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

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.

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.

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.

Patient participation in the clinical pathway-Nurses' perceptions of adults' involvement in haemodialysis

- Andersen-Hollekim, Tone E., Kvangarsnes, Marit, Landstad, Bodil J., Talseth-Palmer, Bente A., Hole, Torstein

TAPES: A tool for assessment and prioritisation in exome studies

- Xavier, Alexandre, 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.

Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome

- Hansen, Maren F., Johansen, Jostein, Sjursen, Wenche, Sylvander, Anna E., Bjørnevoll, Inga, Talseth-Palmer, Bente A., Lavik, Liss A. S., Xavier, Alexandre, Engebretsen, Lars F., Scott, Rodney J., Drabløs, Finn

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.

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

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

Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families

- Talseth-Palmer, Bente A., Bauer, Denis C., Sjursen, Wenche, Evans, Tiffany J., McPhillips, Mary, Proietto, Anthony, Otton, Geoffrey, Spigelman, Allan D., Scott, Rodney J.

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

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.

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.

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.

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.

Genetic modifiers of cancer risk in Lynch syndrome: a review

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

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

The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients

- Talseth-Palmer, Bente A., Wijnen, Juul T., Van Wezel, Tom, Vasen, Hans F. A., Scott, Rodney J., Andreassen, Eva K., Barker, Daniel, Jagmohan-Changur, Shantie, Tops, Carli M., Meldrum, Cliff, The Dutch Cancer Genetics Group, Spigelman, Allan, Hes, Frederik J.