W. Geertsma‐Kleinekoort

Incidence and prognosis of c‐KIT and FLT3 mutations in core binding factor (CBF) acute myeloid leukaemias

J. Reilly, B. Löwenberg, P. Valk, 2003, British journal of haematology.

Integrated genome-wide genotyping and gene expression profiling reveals BCL11B as a putative oncogene in acute myeloid leukemia with 14q32 aberrations

J. V. van Galen, J. Peeters, M. Sanders, 2014, Haematologica.

Regulation of Osteocalcin Production and Bone Resorption by 1,25‐Dihydroxyvitamin D3 in Mouse Long Bones: Interaction with the Bone‐Derived Growth Factors TGF‐β and IGF‐I

J. V. van Leeuwen, A. Staal, J. Birkenhäger, 1998, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia.

Bob Löwenberg, Jurgen R Haanstra, Mathijs A Sanders, 2012, Blood.

Addition of β-mercaptoethanol is a prerequisite for high-quality RNA isolation using QIAsymphony technology as demonstrated by detection of molecular aberrations in hematologic malignancies.

P. Valk, Sonja C van der Poel-van de Luytgaarde, W. M. Geertsma-Kleinekoort, 2013, Genetic testing and molecular biomarkers.

Segmental uniparental disomy as a recurrent mechanism for homozygous CEBPA mutations in acute myeloid leukemia

Bas J. Wouters, M. Sanders, B. Löwenberg, 2007, Leukemia.

SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levels

Sebastiaan Horsman, Bob Löwenberg, Mathijs A Sanders, 2008, BMC Genomics.