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Ribi, Karin; Pagan, Eleonora; Sala, Isabella; Ruggeri, Monica; Bianco, Nadia; Bucci, Eraldo Oreste; Graffeo, Rossella; Borner, Markus; Giordano, Monica; Gianni, Lorenzo; Rabaglio, Manuela; Freschi, Andrea; Cretella, Elisabetta; Seles, Elena; Farolfi, Alberto; Simoncini, Edda; Ciccarese, Mariangela; Rauch, Daniel; Favaretto, Adolfo; Glaus, Agnes; ... (2023). Employment trajectories of young women with breast cancer: an ongoing prospective cohort study in Italy and Switzerland. Journal of Cancer Survivorship, 17(6), pp. 1847-1858. Springer 10.1007/s11764-022-01222-y
Baroutsou, Vasiliki; Duong, Vu; Signorini, Alice; Saccilotto, Ramon; Ciorba, Florina M; Bürki, Nicole; Caiata-Zufferey, Maria; Ryu, Jai Min; Kim, Sung-Won; Lim, Myong Cheol; Monnerat, Christian; Zürrer-Härdi, Ursina; Kim, Jisun; Heinimann, Karl; Graffeo, Rossella; Park, Ji Soo; Rabaglio, Manuela; Chappuis, Pierre Olivier; Kim, Sue and Katapodi, Maria C (2023). Acceptability and Usability of the Family Gene Toolkit for Swiss and Korean Families Harboring BRCA1/BRAC2 Pathogenic Variants: A Web-Based Platform for Cascade Genetic Testing. Cancers, 15(18) MDPI AG 10.3390/cancers15184485
Sarki, Mahesh; Ming, Chang; Aceti, Monica; Fink, Günther; Aissaoui, Souria; Bürki, Nicole; Graffeo, Rossella; Heinimann, Karl; Caiata Zufferey, Maria; Monnerat, Christian; Rabaglio, Manuela; Zürrer-Härdi, Ursina; Chappuis, Pierre O; Katapodi, Maria C (2022). Relatives from Hereditary Breast and Ovarian Cancer and Lynch Syndrome Families Forgoing Genetic Testing: Findings from the Swiss CASCADE Cohort. Journal of personalized medicine, 12(10) MDPI 10.3390/jpm12101740
Salikhanov, Islam; Heinimann, Karl; Chappuis, Pierre; Buerki, Nicole; Graffeo, Rossella; Heinzelmann, Viola; Rabaglio, Manuela; Taborelli, Monica; Wieser, Simon; Katapodi, Maria C (2022). Swiss cost-effectiveness analysis of universal screening for Lynch syndrome of patients with colorectal cancer followed by cascade genetic testing of relatives. Journal of medical genetics, 59(9), pp. 924-930. BMJ Publishing Group 10.1136/jmedgenet-2021-108062
Pedrazzani, Carla; Aceti, Monica; Schweighoffer, Reka; Kaiser-Grolimund, Andrea; Bürki, Nicole; Chappuis, Pierre O; Graffeo, Rossella; Monnerat, Christian; Pagani, Olivia; Rabaglio, Manuela; Katapodi, Maria C; Caiata-Zufferey, Maria (2022). The Communication Chain of Genetic Risk: Analyses of Narrative Data Exploring Proband-Provider and Proband-Family Communication in Hereditary Breast and Ovarian Cancer. Journal of personalized medicine, 12(8) MDPI 10.3390/jpm12081249
Gasparri, Maria Luisa; Di Micco, Rosa; Zuber, Veronica; Taghavi, Katayoun; Bianchini, Giampaolo; Bellaminutti, Serena; Meani, Francesco; Graffeo, Rossella; Candiani, Massimo; Mueller, Michael D.; Papadia, Andrea; Gentilini, Oreste D (2021). Ovarian reserve of women with and without BRCA pathogenic variants: A systematic review and meta-analysis. Breast, 60, pp. 155-162. Elsevier 10.1016/j.breast.2021.09.006
Nikolaidis, Christos; Ming, Chang; Pedrazzani, Carla; van der Horst, Tina; Kaiser-Grolimund, Andrea; Ademi, Zanfina; Bührer-Landolt, Rosmarie; Bürki, Nicole; Caiata-Zufferey, Maria; Champion, Victoria; Chappuis, Pierre O; Kohler, Carmen; Erlanger, Tobias E; Graffeo, Rossella; Hampel, Heather; Heinimann, Karl; Heinzelmann-Schwarz, Viola; Kurzeder, Christian; Monnerat, Christian; Northouse, Laurel L; ... (2018). Challenges and Opportunities for Cancer Predisposition Cascade Screening for Hereditary Breast and Ovarian Cancer and Lynch Syndrome in Switzerland: Findings from an International Workshop. Public health genomics, 21(3-4), pp. 121-132. Karger 10.1159/000496495
Katapodi, Maria C; Viassolo, Valeria; Caiata-Zufferey, Maria; Nikolaidis, Christos; Bührer-Landolt, Rosmarie; Buerki, Nicole; Graffeo, Rossella; Horvath, Henrik Csaba; Kurzeder, Christian; Rabaglio, Manuela; Scharfe, Michael; Urech, Corinne; Erlanger, Tobias E; Probst-Hensch, Nicole; Heinimann, Karl; Heinzelmann-Schwarz, Viola; Pagani, Olivia; Chappuis, Pierre O (2017). Cancer Predisposition Cascade Screening for Hereditary Breast/Ovarian Cancer and Lynch Syndromes in Switzerland: Study Protocol. JMIR research protocols, 6(9), e184. JMIR Publications 10.2196/resprot.8138
