8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome

- Talseth-Palmer, Bente A., Scott, Rodney J., Vasen, Hans F. A., Wijnen, Juul T.

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

- Thompson, Bryony A., Spurdle, Amanda B., du Sart, Desiree, Fabre, Aurelie, Farrell, Michael P., Farrington, Susan M., Frayling, Ian M., Frebourg, Thierry, Goldgar, David E., Heinen, Christopher D., Holinski-Feder, Elke, Kohonen-Corish, Maija, Plazzer, John-Paul, Robinson, Kristina Lagerstedt, Leung, Suet Yi, Martins, Alexandra, Moller, Pat, Morak, Monika, Nystrom, Minna, Peltomaki, Paivi, Pineda, Marta, Qi, Ming, Ramesar, Rajkumar, Greenblatt, Marc S., Rasmussen, Lene Juel, Royer-Pokora, Brigitte, Scott, Rodney J., Sijmons, Rolf, Tavtigian, Sean V., Tops, Carli M., Weber, Thomas, Wijnen, Juul, Woods, Michael O., Macrae, Finlay, Akagi, Kiwamu, Genuardi, Maurizio, Al-Mulla, Fahd, Bapat, Bharati, Bernstein, Inge, Capellá, Gabriel, den Dunnen, John T.

Cell cycle-related genes as modifiers of age of onset of colorectal cancer in Lynch syndrome: a large-scale study in non-Hispanic white patients

- Chen, Jinyun, Pande, Mala, Scott, Rodney J., Frazier, Marsha L., Huang, Yu-Jing, Wei, Chongjuan, Amos, Christopher I., Talseth-Palmer, Bente A., Meldrum, Cliff J., Chen, Wei V., Gorlov, Ivan P., Lynch, Patrick M.

Comparing theory and non-theory based implementation approaches to improving referral practices in cancer genetics: a cluster randomised trial protocol

- Morrow, April, Hogden, Emily, Wolfenden, Luke, Mitchell, Gillian, Macrae, Finlay, Tucker, Kathy, Taylor, Natalie, Kan, Yoon-Jung, Canfell, Karen, Solomon, Michael J., Kench, James G., Gill, Anthony J., Shaw, Tim, Pachter, Nicholas, Parkinson, Bonny

DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome

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

Early changes of endometrial neoplasia revealed by loss of mismatch repair gene protein expression in a patient diagnosed with Lynch syndrome (letter)

- McKenzie, Ross, Scott, Rodney J., Otton, Geoffrey, Scurry, James

Genetic epidemiology studies in hereditary non-polyposis colorectal cancer

- Scott, Rodney, Lubinski, Jan

Genetic modifiers of cancer risk in Lynch syndrome: a review

- Talseth-Palmer, Bente A., Wijnen, Juul T., Grice, Desma M., 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.

Lessons learnt from implementation of a Lynch syndrome screening program for patients with gynaecological malignancy

- Najdawi, Fedaa, Crook, Ashley, Sioson, Loretta, Ahadi, Masha, Turchini, John, Clarkson, Adele, Hogg, Russell, Valmadre, Sue, Gard, Greg, Dooley, Susan J., Scott, Rodney J., Fox, Stephen B., Maidens, Jayne, Field, Michael, Gill, Anthony J., McEvoy, Christopher, Fellowes, Andrew, Pickett, Justine, Ho, Musei, Nevell, David, McIlroy, Kirsten, Sheen, Amy

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

- Burn, John, Gerdes, Anne-Marie, Bisgaard, Marie Louise, Dunlop, Malcolm G., Ho, Judy W. C., Hodgson, Shirley V., Lindblom, Annika, Lubinski, Jan, Morrison, Patrick J., Murday, Victoria, Ramesar, Raj, Side, Lucy, Macrae, Finlay, Scott, Rodney J., Thomas, Huw J. W., Vasen, Hans F., Barker, Gail, Crawford, Gillian, Elliott, Faye, Movahedi, Mohammad, Pylvanainen, Kirsi, Wijnen, Juul T., Fodde, Riccardo, Mecklin, Jukka-Pekka, Lynch, Henry T., Mathers, John C., Bishop, D. Timothy, Moeslein, Gabriela, Olschwang, Sylviane, Eccles, Diane, Evans, D. Gareth, Maher, Eamonn R., Bertario, Lucio

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

- Reeves, Stuart

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.

New EPCAM founder deletion in Polish population

- Dymerska, D., Gołębiewska, K., Szwiec, M., Kilar, E., Huzarski, T., Byrski, T., Lubiński, J., Kurzawski, G., Kuświk, M., Rudnicka, H., Scott, R. J., Billings, R., Pławski, A., Boruń, P., Siołek, M., Kozak-Klonowska, B.

Obesity, aspirin, and risk of colorectal cancer in carriers of hereditary colorectal cancer: a prospective investigation in the CAPP2 study

- Movahedi, Mohammad, Bishop, D. Timothy, Bisgaard, Marie-Luise, Dunlop, Malcolm G., Ho, Judy W. C., Hodgson, Shirley V., Lindblom, Annika, Lubinski, Jan, Morrison, Patrick J., Murday, Victoria, Ramesar, Raj S., Side, Lucy, Macrae, Finlay, Scott, Rodney J., Thomas, Huw J. W., Vasen, Hans F., Burn, John, Mathers, John C., Mecklin, Jukka-Pekka, Moeslein, Gabriela, Olschwang, Sylviane, Eccles, Diana, Evans, D. Gareth, Maher, Eamonn R., Bertario, Lucio

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