Whole genome amplification and its impact on CGH array profiles

- Talseth-Palmer, Bente A., Bowden, Nikola A., Hill, Alyssa, Meldrum, Cliff, Scott, Rodney J.

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

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.

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.

TAPES: A tool for assessment and prioritisation in exome studies

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

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

P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation

- 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.

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

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.

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

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

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

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

Genetic variation and its role in malignancy

- Talseth-Palmer, Bente A., 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.

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.

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.

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.

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.

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.

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