INRASTES
Selected Publications

Selected Publications

(Results: 5)
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Delimitsou, A., Fostira, F., Kalfakakou, D., Apostolou, P., Konstantopoulou, I., Kroupis, C., Papavassiliou, A.G., Kleibl, Z., Stratikos, E., Voutsinas, G.E. and Yannoukakos, D., Functional characterization of CHEK2 variants in a Saccharomyces cerevisiae system Human Mutation, Volume 40, Pages: 631-648, 2019 [doi]
Antoniou, A.C., Casadei, S., Heikkinen, T., Barrowdale, D., Pylkäs, K., Roberts, J., Lee, A., Subramanian, D., De Leeneer, K., Fostira, F., Tomiak, E., Neuhausen, S.L., Teo, Z.L., Khan, S., Aittomäki, K., Moilanen, J.S., Turnbull, C., Seal, S., Mannermaa, A., Kallioniemi, A., Lindeman, G.J., Buys, S.S., Andrulis, I.L., Radice, P., Tondini, C., Manoukian, S., Toland, A.E., Miron, P., Weitzel, J.N., Domchek, S.M., Poppe, B., Claes, K.B.M., Yannoukakos, D., Concannon, P., Bernstein, J.L., James, P.A., Easton, D.F., Goldgar, D.E., Hopper, J.L., Rahman, N., Peterlongo, P., Nevanlinna, H., King, M.-C., Couch, F.J., Southey, M.C., Winqvist, R., Foulkes, W.D. and Tischkowitz, M., Breast-cancer risk in families with mutations in PALB2 New England Journal of Medicine, Volume 371, Pages: 497-506, 2014 [doi]
Zhang, H., Ahearn, T.U., Lecarpentier, J., Barnes, D., Beesley, J., Qi, G., Jiang, X., O’Mara, T.A., Zhao, N., Bolla, M.K., Dunning, A.M., Dennis, J., Wang, Q., Ful, Z.A., Aittomäki, K., Andrulis, I.L., Anton-Culver, H., Arndt, V., Aronson, K.J., Arun, B.K., Auer, P.L., Azzollini, J., Barrowdale, D., Becher, H., Beckmann, M.W., Behrens, S., Benitez, J., Bermisheva, M., Bialkowska, K., Blanco, A., Blomqvist, C., Bogdanova, N.V., Bojesen, S.E., Bonanni, B., Bondavalli, D., Borg, A., Brauch, H., Brenner, H., Briceno, I., Broeks, A., Brucker, S.Y., Brüning, T., Burwinkel, B., Buys, S.S., Byers, H., Caldés, T., Caligo, M.A., Calvello, M., Campa, D., Castelao, J.E., Chang-Claude, J., Chanock, S.J., Christiaens, M., Christiansen, H., Chung, W.K., Claes, K.B.M., Clarke, C.L., Cornelissen, S., Couch, F.J., Cox, A., Cross, S.S., Czene, K., Daly, M.B., Devilee, P., Diez, O., Domchek, S.M., Dörk, T., Dwek, M., Eccles, D.M., Ekici, A.B., Evans, D.G., Fasching, P.A., Figueroa, J., Foretova, L., Fostira, F., Friedman, E., Frost, D., Gago-Dominguez, M., Gapstur, S.M., Garber, J., García-Sáenz, J.A., Gaudet, M.M., Gayther, S.A., Giles, G.G., Godwin, A.K., Goldberg, M.S., Goldgar, D.E., González-Neira, A., Greene, M.H., Gronwald, J., Guénel, P., Häberle, L., Hahnen, E., Haiman, C.A., Hake, C.R., Hall, P., Hamann, U., Harkness, E.F., Heemskerk-Gerritsen, B.A.M., Hillemanns, P., Hogervorst, F.B.L., Holleczek, B., Hollestelle, A., Hooning, M.J., Hoover, R.N., Hopper, J.L., Howell, A., Huebner, H., Hulick, P.J., Imyanitov, E.N., Isaacs, C., Izatt, L., Jager, A., Jakimovska, M., Jakubowska, A., James, P., Janavicius, R., Janni, W., John, E.M., Jones, M.E., Jung, A., Kaaks, R., Kapoor, P.M., Karlan, B.Y., Keeman, R., Khan, S., Khusnutdinova, E., Kitahara, C.M., Ko, Y.-D., Konstantopoulou, I., Koppert, L.B., Koutros, S., Kristensen, V.N., Laenkholm, A.-V., Lambrechts, D., Larsson, S.C., Laurent-Puig, P., Lazaro, C., Lazarova, E., Lejbkowicz, F., Leslie, G., Lesueur, F., Lindblom, A., Lissowska, J., Lo, W.-Y., Loud, J.T., Lubinski, J., Lukomska, A., MacInnis, R.J., Mannermaa, A., Manoochehri, M., Manoukian, S., Margolin, S., Martinez, M.E., Matricardi, L., McGuffog, L., McLean, C., Mebirouk, N., Meindl, A., Menon, U., Miller, A., Mingazheva, E., Montagna, M., Mulligan, A.M., Mulot, C., Muranen, T.A., Nathanson, K.L., Neuhausen, S.L., Nevanlinna, H., Neven, P., Newman, W.G., Nielsen, F.C., Nikitina-Zake, L., Nodora, J., Offit, K., Olah, E., Olopade, O.I., Olsson, H., Orr, N., Papi, L., Papp, J., Park-Simon, T.-W., Parsons, M.T., Peissel, B., Peixoto, A., Peshkin, B., Peterlongo, P., Peto, J., Phillips, K.-A., Piedmonte, M., Plaseska-Karanfilska, D., Prajzendanc, K., Prentice, R., Prokofyeva, D., Rack, B., Radice, P., Ramus, S.J., Rantala, J., Rashid, M.U., Rennert, G., Rennert, H.S., Risch, H.A., Romero, A., Rookus, M.A., Rübner, M., Rüdiger, T., Saloustros, E., Sampson, S., Sandler, D.P., Sawyer, E.J., Scheuner, M.T., Schmutzler, R.K., Schneeweiss, A., Schoemaker, M.J., Schöttker, B., Schürmann, P., Senter, L., Sharma, P., Sherman, M.E., Shu, X.-O., Singer, C.F., Smichkoska, S., Soucy, P., Southey, M.C., Spinelli, J.J., Stone, J., Stoppa-Lyonnet, D., Swerdlow, A.J., Szabo, C.I., Tamimi, R.M., Tapper, W.J., Taylor, J.A., Teixeira, M.R., Terry, M.B., Thomassen, M., Thull, D.L., Tischkowitz, M., Toland, A.E., Tollenaar, R.A.E.M., Tomlinson, I., Torres, D., Troester, M.A., Truong, T., Tung, N., Untch, M., Vachon, C.M., van den Ouweland, A.M.W., van der Kolk, L.E., van Veen, E.M., vanRensburg, E.J., Vega, A., Wappenschmidt, B., Weinberg, C.R., Weitzel, J.N., Wildiers, H., Winqvist, R., Wolk, A., Yang, X.R., Yannoukakos, D., Zheng, W., Zorn, K.K., Milne, R.L., Kraft, P., Simard, J., Pharoah, P.D.P., Michailidou, K., Antoniou, A.C., Schmidt, M.K., Chenevix-Trench, G., Easton, D.F., Chatterjee, N., García-Closas, M., kConFab Investigators, ABCTB Investigators, EMBRACE Study and GEMO Study Collaborators, Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses Nature Genetics, Volume 52, Pages: 572-581, 2020 [doi]
Fostira, F., Kostantopoulou, I., Apostolou, P., Papamentzelopoulou, M.S., Papadimitriou, C., Faliakou, E., Christodoulou, C., Boukovinas, I., Razis, E., Tryfonopoulos, D., Barbounis, V., Vagena, A., Vlachos, I.S., Kalfakakou, D., Fountzilas, G. and Yannoukakos, D., One in three highly selected Greek patients with breast cancer carries a loss-of-function variant in a cancer susceptibility gene Journal of Medical Genetics, Volume 57, Pages: 53-61, 2020 [doi]
Laitman, Y., Friebel, T.M., Yannoukakos, D., Fostira, F., Konstantopoulou, I., Figlioli, G., Bonanni, B., Manoukian, S., Zuradelli, M., Tondini, C., Pasini, B., Peterlongo, P., Plaseska-Karanfilska, D., Jakimovska, M., Majidzadeh, K., Zarinfam, S., Loizidou, M.A., Hadjisavvas, A., Michailidou, K., Kyriacou, K., Behar, D.M., Molho, R.B., Ganz, P., James, P., Parsons, M.T., Sallam, A., Olopade, O.I., Seth, A., Chenevix - Trench, G., Leslie, G., McGuffog, L., Marafie, M.J., Megarbane, A., Al-Mulla, F., Rebbeck, T.R. and Friedman, E., The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries Human Mutation, Volume 40, Pages: e1-e23, 2019 [doi]
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