Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing
Shimelis, Hermela, LaDuca, Holly, Hu, Chunling, Hart, Steven N, Na, Jie, Thomas, Abigail, Akinhanmi, Margaret, Moore, Raymond M, Brauch, Hiltrud, Cox, Angela, Eccles, Diana M, Ewart-Toland, Amanda, Fasching, Peter A, Fostira, Florentia, Garber, Judy, Godwin, Andrew K, Konstantopoulou, Irene, Nevanlinna, Heli, Sharma, Priyanka, Yannoukakos, Drakoulis, Yao, Song, Feng, Bing-Jian, Tippin Davis, Brigette, Lilyquist, Jenna, Pesaran, Tina, Goldgar, David E, Polley, Eric C, Dolinsky, Jill S, Couch, Fergus J
Published in JNCI : Journal of the National Cancer Institute (01.08.2018)
Published in JNCI : Journal of the National Cancer Institute (01.08.2018)
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Genetic Testing of Breast Cancer Patients with Very Early-Onset Breast Cancer (≤30 Years) Yields a High Rate of Germline Pathogenic Variants, Mainly in the BRCA1, TP53, and BRCA2 Genes
Apostolou, Paraskevi, Dellatola, Vasiliki, Papathanasiou, Athanasios, Kalfakakou, Despoina, Fountzilas, Elena, Tryfonopoulos, Dimitrios, Karageorgopoulou, Sofia, Yannoukakos, Drakoulis, Konstantopoulou, Irene, Fostira, Florentia
Published in Cancers (27.06.2024)
Published in Cancers (27.06.2024)
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PALB2 c.2257C>T truncating variant is a Greek founder and is associated with high breast cancer risk
Vagena, Andromachi, Papamentzelopoulou, Myrto, Kalfakakou, Despoina, Kollia, Panagoula, Papadimitriou, Christos, Psyrri, Amanda, Apostolou, Paraskevi, Fountzilas, George, Konstantopoulou, Irene, Yannoukakos, Drakoulis, Fostira, Florentia
Published in Journal of human genetics (01.08.2019)
Published in Journal of human genetics (01.08.2019)
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CHEK2 Pathogenic Variants in Greek Breast Cancer Patients: Evidence for Strong Associations with Estrogen Receptor Positivity, Overuse of Risk-Reducing Procedures and Population Founder Effects
Apostolou, Paraskevi, Dellatola, Vasiliki, Papadimitriou, Christos, Kalfakakou, Despoina, Fountzilas, Elena, Faliakou, Eleni, Fountzilas, Georgios, Romanidou, Ourania, Konstantopoulou, Irene, Fostira, Florentia
Published in Cancers (27.04.2021)
Published in Cancers (27.04.2021)
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Contribution of RAD51D germline mutations in breast and ovarian cancer in Greece
Konstanta, Irene, Fostira, Florentia, Apostolou, Paraskevi, Stratikos, Efstratios, Kalfakakou, Despoina, Pampanos, Andreas, Kollia, Panagoula, Papadimitriou, Christos, Konstantopoulou, Irene, Yannoukakos, Drakoulis
Published in Journal of human genetics (01.11.2018)
Published in Journal of human genetics (01.11.2018)
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Lung cancer as a predominant feature in a patient with Peutz–Jeghers syndrome: Case report
Fostira, Florentia, Fountzilas, Elena, Papadopoulou, Kyriaki, Karaiskos, Theodoros, Mpatsi, Ourania, Pastelli, Nikoleta, Mountzios, Giannis, Konstantopoulou, Irene, Fountzilas, George
Published in Thoracic cancer (01.06.2022)
Published in Thoracic cancer (01.06.2022)
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Characterization and prevalence of two novel CHEK2 large deletions in Greek breast cancer patients
Apostolou, Paraskevi, Fostira, Florentia, Mollaki, Vasiliki, Delimitsou, Angeliki, Vlassi, Metaxia, Pentheroudakis, George, Faliakou, Eleni, Kollia, Panagoula, Fountzilas, George, Yannoukakos, Drakoulis, Konstantopoulou, Irene
Published in Journal of human genetics (01.07.2018)
Published in Journal of human genetics (01.07.2018)
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Prevalence of BRCA1 mutations in familial and sporadic greek ovarian cancer cases
Stavropoulou, Alexandra V, Fostira, Florentia, Pertesi, Maroulio, Tsitlaidou, Marianthi, Voutsinas, Gerassimos E, Triantafyllidou, Olga, Bamias, Aristotelis, Dimopoulos, Meletios A, Timotheadou, Eleni, Pectasides, Dimitrios, Christodoulou, Christos, Klouvas, George, Papadimitriou, Christos, Makatsoris, Thomas, Pentheroudakis, George, Aravantinos, Gerasimos, Karydakis, Vassilis, Yannoukakos, Drakoulis, Fountzilas, George, Konstantopoulou, Irene
Published in PloS one (11.03.2013)
Published in PloS one (11.03.2013)
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A Patient Affected with Serous Ovarian/Peritoneal Carcinoma Carrying the FANCM Mutation
Yannoukakos, Drakoulis, Fostira, Florentia, Pistalmantzian, Nikolaos, Konstantopoulou, Irene, Nikolaidi, Adamantia, Athanasiadis, Ilias
Published in Case reports in oncological medicine (01.01.2019)
Published in Case reports in oncological medicine (01.01.2019)
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A Paternally Inherited BRCA1 Mutation Associated with an Unusual Aggressive Clinical Phenotype
Fostira, Florentia, Tsoukalas, Nikolaos, Konstantopoulou, Irene, Georgoulias, Vassilios, Christophyllakis, Charalambos, Yannoukakos, Drakoulis
Published in Case reports in genetics (01.01.2014)
Published in Case reports in genetics (01.01.2014)
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Prevalence of GJB2 mutations in prelingual deafness in the Greek population
Pampanos, Andreas, Economides, John, Iliadou, Vassiliki, Neou, Polyxeni, Leotsakos, Paulos, Voyiatzis, Nikolaos, Eleftheriades, Nikolaos, Tsakanikos, Michael, Antoniadi, Thalia, Hatzaki, Angeliki, Konstantopoulou, Irene, Yannoukakos, Drakoulis, Gronskov, Karen, Brondum-Nielsen, Karen, Grigoriadou, Maria, Gyftodimou, Jolanda, Iliades, Theophilos, Skevas, Antonios, Petersen, Michael B
Published in International journal of pediatric otorhinolaryngology (02.09.2002)
Published in International journal of pediatric otorhinolaryngology (02.09.2002)
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Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer
Couch, Fergus J, Hart, Steven N, Sharma, Priyanka, Toland, Amanda Ewart, Wang, Xianshu, Miron, Penelope, Olson, Janet E, Godwin, Andrew K, Pankratz, V Shane, Olswold, Curtis, Slettedahl, Seth, Hallberg, Emily, Guidugli, Lucia, Davila, Jaime I, Beckmann, Matthias W, Janni, Wolfgang, Rack, Brigitte, Ekici, Arif B, Slamon, Dennis J, Konstantopoulou, Irene, Fostira, Florentia, Vratimos, Athanassios, Fountzilas, George, Pelttari, Liisa M, Tapper, William J, Durcan, Lorraine, Cross, Simon S, Pilarski, Robert, Shapiro, Charles L, Klemp, Jennifer, Yao, Song, Garber, Judy, Cox, Angela, Brauch, Hiltrud, Ambrosone, Christine, Nevanlinna, Heli, Yannoukakos, Drakoulis, Slager, Susan L, Vachon, Celine M, Eccles, Diana M, Fasching, Peter A
Published in Journal of clinical oncology (01.02.2015)
Published in Journal of clinical oncology (01.02.2015)
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Extending the clinical phenotype associated with biallelic NTHL1 germline mutations
Fostira, Florentia, Kontopodis, Emmanouil, Apostolou, Paraskevi, Fragkaki, Maria, Androulakis, Nikolaos, Yannoukakos, Drakoulis, Konstantopoulou, Irene, Saloustros, Emmanouil
Published in Clinical genetics (01.12.2018)
Published in Clinical genetics (01.12.2018)
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Pathogenic Variants in Breast Cancer Susceptibility Genes in Older Women/Pathogenic Variants in Breast Cancer Susceptibility Genes in Older Women-Reply
Fostira, Florentia, Kalfakakou, Despoina, Konstantopoulou, Irene, Kurian, Allison W, Bernhisel, Ryan, Stefanick, Marcia L
Published in JAMA : the journal of the American Medical Association (28.07.2020)
Published in JAMA : the journal of the American Medical Association (28.07.2020)
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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Fachal, Laura, Beesley, Jonathan, Kar, Siddhartha, Pooley, Karen A, Dennis, Joe, Turman, Constance, Soucy, Penny, Lemaçon, Audrey, Ghoussaini, Maya, Jiang, Xia, Aittomäki, Kristiina, Andrulis, Irene L, Aronson, Kristan J, Benitez, Javier, Blanco, Amie M, Blomqvist, Carl, Brooks-Wilson, Angela, Cai, Qiuyin, Canzian, Federico, Carter, Brian D, Cross, Simon S, Cybulski, Cezary, Dite, Gillian S, Domchek, Susan M, Dörk, Thilo, Fletcher, Olivia, Flyger, Henrik, Foulkes, William D, Friedman, Eitan, Ganz, Patricia A, Gapstur, Susan M, Godwin, Andrew K, González-Neira, Anna, Tibiletti, Maria Grazia, Gronwald, Jacek, Haiman, Christopher A, He, Wei, Healey, Catherine S, Heyworth, Jane, Hooning, Maartje J, Imyanitov, Evgeny N, Jakimovska, Milena, John, Esther M, Johnson, Nichola, Jukkola-Vuorinen, Arja, Jung, Audrey, Kapoor, Pooja Middha, Kirk, Judy, Laitman, Yael, Leslie, Goska, Lester, Jenny, Manoochehri, Mehdi, Manoukian, Siranoush, Matsuo, Keitaro, Mayes, Rebecca, Mebirouk, Noura, Miller, Austin, Montagna, Marco, Muir, Kenneth, Muranen, Taru A, Narod, Steven A, Nikitina-Zake, Liene, Norman, Aaron, Offit, Kenneth, Olah, Edith, Osorio, Ana, Pankratz, V Shane, Park-Simon, Tjoung-Won, Peissel, Bernard, Peto, Julian, Prentice, Ross, Prokofyeva, Darya, Ramus, Susan J, Rau-Murthy, Rohini, Rennert, Gad, Robson, Mark, Sánchez-Herrero, Estela, Scheuner, Maren T, Schoemaker, Minouk J, Singer, Christian F, Smichkoska, Snezhana, Southey, Melissa C, Stoppa-Lyonnet, Dominique, Sutter, Christian, Tapper, William J, Thull, Darcy L, Tung, Nadine, Tzardi, Maria, van Asperen, Christi J, van Rensburg, Elizabeth J, Wappenschmidt, Barbara, Wendt, Camilla, Wildiers, Hans, Chang-Claude, Jenny, García-Closas, Montserrat, Schmidt, Marjanka K, Kristensen, Vessela N, Simard, Jacques, Easton, Douglas F, Kraft, Peter
Published in Nature genetics (01.01.2020)
Published in Nature genetics (01.01.2020)
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Germline deleterious mutations in genes other than BRCA2 are infrequent in male breast cancer
Fostira, Florentia, Saloustros, Emmanouil, Apostolou, Paraskevi, Vagena, Andromahi, Kalfakakou, Despoina, Mauri, Davide, Tryfonopoulos, Dimitrios, Georgoulias, Vassileios, Yannoukakos, Drakoulis, Fountzilas, Georgios, Konstantopoulou, Irene
Published in Breast cancer research and treatment (01.05.2018)
Published in Breast cancer research and treatment (01.05.2018)
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