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Ercan, Ayse Bahar; Aronson, Melyssa; Fernandez, Nicholas R; Chang, Yuan; Levine, Adrian; Liu, Zhihui Amy; Negm, Logine; Edwards, Melissa; Bianchi, Vanessa; Stengs, Lucie; Chung, Jiil; Al-Battashi, Abeer; Reschke, Agnes; Lion, Alex; Ahmad, Alia; Lassaletta, Alvaro; Reddy, Alyssa T; Al-Darraji, Amir F; Shah, Amish C; Van Damme, An; ... (2024). Clinical and biological landscape of constitutional mismatch-repair deficiency syndrome: an International Replication Repair Deficiency Consortium cohort study. The Lancet. Oncology, 25(5), pp. 668-682. Elsevier 10.1016/S1470-2045(24)00026-3
Otth, Maria; Kasteler, Rahel; Mulder, Renée L; Agrusa, Jennifer; Armenian, Saro H; Barnea, Dana; Bergeron, Anne; Bhatt, Neel S; Bourke, Stephen J; Constine, Louis S; Goutaki, Myrofora; Green, Daniel M; Hennewig, Ulrike; Houdouin, Veronique; Hudson, Melissa M; Kremer, Leontien; Latzin, Philipp; Ng, Antony; Oeffinger, Kevin C; Schindera, Christina; ... (2024). Recommendations for surveillance of pulmonary dysfunction among childhood, adolescent, and young adult cancer survivors: a report from the International Late Effects of Childhood Cancer Guideline Harmonization Group. EClinicalMedicine, 69, p. 102487. Elsevier 10.1016/j.eclinm.2024.102487
Hebert, Robyn; Cullinan, Noelle; Armstrong, Linlea; Blood, Katherine A; Brossard, Josee; Brunga, Ledia; Cacciotti, Chantel; Caswell, Kimberly; Cellot, Sonia; Coltin, Hallie; Deyell, Rebecca J; Felton, Kathleen; Fernandez, Conrad V; Fleming, Adam J; Gibson, Paul; Hammad, Rawan; Jabado, Nada; Johnston, Donna L; Lafay-Cousin, Lucie; Larouche, Valérie; ... (2023). Performance of the eHealth decision support tool, MIPOGG, for recognising children with Li-Fraumeni, DICER1, Constitutional mismatch repair deficiency and Gorlin syndromes. Journal of medical genetics, 60(12), pp. 1218-1223. BMJ Publishing Group 10.1136/jmg-2023-109376
Wang, Yuehan; Ronckers, Cécile M; van Leeuwen, Flora E; Moskowitz, Chaya S; Leisenring, Wendy; Armstrong, Gregory T; de Vathaire, Florent; Hudson, Melissa M; Kuehni, Claudia E; Arnold, Michael A; Demoor-Goldschmidt, Charlotte; Green, Daniel M; Henderson, Tara O; Howell, Rebecca M; Ehrhardt, Matthew J; Neglia, Joseph P; Oeffinger, Kevin C; van der Pal, Helena J H; Robison, Leslie L; Schaapveld, Michael; ... (2023). Subsequent female breast cancer risk associated with anthracycline chemotherapy for childhood cancer. Nature medicine, 29(9), pp. 2268-2277. Springer Nature 10.1038/s41591-023-02514-1
Strebel, Sven; Mader, Luzius; Jörger, Philippa; Waespe, Nicolas; Uhlmann, Seraina; von der Weid, Nicolas; Ansari, Marc; Kuehni, Claudia E. (2023). Hearing loss after exposure to vincristine and platinum-based chemotherapy among childhood cancer survivors. EJC Paediatric Oncology, 1, p. 100017. Elsevier 10.1016/j.ejcped.2023.100017
Waespe, Nicolas; Mlakar, Simona Jurkovic; Dupanloup, Isabelle; Rezgui, Mohamed Aziz; Bittencourt, Henrique; Krajinovic, Maja; Kuehni, Claudia E; Nava, Tiago; Ansari, Marc (2023). A novel integrative multi-omics approach to unravel the genetic determinants of rare diseases with application in sinusoidal obstruction syndrome. PLoS ONE, 18(4), e0281892. Public Library of Science 10.1371/journal.pone.0281892
Reulen, Raoul C.; Winter, David L.; Diallo, Ibrahim; Veres, Cristina; Llanas, Damien; Allodji, Rodrigue S.; Bagnasco, Francesca; Bárdi, Edit; Feijen, Elizabeth A.M.; Alessi, Daniela; Fidler-Benaoudia, Miranda M.; Høgsholt, Stine; Teepen, Jop C.; Linge, Helena; Haddy, Nadia; Byrne, Julianne; Debiche, Ghazi; Grabow, Desiree; Gudmundsdottir, Thorgerdur; Fauchery, Romain; ... (2023). Risk Factors for Primary Bone Cancer After Childhood Cancer: A PanCare Childhood and Adolescent Cancer Survivor Care and Follow-Up Studies Nested Case-Control Study. Journal of clinical oncology, 41(21), pp. 3735-3746. American Society of Clinical Oncology 10.1200/JCO.22.02045
Wang, Yuehan; Kremer, Leontien C M; van Leeuwen, Flora E; Armstrong, Gregory T; Leisenring, Wendy; de Vathaire, Florent; Hudson, Melissa M; Kuehni, Claudia E; Arnold, Michael A; Haddy, Nadia; Demoor-Goldschmidt, Charlotte; Diallo, Ibrahima; Howell, Rebecca M; Ehrhardt, Matthew J; Moskowitz, Chaya S; Neglia, Joseph P; van der Pal, Helena J H; Robison, Leslie L; Schaapveld, Michael; Turcotte, Lucie M; ... (2022). Cohort profile: Risk and risk factors for female breast cancer after treatment for childhood and adolescent cancer: an internationally pooled cohort. BMJ open, 12(11), e065910. BMJ Publishing Group 10.1136/bmjopen-2022-065910
Strebel, Sven; Mader, Luzius; Sláma, Tomáš; Waespe, Nicolas; Weiss, Annette; Parfitt, Ross; Am Zehnhoff-Dinnesen, Antoinette; Kompis, Martin; von der Weid, Nicolas X; Ansari, Marc; Kuehni, Claudia E (2022). Severity of hearing loss after platinum chemotherapy in childhood cancer survivors. Pediatric blood & cancer, 69(9), e29755. Wiley-Liss 10.1002/pbc.29755
Guerrini-Rousseau, Léa; Masliah-Planchon, Julien; Waszak, Sebastian M; Alhopuro, Pia; Benusiglio, Patrick R; Bourdeaut, Franck; Brecht, Ines B; Del Baldo, Giada; Dhanda, Sandeep Kumar; Garrè, Maria Luisa; Gidding, Corrie E M; Hirsch, Steffen; Hoarau, Pauline; Jorgensen, Mette; Kratz, Christian; Lafay-Cousin, Lucie; Mastronuzzi, Angela; Pastorino, Lorenza; Pfister, Stefan M; Schroeder, Christopher; ... (2022). Cancer risk and tumour spectrum in 172 patients with a germline SUFU pathogenic variation: a collaborative study of the SIOPE Host Genome Working Group. Journal of medical genetics, 59(11), pp. 1123-1132. BMJ Publishing Group 10.1136/jmedgenet-2021-108385
Uppugunduri, C R S; Huezo-Diaz Curtis, P; Nava, T; Rezgui, M A; Mlakar, V; Mlakar, S Jurkovic; Waespe, N; Théoret, Y; Gumy-Pause, F; Bernard, F; Chalandon, Y; Boelens, J J; Bredius, R G M; Dalle, J H; Nath, C; Corbacioglu, S; Peters, C; Bader, P; Shaw, P; Bittencourt, H; ... (2022). Association study of candidate DNA-repair gene variants and acute graft versus host disease in pediatric patients receiving allogeneic hematopoietic stem-cell transplantation. Pharmacogenomics journal, 22(1), pp. 9-18. Nature Publishing Group 10.1038/s41397-021-00251-7
Waespe, Nicolas; Strebel, Sven; Nava, Tiago; Uppugunduri, Chakradhara Rao S; Marino, Denis; Mattiello, Veneranda; Otth, Maria; Gumy-Pause, Fabienne; Von Bueren, André O; Baleydier, Frederic; Mader, Luzius; Spoerri, Adrian; Kuehni, Claudia E; Ansari, Marc (2022). Cohort-based association study of germline genetic variants with acute and chronic health complications of childhood cancer and its treatment: Genetic Risks for Childhood Cancer Complications Switzerland (GECCOS) study protocol. BMJ open, 12(1), e052131. BMJ Publishing Group 10.1136/bmjopen-2021-052131
Jurkovic Mlakar, Simona; Uppugunduri, Satyanarayana Chakradhara Rao; Nava, Tiago; Mlakar, Vid; Golay, Hadrien; Robin, Shannon; Waespe, Nicolas; Rezgui, Mohamed Aziz; Chalandon, Yves; Boelens, Jaap Jan; Bredius, Robert G M; Dalle, Jean-Hugues; Peters, Christina; Corbacioglu, Selim; Bittencourt, Henrique; Krajinovic, Maja; Ansari, Marc (2022). GSTM1 and GSTT1 double null genotypes determining cell fate and proliferation as potential risk factors of relapse in children with hematological malignancies after hematopoietic stem cell transplantation. Journal of cancer research and clinical oncology, 148(1), pp. 71-86. Springer 10.1007/s00432-021-03769-2
Goudie, Catherine; Witkowski, Leora; Cullinan, Noelle; Reichman, Lara; Schiller, Ian; Tachdjian, Melissa; Armstrong, Linlea; Blood, Katherine A; Brossard, Josée; Brunga, Ledia; Cacciotti, Chantel; Caswell, Kimberly; Cellot, Sonia; Clark, Mary Egan; Clinton, Catherine; Coltin, Hallie; Felton, Kathleen; Fernandez, Conrad V; Fleming, Adam J; Fuentes-Bolanos, Noemi; ... (2021). Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes. JAMA oncology, 7(12), pp. 1806-1814. American Medical Association 10.1001/jamaoncol.2021.4536
Vogel, Nicole; Schmugge, Markus; Renella, Raffaele; Waespe, Nicolas; Hengartner, Heinz (2021). The landscape of pediatric Diamond-Blackfan anemia in Switzerland: genotype and phenotype characteristics. European journal of pediatrics, 180(12), pp. 3581-3585. Springer-Verlag 10.1007/s00431-021-04146-4
Waespe, Nicolas; Strebel, Sven; Marino, Denis; Mattiello, Veneranda; Muet, Fanny; Nava, Tiago; Schindera, Christina; Belle, Fabien N.; Mader, Luzius; Spoerri, Adrian; Kuehni, Claudia E.; Ansari, Marc (2021). Predictors for participation in DNA self-sampling of childhood cancer survivors in Switzerland. BMC Medical research methodology, 21(1), p. 236. BioMed Central 10.1186/s12874-021-01428-1
Guerrini-Rousseau, L; Smith, M J; Kratz, C P; Doergeloh, B; Hirsch, S; Hopman, S M J; Jorgensen, M; Kuhlen, M; Michaeli, O; Milde, T; Ridola, V; Russo, A; Salvador, H; Waespe, N; Claret, B; Brugieres, L; Evans, D G (2021). Current recommendations for cancer surveillance in Gorlin syndrome: a report from the SIOPE host genome working group (SIOPE HGWG). Familial Cancer, 20(4), pp. 317-325. Springer 10.1007/s10689-021-00247-z
Strebel, Sven; Waespe, Nicolas; Kuehni, Claudia E (2021). Hearing loss in childhood cancer survivors. The Lancet. Child & adolescent health, 5(5), e17. Elsevier 10.1016/S2352-4642(21)00099-7
Waespe, Nicolas; Strebel, Sven; Jurkovic Mlakar, Simona; Krajinovic, Maja; Kuehni, Claudia Elisabeth; Nava, Tiago; Ansari, Marc (2021). Genetic Predictors for Sinusoidal Obstruction Syndrome-A Systematic Review. Journal of personalized medicine, 11(5), p. 347. MDPI 10.3390/jpm11050347
Waespe, Nicolas; Belle, Fabiën N.; Redmond, Shelagh; Schindera, Christina; Spycher, Ben D.; Rössler, Jochen; Ansari, Marc; Kuehni, Claudia E. (2021). Cancer predisposition syndromes as a risk factor for early second primary neoplasms after childhood cancer - A national cohort study. European journal of cancer, 145, pp. 71-80. Elsevier 10.1016/j.ejca.2020.11.042
Baenziger, Julia; Roser, Katharina; Mader, Luzius; Harju, Erika; Ansari, Marc; Waespe, Nicolas; Scheinemann, Katrin; Michel, Gisela (2020). Post-traumatic stress in parents of long-term childhood cancer survivors compared to parents of the Swiss general population. Journal of psychosocial oncology research and practice, 2(3), e024. Wolters Kluwer Health 10.1097/OR9.0000000000000024
