Talseth-Palmer, Bente A., Scott, Rodney J.. Master Publishing Group; 2011. Genetic variation and its role in malignancy.

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.. Nature Publishing Group; 2021. A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants.

Talseth-Palmer, Bente A., Wijnen, Juul T., Grice, Desma M., Scott, Rodney J.. Springer Netherlands; 2013. Genetic modifiers of cancer risk in Lynch syndrome: a review.

Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, Grice, Desma M., Hannan, Garry N., Scott, Rodney J.. BioMed Central; 2014. Expanding the genetic basis of copy number variation in familial breast cancer.

Talseth-Palmer, Bente A., Bowden, Nikola A., Hill, Alyssa, Meldrum, Cliff, Scott, Rodney J.. Biomed Central; 2008. Whole genome amplification and its impact on CGH array profiles.

Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, Grice, Desma M., Duesing, Konsta, Hannan, Garry N., Scott, Rodney J.. MDPI; 2013. Copy number variation in hereditary non-polyposis colorectal cancer.

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.. BioMed Central; 2013. The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients.

Xavier, Alexandre, Olsen, Maren Fridtjofsen, Lavik, Liss A., Johansen, Jostein, Singh, Ashish Kumar, Sjursen, Wenche, Scott, Rodney J., Talseth-Palmer, Bente A.. John Wiley & Sons; 2019. Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome.

Talseth-Palmer, Bente A., Scott, Rodney J., Vasen, Hans F. A., Wijnen, Juul T.. Nature Publishing Group; 2012. 8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome.

Holmes, Merran, Connor, Toni, Oldmeadow, Christopher, Pockney, Peter G., Scott, Rodney J., Talseth-Palmer, Bente A.. BMC; 2018. CD36-a plausible modifier of disease phenotype in familial adenomatous polyposis.

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.. BioMed Central Ltd; 2013. Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.

Sjursen, Wenche, McPhillips, Mary, Scott, Rodney J., Talseth-Palmer, Bente A.. John Wiley & Sons; 2016. Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.

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. BMJ Group; 2011. Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome.

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. Public Library of Science; 2013. Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility.

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.. Oxford University Press; 2013. 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.

Talseth-Palmer, Bente A., Bauer, Denis C., Sjursen, Wenche, Evans, Tiffany J., McPhillips, Mary, Proietto, Anthony, Otton, Geoffrey, Spigelman, Allan D., Scott, Rodney J.. John Wiley & Sons; 2016. Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families.

Røyset, Bodil, Talseth-Palmer, Bente A., Lydersen, Stian, Farup, Per G.. Dove Medical Press; 2019. Effects of a fall prevention program in elderly: A pragmatic observational study in two orthopedic departments.

Andersen-Hollekim, Tone E., Kvangarsnes, Marit, Landstad, Bodil J., Talseth-Palmer, Bente A., Hole, Torstein. Wiley-Blackwell; 2019. Patient participation in the clinical pathway-Nurses' perceptions of adults' involvement in haemodialysis.

Xavier, Alexandre, Scott, Rodney J., Talseth-Palmer, Bente A.. Public Library of Science (PLoS); 2019. TAPES: A tool for assessment and prioritisation in exome studies.

Avery-Kiejda, Kelly A., Bowden, Nikola A., Hersey, Peter, Croft, Amanda J., Scurr, Lyndee L., Kairupan, Carla F., Ashton, Katie A., Talseth-Palmer, Bente A., Rizos, Helen, Zhang, Xu D., Scott, Rodney J.. BioMed Central; 2011. P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation.

Talseth-Palmer, Bente A., McPhillips, Mary, Groombridge, Claire, Spigelman, Allan, Scott, Rodney J.. BioMed Central; 2010. MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer.

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. Wiley-Blackwell; 2017. Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.

Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, McElduff, Patrick, Spigelman, Allan D., Hannan, Garry N., Scott, Rodney J.. Elsevier; 2016. Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients.

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. John Wiley & Sons; 2013. Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers.

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. John Wiley & Sons; 2009. Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age.

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. Nature Publishing Group; 2023. MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome.

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. Public Library of Science; 2014. Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures.