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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
Sarki, Mahesh; Ming, Chang; Aissaoui, Souria; Bürki, Nicole; Caiata-Zufferey, Maria; Erlanger, Tobias Ephraim; Graffeo-Galbiati, Rossella; Heinimann, Karl; Heinzelmann-Schwarz, Viola; Monnerat, Christian; Probst-Hensch, Nicole; Rabaglio, Manuela; Zürrer-Härdi, Ursina; Chappuis, Pierre Olivier; Katapodi, Maria C (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(7) MDPI AG 10.3390/cancers14071636
Pedrazzani, Carla; Ming, Chang; Bürki, Nicole; Caiata-Zufferey, Maria; Chappuis, Pierre O; Duquette, Debra; Heinimann, Karl; Heinzelmann-Schwarz, Viola; Graffeo-Galbiati, Rossella; Merajver, Sofia D; Milliron, Kara J; Monnerat, Christian; Pagani, Olivia; Rabaglio, Manuela; Katapodi, Maria C (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) MDPI AG 10.3390/cancers13246254
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
Vogt, Alexia; Schmid, Sabine; Heinimann, Karl; Frick, Harald; Herrmann, Christian; Cerny, Thomas; Omlin, Aurelius Gabriel (2017). Multiple primary tumours: challenges and approaches, a review. ESMO open, 2(2), e000172. BMJ 10.1136/esmoopen-2017-000172
Suter, Aude-Annick; Itin, Peter; Heinimann, Karl; Ahmed, Munaza; Ashraf, Tazeen; Fryssira, Helen; Kini, Usha; Lapunzina, Pablo; Miny, Peter; Sommerlund, Mette; Suri, Mohnish; Vaeth, Signe; Vasudevan, Pradeep; Gallati, Sabina (2016). Rothmund-Thomson Syndrome: novel pathogenic mutations and frequencies of variants in the RECQL4 and USB1 (C16orf57) gene. Molecular genetics & genomic medicine, 4(3), pp. 359-366. Wiley 10.1002/mgg3.209
Ferrarini, Alessandra; Auteri-Kaczmarek, Agnes; Pica, Alessia; Boesch, Nemya; Heinimann, Karl; Schäfer, Stephan C; Vesnaver-Megalo, Sara; Cina, Viviane; Beckmann, Jacques S; Monnerat, Christian (2011). Early occurrence of lung adenocarcinoma and breast cancer after radiotherapy of a chest wall sarcoma in a patient with a de novo germline mutation in TP53. Familial Cancer, 10(2), pp. 187-92. Dordrecht: Springer 10.1007/s10689-010-9415-9
von Kanel, Thomas; Gerber, Dominik; Schaller, André; Baumer, Alessandra; Wey, Eva; Jackson, Christopher B; Gisler, Franziska M; Heinimann, Karl; Gallati, Sabina (2010). Quantitative 1-Step DNA Methylation Analysis with Native Genomic DNA as Template. Clinical chemistry, 56(7), pp. 1098-106. Washington, D.C.: American Association for Clinical Chemistry 10.1373/clinchem.2009.142828
Montani, Matteo; Heinimann, Karl; von Teichman, Adriana; Rudolph, Thomas; Perren, Aurel; Moch, Holger (2010). VHL-gene deletion in single renal tubular epithelial cells and renal tubular cysts: further evidence for a cyst-dependent progression pathway of clear cell renal carcinoma in von Hippel-Lindau disease. The American journal of surgical pathology, 34(6), pp. 806-15. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1097/PAS.0b013e3181ddf54d
Rüegg, Stephan; Lehky Hagen, Monique; Hohl, Ursula; Kappos, Ludwig; Fuhr, Peter; Plasilov, Martina; Müller, Hansjakob; Heinimann, Karl (2005). Oculopharyngeal muscular dystrophy - an under-diagnosed disorder? Swiss medical weekly, 39-40(135), pp. 574-86. Muttenz: EMH Schweizerischer Ärzteverlag
Heinimann, Karl; Perren, Aurel (2019). Erbliche Tumorerkrankungen und Phakomatosen. In: Cerny, Thomas; Karlin, Kirill (eds.) PathoMaps. Springer-Lehrbuch (pp. 177-181). Springer-Verlag 10.1007/978-3-662-57439-3_25
