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Genetic Testing and Molecular Biomarkers|March 15, 2013
Detection of CEBPA double mutants in acute myeloid leukemia using a custom gene expression arrayMartin H van Vliet, Pia Burgmer, Linda de Quartel, et al.
Cancer Research|February 12, 2005
Comparative genomic hybridization profiles in human BRCA1 and BRCA2 breast tumors highlight differential sets of genomic aberrationsErik H van Beers, Tibor van Welsem, Lodewyk F A Wessels, et al.
Breast Cancer Research and Treatment|August 16, 2008
Prediction of BRCA1-association in hereditary non-BRCA1/2 breast carcinomas with array-CGHSimon A Joosse, Erik H van Beers, Ivon H G Tielen, et al.
Blood|September 3, 2015
Prediction of high- and low-risk multiple myeloma based on gene expression and the International Staging SystemRowan Kuiper, Mark van Duin, Martin H van Vliet, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approachMarc Tischkowitz, Nancy Hamel, Marcelo A Carvalho, et al.
Genes, Chromosomes & Cancer|July 30, 2008
Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locusRogier A Oldenburg, Karin H G Kroeze-Jansema, Jeanine J Houwing-Duistermaat, et al.
Blood Advances|December 22, 2020
Prognostic and predictive performance of R-ISS with SKY92 in older patients with multiple myeloma: the HOVON-87/NMSG-18 trialRowan Kuiper, Sonja Zweegman, Mark van Duin, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2007
Analysis of PALB2/FANCN-associated breast cancer familiesMarc Tischkowitz, Bing Xia, Nelly Sabbaghian, et al.
Clinical Lymphoma, Myeloma & Leukemia|July 25, 2017
Prognostic Validation of SKY92 and Its Combination With ISS in an Independent Cohort of Patients With Multiple MyelomaErik H van Beers, Martin H van Vliet, Rowan Kuiper, et al.
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