Objects
Thompson, Bryony A., Spurdle, Amanda B., du Sart, Desiree, Fabre, Aurelie, Farrell, Michael P., Farrington, Susan M., Frayling, Ian M., Frebourg, Thierry, Goldgar, David E., Heinen, Christopher D., Holinski-Feder, Elke, Kohonen-Corish, Maija, Plazzer, John-Paul, Robinson, Kristina Lagerstedt, Leung, Suet Yi, Martins, Alexandra, Moller, Pat, Morak, Monika, Nystrom, Minna, Peltomaki, Paivi, Pineda, Marta, Qi, Ming, Ramesar, Rajkumar, Greenblatt, Marc S., Rasmussen, Lene Juel, Royer-Pokora, Brigitte, Scott, Rodney J., Sijmons, Rolf, Tavtigian, Sean V., Tops, Carli M., Weber, Thomas, Wijnen, Juul, Woods, Michael O., Macrae, Finlay, Akagi, Kiwamu, Genuardi, Maurizio, Al-Mulla, Fahd, Bapat, Bharati, Bernstein, Inge, Capellá, Gabriel, den Dunnen, John T.. Nature Publishing Group; 2014. Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
Out, Astrid A., Tops, Carli M. J., Fostira, Florentia, Franken, Patrick F., Gaustadnes, Mette, Heinimann, Karl, Hodgson, Shirley V., Hogervorst, Frans B. L., Holinski-Feder, Elke, Lagerstedt-Robinson, Kristina, Olschwang, Sylviane, van den Ouweland , Ans M. W., Nielsen, Maartje, Scott, Rodney J., Weiss, Marjan M., van Minderhout, Ivonne J. H. M., Fokkema, Ivo F. A. C., Buisine, Marie-Pierre, Claes, Kathleen, Colas, Chrystelle, Fodde, Riccardo. John Wiley & Sons; 2010. Leiden Open Variation Database of the MUTYH gene.
Seppala, Toni T., Ahadova, Aysel, Bernstein, Inge, Holinski-Feder, Elke, Pylvanainen, Kirsi, Renkonen-Sinisalo, Laura, Lepisto, Anna, Lautrup, Charlotte Kvist, Lindblom, Annika, Plazzer, John-Paul, Winship, Ingrid, Tjandra, Douglas, Dominguez-Valentin, Mev, Katz, Lior H., Aretz, S, Hueneburg, R, Holzapfel, S, Heinimann, K, Della Valle, A, Neffa, F, Gluck, N, Cappel, WHDVTN, Vasen, H, Macrae, Finlay, Morak, M, Steinke-Lange, V, Engel, C, Rahner, N, Schmiegel, W, Vangala, D, Thomas, H, Green, K, Lalloo, F, Crosbie, EJ, Evans, D. Gareth, Hill, J, Capella, G, Pineda, M, Navarro, M, Blanco, I, ten Broeke, S, Nielsen, M, Ljungmann, K, Nakken, S, Lindor, N, Therkildsen, Christina, Frayling, I, Hovig, E, Sunde, L, Kloor, M, Mecklin, J-P, Kalager, M, Moller, P, Sampson, Julian, Scott, Rodney, Burn, John, Moeslein, Gabriela. BioMed Central; 2019. Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report.
Ahadova, Aysel, Seppälä, Toni T., Laghi, Luigi, Dominguez-Valentin, Mev, Capella, Gabriel, Macrae, Finlay, Scott, Rodney, Hüneburg, Robert, Nattermann, Jacob, Hoffmeister, Michael, Brenner, Hermann, Bläker, Hendrik, Engel, Christoph, von Knebel Doeberitz, Magnus, Sampson, Julien R., Vasen, Hans, Mecklin, Jukka-Pekka, Møller, Pal, Kloor, Matthias, Gallon, Richard, Burn, John, Holinski-Feder, Elke, Steinke-Lange, Verena, Möslein, Gabriela, Nielsen, Maartje, ten Broeke, Sanne W.. John Wiley & Sons; 2021. The "unnatural" history of colorectal cancer in Lynch syndrome: lessons from colonoscopy surveillance.