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Evenepoel, Lucie; van Nederveen, Francien H; Oudijk, Lindsey; Papathomas, Thomas G; Restuccia, David F; Belt, Eric J T; de Herder, Wouter W; Feelders, Richard A; Franssen, Gaston J H; Hamoir, Marc; Maiter, Dominique; Perren, Aurel; Timmers, Henri J L M; van Eeden, Susanne; Vroonen, Laurent; Aydin, Selda; Robledo, Mercedes; Vikkula, Miikka; de Krijger, Ronald R; Dinjens, Winand N M; ... (2018). Expression of Contactin 4 is associated with malignant behavior in pheochromocytomas and paragangliomas. The Journal of clinical endocrinology and metabolism, 103(1), pp. 46-55. The Endocrine Society 10.1210/jc.2017-01314
Letouzé, Eric; Rosati, Roberto; Komechen, Heloisa; Doghman, Mabrouka; Marisa, Laetitia; Flück, Christa; de Krijger, Ronald R; van Noesel, Max M; Mas, Jean-Christophe; Pianovski, Mara A D; Zambetti, Gerard P; Figueiredo, Bonald C; Lalli, Enzo (2012). SNP array profiling of childhood adrenocortical tumors reveals distinct pathways of tumorigenesis and highlights candidate driver genes. Journal of clinical endocrinology and metabolism, 97(7), E1284-93. Chevy Chase, Md.: Endocrine Society 10.1210/jc.2012-1184
Swarts, Dorian R A; Claessen, Sandra M H; Jonkers, Yvonne M H; van Suylen, Robert-Jan; Dingemans, Anne-Marie C; de Herder, Wouter W; de Krijger, Ronald R; Smit, Egbert F; Thunnissen, Frederik B J M; Seldenrijk, Cornelis A; Vink, Aryan; Perren, Aurel; Ramaekers, Frans C S; Speel, Ernst-Jan M (2011). Deletions of 11q22.3-q25 are associated with atypical lung carcinoids and poor clinical outcome. American journal of pathology, 179(3), pp. 1129-37. New York, N.Y.: Elsevier 10.1016/j.ajpath.2011.05.028
van Nederveen, Francien H; Gaal, José; Favier, Judith; Korpershoek, Esther; Oldenburg, Rogier A; de Bruyn, Elly M C A; Sleddens, Hein F B M; Derkx, Pieter; Rivière, Julie; Dannenberg, Hilde; Petri, Bart-Jeroen; Komminoth, Paul; Pacak, Karel; Hop, Wim C J; Pollard, Patrick J; Mannelli, Massimo; Bayley, Jean-Pierre; Perren, Aurel; Niemann, Stephan; Verhofstad, Albert A; ... (2009). An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis. Lancet oncology, 10(8), pp. 764-71. Oxford: Elsevier 10.1016/S1470-2045(09)70164-0
