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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
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
Kasteler, Rahel; Kam, Linda; Weiss, Annette; Waespe, Nicolas; Sommer, Grit; Singer, Florian; von der Weid, Nicolas X; Ansari, Marc; Kuehni, Claudia E; Oncology Group (SPOG), Swiss Pediatric (2018). Monitoring pulmonary health in Swiss childhood cancer survivors. Pediatric blood & cancer, 65(10), e27255. Wiley-Liss 10.1002/pbc.27255
