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Journal of Virology|October 28, 2004
Conditionally replicating adenoviruses kill tumor cells via a basic apoptotic machinery-independent mechanism that resembles necrosis-like programmed cell deathMohamed A I Abou El Hassan, Ida van der Meulen-Muileman, Saman Abbas, et al.
Blood|June 19, 2013
A capture-sequencing strategy identifies IRF8, EBF1, and APRIL as novel IGH fusion partners in B-cell lymphomaHakim Bouamar, Saman Abbas, An-Ping Lin, et al.
Blood|May 23, 2012
Thrombopoietin/MPL participates in initiating and maintaining RUNX1-ETO acute myeloid leukemia via PI3K/AKT signalingJohn Anto Pulikkan, Dmitri Madera, Liting Xue, et al.
Haematologica|November 8, 2011
Acquired mutations in ASXL1 in acute myeloid leukemia: prevalence and prognostic valueMarta Pratcorona, Saman Abbas, Mathijs A Sanders, et al.
Haematologica|October 8, 2008
Prediction of molecular subtypes in acute myeloid leukemia based on gene expression profilingRoel G W Verhaak, Bas J Wouters, Claudia A J Erpelinck, et al.
Blood|May 21, 2011
Risk stratification of intermediate-risk acute myeloid leukemia: integrative analysis of a multitude of gene mutation and gene expression markersVeronika Rockova, Saman Abbas, Bas J Wouters, et al.
BMC Genomics|January 29, 2008
SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levelsMathijs A Sanders, Roel G W Verhaak, Wendy M C Geertsma-Kleinekoort, et al.
Blood|June 12, 2010
Acquired mutations in the genes encoding IDH1 and IDH2 both are recurrent aberrations in acute myeloid leukemia: prevalence and prognostic valueSaman Abbas, Sanne Lugthart, François G Kavelaars, et al.
Blood|April 12, 2012
Mutant DNMT3A: a marker of poor prognosis in acute myeloid leukemiaAna Flávia Tibúrcio Ribeiro, Marta Pratcorona, Claudia Erpelinck-Verschueren, et al.
Haematologica|January 21, 2014
Integrated genome-wide genotyping and gene expression profiling reveals BCL11B as a putative oncogene in acute myeloid leukemia with 14q32 aberrationsSaman Abbas, Mathijs A Sanders, Annelieke Zeilemaker, et al.
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