8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome

- Talseth-Palmer, Bente A., Scott, Rodney J., Vasen, Hans F. A., Wijnen, Juul T.

A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants

- Wiik, Mariann Unhjem, Evans, Tiffany-Jane, Belhadj, Sami, Bolton, Katherine A., Dymerska, Dagmara, Jagmohan-Changur, Shantie, Capellá, Gabriel, Kurzawski, Grzegorz, Wijnen, Juul T., Valle, Laura, Vasen, Hans F. A., Lubinski, Jan, Scott, Rodney J., Talseth-Palmer, Bente A.

CD36-a plausible modifier of disease phenotype in familial adenomatous polyposis

- Holmes, Merran, Connor, Toni, Oldmeadow, Christopher, Pockney, Peter G., Scott, Rodney J., Talseth-Palmer, Bente A.

Cell cycle-related genes as modifiers of age of onset of colorectal cancer in Lynch syndrome: a large-scale study in non-Hispanic white patients

- Chen, Jinyun, Pande, Mala, Scott, Rodney J., Frazier, Marsha L., Huang, Yu-Jing, Wei, Chongjuan, Amos, Christopher I., Talseth-Palmer, Bente A., Meldrum, Cliff J., Chen, Wei V., Gorlov, Ivan P., Lynch, Patrick M.

Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome

- Talseth-Palmer, Bente A., Brenne, Ingvild S., Scott, Rodney J., Ashton, Katie A., Evans, Tiffany-Jane, McPhillips, Mary, Groombridge, Claire, Suchy, Janina, Kurzawski, Grzegorz, Spigelman, Allan, Lubinski, Jan

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

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.

Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures

- Evans, Tiffany-Jane, Milne, Elizabeth, Richardson, Ebony, Lavis, Laura, Catchpoole, Daniel, Attia, John R., Armstrong, Bruce K., Clavel, Jacqueline, Scott, Rodney J., Anderson, Denise, de Klerk, Nicholas H., Jamieson, Sarra E., Talseth-Palmer, Bente A., Bowden, Nikola A., Holliday, Elizabeth G., Rudant, Jéremié, Orsi, Laurent

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.

Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients

- Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, McElduff, Patrick, Spigelman, Allan D., Hannan, Garry N., Scott, Rodney J.

Copy number variation in hereditary non-polyposis colorectal cancer

- Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, Grice, Desma M., Duesing, Konsta, Hannan, Garry N., Scott, Rodney J.

Effects of a fall prevention program in elderly: A pragmatic observational study in two orthopedic departments

- Røyset, Bodil, Talseth-Palmer, Bente A., Lydersen, Stian, Farup, Per G.

Expanding the genetic basis of copy number variation in familial breast cancer

- Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, Grice, Desma M., Hannan, Garry N., Scott, Rodney J.

Genetic modifiers of cancer risk in Lynch syndrome: a review

- Talseth-Palmer, Bente A., Wijnen, Juul T., Grice, Desma M., Scott, Rodney J.

Genetic variation and its role in malignancy

- Talseth-Palmer, Bente A., Scott, Rodney J.

Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age

- Shi, Zumin, Johnstone, Daniel, Lubinski, Jan, Scott, Rodney J., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, Spigelman, Allan D., Groombridge, Claire, Milward, Elizabeth A., Olynyk, John K., Suchy, Janina, Kurzawski, Grzegorz

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

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

Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility

- Picelli, Simone, Lorenzo Bermejo, Justo, Pardini, Barbara, Vodickova, Ludmila, Mueller, Heiko, Talseth-Palmer, Bente A., Stibbard, Geoffrey, Peterlongo, Paolo, Nici, Carmela, Veneroni, Silvia, Li, Li, Casey, Graham, Chang-Claude, Jenny, Tenesa, Albert, Farrington, Susan M., Tomlinson, Ian, Moreno, Victor, van Wezel, Tom, Wijnen, Juul, Dunlop, Malcolm, Radice, Paolo, Scott, Rodney J., Vodicka, Pavel, Hoffmeister, Michael, Ruiz-Ponte, Clara, Brenner, Hermann, Buch, Stephan, Voelzke, Henry, Hampe, Jochen, Schafmayer, Clemens, Lindblom, Annika, Fernandez-Rozadilla, Ceres, Carracedo, Angel, Castells, Antoni, Castellvi-Bel, Sergi, The EPICOLON Consortium, Naccarati, Alessio

MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer

- Talseth-Palmer, Bente A., McPhillips, Mary, Groombridge, Claire, Spigelman, Allan, Scott, Rodney J.

MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome

- Wiik, Mariann Unhjem, Negline, Mia, Klinkhammer, Hannah, Spier, Isabel, Perne, Claudia, Mayr, Andreas, Valle, Laura, Lubinski, Jan, Sjursen, Wenche, Scott, Rodney J., Talseth-Palmer, Bente A., Beisvåg, Vidar, Clapham, Matthew, Holliday, Elizabeth, Dueñas, Nuria, Brunet, Joan, Pineda, Marta, Bonifaci, Nuria, Aretz, Stefan