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

- Weber, W., Scott, Rodney J

CD36 polymorphisms and the age of disease onset in patients with pathogenic variants within the mutation cluster region of APC

- Connor, T, McPhillips, M, Scott, RJ, Hipwell, M, Ziolkowski, A, Oldmeadow, C, Clapham, M, Pockney, PG, Lis, E, Banasiewicz, T, Plawski, 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.

Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

- Moller, Pal, Seppala, Toni, Capella, Gabriel, Poplawski, N, Hoogerbrugge, N, Morrison, PJ, James, P, Lee, G, Chen-Shtoyerman, R, Ankathil, R, Pai, R, Ward, R, Parry, S, Evans, Dafydd Gareth, Debniak, T, John, T, van Overeem Hansen, T, Caldes, T, Yamaguchi, T, Barca-Tierno, V, Garre, P, Cavestro, GM, Weitz, J, Redler, S, Burn, John, Buettner, R, Heuveline, V, Hopper, JL, Win, AK, Lindor, N, Gallinger, S, Le Marchand, L, Newcomb, PA, Figueiredo, J, Buchanan, DD, Holinski-Feder, Elke, Thibodeau, SN, ten Broeke, SW, Hovig, E, Nakken, S, Pineda, M, Duenas, N, Brunet, J, Green, K, Lalloo, F, Newton, K, Bertario, Lucio, Crosbie, EJ, Mints, M, Tjandra, D, Neffa, F, Esperon, P, Kariv, R, Rosner, G, Pavicic, WH, Kalfayan, P, Torrezan, GT, Bonanni, Bernardo, Bassaneze, T, Martin, C, Moslein, G, Ahadova, A, Kloor, M, Sampson, JR, Jenkins, MA, Lindblom, Annika, Levi, Zohar, Macrae, Finlay, Winship, Ingrid, Dowty, James G., Plazzer, John-Paul, Sijmons, R, Laghi, L, Della Valle, A, Heinimann, K, Half, E, Lopez-Koestner, F, Alvarez-Valenzuela, K, Scott, Rodney J., Katz, L, Haupt, Saskia, Laish, I, Vainer, E, Vaccaro, CA, Carraro, DM, Gluck, N, Abu-Freha, N, Stakelum, A, Kennelly, R, Winter, D, Rossi, BM, Dominguez-Valentin, Mev, Greenblatt, M, Bohorquez, M, Sheth, H, Tibiletti, MG, Lino-Silva, LS, Horisberger, K, Portenkirchner, C, Nascimento, I, Rossi, NT, da Silva, LA, Sunde, Lone, Thomas, H, Zarand, A, Mecklin, J-P, Pylvanainen, K, Renkonen-Sinisalo, L, Lepisto, A, Peltomaki, P, Therkildsen, C, Lindberg, LJ, Thorlacius-Ussing, O, Bernstein, Inge, von Knebel Doeberitz, M, Loeffler, M, Rahner, N, Steinke-Lange, V, Schmiegel, W, Vangala, D, Perne, C, Hueneburg, R, de Vargas, AF, Latchford, A, Engel, Christoph, Gerdes, A-M, Backman, A-S, Guillen-Ponce, C, Snyder, C, Lautrup, CK, Amor, D, Palmero, E, Stoffel, E, Duijkers, F, Hall, MJ, Aretz, Stefan, Hampel, H, Williams, H, Okkels, H, Lubinski, J, Reece, J, Ngeow, J, Guillem, JG, Arnold, J, Wadt, K, Monahan, K, Nielsen, Maartje, Senter, L, Rasmussen, LJ, van Hest, LP, Ricciardiello, L, Kohonen-Corish, MRJ, Ligtenberg, MJL, Southey, M, Aronson, M, Zahary, MN, Samadder, NJ

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

Dupuytren's disease and the risk of malignant neoplasms

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

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.

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.

Gene expression profiling of Xeroderma pigmentosum

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

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.

Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

- Seppala, Toni T., Ahadova, Aysel, Bernstein, Inge, Holinski-Feder, Elke, Pylvanainen, Kirsi, Renkonen-Sinisalo, Laura, Lepisto, Anna, Lautrup, Charlotte Kvist, Lindblom, Annika, Plazzer, John-Paul, Winship, Ingrid, Tjandra, Douglas, Dominguez-Valentin, Mev, Katz, Lior H., Aretz, S, Hueneburg, R, Holzapfel, S, Heinimann, K, Della Valle, A, Neffa, F, Gluck, N, Cappel, WHDVTN, Vasen, H, Macrae, Finlay, Morak, M, Steinke-Lange, V, Engel, C, Rahner, N, Schmiegel, W, Vangala, D, Thomas, H, Green, K, Lalloo, F, Crosbie, EJ, Evans, D. Gareth, Hill, J, Capella, G, Pineda, M, Navarro, M, Blanco, I, ten Broeke, S, Nielsen, M, Ljungmann, K, Nakken, S, Lindor, N, Therkildsen, Christina, Frayling, I, Hovig, E, Sunde, L, Kloor, M, Mecklin, J-P, Kalager, M, Moller, P, Sampson, Julian, Scott, Rodney, Burn, John, Moeslein, Gabriela

Lynch syndrome testing of colorectal cancer patients in a high-income country with universal healthcare: a retrospective study of current practice and gaps in seven australian hospitals

- Steinberg, Julia, Chan, Priscilla, Pearn, Amy, Nichols, Cassandra, McKay, Skye, Hayward, Anne, Egoroff, Natasha, Engel, Alexander, Gibbs, Peter, Goodwin, Annabel, Harris, Marion, Kench, James G., Hogden, Emily, Pachter, Nicholas, Parkinson, B, Pockney, Peter, Ragunathan, A, Smyth, C, Solomon, M, Steffens, D, Toh, JWT, Wallace, M, Canfell, K, Tiernan, Gabriella, Gill, A, Macrae, F, Tucker, K, Taylor, N, Morrow, April, Kang, Yoon-Jung, He, Emily, Venchiarutti, Rebecca, Titterton, Leanna, Sankey, Lucien

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

Modifier genes and Lynch syndrome: some considerations

- 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.

Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report

- Dominguez-Valentin, Mev, Seppälä, Toni T., Sampson, Julian R., Macrae, Finlay, Winship, Ingrid, Evans, D. Gareth, Scott, Rodney J., Burn, John, Möslein, Gabriela, Bernstein, Inge, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, Anna, Lindblom, Annika, Plazzer, John-Paul, Tjandra, Douglas, Thomas, Huw, Green, Kate, Lalloo, Fiona, Crosbie, Emma J.

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.

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