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Grant Proposals (funded, non-ehealth) (69)

Published on in Vol 6, No 9 (2017): September

Cancer Predisposition Cascade Screening for Hereditary Breast/Ovarian Cancer and Lynch Syndromes in Switzerland: Study Protocol

Cancer Predisposition Cascade Screening for Hereditary Breast/Ovarian Cancer and Lynch Syndromes in Switzerland: Study Protocol

Cancer Predisposition Cascade Screening for Hereditary Breast/Ovarian Cancer and Lynch Syndromes in Switzerland: Study Protocol

Authors of this article:

Maria C Katapodi1, 2 Author Orcid Image ;   Valeria Viassolo3 Author Orcid Image ;   Maria Caiata-Zufferey4 Author Orcid Image ;   Christos Nikolaidis1 Author Orcid Image ;   Rosmarie Bührer-Landolt5 Author Orcid Image ;   Nicole Buerki6 Author Orcid Image ;   Rossella Graffeo7 Author Orcid Image ;   Henrik Csaba Horváth8 Author Orcid Image ;   Christian Kurzeder6 Author Orcid Image ;   Manuela Rabaglio5 Author Orcid Image ;   Michael Scharfe9 Author Orcid Image ;   Corinne Urech6 Author Orcid Image ;   Tobias E Erlanger9 Author Orcid Image ;   Nicole Probst-Hensch10 Author Orcid Image ;   Karl Heinimann11 Author Orcid Image ;   Viola Heinzelmann-Schwarz6 Author Orcid Image ;   Olivia Pagani7 Author Orcid Image ;   Pierre O. Chappuis3, 12 Author Orcid Image
Article Authors Cited by (27) Tweetations (2) Metrics

Journals

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  11. Kim S, Aceti M, Baroutsou V, Bürki N, Caiata-Zufferey M, Cattaneo M, Chappuis P, Ciorba F, Graffeo-Galbiati R, Heinzelmann-Schwarz V, Jeong J, Jung M, Kim S, Kim J, Lim M, Ming C, Monnerat C, Park H, Park S, Pedrazzani C, Rabaglio M, Ryu J, Saccilotto R, Wieser S, Zürrer-Härdi U, Katapodi M. Using a Tailored Digital Health Intervention for Family Communication and Cascade Genetic Testing in Swiss and Korean Families With Hereditary Breast and Ovarian Cancer: Protocol for the DIALOGUE Study. JMIR Research Protocols 2021;10(6):e26264 View
  12. Baroutsou V, Cerqueira Gonzalez Pena R, Schweighoffer R, Caiata-Zufferey M, Kim S, Hesse-Biber S, Ciorba F, Lauer G, Katapodi M. Predicting Openness of Communication in Families With Hereditary Breast and Ovarian Cancer Syndrome: Natural Language Processing Analysis. JMIR Formative Research 2023;7:e38399 View
  13. Frey M, Finch A, Kulkarni A, Akbari M, Chapman-Davis E. Genetic Testing for All: Overcoming Disparities in Ovarian Cancer Genetic Testing. American Society of Clinical Oncology Educational Book 2022;(42):471 View
  14. Bommer C, Lupatsch J, Bürki N, Schwenkglenks M. Cost–utility analysis of risk-reducing strategies to prevent breast and ovarian cancer in BRCA-mutation carriers in Switzerland. The European Journal of Health Economics 2022;23(5):807 View
  15. Sarki M, Ming C, Aceti M, Fink G, Aissaoui S, Bürki N, Graffeo R, Heinimann K, Caiata Zufferey M, Monnerat C, Rabaglio M, Zürrer-Härdi U, Chappuis P, Katapodi M. Relatives from Hereditary Breast and Ovarian Cancer and Lynch Syndrome Families Forgoing Genetic Testing: Findings from the Swiss CASCADE Cohort. Journal of Personalized Medicine 2022;12(10):1740 View
  16. Frey M, Ahsan M, Bergeron H, Lin J, Li X, Fowlkes R, Narayan P, Nitecki R, Rauh-Hain J, Moss H, Baltich Nelson B, Thomas C, Christos P, Hamilton J, Chapman-Davis E, Cantillo E, Holcomb K, Kurian A, Lipkin S, Offit K, Sharaf R. Cascade Testing for Hereditary Cancer Syndromes: Should We Move Toward Direct Relative Contact? A Systematic Review and Meta-Analysis. Journal of Clinical Oncology 2022;40(35):4129 View
  17. Pedrazzani C, Aceti M, Schweighoffer R, Kaiser-Grolimund A, Bürki N, Chappuis P, Graffeo R, Monnerat C, Pagani O, Rabaglio M, Katapodi M, Caiata-Zufferey M. 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 2022;12(8):1249 View
  18. Kahn R, Ahsan M, Chapman-Davis E, Holcomb K, Nitecki R, Rauh-Hain J, Fowlkes R, Tubito F, Pires M, Christos P, Tkachuk K, Krinsky H, Sharaf R, Offit K, Lipkin S, Frey M. Barriers to completion of cascade genetic testing: how can we improve the uptake of testing for hereditary breast and ovarian cancer syndrome?. Familial Cancer 2023;22(2):127 View
  19. Nikolaidis C, Ming C, Pedrazzani C, van der Horst T, Kaiser-Grolimund A, Ademi Z, Bührer-Landolt R, Bürki N, Caiata-Zufferey M, Champion V, Chappuis P, Kohler C, Erlanger T, Graffeo R, Hampel H, Heinimann K, Heinzelmann-Schwarz V, Kurzeder C, Monnerat C, Northouse L, Pagani O, Probst-Hensch N, Rabaglio M, Schoenau E, Sijbrands E, Taborelli M, Urech C, Viassolo V, Wieser S, Katapodi M. 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 2018;21(3-4):121 View
  20. Frey M, Ahsan M, Badiner N, Lin J, Narayan P, Nitecki R, Rauh‐Hain J, Moss H, Fowlkes R, Thomas C, Bergeron H, Christos P, Levi S, Blank S, Holcomb K, Cantillo E, Sharaf R, Lipkin S, Offit K, Chapman‐Davis E. What happens in the long term: Uptake of cancer surveillance and prevention strategies among at‐risk relatives with pathogenic variants detected via cascade testing. Cancer 2022;128(24):4241 View
  21. Sarki M, Ming C, Aissaoui S, Bürki N, Caiata-Zufferey M, Erlanger T, Graffeo-Galbiati R, Heinimann K, Heinzelmann-Schwarz V, Monnerat C, Probst-Hensch N, Rabaglio M, Zürrer-Härdi U, Chappuis P, Katapodi M. Intention to Inform Relatives, Rates of Cascade Testing, and Preference for Patient-Mediated Communication in Families Concerned with Hereditary Breast and Ovarian Cancer and Lynch Syndrome: The Swiss CASCADE Cohort. Cancers 2022;14(7):1636 View
  22. Pedrazzani C, Ming C, Bürki N, Caiata-Zufferey M, Chappuis P, Duquette D, Heinimann K, Heinzelmann-Schwarz V, Graffeo-Galbiati R, Merajver S, Milliron K, Monnerat C, Pagani O, Rabaglio M, Katapodi M. Genetic Literacy and Communication of Genetic Information in Families Concerned with Hereditary Breast and Ovarian Cancer: A Cross-Study Comparison in Two Countries and within a Timeframe of More Than 10 Years. Cancers 2021;13(24):6254 View
  23. Barnoy S, Dagan E, Kim S, Caiata-Zufferey M, Katapodi M. Privacy and utility of genetic testing in families with hereditary cancer syndromes living in three countries: the international cascade genetic screening experience. Frontiers in Genetics 2023;14 View
  24. Baroutsou V, Duong V, Signorini A, Saccilotto R, Ciorba F, Bürki N, Caiata-Zufferey M, Ryu J, Kim S, Lim M, Monnerat C, Zürrer-Härdi U, Kim J, Heinimann K, Graffeo R, Park J, Rabaglio M, Chappuis P, Kim S, Katapodi M. 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 2023;15(18):4485 View
  25. Joder C, Gmür A, Solass W, Christe L, Rabaglio M, Fluri M, Rau T, Saner F, Knabben L, Imboden S, Mueller M, Siegenthaler F. Real-World Data on Institutional Implementation of Screening for Mismatch Repair Deficiency and Lynch Syndrome in Endometrial Cancer Patients. Cancers 2024;16(3):671 View
  26. Aceti M, Caiata-Zufferey M, Pedrazzani C, Schweighoffer R, Kim S, Baroutsou V, Katapodi M, Kim S. Modes of responsibility in disclosing cancer genetic test results to relatives: An analysis of Swiss and Korean narrative data. Patient Education and Counseling 2024;123:108202 View

Books/Policy Documents

  1. . Constitutional Oncogenetics. View