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

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.

Modifier genes in Lynch syndrome: functional genomics and its consequence on disease expression

- Reeves, Stuart

Genetic epidemiology studies in hereditary non-polyposis colorectal cancer

- Scott, Rodney, Lubinski, Jan

Genetic variation and risk of endometrial cancer

- Ashton, Katie

MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer

- Reeves, Stuart G., Meldrum, Cliff, Groombridge, Claire, Spigelman, Allan D., Suchy, Janina, Kurzawski, Grzegorz, Lubinski, Jan, McElduff, Patrick, Scott, Rodney J.

Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer

- Talseth, Bente A., Ashton, Katie A., Meldrum, Cliff, Suchy, Janina, Kurzawski, Grzegorz, Lubinski, Jan, Scott, Rodney J.

IGF1 is a modifier of disease risk in hereditary non-polyposis colorectal cancer

- Reeves, Stuart G., Rich, Dominique, Meldrum, Cliff J., Colyvas, Kim, Kurzawski, Grzegorz, Suchy, Janina, Lubinski, Jan, Scott, Rodney J.

Variable phenotypic expression in HNPCC and the search for modifier genes

- Scott, Rodney J.

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

- Weber, W., Scott, Rodney J

Deletion mutations in an Australian series of HNPCC patients

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

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.