goergens, Heike; Morak, Monika; Holzapfel, Stefanie; Hueneburg, Robert; Doeberitz, Magnus von Knebel; Loeffler, Markus; Rahner, Nils; Weitz, Jurgen; Pylvanainen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Auranen, Annika; Hopper, John L.; Win, Aung Ko; Haile, Robert W.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loic; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Okkels, Henrik; Ketabi, Zohreh; Denton, Oliver G.; Rodland, Einar Andreas; Vasen, Hans; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Sampson, Julian R.; Evans, D. Gareth; Seppala, Toni T. und Moller, Pal
(2020):
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.
In: Genetics in Medicine, Bd. 23, Nr. 4: S. 705-712
2019
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, Stephane; Bien, Stephanie; Bloomer, Amanda; Boehm, Jürgen; 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; Correa, Marcia Cruz; Curtis, Keith R.; Duggan, David; Easton, Douglas F.; English, Dallas; Feskens, Edith J. M.; 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; Kühn, Tilman; Kury, Sebastien; LaCroix, Andrea; Laurie, Cecelia A.; Lejbkowicz, Flavio; Lemire, Mathieu; Lenz, Heinz-Josef; Levine, David; Li, Christopher I.; Li, Li; Lieb, Wolfgang; Lin, Yi; Lindor, Noralane M.; Liu, Yun-Ru; Loupakis, Fotios; Lu, Yingchang; Luh, Frank; Ma, Jing; Mancao, Christoph; Manion, Frank J.; Markowitz, Sanford D.; Martin, Vicente; Matsuda, Koichi; Matsuo, Keitaro; McDonnell, Kevin J.; McNeil, Caroline E.; Milne, Roger; Molina, Antonio J.; Mukherjee, Bhramar; Murphy, Neil; Newcomb, Polly A.; Offit, Kenneth; Omichessan, Hanane; Palli, Domenico; Cotore, Jesus P. Paredes; Perez-Mayoral, Julyann; Pharoah, Paul D.; Potter, John D.; Qu, Conghui; Raskin, Leon; Rennert, Gad; Rennert, Hedy S.; Riggs, Bridget M.; Schafmayer, Clemens; Schön, Robert E.; Sellers, Thomas A.; Seminara, Daniela; Severi, Gianluca; Shi, Wei; Shibata, David; Shu, Xiao-Ou; Siegel, Erin M.; Slattery, Martha L.; Southey, Melissa; Stadler, Zsofia K.; Stern, Mariana C.; Stintzing, Sebastian; Taverna, Darin; Thibodeau, Stephen N.; Thomas, Duncan C.; Trichopoulou, Antonia; Tsugane, Shoichiro; Ulrich, Cornelia M.; van Duijnhoven, Franzel J. B.; van Guelpan, Bethany; Vijai, Joseph; Virtamo, Jarmo; Weinstein, Stephanie J.; White, Emily; Win, Aung Ko; Wolk, Alicja; Woods, Michael; Wu, Anna H.; Wu, Kana; Xiang, Yong-Bing; Yen, Yun; Zanke, Brent W.; Zeng, Yi-Xin; Zhang, Ben; Zubair, Niha; Kweon, Sun-Seog; Figueiredo, Jane C.; Zheng, Wei; Le Marchand, Loic; Lindblom, Annika; Moreno, Victor; Peters, Ulrike; Casey, Graham; Hsu, Li; Conti, David V. und Gruber, Stephen B.
(2019):
Novel Common Genetic Susceptibility Loci for Colorectal Cancer.
In: Jnci-Journal of the National Cancer Institute, Bd. 111, Nr. 2: S. 146-157
2018
Broeke, Sanne W. ten; Klift, Heleen M. van der; Tops, Carli M. J.; Aretz, Stefan; Bernstein, Inge; Buchanan, Daniel D.; Chapelle, Albert de la; Capella, Gabriel; Clendenning, Mark; Engel, Christoph; Gallinger, Steven; Gomez Garcia, Encarna; Figueiredo, Jane C.; Haile, Robert; Hampel, Heather L.; Hopper, John L.; Hoogerbrugge, Nicoline; Knebel Doeberitz, Magnus von; Le Marchand, Loic; Lettebör, Tom G. W.; Jenkins, Mark A.; Lindblom, Annika; Lindor, Noralane M.; Mensenkamp, Arjen R.; Moller, Pal; Newcomb, Polly A.; Os, Theo A. M. van; Pearlman, Rachel; Pineda, Marta; Rahner, Nils; Redeker, Egbert J. W.; Olderode-Berends, Maran J. W.; Rosty, Christophe; Schackert, Hans K.; Scott, Rodney; Senter, Leigha; Spruijt, Liesbeth; Steinke-Lange, Verena; Suerink, Manon; Thibodeau, Stephen; Vos, Yvonne J.; Wagner, Anja; Winship, Ingrid; Hes, Frederik J.; Vasen, Hans F. A.; Wijnen, Juul T.; Nielsen, Maartje und Win, Aung Ko
(2018):
Cancer Risks for PMS2-Associated Lynch Syndrome.
In: Journal of Clinical Oncology, Bd. 36, Nr. 29: S. 2961-2968
2017
Gu, Fangyi; Zhang, Han; Hyland, Paula L.; Berndt, Sonja; Gapstur, Susan M.; Wheeler, William; Amos, Christopher I.; Bezieau, Stephane; Bickeboller, Heike; Brenner, Hermann; Brennan, Paul; Chang-Claude, Jenny; Conti, David V.; Doherty, Jennifer Anne; Gruber, Stephen B.; Harrison, Tabitha A.; Hayes, Richard B.; Hoffmeister, Michael; Houlston, Richard S.; Hung, Rayjean J.; Jenkins, Mark A.; Kraft, Peter; Lawrenson, Kate; Mckay, James; Markt, Sarah; Mucci, Lorelei; Phelan, Catherine M.; Qu, Conghui; Risch, Angela; Rossing, Mary Anne; Wichmann, H.-Erich; Shi, Jianxin; Schernhammer, Eva; Yu, Kai; Landi, Maria Teresa und Caporaso, Neil E.
(2017):
Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia.
In: International Journal of Cancer, Bd. 141, Nr. 9: S. 1794-1802