Browsing byAuthorHampel, H

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Showing results 1 to 5 of 5
Issue DateTitleAuthor(s)
2023A mainstreaming oncogenomics model: improving the identification of Lynch syndrome.O'Shea, R; Crook, A; Jacobs, C; Kentwell, M; Gleeson, M; Tucker, KM; Hampel, H; Rahm, AK; Taylor, N; Lewis, S; Rankin, NM
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),
2003-08-01Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathwayZhou, XP; Waite, KA; Pilarski, R; Hampel, H; Fernandez, MJ; Bos, C; Dasouki, M; Feldman, GL; Greenberg, LA; Ivanovich, J; Matloff, E; Patterson, A; Pierpont, ME; Russo, D; Nassif, NT; Eng, C
2010-06-01Phenotypic diversity in patients with multiple serrated polyps: A genetics clinic studyBuchanan, DD; Sweet, K; Drini, M; Jenkins, MA; Win, AK; Gattas, M; Walsh, MD; Clendenning, M; McKeone, D; Walters, R; Roberts, A; Young, A; Hampel, H; Hopper, JL; Goldblatt, J; George, J; Suthers, GK; Phillips, K; Young, GP; Chow, E; Parry, S; Woodall, S; Tucker, K; Muir, A; Field, M; Greening, S; Gallinger, S; Green, J; Woods, MO; Spaetgens, R; De La Chapelle, A; MacRae, F; Walker, NI; Jass, JR; Young, JP
2021-11Stakeholders' views of integrating universal tumour screening and genetic testing for colorectal and endometrial cancer into routine oncology.O'Shea, R; Rankin, NM; Kentwell, M; Gleeson, M; Tucker, KM; Hampel, H; Taylor, N; Lewis, S