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Issue DateTitleAuthor(s)
2019-12-01Development and validation of a targeted gene sequencing panel for application to disparate cancersMcCabe, MJ; Gauthier, MEA; Chan, CL; Thompson, TJ; De Sousa, SMC; Puttick, C; Grady, JP; Gayevskiy, V; Tao, J; Ying, K; Cipponi, A; Deng, N; Swarbrick, A; Thomas, ML; Lord, RV; Johns, AL; Kohonen-Corish, M; O’Toole, SA; Clark, J; Mueller, SA; Gupta, R; McCormack, AI; Dinger, ME; Cowley, MJ; Aghmesheh, M; Amor, D; Andrews, L; Antill, Y; Armitage, S; Arnold, L; Balleine, R; Bastick, P; Beesley, J; Beilby, J; Bennett, I; Blackburn, A; Bogwitz, M; Botes, L; Brennan, M; Brown, M; Buckley, M; Burgess, M; Burke, J; Butow, P; Caldon, L; Callen, D; Campbell, I; Chauhan, D; Chauhan, M; Chenevix-Trench, G; Christian, A; Clarke, C; Cohen, P; Colley, A; Crook, A; Cui, J; Culling, B; Cummings, M; Dawson, SJ; deFazio, A; Delatycki, M; Dickson, R; Dixon, J; Dobrovic, A; Dudding, T; Edkins, T; Edwards, S; Eisenbruch, M; Farshid, G; Fellows, A; Fenton, G; Field, M; Flanagan, J; Fong, P; Forrest, L; Fox, S; French, J; Friedlander, M; Gaff, C; Ortega, DG; Gattas, M; George, P; Giles, G; Gill, G; Greening, S; Haan, E; Harris, M; Hart, S; Hayward, N; Heiniger, L; Hopper, J; Hunt, C; James, P; Jenkins, M; Kefford, R; Kidd, A; Kirk, J; Koehler, J; Kollias, J; Lakhani, S
2022-10-01Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.Møller, P; Seppälä, T; Dowty, JG; Haupt, S; Dominguez-Valentin, M; Sunde, L; Bernstein, I; Engel, C; Aretz, S; Nielsen, M; Capella, G; Evans, DG; Burn, J; Holinski-Feder, E; Bertario, L; Bonanni, B; Lindblom, A; Levi, Z; Macrae, F; Winship, I; Plazzer, J-P; Sijmons, R; Laghi, L; Valle, AD; Heinimann, K; Half, E; Lopez-Koestner, F; Alvarez-Valenzuela, K; Scott, RJ; Katz, L; Laish, I; Vainer, E; Vaccaro, CA; Carraro, DM; Gluck, N; Abu-Freha, N; Stakelum, A; Kennelly, R; Winter, D; Rossi, BM; Greenblatt, M; Bohorquez, M; Sheth, H; Tibiletti, MG; Lino-Silva, LS; Horisberger, K; Portenkirchner, C; Nascimento, I; Rossi, NT; da Silva, LA; Thomas, H; Zaránd, A; Mecklin, J-P; Pylvänäinen, K; Renkonen-Sinisalo, L; Lepisto, A; Peltomäki, P; Therkildsen, C; Lindberg, LJ; Thorlacius-Ussing, O; von Knebel Doeberitz, M; Loeffler, M; Rahner, N; Steinke-Lange, V; Schmiegel, W; Vangala, D; Perne, C; Hüneburg, R; de Vargas, AF; Latchford, A; Gerdes, A-M; Backman, A-S; Guillén-Ponce, C; Snyder, C; Lautrup, CK; Amor, D; Palmero, E; Stoffel, E; Duijkers, F; Hall, MJ; Hampel, H; Williams, H; Okkels, H; Lubiński, J; Reece, J; Ngeow, J; Guillem, JG; Arnold, J; Wadt, K; Monahan, K; Senter, L; Rasmussen, LJ; van Hest, LP; Ricciardiello, L; Kohonen-Corish, MRJ; Ligtenberg, MJL; Southey, M; Aronson, M; Zahary, MN; Samadder, NJ; Poplawski, N; Hoogerbrugge, N; Morrison, PJ; James, P; Lee, G; Chen-Shtoyerman, R; Ankathil, R; Pai, R; Ward, R; Parry, S; Dębniak, T; John, T; van Overeem Hansen, T; Caldés, T; Yamaguchi, T; Barca-Tierno, V; Garre, P; Cavestro, GM; Weitz, J; Redler, S; Büttner, R; Heuveline, V; Hopper, JL; Win, AK; Lindor, N; Gallinger, S; Le Marchand, L; Newcomb, PA; Figueiredo, J; Buchanan, DD; Thibodeau, SN; Ten Broeke, SW; Hovig, E; Nakken, S; Pineda, M; Dueñas, N; Brunet, J; Green, K; Lalloo, F; Newton, K; Crosbie, EJ; Mints, M; Tjandra, D; Neffa, F; Esperon, P; Kariv, R; Rosner, G; Pavicic, WH; Kalfayan, P; Torrezan, GT; Bassaneze, T; Martin, C; Moslein, G; Ahadova, A; Kloor, M; Sampson, JR; Jenkins, MA; European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC),
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