Browsing by Author Nakken, Sigve

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Issue DateTitleAuthor(s)
9-Dec-2015A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.Alioto, Tyler S.; Buchhalter, Ivo; Derdak, Sophia; Hutter, Barbara; Eldridge, Matthew D.; Hovig, Eivind; Heisler, Lawrence E.; Beck, Timothy A.; Simpson, Jared T.; Tonon, Laurie; Sertier, Anne-Sophie; Patch, Ann-Marie; Jäger, Natalie; Ginsbach, Philip; Drews, Ruben; Paramasivam, Nagarajan; Kabbe, Rolf; Chotewutmontri, Sasithorn; Diessl, Nicolle; Previti, Christopher; Schmidt, Sabine; Brors, Benedikt; Feuerbach, Lars; Heinold, Michael; Gröbner, Susanne; Korshunov, Andrey; Tarpey, Patrick; Butler, Adam P.; Hinton, Jonathan; Jones, David T.W.; Menzies, Andrew; Raine, Keiran; Shepherd, Rebecca; Stebbings, Lucy; Teague, John W.; Ribeca, Paolo; Castro Giner, Francesc; Beltran i Agulló, Sergi; Raineri, Emanuele; Dabad, Marc; Heath, Simon C.; Gut, Marta; Denroche, Robert E.; Harding, Nicholas J.; Yamaguchi, Takafumi N.; Nakagawa, Hidewaki; Quesada, Victor; Valdés Mas, Rafael; Nakken, Sigve; Vodák, Daniel; Bower, Lawrence; Lynch, Andrew G.; Anderson, Charlotte L.; Waddell, Nicola; Pearson, John V.; Grimmond, Sean M.; Peto, Myron; Spellman, Paul; He, Minghui; Kandoth, Cyriac; Lee, Semin; Zhang, John; Létourneau, Louis; Ma, Singer; Seth, Sahil; Torrents Arenales, David; Xi, Liu; Wheeler, David A.; López-Otin, Carlos; Campo Güerri, Elias; Campbell, Peter J.; Boutros, Paul C.; Puente, Xose S.; Gerhard, Daniela S.; Pfister, Stefan M.; McPherson, John D.; Hudson, Thomas J.; Schlesner, Matthias; Lichter, Peter; Eils, Roland; Jones, David T.W.; Gut, Ivo G.
28-Jul-2017Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome DatabaseMøller, Pål; Seppälä, Toni T.; Bernstein, Inge; Holinski Feder, Elke; Sala, Paulo; Gareth Evans, D.; Lindblom, Annika; Macrae, Finlay; Blanco Guillermo, Ignacio; Sijmons, Rolf H.; Jeffries, Jacqueline; Vasen, Hans; Burn, John; Nakken, Sigve; Hovig, Eivind; Rødland, Einar Andreas; Tharmaratnam, Kukatharmini; de Vos Tot Nederveen Cappel, Wouter H.; Hill, James; Wijnen, Juul T.; Jenkins, Mark A.; Green, Kate; Lalloo, Fiona; Sunde, Lone; Mints, Miriam; Bertario, Lucio; Pineda Riu, Marta; Navarro García, Matilde; Morak, Monika; Renkonen Sinisalo, Laura; Dominguez Valentin, Mev; Frayling, Ian M.; Plazzer, John Paul; Pylvanainen, Kirsi; Genuardi, Maurizio; Mecklin, Jukka-Pekka; Moeslein, Gabriela; Sampson, Julian R.; Capellá, G. (Gabriel); Mallorca Group
1-Jan-2020Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseDominguez 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; Capellá, G. (Gabriel); Balaguer Prunés, 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 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; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Schackert, Hans K.
10-Oct-2017Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a prospective lynch syndrome databaseSeppälä, Toni T.; Pylvänäinen, Kirsi; Evans, D. Gareth; Järvinen, Heikki; Renkonen-Sinisalo, Laura; Bernstein, Inge; Holinski-Feder, Elke; Sala, Paola; Lindblom, Annika; Macrae, Finlay; Blanco, Inlay; Sijmons, Rolf; Jeffries, Jacqueline; Vasen, Hans; Burn, John; Nakken, Sigve; Hovig, Eivind; Rødland, Einar Andreas; Tharmaratnam, Kukatharmini; De Vos Tot Nederveen Cappel, Wouter H.; Hill, James; Wijnen, Juul; Jenkins, Mark A.; Genuardi, Maurizio; Green, Kate; Lalloo, Fiona; Sunde, Lone; Mints, Miriam; Bertario, Lucio; Pineda Riu, Marta; Navarro, Matilde; Morak, Monika; Frayling, Ian M.; Plazzer, John-Paul; Sampson, Julian R.; Capellá, G. (Gabriel); Möslein, Gabriela; Mecklin, Jukka-Pekka; Møller, Pål; Mallorca Group
1-Oct-2022Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortiumMøller, Pål; Seppälä, Toni T.; Dowty, James G.; Haupt, Saskia; Dominguez Valentin, Mev; Sunde, Lone; Bernstein, Inge; Engel, Christoph; Aretz, Stefan; Nielsen, Maartje; Capellá, G. (Gabriel); Lindblom, Annika; Gluck, Nathan; Kalfayan, Pablo; Torrezan, Giovana Tardin; Winship, Ingrid; Plazzer, John Paul; Sijmons, Rolf; Backman, Ann Sofie; De Vargas, Aída Falcón; Vangala, Deepak; Lautrup, Charlotte K.; Laghi, Luigi; Valle, Adriana Della; Abu Freha, Naim; Winter, Des; Bohorquez, Mabel; Horisberger, Karoline; Heinimann, Karl; Half, Elizabeth; Lopez Koestner, Francisco; Alvarez Valenzuela, Karin; Van Hest, Liselotte P.; Scott, Rodney J.; Ligtenberg, Marjolijn J. L.; Katz, Lior; Da Silva, Leandro Apolinário; Zahary, Mohd N.; Laish, Ido; Rossi, Norma Teresa; Morrison, Patrick J.; Vainer, Elez; Nascimento, Ivana; Steinke Lange, Verena; Vaccaro, Carlos Alberto; Carraro, Dirce Maria; Thomas, Huw; Zaránd, Attila; Poplawski, Nicola; Aronson, Melyssa; Kohonen Corish, Maija R. J.; Lee, Grant; Mecklin, Jukka Pekka; Pylvänäinen, Kirsi; Schmiegel, Wolff; Hüneburg, Robert; Gerdes, Anne Marie; Snyder, Carrie; Renkonen Sinisalo, Laura; Lepisto, Anna; Peltomäki, Päivi; Therkildsen, Christina; Lindberg, Lars Joachim; Lindor, Noralane; Thorlacius Ussing, Ole; Stoffel, Elena; Newcomb, Polly A.; Von Knebel Doeberitz, Magnus; Palmero, Edenir; Thibodeau, Stephen N.; Loeffler, Markus; Amor, David; Hoogerbrugge, Nicoline; Rahner, Nils; Duijkers, Floor; Hall, Michael J.; Buchanan, Daniel D.; Le Marchand, Loïc; Win, Aung Ko; Hovig, Eivind; Hampel, Heather; Williams, Heinric; Ricciardiello, Luigi; Southey, Melissa; Samadder, N. Jewel; James, Paul; Okkels, Henrik; Lubiński, Jan; Reece, Jeanette; Ngeow, Joanne; Bassaneze, Thiago; Guillem, Jose G.; Ahadova, Aysel; Arnold, Julie; Pai, Rish; Jenkins, Mark A.; Wadt, Karin; Ankathil, Ravindran; Holinski Feder, Elke; Monahan, Kevin; Chen Shtoyerman, Rakefet; Heuveline, Vincent; Senter, Leigha; Rasmussen, Lene J.; Ward, Robyn; Parry, Susan; Evans, D. Gareth; Sampson, Julian R.; Moslein, Gabriela; Bonanni, Bernardo; Dębniak, Tadeusz; John, Thomas; Hopper, John L.; Gallinger, Steven; Figueiredo, Jane; Ten Broeke, Sanne W.; Van Overeem Hansen, Thomas; Caldés, Trinidad; Yamaguchi, Tatsuro; Barca Tierno, Verónica; Garre, Pilar; Kennelly, Rory; Cavestro, Giulia Martina; Dueñas, Nuria; Greenblatt, Marc; Weitz, Jürgen; Pineda, Marta; Lino Silva, Leonardo S.; Redler, Silke; Nakken, Sigve; Burn, John; Büttner, Reinhard; Brunet, Joan; Green, Kate; Sheth, Harsh; Rossi, Benedito Mauro; Stakelum, Aine; Portenkirchner, Carmen; Lalloo, Fiona; Newton, Katie; Martin, Claudia; Kloor, Matthias; The European Hereditary Tumour Group (ehtg) And The International Mismatch Repair Consortium (imrc); Bertario, Lucio; Crosbie, Emma J.; Mints, Miriam; Tjandra, Douglas; Neffa, Florencia; Perne, Claudia; Esperon, Patricia; Latchford, Andrew; Kariv, Revital; Macrae, Finlay; Guillén Ponce, Carmen; Rosner, Guy; Levi, Zohar; Tibiletti, Maria Grazia; Pavicic, Walter Hernán
Sep-2017Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome databaseMøller, Pål; Seppälä, Toni T.; Bernstein, Inge; Holinski Feder, Elke; Sala, Paulo; Evans, D. Gareth; Lindblom, Annika; Macrae, Finlay; Blanco Guillermo, Ignacio; Sijmons, Rolf H.; Jeffries, Jacqueline; Vasen, Hans; Burn, John; Nakken, Sigve; Hovig, Eivind; Rødland, Einar Andreas; Tharmaratnam, Kukatharmini; de Vos Tot Nederveen Cappel, Wouter H.; Hill, James; Wijnen, Juul T.; Jenkins, Mark A.; Green, Kate; Lalloo, Fiona; Sunde, Lone; Mints, Miriam; Bertario, Lucio; Pineda Riu, Marta; Navarro García, Matilde; Morak, Monika; Renkonen Sinisalo, Laura; Frayling, Ian M.; Plazzer, John Paul; Pylvanainen, Kirsi; Genuardi, Maurizio; Mecklin, Jukka-Pekka; Möslein, Gabriela; Sampson, Julian R.; Capellá, G. (Gabriel); Mallorca Group
28-Feb-2019Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database reportSeppälä, Toni T.; Ahadova, Aysel; Dominguez Valentin, Mev; Macrae, Finlay; Evans, D. Gareth; Therkildsen, Christina; Sampson, Julian R.; Scott, RodneyJ.; Burn, John; Moslein, Gabriela; Bernstein, Inge; Holinski-Feder, Elke; Pylvanainen, Kirsi; Renkonen Sinisalo; Lepisto, Anna; Lautrup, Charlotte K.; Lindblom, Annika; Plazzer, John Paul; Winship, Ingrid; Tjandra, Douglas; Katz, Lior; Aretz, Stefan; Hüneburg, Robert; Holzapfel, Stefanie; Heinimann, Karl; Della Valle, Adriana; Neffa, Florencia; Gluck, Nathan; De Vos Tot Nederveen Cappel, Wouter H. WH.; Vasen, Hans; Morak, Monika; Steinke-Lange, Verena; Engel, Christoph; Rahner, Nils; Schmiegel, Wolff; Vangala, Deepak; Thomas, Huw; Green, Kate; Lalloo, Fiona; Crosbie, Emma J.; Hill, James; Capellá, G. (Gabriel); Pineda Riu, Marta; Navarro, Matilde; Blanco Guillermo, Ignacio; ten Broeke, Sanne W.; Nielsen, Maartje; Ljungmann, Ken; Nakken, Sigve; Lindor, Noralane; Frayling, Ian M.; Hovig, Eivind; Sunde, Lone; Kloor, Matthias; Mecklin, Jukka-Pekka; Kalager, Mette; Møller, Pål
20-Mar-2023Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database.Dominguez Valentin, Mev; Haupt, Saskia; Seppälä, Toni T.; Sampson, Julian R.; Sunde, Lone; Bernstein, Inge; Jenkins, Mark A.; Engel, Christoph; Aretz, Stefan; Nielsen, Maartje; Capellá, G. (Gabriel); Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Buchanan, Daniel D; Thibodeau, Steven N.; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Redler, Silke; Schröck, Evelin; Steinke-Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Hüneburg, Robert; Büttner, Reinhard; Weitz, Jürgen; Pineda Riu, Marta; Dueñas, Nuria; Brunet, Joan; Moreira, Leticia; Sánchez, Ariadna; Hovig, Eivind; Nakken, Sigve; Tjandra, Douglas; Green, Kate; Lalloo, Fiona; Hill, James; Crosbie, Emma J.; Mints, Miriam; Goldberg, Yael; Ten Broeke, Sanne W.; Kariv, Revital; Rosner, Guy; Advani, Suresh H.; Thomas, Lidiya; Shah, Pankaj; Shah, Mithun; Neffa, Florencia; Esperon, Patricia; Balaguer Prunés, Francesc; Pavicic, Walter Hernán; Torrezan, Giovana Tardin; Bassaneze, Thiago; Martin, Claudia; Möslein, Gabriela; Møller, Pål; Evans, D. 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; Dębniak, Tadeusz; Fruscio, Robert; López-Koestner, Francisco; Alvarez-Valenzuela, Karin; Katz, Lior H.; Laish, Ido; Vainer, Elez; Vaccaro, Carlos Alberto; Carraro, Dirce Maria; Monahan, Kevin; Half, Elizabeth; Stakelum, Aine; Winter, Des; Kennelly, Rory; Gluck, Nathan; Sheth, Harsh; Abu-Freha, Naim; Greenblatt, Marc; Rossi, Benedito Mauro; Bohorquez, Mabel; Cavestro, Giulia Martina; Lino-Silva, Leonardo S.; Horisberger, Karoline; Tibiletti, Maria Grazia; Nascimento, Ivana; Thomas, Huw; Rossi, Norma Teresa; Apolinário da Silva, Leandro; Zaránd, Attila; Ruiz Bañobre, Juan; Heuveline, Vincent; Mecklin, Jukka Pekka; Pylvänäinen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Peltomäki, Päivi; Therkildsen, Christina; Madsen, Mia Gebauer; Burgdorf, Stefan Kobbelgaard; Hopper, John L.; Ko Win, Aung; Haile, Robert W.
28-Jun-2021No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database StudyDominguez Valentin, Mev; Plazzer, John Paul; Sampson, Julian R.; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capellá, G. (Gabriel); Balaguer Prunés, Francesc; Macrae, Finlay; Winship, Ingrid M.; Thomas, Huw; Evans, D. Gareth; Burn, John; Greenblatt, Marc; de Vos Tot Nederveen Cappel, Wouter H.; Sijmons, Rolf H.; Nielsen, Maartje; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Valle, Adriana Della; Lopez Kostner, Francisco; Alvarez Valenzuela, Karin; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Nakken, Sigve; Hovig, Eivind; Green, Kate; Lalloo, Fiona; Hill, James; Vasen, Hans; Perne, Claudia; Büttner, Reinhard; Görgens, Heike; Holinski Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Weitz, Jürgen; Steinke Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Crosbie, Emma J.; Pineda, Marta; Navarro, Matilde; Brunet, Joan; Moreira, Leticia; Sánchez, Ariadna; Serra Burriel, Miquel; Mints, Miriam; Kariv, Revital; Rosner, Guy; Piñero, Tamara Alejandra; Pavicic, Walter Hernán; Kalfayan, Pablo; ten Broeke, Sanne W.; Mecklin, Jukka-Pekka; Pylvänäinen, Kirsi; Renkonen Sinisalo, Laura; Lepistö, Anna; Peltomäki, Päivi; Hopper, John L.; Ko Win, Aung; Buchanan, Daniel D.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Hansen, Thomas V. O.; Lindberg, Lars; Rødland, Einar Andreas; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Seppälä, Toni T.; Møller, Pål
6-Dec-2019Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testingDominguez Valentin, Mev; Nakken, Sigve; Tubeuf, Hélène; Vodák, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Holth, Arild; Capellá, G. (Gabriel); Davidson, Ben; Evans, D. Gareth; Martins, Alexandra; Møller, Pål; Hovig, Eivind
1-Dec-2020Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.Dominguez Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capellá, G. (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 Riu, Marta; Navarro, Matilde; Brunet, Joan; Kariv, Revital; Rosner, Guy; Piñero, Tamara Alejandra; González, María Laura; Kalfayan, Pablo; Ryan, Neil A. J.; Ten Broeke, Sanne W.; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Burn, John; Greenblatt, Marc; de Vos Tot Nederveen Cappel, Wouter H.; Della Valle, Adriana; Lopez Kostner, Francisco; Alvarez Valenzuela, Karin; Büttner, Reinhard; Görgens, Heike; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Weitz, Jürgen; Pylvänäinen, Kirsi; Renkonen Sinisalo, Laura; Lepistö, Anna; Auranen, Annika; Hopper, John L.; Ko Win, Aung; Haile, Robert W.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Okkels, Henrik; Ketabi, Zohreh; Denton, Oliver G.; Rødland, Einar A.; Vasen, Hans; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Sampson, Julian R.; Evans, D. Gareth; Seppälä, Toni T.; Møller, Pål
14-Oct-2019Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database reportDominguez Valentin, Mev; Seppälä, Toni T.; Sampson, Julian R.; Macrae, Finlay; Winship, Ingrid; Evans, D. Gareth; Scott, RodneyJ.; Burn, John; Moslein, Gabriela; Bernstein, Inge; Pylvanainen, Kirsi; Renkonen Sinisalo, Laura; Lepisto, Anna; Lindblom, Annika; Plazzer, John-Paul; Tjandra, Douglas; Thomas, Huw; Green, Kate; Lalloo, Fiona; Crosbie, Emma J.; Hill, James; Capellá, G. (Gabriel); Pineda Riu, Marta; Navarro, Matilde; Brunet, Joan; Ronlund, Karina; Nielsen, Randi Thyregaard; Yilmaz, Mette; Elvang, Louise Laurberg; Katz, Lior; Nielsen, Maartje; ten Broeke, Sanne W.; Nakken, Sigve; Hovig, Eivind; Sunde, Lone; Kloor, Matthias; Knebel Doeberitz, Magnus v; Ahadova, Aysel; Lindor, Noralane; Steinke Lange, Verena; Holinski Feder, Elke; Mecklin, Jukka-Pekka; Møller, Pål