Jessica G. C. A. M. Buijs-Gladdines

Integrated Transcript and Genome Analyses Reveal NKX2-1 and MEF2C as Potential Oncogenes in T Cell Acute Lymphoblastic Leukemia

Irene Homminga, Rob Pieters, Anton W. Langerak et al. · Cancer Cell · 2011 · 378 citations · Full text

Hematological Malignancy, Mixed-phenotype Acute Leukemia, Immunology +4

The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia

Pieter Van Vlierberghe, Martine van Grotel, Joëlle Tchinda et al. · Blood · 2008 · 222 citations · Full text

The cryptic chromosomal deletion del(11)(p12p13) as a new activation mechanism of LMO2 in pediatric T-cell acute lymphoblastic leukemia

Pieter Van Vlierberghe, Martine van Grotel, H. Berna Beverloo et al. · Blood · 2006 · 165 citations · Full text

Prognostic significance of molecular-cytogenetic abnormalities in pediatric T-ALL is not explained by immunophenotypic differences

Martine van Grotel, Jules P.P. Meijerink, Elisabeth R. van Wering et al. · Leukemia · 2007 · 142 citations · Full text

Pediatric T-all, Autoimmune Disease, Genetic Disorder +13

NOTCH1 and/or FBXW7 mutations predict for initial good prednisone response but not for improved outcome in pediatric T-cell acute lymphoblastic leukemia patients treated on DCOG or COALL protocols

Linda Zuurbier, Irene Homminga, Valerie Calvert et al. · Leukemia · 2010 · 140 citations

Hematological Malignancy, Pediatric Hematology, Medicine +9