Mirjam van der Burg
Mirjam van der Burg
Leiden University Medical Center, Dept. of Pediatrics, Laboratory for Immunology
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Targeted genome editing in human repopulating haematopoietic stem cells
P Genovese, G Schiroli, G Escobar, T Di Tomaso, C Firrito, A Calabria, ...
Nature 510 (7504), 235-240, 2014
An Antibody-Deficiency Syndrome Due to Mutations in the CD19 Gene
MC Van Zelm, I Reisli, M Van Der Burg, D Castaño, CJM Van Noesel, ...
New England Journal of Medicine 354 (18), 1901-1912, 2006
CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency
MC Van Zelm, J Smet, B Adams, F Mascart, L Schandené, F Janssen, ...
The Journal of clinical investigation 120 (4), 1265-1274, 2010
Human memory B cells originate from three distinct germinal center-dependent and-independent maturation pathways
MA Berkowska, GJA Driessen, V Bikos, C Grosserichter-Wagener, ...
Blood, The Journal of the American Society of Hematology 118 (8), 2150-2158, 2011
Circulating CD21low B cells in common variable immunodeficiency resemble tissue homing, innate-like B cells
M Rakhmanov, B Keller, S Gutenberger, C Foerster, M Hoenig, ...
Proceedings of the National Academy of Sciences 106 (32), 13451-13456, 2009
The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency
V Bigley, M Haniffa, S Doulatov, XN Wang, R Dickinson, N McGovern, ...
Journal of Experimental Medicine 208 (2), 227-234, 2011
Replication history of B lymphocytes reveals homeostatic proliferation and extensive antigen-induced B cell expansion
MC Van Zelm, T Szczepański, M Van Der Burg, JJM Van Dongen
The Journal of experimental medicine 204 (3), 645-655, 2007
Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiency
K Warnatz, L Bossaller, U Salzer, A Skrabl-Baumgartner, W Schwinger, ...
Blood 107 (8), 3045-3052, 2006
A DNA-PKcs mutation in a radiosensitive TB SCID patient inhibits Artemis activation and nonhomologous end-joining
M Van Der Burg, H IJspeert, NS Verkaik, T Turul, WW Wiegant, ...
The Journal of clinical investigation 119 (1), 91-98, 2009
Heteroduplex PCR analysis of rearranged T cell receptor genes for clonality assessment in suspect T cell proliferations
AW Langerak, T Szczepański, M van der Burg, ILM Wolvers-Tettero, ...
Leukemia 11 (12), 2192-2199, 1997
Immunoglobulin gene rearrangements and the pathogenesis of multiple myeloma
D González, M van der Burg, R García-Sanz, JA Fenton, AW Langerak, ...
Blood, The Journal of the American Society of Hematology 110 (9), 3112-3121, 2007
Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathies
H Debiec, J Nauta, F Coulet, M van der Burg, V Guigonisy, T Schurmans, ...
The Lancet 364 (9441), 1252-1259, 2004
Non-homologous end-joining, a sticky affair
DC Van Gent, M van der Burg
Oncogene 26 (56), 7731-7740, 2007
A new type of radiosensitive TBNK+ severe combined immunodeficiency caused by a LIG4 mutation
M van der Burg, LR van Veelen, NS Verkaik, WW Wiegant, NG Hartwig, ...
The Journal of clinical investigation 116 (1), 137-145, 2006
Comparative analysis of Ig and TCR gene rearrangements at diagnosis and at relapse of childhood precursor-B–ALL provides improved strategies for selection of stable PCR targets …
T Szczepanski, MJ Willemse, B Brinkhof, ER van Wering, M van der Burg, ...
Blood, The Journal of the American Society of Hematology 99 (7), 2315-2323, 2002
Ig gene rearrangement steps are initiated in early human precursor B cell subsets and correlate with specific transcription factor expression
MC Van Zelm, M Van Der Burg, D De Ridder, BH Barendregt, ...
The Journal of Immunology 175 (9), 5912-5922, 2005
Educational paper
M van der Burg, AR Gennery
European journal of pediatrics 170 (5), 561-571, 2011
Targeted next-generation sequencing: a novel diagnostic tool for primary immunodeficiencies
IJ Nijman, JM van Montfrans, M Hoogstraat, ML Boes, L van de Corput, ...
Journal of Allergy and Clinical Immunology 133 (2), 529-534. e1, 2014
Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2
JC De Greef, J Wang, J Balog, JT Den Dunnen, RR Frants, ...
The American Journal of Human Genetics 88 (6), 796-804, 2011
TREC based newborn screening for severe combined immunodeficiency disease: a systematic review
J van der Spek, RHH Groenwold, M van der Burg, JM van Montfrans
Journal of clinical immunology 35 (4), 416-430, 2015
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