The "unnatural" history of colorectal cancer in Lynch syndrome: lessons from colonoscopy surveillance
- Creator: 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.
- Resource Type: journal article
- Date: 2021
Identification of new causative genes in inherited colorectal cancer
- Creator: Xavier, Alexandre
- Resource Type: thesis
- Date: 2020
Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome
- Creator: Xavier, Alexandre , Olsen, Maren Fridtjofsen , Lavik, Liss A. , Johansen, Jostein , Singh, Ashish Kumar , Sjursen, Wenche , Scott, Rodney J. , Talseth-Palmer, Bente A.
- Resource Type: journal article
- Date: 2019
Cancer Risks for PMS2-Associated Lynch Syndrome.
- Creator: 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
- Resource Type: journal article
- Date: 2018
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations
- Creator: Sjursen, Wenche , McPhillips, Mary , Scott, Rodney J. , Talseth-Palmer, Bente A.
- Resource Type: journal article
- Date: 2016
Colonoscopy findings in high-risk individuals compared to an average-risk control population
- Creator: Forsberg, Anna , Kjellström, Lars , Andreasson, Anna , Jaramillo, Erik , Rubio, Carlos A. , Björck, Erik , Agréus, Lars , Talley, Nicholas J. , Lindblom, Annika
- Resource Type: journal article
- Date: 2015
Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers
- Creator: 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
- Resource Type: journal article
- Date: 2013
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
- Creator: 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.
- Resource Type: journal article
- Date: 2013