Blood molybdenum level as a marker of cancer risk on BRCA1 carriers

- Matuszczak, Milena, Kiljańczyk, Adam, Huzarski, Tomasz, Lener, Marcin, Jakubowska, Anna, Pietrzak, Sandra, Szwiec, Marek, Stawicka-Niełacna, Małgorzata, Godlewski, Dariusz, Prusaczyk, Artur, Jasiewicz, Andrzej, Kluz, Tomasz, Marciniak, Wojciech, Tomiczek-Szwiec, Joanna, Kilar-Kobierzycka, E, Siolek, M, Posmyk, R, Jarkiewicz-Tretyn, J, Scott, Rodney, Narod, S, Lubiński, J, Derkacz, Róża, Stempa, Klaudia, Baszuk, Piotr, Bryśkiewicz, Marta, Cybulski, Cezary, Dębniak, Tadeusz, Jacek, Gronwald

Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statement.

- Møller, Pal, Seppälä, Toni T., Kohut, Kelly E., Ryan, Neil, Bauerfeind, Peter, Thomas, Laura E., Evans, D. Gareth, Aretz, Stefan, Sijmons, Rolf H., Half, Elizabeth, Heinimann, Karl, Horisberger, Karoline, Ahadova, Aysel, Monahan, Kevin, .,, Crosbie, Emma J., Holinski-Feder, Elke, Scott, Rodney, Haupt, Saskia, Möslein, Gabriela, Winship, Ingrid, Bajwa-ten Broeke, Sanne W.

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

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

Modifier genes and Lynch syndrome: some considerations

- 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

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

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

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.

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.

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

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.

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

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.

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.

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.

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.

Gene expression profiling of Xeroderma pigmentosum

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