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Nature Genetics|November 13, 2012
Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencingJulia Richter, Matthias Schlesner, Steve Hoffmann, et al.
Nature Genetics|July 6, 2010
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disordersThomas Ernst, Andrew J Chase, Joannah Score, et al.
In Vitro Cellular & Developmental Biology. Animal|July 9, 2010
Recommendation of short tandem repeat profiling for authenticating human cell lines, stem cells, and tissuesRita Barallon, Steven R Bauer, John Butler, et al.
Nature Genetics|October 6, 2015
DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional controlHelene Kretzmer, Stephan H Bernhart, Wei Wang, et al.
Haematologica|April 16, 2017
Epigenetically induced ectopic expression of UNCX impairs the proliferation and differentiation of myeloid cellsGiulia Daniele, Giorgia Simonetti, Caterina Fusilli, et al.
Genes, Chromosomes & Cancer|July 16, 2015
The PCBP1 gene encoding poly(rC) binding protein I is recurrently mutated in Burkitt lymphomaRabea Wagener, Sietse M Aukema, Matthias Schlesner, et al.
Ejhaem|September 2, 2022
B-cell receptors of EBV-negative Burkitt lymphoma bind modified isoforms of autoantigensTheresa Bock, Moritz Bewarder, Onur Cetin, et al.
Blood|October 5, 2018
IG-MYC + neoplasms with precursor B-cell phenotype are molecularly distinct from Burkitt lymphomasRabea Wagener, Cristina López, Kortine Kleinheinz, et al.
Haematologica|July 9, 2016
Alterations of microRNA and microRNA-regulated messenger RNA expression in germinal center B-cell lymphomas determined by integrative sequencing analysisKebria Hezaveh, Andreas Kloetgen, Stephan H Bernhart, et al.
Blood|September 28, 2016
Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphomaLarry Mansouri, Daniel Noerenberg, Emma Young, et al.
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