Heritable defects in telomere and mitotic function selectively predispose to sarcomas

- Ballinger, Mandy L., Pattnaik, Swetansu, van der Graaf, Winette T. A., Fennelly, V, Wicht, A, Zielony, B, Galligan, E, Glavich, G, Stoeckert, J, Williams, L, Djandjgava, L, Buettner, I, Osinki, C, Puri, Ajay, Stephens, S, Rogasik, M, Bouclier, L, Girodet, M, Charreton, A, Fayet, Y, Crasto, S, Sandupatla, B, Yoon, Y, Je, N, Duffaud, Florence, Thompson, L, Fowler, T, Johnson, B, Petrikova, G, Hambridge, T, Hutchins, A, Bottero, D, Scanlon, D, Stokes-Denson, J, Génin, E, Le Cesne, Axel, Campion, D, Dartigues, J-F, Deleuze, J-F, Lambert, J-C, Redon, R, Ludwig, T, Grenier-Boley, B, Letort, S, Lindenbaum, P, Meyer, V, Seddon, Beatrice, Quenez, O, Dina, C, Bellenguez, C, Le Clézio, CC, Giemza, J, Chatel, S, Férec, C, Le Marec, H, Letenneur, L, Nicolas, G, Chandrasekar, Coonoor, Rouault, K, Schiffman, Joshua D., Brohl, Andrew S., James, Paul A., Kurtz, Jean-Emmanuel, Mundra, Piyushkumar A., Penel, Nicolas, Myklebost, Ola, Meza-Zepeda, LA, Pickett, H, Kansara, M, Waddell, N, Kondrashova, O, Pearson, JV, Barbour, AP, Li, S, Zaheed, Milita, Nguyen, TL, Fatkin, D, Graham, RM, Giannoulatou, E, Green, MJ, Kaplan, W, Ravishankar, S, Copty, J, Powell, JE, Cuppen, E, Rath, Emma, van Eijk, K, Veldink, J, Ahn, J-H, Kim, JE, Randall, RL, Tucker, K, Judson, I, Sarin, R, Genin, E, Priestley, Peter, French Exome Project Consortium,, Haber, M, Marshall, G, Cairns, Murray J., Blay, J-Y, International Sarcoma Kindred Study,, Thomas, DM, Tattersall, M, Neuhaus, S, Baber, Jonathan, Lewis, C, Carey-Smith, R, Wood, D, Porceddu, S, Dickinson, I, Thorne, H, James, P, Ray-Coquard, I, Ray-Coquard, Isabelle, Cassier, P, Le Cesne, A, Duffaud, F, Penel, N, Isambert, N, Kurtz, J-E, Puri, A, Isambert, Nicholas, Ward, I, van der Graaf, W, Seddon, B, Chandrasekar, C, Rickar, R, Hennig, I, Schiffman, J, Silvestri, A, Causeret, Sylvain, Zaratzian, A, Tayao, M, Walwyn, K, Niedermayr, E, Mang, D, Clark, R, Thorpe, T, MacDonald, J, Riddell, K, Mar, J

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

Homologous recombination DNA repair defects in PALB2-associated breast cancers

- Li, Anqi, Mane, G, Marsh, D, Mclachlan, S-A, Meiser, B, Milne, R, Nightingale, S, O'Connell, S, Pachter, N, Patterson, B, Phillips, K, Saleh, M, Salisbury, E, Saunders, C, Saunus, J, Scott, C, Scott, R, Sexton, A, Shelling, A, Simpson, P, Spigelman, A, Spurdle, M, Stone, J, Taylor, J, Thorne, H, Trainer, A, Trench, G, Tucker, K, Visvader, J, Walker, L, Wallis, M, Williams, R, Winship, I, Wu, K, Young, MA, Geyer, Felipe C., Bi, Rui, Piscuoglio, Salvatore, Wen, Hannah Y., Lozada, John R., Gularte-Merida, Rodrigo, Cavallone, Luca, Rezoug, Zoulikha, Nguyen-Dumont, Tu, Peterlongo, Paolo, Tondini, Carlo, Blecua, Pedro, Terkelsen, Thorkild, Ronlund, K, Boonen, SE, Mannerma, A, Winqvist, R, Janatova, M, Rajadurai, P, Xia, B, Norton, L, Robson, ME, Lee, Ju Youn, Ng, P-S, Looi, L-M, Southey, MC, Weigelt, B, Soo-Hwang, T, Tischkowitz, M, Foulkes, WD, Reis-Filho, JS, Aghmesheh, M, Amor, D, Selenica, Pier, Andrews, L, Antill, Y, Balleine, R, Beesley, J, Blackburn, A, Bogwitz, M, Brown, M, Burgess, M, Burke, J, Butow, P, Brown, David N., Caldon, L, Campbell, I, Christian, A, Clarke, C, Cohen, P, Crook, A, Cui, J, Cummings, M, Dawson, S-J, De Fazio, A, Pareja, Fresia, Delatycki, M, Dobrovic, A, Dudding, T, Duijf, P, Edkins, E, Edwards, S, Farshid, G, Fellows, A, Field, M, Flanagan, J, Lee, Simon S. K., Fong, P, Forbes, John, Forrest, L, Fox, S, French, J, Friedlander, M, Ortega, DG, Gattas, M, Giles, G, Gill, G, Kumar, Rahul, Gleeson, M, Greening, S, Haan, E, Harris, M, Hayward, N, Hickie, I, Hopper, J, Hunt, C, James, P, Jenkins, M, Rivera, Barbara, Kefford, R, Kentwell, M, Kirk, J, Kollias, J, Lakhani, S, Lindeman, G, Lipton, L, Lobb, L, Lok, S, Macrea, F