Tomlinson, I. P. M., Dunlop, M., Aaltonen, L. A., Hemminki, K., Lindblom, A., Forsti, A., Sieber, O., Lipton, L., van Wezel , T., Morreau, H., Wijnen, J. T., Devilee, P., Campbell, H., Scott, R., Zanke, B., Gallinger, S., Hudson, T., Koessler, T., Pharoah, P. D., Niittymakix, I., Tuupanenx, S.. H. K. Lewis; 2009. COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer.

Darabi, Hatef, McCue, Karen, Dennis, Joe, Cox, A., Cross, S. S., Luben, R., Khaw, K.-T., Choi, J.-Y., Kang, D., Hartman, M., Lim, W. Y., Kabisch, M., Torres, D., Wang, Qin, Jakubowska, A., Lubinski, J., McKay, J., Sangrajrang, S., Toland, A. E., Yannoukakos, D., Shen, C.-Y., Yu, J.-C., Ziogas, A., Schoemaker, M. J., Canisius, Sander, Swerdlow, A., Borresen-Dale, A.-L., Kristensen, V., French, J. D., Edwards, S. L., Dunning, A. M., Easton, D. F., Hall, P., Chenevix-Trench, G., Scott, Christopher G., Apicella, Carmel, Hopper, John L., Southey, Melissa C., Stone, Jennifer, Broeks, Annegien, Schmidt, Marjanka K., Beesley, Jonathan, Scott, Rodney J., Lophatananon, Artitaya, Muir, Kenneth, Beckmann, Matthias W., Ekici, Arif B., Fasching, Peter A., Heusinger, Katharina, dos-Santos-Silva, Isabel, Peto, Julian, Tomlinson, Ian, Michailidou, Kyriaki, Sawyer, Elinor J., Burwinkel, Barbara, Marme, Frederik, Guénel, Pascal, Truong, Thérèse, Bojesen, Stig E., Flyger, Henrik, Benitez, Javier, González-Neira, Anna, Anton-Culver, Hoda, Nord, Silje, Neuhausen, Susan L., Arndt, Volker, Brenner, Hermann, Engel, Christoph, Meindl, Alfons, Schmutzler, Rita K., Arnold, Norbert, Brauch, Hiltrud, Hamann, Ute, Chang-Claude, Jenny, Kar, Siddhartha, Khan, Sofia, Nevanlinna, Heli, Ito, Hidemi, Matsuo, Keitaro, Bogdanova, Natalia V., Dörk, Thilo, Lindblom, Annika, Margolin, Sara, Kosma, Veli-Matti, Mannermaa, Arto, Humphreys, Keith, Tseng, Chiu-chen, Wu, Anna H., Floris, Giuseppe, Lambrechts, Diether, Rudolph, Anja, Peterlongo, Paolo, Radice, Paolo, Couch, F. J., Vachon, C., Giles, G. G., Thompson, Deborah, McLean, C., Milne, R. L., Dugué, P.-A., Haiman, C. A., Maskarinec, G., Woolcott, C., Henderson, B. E., Goldberg, M. S., Simard, J., Teo, S. H., Ghoussaini, Maya, Mariapun, S., Helland, A., Haakensen, V., Zheng, W., Beeghly-Fadiel, A., Tamimi, R., Jukkola-Vuorinen, A., Winqvist, R., Andrulis, I. L., Knight, J. A., Bolla, Manjeet K., Devilee, P., Tollenaar, R. A. E. M., Figueroa, J., García-Closas, M., Czene, K., Hooning, M. J., Tilanus-Linthorst, M., Li, J., Gao, Y.-T., Shu, X.-O.. Cell Press; 2015. Polymorphisms in a putative enhancer at the 10q21.2 breast cancer risk locus regulate NRBF2 expression.

Jakubowska, A., Rozkrut, D., Antoniou, A., Hamann, U., Scott, R. J., McGuffog, L., Healy, S., Sinilnikova, O. M., Rennert, G., Lejbkowicz, F., Flugelman, A., Andrulis, I. L., Glendon, G., Ozcelik, H., Thomassen, M., Paligo, M., Aretini, P., Kantala, J., Aroer, B., Von Wachenfeldt, A., van der Luijt, B., Devilee, P., EMBRACE,, Easton, D. F., Peock, S., Frost, D., Platte, R., Ellis, S. D., Fineberg, E., Evans, D. G., Lalloo, F., Eeles, R., Jacobs, C., Adlard, J., Davidson, R., Eccles, D., Cole, T., Cook, J., Godwin, A., Bove, B., GEMO Study Collaborators,, Stoppa-Lyonnet, D., Caux-Moncoutier, V., Coupier, I., Peyrat, J.-P., Vennin, P., Muller, D., Fricker, J. P., Venat-Bouvet, L., Johannsson, O. Th., Isaacs, C., Schmutzler, R., Wappenschmidt, B., Meindl, A., Arnold, N., Varon-Mateeva, R., Niederacher, D., Sutter, C., Deissler, H., Preisler-Adams, S., Simard, J., Soucy, P., Durocher, F., Chenevix-Trench, G., Beesley, J., Chen, X., ConFab, K., Rebbeck, T., Couch, F., Wang, X., Lindor, N., Fredericksen, Z., Pankratz, V. S., Peterlongo, P., Bonanni, B., Fortuzzi, S., Peissel, B., Szabo, C., Mai, P. L., Loud, J. T., Lubinski, J., Liljegren, A., Loman, N., Herbst, K., Kristoffersson, U., Rosenquist, R., Karlsson, P., Stenmark-Askmalm, M., Melin, B., Nathanson, K. L., Domchek, S. M., Byrski, T., Huzarski, T., Gronwald, J., Menkiszak, J., Cybulski, C., Serrano, P., Osorio, A., Cajal, T. R., Tsitlaidou, M., Benitez, J., Gilbert, M., Rookus, M., Aalfs, C. M., Kluijt, I., Boessenkool-Pape, J. L., Meijers-Heijboer, H. E. J., Oosterwijk, J. C., Van Asperen, C. J., Blok, M. J., Nelen, M. R., Van Den Ouweland, A. M. W., Seynaeve, C.. Nature Publishing Group; 2012. Association of PHB 1630 C > T and MTHFR 677 C > T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study.