Items where Author is "Chappuis, P"

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Number of items: 16.

Pedrazzani, Carla Ambrogina and Aceti, M and Schweighoffer, R and Kaiser-Grolimund, A and Bürki, N and Chappuis, P and Graffeo, R and Monnerat, C and Pagani, Olivia and Rabaglio, M and Katapodi, M and 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). p. 1249.

Sarki, M and Ming, C and Aissaoui, S and Burki, N and Caiata Zufferey, Maria and Erlanger, T and Graffeo-Galbiati, R and Heinimann, K and Heinzelmann-Schwarz, V and Monnerat, C and Probst-Hensch, N and Rabaglio, M and Zürrer, U and Chappuis, P and Katapodi, M (2022) Differences in intention to inform relatives and rates of cascade testing in families concerned with hereditary breast and ovarian cancer and Lynch syndrome: The Swiss CASCADE cohort. In: European Human Genetics Conference, 11-14.6.2022, Wien.

Schweighoffer, R and Aceti, M and Caiata Zufferey, Maria and Baroutsou, V and Pedrazzani, Carla Ambrogina and Kim, S and Burki, N and Chappuis, P and Graffeo-Galbiati, R and Monnerat, C and Rabaglio, M and Katapodi, M (2022) Determinants for or against prophylactic mastectomy and/or salpingo-oophorectomy in unaffected women with BRCA1 or BRCA2 pathogenic variants in Switzerland: A Mixed-Methods Study. In: 11th Global Breast Cancer Conference, 28-30.4.2022, Seoul, South Korea.

Sarki, M and Ming, C and Aissaoui, S and Burki, N and Caiata Zufferey, Maria and Erlanger, T and Monnerat, C and Graffeo-Galbiati, R and Heinimann, K and Heinzelmann-Schwarz, V and Koechlin, H and Probst-Hensch, N and Rabaglio, M and Zürrer, U and Chappuis, P and Katapodi, M (2022) 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, 14 (1636).

Aceti, M and Caiata Zufferey, Maria and Pedrazzani, Carla Ambrogina and Schweighoffer, Reka and Baroutsou, V and Burki, N and Chappuis, P and Graffeo-Galbiati, R and Monnerat, C and Katapodi, M (2022) Life Course Perspective on the decision-making process to undergo genetic testing in hereditary cancer at risk families. In: 19th Biennal European Society for Health and Medical Sociology Conference, 25-27.8.2022, Bologna.

Schweighoffer, R and Katapodi, M and Aceti, M and Pedrazzani, Carla Ambrogina and Burki, N and Chappuis, P and Graffeo-Galbiati, R and Monnerat, C and Rabaglio, M and Pagani, Olivia and Membrez, Véronique and Unger, Sheila and Caiata Zufferey, Maria (2022) Making the right choice. How unaffected women carrying BRCA1/BRCA2 germline mutations decide for prophylactic mastectomy to reduce cancer risk. In: European Human Genetics Conference, 11-14.6.2022, Wien.

Sarki, M and Ming, C and Aceti, M and Fink, Günther and Aissaoui, S and Burki, N and Graffeo, R and Heinimann, K and Caiata Zufferey, Maria and Monnerat, C and Rabaglio, Manuela and Zürrer-Härdi, Ursina and Chappuis, P and Katapodi, M (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 (1740).

Aceti, M and Baroutsou, V and Kaiser-Grolimund, A and Pedrazzani, Carla Ambrogina and Rudaz, M and Burki, N and Chappuis, P and Graffeo-Galbiati, R and Monnerat, C and Rabaglio, M and Kim, S and Katapodi, M and Caiata Zufferey, Maria (2021) Bottom-up approach: soliciting participants’ input for developing a digital platform to support cancer coping and family communication about hereditary cancer risks in Switzerland and Korea. In: Clinical Research Day of the Department of Clinical Research of the University of Basel, 28.1.2021, Basel, Switzerland.

Pedrazzani, Carla Ambrogina and Ming, C and Burki, N and Caiata Zufferey, Maria and Chappuis, P and Duquette, D and Heinimann, K and Heinzelmann-Schwarz, V and Graffeo-Galbiati, R and Merajver, SD and Milliron, KJ and Monnerat, C and Pagani, Olivia and Rabaglio, M and Katapodi, M (2021) 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, 13 (24). p. 6254.

Aceti, M and Baroutsou, V and Kaiser-Grolimund, A and Pedrazzani, Carla Ambrogina and Rudaz, M and Burki, N and Chappuis, P and Graffeo-Galbiati, R and Monnerat, C and Kim, S and Caiata Zufferey, Maria and Katapodi, M (2021) Implementing a digital platform to support family communication about hereditary cancer risks. In: Clinical Research Day of the Department of Clinical Research of the University of Basel, 28.1.2021, Basel, Switzerland.

Caiata Zufferey, Maria and Pedrazzani, Carla Ambrogina and Aceti, Monica and Kaiser-Grolimund, A and Rudaz, M and Baroutsou, V and Kim, S and Burki, N and Chappuis, P and Graffeo-Galbiati, R and Monnerat, C and Rabaglio, M and Katapodi, M (2021) To say or not to say: A qualitative study on barriers and facilitators in family communication about genetic cancer risk. In: 10th Global Breast Cancer Conference, 8-10.4.2021, Seoul, South Korea.

Kim, S. and Aceti, M. and Baroutsou, V. and Burki, N and Caiata Zufferey, Maria and Cattaneo, M. and Chappuis, P and Ciorba, F. and Graffeo-Galbiati, R and Heinzelmann-Schwarz, V and Jeong, J. and Jung, M. and Kim, S.W. and Kim, J. and Lim, M.C. and Ming, C. and Monnerat, C and Park, H.S. and Park, S. and Pedrazzani, C. and Rabaglio, M. and Ryu, J.M. and Saccilotto, R. and Wieser, S. and Zürrer-Härdi, U. and Katapodi, M.C. (2021) Using a tailored digital health intervention for family communication and cascade genetic testing in Swiss and Korean families with hereditary breast/ovarian cancer: Protocol for the DIALOGUE study. Journal of Medical Internet Research, 10 (6). e26264.

Fadda, Marta and Chappuis, P and Katapodi, M and Pagani, Olivia and Monnerat, Christian and Membrez, Véronique and Unger, Sheila and Caiata Zufferey, Maria (2020) Physicians communicating with women at genetic risk of breast and ovarian cancer: are we in the middle of the ford between contradictory messages and unshared decision making ? PLOS ONE. (In Press)

Katapodi, M and Burki, N and Graffeo-Galbiati, R and Monnerat, C and Rabaglio, M and Viassolo, V and Pedrazzani, C and Fluri, M and Kaiser-Grolimund, A and Ming, C and Schoneau, E and Caiata Zufferey, Maria and Erlangen, T and Heinimann, K and Heinzelmann-Schwarz, V and Kurzeder, C and Koechlin, H and Taborelli, M and Pagani, Olivia and Chappuis, P (2020) THE SWISS CASCADE: A SPRINGBOARD FOR INTERNATIONAL COLLABORATION. In: Global Breast Cancer Conference, 9-11.4.2020, Seoul, Korea. (In Press)

Nikolaidis, C and Ming, C and Pedrazzani, C and van der Horst, T and Kaiser-Grolimund, A and Ademi, Z and Bührer-Landolt, R and Burki, N and Caiata Zufferey, Maria and Champion, V and Chappuis, P and Kohler, C and Erlanger, T and Graffeo-Galbiati, R and Hampel, H and Heinimann, K and Heinzelmann-Schwarz, V and Kurzeder, C and Monnerat, C and Northouse, L and Pagani, O and Probst, N and Rabaglio, M and Schoenau, E and Sijbrands, E and Taborelli, M and Urech, C and Viassolo, V and Wieser, S and Katapodi, M (2019) 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. (In Press)

Katapodi, M and Viassolo, V and Caiata Zufferey, Maria and Nikolaidis, C and Bührer-Landolt, R and Bürki, N and Graffeo, R and Horváth, H and Kurzeder, C and Rabaglio, M and Scharfe, M and Urech, C and Erlanger, T and Probst-Hensch, N and Heinimann, K and Heinzelmann-Schwarz, V and Pagani, Olivia and Chappuis, P (2017) Swiss Cancer Predisposition Cascade Screening Consortium regarding the use and impact of genetic testing in hereditary breast/ovarian cancer and Lynch syndromes: the CASCADE study. Journal of Medical Internet Research. (In Press)

This list was generated on Tue Apr 16 18:47:13 2024 CEST.