High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with Cancer
Diets, Illja J, Waanders, Esmé, Ligtenberg, Marjolijn J, van Bladel, Diede A G, Kamping, Eveline J, Hoogerbrugge, Peter M, Hopman, Saskia, Olderode-Berends, Maran J, Gerkes, Erica H, Koolen, David A, Marcelis, Carlo, Santen, Gijs W, van Belzen, Martine J, Mordaunt, Dylan, McGregor, Lesley, Thompson, Elizabeth, Kattamis, Antonis, Pastorczak, Agata, Mlynarski, Wojciech, Ilencikova, Denisa, van Silfhout, Anneke Vulto, Gardeitchik, Thatjana, de Bont, Eveline S, Loeffen, Jan, Wagner, Anja, Mensenkamp, Arjen R, Kuiper, Roland P, Hoogerbrugge, Nicoline, Jongmans, Marjolijn C
Published in Clinical cancer research (01.04.2018)
Published in Clinical cancer research (01.04.2018)
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Multiclonal complexity of pediatric acute lymphoblastic leukemia and the prognostic relevance of subclonal mutations
Antić, Željko, Yu, Jiangyan, Van Reijmersdal, Simon V, Van Dijk, Anke, Dekker, Linde, Segerink, Wouter H, Sonneveld, Edwin, Fiocco, Marta, Pieters, Rob, Hoogerbrugge, Peter M, Van Leeuwen, Frank N, Van Kessel, Ad Geurts, Waanders, Esme, Kuiper, Roland P
Published in Haematologica (Roma) (01.12.2021)
Published in Haematologica (Roma) (01.12.2021)
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Independent prognostic value of BCR-ABL1-like signature and IKZF1 deletion, but not high CRLF2 expression, in children with B-cell precursor ALL
van der Veer, Arian, Waanders, Esmé, Pieters, Rob, Willemse, Marieke E., Van Reijmersdal, Simon V., Russell, Lisa J., Harrison, Christine J., Evans, William E., van der Velden, Vincent H.J., Hoogerbrugge, Peter M., Van Leeuwen, Frank, Escherich, Gabriele, Horstmann, Martin A., Mohammadi Khankahdani, Leila, Rizopoulos, Dimitris, De Groot-Kruseman, Hester A., Sonneveld, Edwin, Kuiper, Roland P., Den Boer, Monique L.
Published in Blood (10.10.2013)
Published in Blood (10.10.2013)
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Recognition of genetic predisposition in pediatric cancer patients: An easy-to-use selection tool
Jongmans, Marjolijn C.J, Loeffen, Jan L.C.M, Waanders, Esmé, Hoogerbrugge, Peter M, Ligtenberg, Marjolijn J.L, Kuiper, Roland P, Hoogerbrugge, Nicoline
Published in European journal of medical genetics (01.03.2016)
Published in European journal of medical genetics (01.03.2016)
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Relapse-Fated Latent Diagnosis Subclones in Acute B Lineage Leukemia Are Drug Tolerant and Possess Distinct Metabolic Programs
Dobson, Stephanie M, García-Prat, Laura, Vanner, Robert J, Wintersinger, Jeffrey, Waanders, Esmé, Gu, Zhaohui, McLeod, Jessica, Gan, Olga I, Grandal, Ildiko, Payne-Turner, Debbie, Edmonson, Michael N, Ma, Xiaotu, Fan, Yiping, Voisin, Veronique, Chan-Seng-Yue, Michelle, Xie, Stephanie Z, Hosseini, Mohsen, Abelson, Sagi, Gupta, Pankaj, Rusch, Michael, Shao, Ying, Olsen, Scott R, Neale, Geoffrey, Chan, Steven M, Bader, Gary, Easton, John, Guidos, Cynthia J, Danska, Jayne S, Zhang, Jinghui, Minden, Mark D, Morris, Quaid, Mullighan, Charles G, Dick, John E
Published in Cancer discovery (01.04.2020)
Published in Cancer discovery (01.04.2020)
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Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors
Sabatella, Mariangela, Mantere, Tuomo, Waanders, Esmé, Neveling, Kornelia, Mensenkamp, Arjen R, Dijk, Freerk, Hehir‐Kwa, Jayne Y, Derks, Ronnie, Kwint, Michael, O'Gorman, Luke, Tropa Martins, Madalena, Gidding, Corrie EM, Lequin, Maarten H, Küsters, Benno, Wesseling, Pieter, Nelen, Marcel, Biegel, Jacklyn A, Hoischen, Alexander, Jongmans, Marjolijn C, Kuiper, Roland P
Published in The Journal of pathology (01.10.2021)
Published in The Journal of pathology (01.10.2021)
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TRIM28 haploinsufficiency predisposes to Wilms tumor
Diets, Illja J., Hoyer, Juliane, Ekici, Arif B., Popp, Bernt, Hoogerbrugge, Nicoline, Reijmersdal, Simon V., Bhaskaran, Rajith, Hadjihannas, Michel, Vasileiou, Georgia, Thiel, Christian T., Seven, Didem, Uebe, Steffen, Ilencikova, Denisa, Waanders, Esmé, Mavinkurve‐Groothuis, Annelies M.C., Roeleveld, Nel, Krijger, Ronald R., Wegert, Jenny, Graf, Norbert, Vokuhl, Christian, Agaimy, Abbas, Gessler, Manfred, Reis, André, Kuiper, Roland P., Jongmans, Marjolijn C.J., Metzler, Markus
Published in International journal of cancer (15.08.2019)
Published in International journal of cancer (15.08.2019)
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Outcome of children with hypodiploid ALL treated with risk-directed therapy based on MRD levels
Mullighan, Charles G., Jeha, Sima, Pei, Deqing, Payne-Turner, Debbie, Coustan-Smith, Elaine, Roberts, Kathryn G., Waanders, Esmé, Choi, John K., Ma, Xiaotu, Raimondi, Susana C., Fan, Yiping, Yang, Wenjian, Song, Guangchun, Yang, Jun J., Inaba, Hiroto, Downing, James R., Leung, Wing H., Bowman, W. Paul, Relling, Mary V., Evans, William E., Zhang, Jinghui, Campana, Dario, Pui, Ching-Hon
Published in Blood (24.12.2015)
Published in Blood (24.12.2015)
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Mutational Landscape and Patterns of Clonal Evolution in Relapsed Pediatric Acute Lymphoblastic Leukemia
Waanders, Esmé, Gu, Zhaohui, Dobson, Stephanie M., Antić, Željko, Crawford, Jeremy Chase, Ma, Xiaotu, Edmonson, Michael N., Payne-Turner, Debbie, van de Vorst, Maartje, Jongmans, Marjolijn C.J., McGuire, Irina, Zhou, Xin, Wang, Jian, Shi, Lei, Pounds, Stanley, Pei, Deqing, Cheng, Cheng, Song, Guangchun, Fan, Yiping, Shao, Ying, Rusch, Michael, McCastlain, Kelly, Yu, Jiangyan, van Boxtel, Ruben, Blokzijl, Francis, Iacobucci, Ilaria, Roberts, Kathryn G., Wen, Ji, Wu, Gang, Ma, Jing, Easton, John, Neale, Geoffrey, Olsen, Scott R., Nichols, Kim E., Pui, Ching-Hon, Zhang, Jinghui, Evans, William E., Relling, Mary V., Yang, Jun J., Thomas, Paul G., Dick, John E., Kuiper, Roland P., Mullighan, Charles G.
Published in Blood cancer discovery (01.07.2020)
Published in Blood cancer discovery (01.07.2020)
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De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism
Diets, Illja J., van der Donk, Roos, Baltrunaite, Kristina, Waanders, Esmé, Reijnders, Margot R.F., Dingemans, Alexander J.M., Pfundt, Rolph, Vulto-van Silfhout, Anneke T., Wiel, Laurens, Gilissen, Christian, Thevenon, Julien, Perrin, Laurence, Afenjar, Alexandra, Nava, Caroline, Keren, Boris, Bartz, Sarah, Peri, Bethany, Beunders, Gea, Verbeek, Nienke, van Gassen, Koen, Thiffault, Isabelle, Cadieux-Dion, Maxime, Huerta-Saenz, Lina, Wagner, Matias, Konstantopoulou, Vassiliki, Vodopiutz, Julia, Griese, Matthias, Boel, Annekatrien, Callewaert, Bert, Brunner, Han G., Kleefstra, Tjitske, Hoogerbrugge, Nicoline, de Vries, Bert B.A., Hwa, Vivian, Dauber, Andrew, Hehir-Kwa, Jayne Y., Kuiper, Roland P., Jongmans, Marjolijn C.J.
Published in American journal of human genetics (04.04.2019)
Published in American journal of human genetics (04.04.2019)
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Heterozygosity for bisphosphoglycerate mutase deficiency expressing clinically as congenital erythrocytosis: A case series and literature review
Dijk, Myrthe J., Oirschot, Brigitte A., Stam‐Slob, Manon C., Waanders, Esmé, Zwaag, Bert, Beers, Eduard J., Jans, Judith J. M., Linden, Peter Willem, Torregrosa Diaz, Jose M., Gardie, Betty, Girodon, François, Schots, Rik, Thielen, Noortje, Wijk, Richard
Published in British journal of haematology (01.01.2023)
Published in British journal of haematology (01.01.2023)
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The origin and nature of tightly clustered BTG1 deletions in precursor B-cell acute lymphoblastic leukemia support a model of multiclonal evolution
Waanders, Esmé, Scheijen, Blanca, van der Meer, Laurens T, van Reijmersdal, Simon V, van Emst, Liesbeth, Kroeze, Yvet, Sonneveld, Edwin, Hoogerbrugge, Peter M, van Kessel, Ad Geurts, van Leeuwen, Frank N, Kuiper, Roland P
Published in PLoS genetics (01.02.2012)
Published in PLoS genetics (01.02.2012)
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European standard clinical practice – Key issues for the medical care of individuals with familial leukemia
Förster, Alisa, Davenport, Claudia, Duployez, Nicolas, Erlacher, Miriam, Ferster, Alina, Fitzgibbon, Jude, Göhring, Gudrun, Hasle, Henrik, Jongmans, Marjolijn C., Kolenova, Alexandra, Kronnie, Geertruijte, Lammens, Tim, Mecucci, Cristina, Mlynarski, Wojciech, Niemeyer, Charlotte M., Sole, Francesc, Szczepanski, Tomasz, Waanders, Esmé, Biondi, Andrea, Wlodarski, Marcin, Schlegelberger, Brigitte, Ripperger, Tim
Published in European journal of medical genetics (01.04.2023)
Published in European journal of medical genetics (01.04.2023)
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Characteristics of white blood cell count in acute lymphoblastic leukemia: A COST LEGEND phenotype–genotype study
Helenius, Marianne, Vaitkeviciene, Goda, Abrahamsson, Jonas, Jonsson, Ólafur Gisli, Lund, Bendik, Harila‐Saari, Arja, Vettenranta, Kim, Mikkel, Sirje, Stanulla, Martin, Lopez‐Lopez, Elixabet, Waanders, Esmé, Madsen, Hans O., Marquart, Hanne Vibeke, Modvig, Signe, Gupta, Ramneek, Schmiegelow, Kjeld, Nielsen, Rikke Linnemann
Published in Pediatric blood & cancer (01.06.2022)
Published in Pediatric blood & cancer (01.06.2022)
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Journal Article
Clonal dynamics in pediatric B‐cell precursor acute lymphoblastic leukemia with very early relapse
Antić, Željko, Yu, Jiangyan, Bornhauser, Beat C., Lelieveld, Stefan H., Ham, Cedric G., Reijmersdal, Simon V., Morgado, Lionel, Elitzur, Sarah, Bourquin, Jean‐Pierre, Cazzaniga, Giovanni, Eckert, Cornelia, Camós, Mireia, Sutton, Rosemary, Cavé, Hélène, Moorman, Anthony V., Sonneveld, Edwin, Geurts van Kessel, Ad, Leeuwen, Frank N., Hoogerbrugge, Peter M., Waanders, Esmé, Kuiper, Roland P.
Published in Pediatric blood & cancer (01.01.2022)
Published in Pediatric blood & cancer (01.01.2022)
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Journal Article
Accurate detection of low-level mosaic mutations in pediatric acute lymphoblastic leukemia using single molecule tagging and deep-sequencing
Yu, Jiangyan, Antić, Željko, van Reijmersdal, Simon V., Hoischen, Alexander, Sonneveld, Edwin, Waanders, Esmé, Kuiper, Roland P.
Published in Leukemia & lymphoma (03.07.2018)
Published in Leukemia & lymphoma (03.07.2018)
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Late Recurrence of Childhood T-Cell Acute Lymphoblastic Leukemia Frequently Represents a Second Leukemia Rather Than a Relapse: First Evidence for Genetic Predisposition
SZCZEPANSKI, Tomasz, VAN DER VELDEN, Vincent H. J, ZUR STADT, Udo, CAMPANA, Dario, SCHRAUDER, André, SUTTON, Rosemary, VAN WERING, Elisabeth, MEIJERINK, Jules P. P, VAN DONGEN, Jacques J. M, WAANDERS, Esmé, KUIPER, Roland P, VAN VLIERBERGHE, Pieter, GRUHN, Bernd, ECKERT, Cornelia, PANZER-GRÜMAYER, Renate, BASSO, Giuseppe, CAVE, Hélène
Published in Journal of clinical oncology (20.04.2011)
Published in Journal of clinical oncology (20.04.2011)
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Congenital disorders of glycosylation in hepatology: The example of polycystic liver disease
Janssen, Manoe J, Waanders, Esmé, Woudenberg, Jannes, Lefeber, Dirk J, Drenth, Joost P.H
Published in Journal of hepatology (01.03.2010)
Published in Journal of hepatology (01.03.2010)
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