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A new bioinformatics tool to help assess the significance of BRCA1 variants Cusin, Isabelle; Teixeira, Daniel; Zahn-Zabal, Monique; de Laval, Valentine Rech; Gleizes, Anne; Viassolo, Valeria; Chappuis, Pierre O.; Hutter, Pierre; Bairoch, Amos; Gaudet, Pascale 分享 收藏
Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci Al Olama, Ali Amin; Benlloch, Sara; Antoniou, Antonis C.; Giles, Graham G.; Severi, Gianluca; Neal, David E.; Hamdy, Freddie C.; Donovan, Jenny L.; Muir, Kenneth; Schleutker, Johanna; Henderson, Brian E.; Haiman, Christopher A.; Schumacher, Fredrick R.; Pashayan, Nora; Pharoah, Paul D. P.; Ostrander, Elaine A.; Stanford, Janet L.; Batra, Jyotsna; Clements, Judith A.; Chambers, Suzanne K.; Weischer, Maren; Nordestgaard, Borge G.; Ingles, Sue A.; Sorensen, Karina D.; Orntoft, Torben F.; Park, Jong Y.; Cybulski, Cezary; Maier, Christiane; Doerk, Thilo; Dickinson, Joanne L.; Cannon-Albright, Lisa; Brenner, Hermann; Rebbeck, Timothy R.; Zeigler-Johnson, Charnita; Habuchi, Tomonori; Thibodeau, Stephen N.; Cooney, Kathleen A.; Chappuis, Pierre O.; Hutter, Pierre; Kaneva, Radka P.; Foulkes, William D.; Zeegers, Maurice P.; Lu, Yong-Jie; Zhang, Hong-Wei; Stephenson, Robert; Cox, Angela; Southey, Melissa C.; Spurdle, Amanda B.; FitzGerald, Liesel; Leongamornlert, Daniel; Saunders, Edward; Tymrakiewicz, Malgorzata; Guy, Michelle; Dadaev, Tokhir; Little, Sarah J.; Govindasami, Koveela; Sawyer, Emma; Wilkinson, Rosemary; Herkommer, Kathleen; Hopper, John L.; Lophatonanon, Aritaya; Rinckleb, Antje E.; Kote-Jarai, Zsofia; Eeles, Rosalind A.; Easton, Douglas F. 分享 收藏
High-Resolution Breakpoint Analysis Provides Evidence for the Sequence-Directed Nature of Genome Rearrangements in Hereditary Disorders Kovac, Michal B.; Kovacova, Monika; Bachraty, Hynek; Bachrata, Katarina; Piscuoglio, Salvatore; Hutter, Pierre; Ilencikova, Denisa; Bartosova, Zdena; Tomlinson, Ian; Roethlisberger, Benno; Heinimann, Karl 分享 收藏
Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012 Rahner, Nils; Steinke, Verena; Schlegelberger, Brigitte; Eisinger, Francois; Hutter, Pierre; Olschwang, Sylviane 分享 收藏
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Recurrence and Variability of Germline EPCAM Deletions in Lynch Syndrome Kuiper, Roland P.; Vissers, Lisenka E. L. M.; Venkatachalam, Ramprasath; Bodmer, Danielle; Hoenselaar, Eveline; Goossens, Monique; Haufe, Aline; Kamping, Eveline; Niessen, Renee C.; Hogervorst, Frans B. L.; Gille, Johan J. P.; Redeker, Bert; Tops, Carli M. J.; van Gijn, Marielle E.; van den Ouweland, Ans M. W.; Rahner, Nils; Steinke, Verena; Kahl, Philip; Holinski-Feder, Elke; Morak, Monika; Kloor, Matthias; Stemmler, Susanne; Betz, Beate; Hutter, Pierre; Bunyan, David J.; Syngal, Sapna; Culver, Julie O.; Graham, Tracy; Chan, Tsun L.; Nagtegaal, Iris D.; van Krieken, J. Han J. M.; Schackert, Hans K.; Hoogerbrugge, Nicoline; van Kessel, Ad Geurts; Ligtenberg, Marjolijn J. L. 分享 收藏
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Multiple novel prostate cancer predisposition loci confirmed by an international study:: The PRACTICAL consortium Kote-Jarai, Zsofia; Easton, Douglas F.; Stanford, Janet L.; Ostrander, Elaine A.; Schleutker, Johanna; Ingles, Sue A.; Schaid, Daniel; Thibodeau, Stephen; Doerk, Thilo; Neal, David; Cox, Angela; Maier, Christiane; Vogel, Walter; Guy, Michelle; Muir, Kenneth; Lophatananon, Artitaya; Kedda, Mary-Anne; Spurdle, Amanda; Steginga, Suzanne; John, Esther M.; Giles, Graham; Hopper, John; Chappuis, Pierre O.; Hutter, Pierre; Foulkes, William D.; Hamel, Nancy; Salinas, Claudia A.; Koopmeiners, Joseph S.; Karyadi, Danielle M.; Johanneson, Bo; Wahlfors, Tiina; Tammela, Teuvo L.; Stern, Mariana C.; Corral, Roman; McDonnell, Shannon K.; Schuermann, Peter; Meyer, Andreas; Kuefer, Rainer; Leongamornlert, Daniel A.; Tymrakiewicz, Malgorzata; Liu, Jo-fen; O'Mara, Tracy; Gardiner, R. A. (Frank); Aitken, Joanne; Joshi, Amit D.; Severi, Gianluca; English, Dallas R.; Southey, Melissa; Edwards, Stephen M.; Al Olama, Ali Amin; Eeles, Rosalind A. 分享 收藏
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Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary Nonpolyposis colorectal cancer (HNPCC) van der Klift, H; Wijnen, J; Wagner, A; Verkuilen, P; Tops, C; Otway, R; Kohonen-Corish, M; Vasen, H; Oliani, C; Barana, D; Moller, P; DeLozier-Blanchet, C; Hutter, P; Foulkes, W; Lynch, H; Burn, J; Möslein, G; Fodde, R 分享 收藏
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The murine orthologue of the golgi-localized TPTE protein provides clues to the evolutionary history of the human TPTE gene family Guipponi, M; Tapparel, C; Jousson, O; Sacmuffa, N; Mas, C; Rossier, C; Hutter, P; Meda, P; Lyle, R; Reymond, A; Antonarakis, SE 分享 收藏
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Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation Hutter, P; Couturier, A; Scott, RJ; Alday, P; DelozierBlanchet, C; Cachat, F; Antonarakis, SE; Joris, F; Gaudin, M; DAmato, L; Buerstedde, JM 分享 收藏
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