Mitochondrial D310 mutation as clonal marker for solid tumors

by Geurts-Giele, Willemina R. R., Gathier, Gerard H. G. K., Atmodimedjo, Peggy N., Dubbink, Hendrikus J., Dinjens, Winand N. M.
Published 2015

Early onset esophageal adenocarcinoma: a distinct molecular entity?

by van Nistelrooij, Anna M.J., van Marion, Ronald, Biermann, Katharina, Spaander, Manon C.W., van Lanschot, J. Jan B., Wijnhoven, Bas P.L., Dinjens, Winand N.M.
Published 2016

Prevalence of c-KIT Mutations in Gonadoblastoma and Dysgerminomas of Patients with Disorders of Sex Development (DSD) and Ovarian Dysgerminomas

by Hersmus, Remko, Stoop, Hans, van de Geijn, Gert Jan, Eini, Ronak, Biermann, Katharina, Oosterhuis, J. Wolter, DHooge, Catharina, Schneider, Dominik T., Meijssen, Isabelle C., Dinjens, Winand N. M., Dubbink, Hendrikus Jan, Drop, Stenvert L. S., Looijenga, Leendert H. J.
Published 2012

Adrenal Medullary Hyperplasia Is a Precursor Lesion for Pheochromocytoma in MEN2 Syndrome12

by Korpershoek, Esther, Petri, Bart-Jeroen, Post, Edward, van Eijck, Casper H.J., Oldenburg, Rogier A., Belt, Eric J.T., de Herder, Wouter W., de Krijger, Ronald R., Dinjens, Winand N.M.
Published 2014

Vascular Pattern Analysis for the Prediction of Clinical Behaviour in Pheochromocytomas and Paragangliomas

by Oudijk, Lindsey, van Nederveen, Francien, Badoual, Cécile, Tissier, Frédérique, Tischler, Arthur S., Smid, Marcel, Gaal, José, Lepoutre-Lussey, Charlotte, Gimenez-Roqueplo, Anne-Paule, Dinjens, Winand N.M., Korpershoek, Esther, de Krijger, Ronald, Favier, Judith
Published 2015

IL-7 Receptor Mutations and Steroid Resistance in Pediatric T cell Acute Lymphoblastic Leukemia: A Genome Sequencing Study

by Li, Yunlei, Buijs-Gladdines, Jessica G. C. A. M., Canté-Barrett, Kirsten, Stubbs, Andrew P., Vroegindeweij, Eric M., Smits, Willem K., van Marion, Ronald, Dinjens, Winand N. M., Horstmann, Martin, Kuiper, Roland P., Buijsman, Rogier C., Zaman, Guido J. R., van der Spek, Peter J., Pieters, Rob, Meijerink, Jules P. P.
Published 2016

Single nucleotide polymorphisms in CRTC1 and BARX1 are associated with esophageal adenocarcinoma

by van Nistelrooij, Anna M. J., van der Korput, Hetty A. G. M., Broer, Linda, van Marion, Ronald, van Berge Henegouwen, Mark I., van Noesel, Carel J., Biermann, Katharina, Spaander, Manon C. W., Tilanus, Hugo W., van Lanschot, J. Jan B., Hofman, Albert, Uitterlinden, André G., Wijnhoven, Bas P. L., Dinjens, Winand N. M.
Published 2015