Tom van Wezel

Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer.

Julian Peto, Sergi Castellví-Bel, Jean-Baptiste Cazier, 2008, Human molecular genetics.

DNA repair genes are selectively mutated in diffuse large B cell lymphomas

Mats Nilsson, David Kipling, Konstantinos Georgiou, 2013, The Journal of experimental medicine.

Progression and Tumor Heterogeneity Analysis in Early Rectal Cancer

Jan Oosting, Paul H C Eilers, Hans Morreau, 2008, Clinical Cancer Research.

Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer

Ekaterina S Jordanova, Jan Oosting, Karoly Szuhai, 2007, BMC Genomics.

Macrodissection versus microdissection of rectal carcinoma: minor influence of stroma cells to tumor cell gene expression profiles

J Han JM van Krieken, Jan Paul Medema, P. Eilers, 2005, BMC Genomics.

High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays.

Cisca Wijmenga, Jan Oosting, Paul H C Eilers, 2007, Genome research.

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer

Ian J. Deary, Archie Campbell, Sergi Castellví-Bel, 2015, Scientific Reports.

Allelic Variation at the 8q23.3 Colorectal Cancer Risk Locus Functions as a Cis-Acting Regulator of EIF3H

Miguel Manzanares, Yussanne Ma, Richard S. Houlston, 2010, PLoS genetics.

Reliable high-throughput genotyping and loss-of-heterozygosity detection in formalin-fixed, paraffin-embedded tumors using single nucleotide polymorphism arrays.

Cisca Wijmenga, Jan Oosting, Paul H C Eilers, 2005, Cancer research.