Resultados da pesquisa - Simon V. van Reijmersdal

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  1. 1
    The Origin and Nature of Tightly Clustered BTG1 Deletions in Precursor B-Cell Acute Lymphoblastic Leukemia Support a Model of Multiclonal Evolution

    The Origin and Nature of Tightly Clustered BTG1 Deletions in Precursor B-Cell Acute Lymphoblastic Leukemia Support a Model of Multiclonal Evolution Por Esmé Waanders, Blanca Scheijen, Laurens T. van der Meer, Simon V. van Reijmersdal, Liesbeth van Emst, Yvet Kroeze, Edwin Sonneveld, Peter M. Hoogerbrugge, Ad Geurts van Kessel, Frank N. van Leeuwen, Roland P. Kuiper

    Publicado em 2012
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  2. 2
    Validation Study of Existing Gene Expression Signatures for Anti-TNF Treatment in Patients with Rheumatoid Arthritis

    Validation Study of Existing Gene Expression Signatures for Anti-TNF Treatment in Patients with Rheumatoid Arthritis Por Erik J. M. Toonen, Christian Gilissen, Barbara Franke, Wietske Kievit, A M M Eijsbouts, Alfons A den Broeder, Simon V. van Reijmersdal, Joris A. Veltman, Hans Scheffer, Timothy R. D. J. Radstake, Piet L. C. M. van Riel, Pilar Barrera, Marieke J. H. Coenen

    Publicado em 2012
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  3. 3
    Prevalence of (Epi)genetic Predisposing Factors in a 5-Year Unselected National Wilms Tumor Cohort: A Comprehensive Clinical and Genomic Characterization

    Prevalence of (Epi)genetic Predisposing Factors in a 5-Year Unselected National Wilms Tumor Cohort: A Comprehensive Clinical and Genomic Characterization Por Janna A. Hol, Roland P. Kuiper, Freerk van Dijk, Esmé Waanders, Sophie E. van Peer, Marco J. Koudijs, Reno S. Bladergroen, Simon V. van Reijmersdal, Lionel Morgado, Jet Bliek, Maria Lombardi, Saskia Hopman, Jarno Drost, Ronald R. de Krijger, Marry M. van den Heuvel‐Eibrink, Marjolijn C.J. Jongmans

    Publicado em 2022
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  4. 4
    Genetic Screening for TLR7 Variants in Young and Previously Healthy Men With Severe COVID-19

    Genetic Screening for TLR7 Variants in Young and Previously Healthy Men With Severe COVID-19 Por Xavier Solanich, Gardenia Vargas‐Parra, Caspar I. van der Made, Annet Simons, Janneke Schuurs-Hoeijmakers, Arnau Antolí, Jesús Del Valle, Gemma Rocamora-Blanch, Fernando Setién, Manel Esteller, Simon V. van Reijmersdal, Antoni Riera‐Mestre, Joan Sabater‐Riera, Gabriel Capellà, Frank L. van de Veerdonk, Ben van der Hoven, Xavier Corbella, Alexander Hoischen, Conxi Lázaro

    Publicado em 2021
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  5. 5
    Diagnostic Genome Profiling in Mental Retardation

    Diagnostic Genome Profiling in Mental Retardation Por Bert B.A. de Vries, Rolph Pfundt, M.A.R. Leisink, David A. Koolen, Lisenka E.L.M. Vissers, Irene M. Janssen, Simon V. van Reijmersdal, Willy M. Nillesen, Erik Huys, Nicole de Leeuw, Dominique Smeets, Erik A. Sistermans, Ton Feuth, Conny M.A. van Ravenswaaij‐Arts, Ad Geurts van Kessel, Eric Schoenmakers, Han G. Brunner, Joris A. Veltman

    Publicado em 2005
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  6. 6
    Independent prognostic value of BCR-ABL1-like signature and IKZF1 deletion, but not high CRLF2 expression, in children with B-cell precursor ALL

    Independent prognostic value of BCR-ABL1-like signature and IKZF1 deletion, but not high CRLF2 expression, in children with B-cell precursor ALL Por Arian van der Veer, Esmé Waanders, Rob Pieters, Marieke E. Willemse, Simon V. van Reijmersdal, Lisa J. Russell, Christine J. Harrison, William E. Evans, Vincent H. J. van der Velden, Peter M. Hoogerbrugge, Frank N. van Leeuwen, Gabriele Escherich, Martin A. Horstmann, Leila mohammadi Khankahdani, Dimitris Rizopoulos, Hester A. de Groot‐Kruseman, Edwin Sonneveld, Roland P. Kuiper, Monique L. den Boer

    Publicado em 2013
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  7. 7
    <i>TRIM28</i> haploinsufficiency predisposes to Wilms tumor

    <i>TRIM28</i> haploinsufficiency predisposes to Wilms tumor Por Illja J. Diets, Juliane Hoyer, Arif B. Ekici, Bernt Popp, Nicoline Hoogerbrugge, Simon V. van Reijmersdal, Rajith Bhaskaran, Michel V. Hadjihannas, Georgia Vasileiou, Christian T. Thiel, Didem Seven, Steffen Uebe, Denisa Ilenčíková, Esmé Waanders, Annelies M. C. Mavinkurve‐Groothuis, Nel Roeleveld, Ronald R. de Krijger, Jenny Wegert, Norbert Graf, Christian Vokuhl, Abbas Agaimy, Manfred Gessler, André Reis, Roland P. Kuiper, Marjolijn C.J. Jongmans, Markus Metzler

    Publicado em 2019
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  8. 8
    Presence of Genetic Variants Among Young Men With Severe COVID-19

    Presence of Genetic Variants Among Young Men With Severe COVID-19 Por Caspar I. van der Made, Annet Simons, Janneke Schuurs-Hoeijmakers, Guus van den Heuvel, Tuomo Mantere, Simone Kersten, Rosanne C. van Deuren, Marloes Steehouwer, Simon V. van Reijmersdal, Martin Jaeger, Tom Hofste, Galuh Astuti, Jordi Corominas Galbany, Vyne van der Schoot, Hans van der Hoeven, Wanda Hagmolen of ten Have, Eva Klijn, Catrien van den Meer, Jeroen Fiddelaers, Quirijn de Mast, Chantal P. Bleeker‐Rovers, Leo A. B. Joosten, Helger G. Yntema, Christian Gilissen, Marcel Nelen, J.W.M. van der Meer, Han G. Brunner, Mihai G. Netea, Frank L. van de Veerdonk, Alexander Hoischen

    Publicado em 2020
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