INRASTES
Selected Publications

Selected Publications

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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., 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]
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., Kalfakakou, D. and Konstantopoulou, I., Pathogenic Variants in Breast Cancer Susceptibility Genes in Older Women JAMA, Volume 324, Pages: 397, 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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