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Επιλεγμένες Δημοσιεύσεις

Επιλεγμένες Δημοσιεύσεις

(Αποτελέσματα: 5)
Καθαρισμός
Fostira, F., Koutsodontis, G., Vagia, E., Economopoulou, P., Kotsantis, I., Sasaki, C., Rontogianni, D., Perisanidis, C. and Psyrri, A., Predisposing germline mutations in young patients with squamous cell cancer of the oral cavity JCO Precision Oncology, Volume 2, 2018 [doi]
Fostira, F., Kontopodis, E., Apostolou, P., Fragkaki, M., Androulakis, N., Yannoukakos, D., Konstantopoulou, I. and Saloustros, E., Extending the clinical phenotype associated with biallelic NTHL1 germline mutations Clinical Genetics, Volume 94, Pages: 588-589, 2018 [doi]
Fostira, F., Kalfakakou, D. and Konstantopoulou, I., Pathogenic Variants in Breast Cancer Susceptibility Genes in Older Women JAMA, Volume 324, Pages: 397, 2020 [doi]
Yang, X., Leslie, G., Doroszuk, A., Schneider, S., Allen, J., Decker, B., Dunning, A.M., Redman, J., Scarth, J., Plaskocinska, I., Luccarini, C., Shah, M., Pooley, K., Dorling, L., Leei, A., Adank, M.A., Adlard, J., Aittomäki, K., Andrulis, I.L., Ang, P., Barwell, J., Bernstein, J.L., Bobolis, K., Borg, Å., Blomqvist, C., Claes, K.B.M., Concannon, P., Cuggia, A., Culver, J.O., Damiola, F., De Pauw, A., Diez, O., Dolinsky, J.S., Domchek, S.M., Engel, C., Evans, D.G., Fostira, F., Garber, J., Golmard, L., Goode, E.L., Gruber, S.B., Hahnen, E., Hake, C., Heikkinen, T., Hurley, J.E., Janavicius, R., Kleibl, Z., Kleiblova, P., Konstantopoulou, I., Kvist, A., Laduca, H., Lee, A.S.G., Lesueur, F., Maher, E.R., Mannermaa, A., Manoukian, S., McFarland, R., McKinnon, W., Meindl, A., Metcalfe, K., Taib, N.A.M., Moilanen, J., Nathanson, K.L., Neuhausen, S., Ng, P.S., Nguyen-Dumont, T., Nielsen, S.M., Obermair, F., Offit, K., Olopade, O.I., Ottini, L., Penkert, J., Pylkäs, K., Radice, P., Ramus, S.J., Rudaitis, V., Side, L., Silva-Smith, R., Silvestri, V., Skytte, A.-B., Slavin, T., Soukupova, J., Tondini, C., Trainer, A.H., Unzeitig, G., Usha, L., Van Overeem Hansen, T., Whitworth, J., Wood, M., Yip, C.H., Yoon, S.-Y., Yussuf, A., Zogopoulos, G., Goldgar, D., Hopper, J.L., Chenevix-Trench, G., Pharoah, P., George, S.H.L., Balmaña, J., Houdayer, C., James, P., El-Haffaf, Z., Ehrencrona, H., Janatova, M., Peterlongo, P., Nevanlinna, H., Schmutzler, R., Teo, S.-H., Robson, M., Pal, T., Couch, F., Weitzel, J.N., Elliott, A., Southey, M., Winqvist, R., Easton, D.F., Foulkes, W.D., Antoniou, A.C. and Tischkowitz, M., Cancer risks associated with germline PALB2 pathogenic variants: An international study of 524 families Journal of Clinical Oncology, Volume 38, Pages: 674-685, 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]
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