Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families

- Dębniak, Tadeusz, Gromowski, Tomasz, Cybulski, Cezary, Serrano-Fernandez, Pablo, Lubiński, Jan, Scott, Rodney J., Gronwald, Jacek, Huzarski, Tomasz, Byrski, Tomasz, Kurzawski, Grzegorz, Dymerska, Dagmara, Górski, Bohdan, Paszkowska-Szczur, Katarzyna

Genetic variants in MUTYH are not associated with endometrial cancer risk

- Ashton, Katie A., Proietto, Anthony, Otton, Geoffrey, Symonds, Ian, Scott, Rodney J.

Hereditary cancer in clinical practice transfers to BioMed Central (editorial)

- Lubiński, Jan, Sijmons, Rolf H., Scott, Rodney J.

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.

Colorectal carcinoma in the course of inflammatory bowel diseases

- Hnatyszyn, Andrzej, Hryhorowicz, Szymon, Kaczmarek-Rys, Marta, Lis, Emilia, Slomski, Ryszard, Scott, Rodney J., Plawski, Andrzej

Deletion mutations in an Australian series of HNPCC patients

- McPhillips, Mary, Meldrum, C. J., Scott, Rodney J, Creegan, Rhona, Edkins, Edward

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.

Gene expression profiling of Xeroderma pigmentosum

- Bowden, Nikola A., Tooney, Paul A., Scott, Rodney J.

Dupuytren's disease and the risk of malignant neoplasms

- Żyluk, Andrzej, Paszkowska-Szczur, Katarzyna, Gupta, Satish, Scott, Rodney J., Lubiński, Jan, Dębniak, Tadeusz

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.

Case report: familial gastric cancer and chordoma in the same family

- Weber, W., Scott, Rodney J

The potential role of miRNAs in therapy of breast and ovarian cancers associated with BRCA1 mutation

- Strumidło, Agnieszka, Skiba, Sylwia, Scott, Rodney J., Lubiński, Jan

Frequency of the common MYH mutations (G382D and Y165C) in MMR mutation positive and negative HNPCC patients

- Ashton, Katie A., Kairupan, C. F., Scott, Rodney J., Meldrum, C. J., McPhillips, M. L.

When is a mutation not a mutation: the case of the c.594-2A>C splice variant in a woman harbouring another BRCA1 mutation in trans

- Wong-Brown, Michelle, McPhillips, Mary, Gleeson, Margaret, Spigelman, Allan D., Meldrum, Cliff J., Dooley, Susan, Scott, Rodney J.