Browsing by Author Vasen, Hans F. A.

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 6 of 6
Issue DateTitleAuthor(s)
31-May-2021A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variantsUnhjem Wiik, Mariann; Evans, Tiffany Jane; Belhadj, Sami; Bolton, Katherine A.; Dymerska, Dagmara; Jagmohan Changur, Shantie; Capellá, G. (Gabriel); Kurzawski, Grzegorz; Wijnen, Juul T.; Valle, Laura; Vasen, Hans F. A.; Lubinski, Jan; Scott, Rodney J.; Talseth Palmer, Bente A.
10-Oct-2017Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a prospective lynch syndrome databaseSeppälä, Toni; 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 F. A.; 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
2008Guidelines for the clinical management of familial adenomatous polyposis (FAP)Vasen, Hans F. A.; Möslein, Gabriela; Alonso, A.; Aretz, S.; Bernstein, Inge; Bertario, Lucio; Blanco Guillermo, Ignacio; Bülow, S.; Burn, John; Capellá, G. (Gabriel); Colas, Chrystelle; Engel, Christoph; Frayling, Ian M.; Friedl, W.; Hes, F. J.; Hodgson, Shirley; Järvinen, Heikki; Mecklin, Jukka-Pekka; Møller, Pål; Myrhoi, T.; Nagengast, F. M.; Parc, Yann; Phillips, R.; Clark, Susan K.; Ponz de Leon, Maurizio; Renkonen-Sinisalo, Laura; Sampson, J. R.; Stormorken, A.; Tejpar, Sabine; Thomas, H. J. W.; Wijnen, Juul
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, Dafydd 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, 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; 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
2010Peutz-Jeghers syndrome: a systematic review and recommendations for managementBeggs, A. D.; Latchford, A. R.; Vasen, Hans F. A.; Möslein, Gabriela; Alonso, A.; Aretz, S.; Bertario, Lucio; Blanco Guillermo, Ignacio; Bülow, S.; Burn, John; Capellá, G. (Gabriel); Colas, Chrystelle; Friedl, W.; Møller, Pål; Hes, F. J.; Järvinen, Heikki; Mecklin, Jukka-Pekka; Nagengast, F. M.; Parc, Yann; Phillips, R. K. S.; Hyer, W.; Ponz de Leon, Maurizio; Renkonen-Sinisalo, Laura; Sampson, J. R.; Stormorken, A.; Tejpar, Sabine; Thomas, H. J. W.; Wijnen, Juul; Clark, Susan K.; Hodgson, Shirley V.
8-Feb-2013Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility AllelesGracia Aznarez, Francisco Javier; Fernandez, Victoria; Pita, Guillermo; Peterlongo, Paolo; Dominguez, Orlando; Hoya, Miguel de la; Durán, Mercedes; Osorio, Ana; Moreno, Leticia; González Neira, Anna; Rosa Rosa, Juan Manuel; Sinilnikova, Olga M.; Mazoyer, Sylvie; Hopper, John L.; Lázaro García, Conxi; Southey, Melissa C.; Odefrey, Fabrice; Manoukian, Siranoush; Catucci, Irene; Caldes, Trinidad; Lynch, Henry T.; Hilbers, Florentine S. M.; van Asperen, Christi J.; Vasen, Hans F. A.; Goldgar, David E.; Radice, Paolo; Devilee, Peter; Benitez, Javier