The "unnatural" history of colorectal cancer in Lynch syndrome: lessons from colonoscopy surveillance

- 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.

Identification of new causative genes in inherited colorectal cancer

- Xavier, Alexandre

Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome

- Xavier, Alexandre, Olsen, Maren Fridtjofsen, Lavik, Liss A., Johansen, Jostein, Singh, Ashish Kumar, Sjursen, Wenche, Scott, Rodney J., Talseth-Palmer, Bente A.

Cancer Risks for PMS2-Associated Lynch Syndrome.

- Ten Broeke, Sanne W., van der Klift, Heleen M., Gallinger, Steven, Gomez Garcia, Encarna, Figueiredo, Jane C., Haile, Robert, Hampel, Heather L., Hopper, John L., Hoogerbrugge, Nicoline, von Knebel Doeberitz, Magnus, Le Marchand, Loic, Letteboer, Tom G. W., Tops, Carli M. J., Jenkins, MA, Lindblom, A, Lindor, NM, Mensenkamp, AR, Møller, P, Newcomb, PA, van Os, TAM, Pearlman, R, Pineda, M, Rahner, N, Aretz, Stefan, Redeker, EJW, Olderode-Berends, MJW, Rosty, C, Schackert, HK, Scott, Rodney, Senter, L, Spruijt, L, Steinke-Lange, V, Suerink, M, Thibodeau, S, Bernstein, Inge, Vos, YJ, Wagner, A, Winship, I, Hes, FJ, Vasen, HFA, Wijnen, JT, Nielsen, M, Win, AK, Buchanan, Daniel D., de la Chapelle, Albert, Capella, Gabriel, Clendenning, Mark, Engel, Christoph

Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations

- Sjursen, Wenche, McPhillips, Mary, Scott, Rodney J., Talseth-Palmer, Bente A.

Colonoscopy findings in high-risk individuals compared to an average-risk control population

- Forsberg, Anna, Kjellström, Lars, Andreasson, Anna, Jaramillo, Erik, Rubio, Carlos A., Björck, Erik, Agréus, Lars, Talley, Nicholas J., Lindblom, Annika

Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers

- Talseth-Palmer, Bente A., Wijnen, Juul T., Suchy, Janina, Kurzawski, Grzegorz, The Dutch Cancer Genetics Group,, Spigelman, Allan, Møller, Pål, Morreau, Hans M., Van Wezel, Tom, Lubinski, Jan, Vasen, Hans F. A., Scott, Rodney J., Brenne, Ingvild S., Jagmohan-Changur, Shantie, Barker, Daniel, Ashton, Katie A., Tops, Carli M., Evans, Tiffany-Jane, McPhillips, Mary, Groombridge, Claire

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients

- Talseth-Palmer, Bente A., Holliday, Elizabeth G., Evans, Tiffany-Jane, McEvoy, Mark, Attia, John, Grice, Desma M., Masson, Amy L., Meldrum, Cliff, Spigelman, Allan, Scott, Rodney J.