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Genome Medicine|December 6, 2019
Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variantsSjors Middelkamp, Judith M Vlaar, Jacques Giltay, et al.
Hemasphere|December 11, 2025
Posttransplantation clonal dynamics of hematopoietic stem cells carrying prenatal and early-life DNMT3A mutationsLucca L M Derks, Konradin F Müskens, Markus J van Roosmalen, et al.
Nature Communications|June 7, 2020
Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencingChristina Stangl, Sam de Blank, Ivo Renkens, et al.
Cancer Discovery|January 24, 2025
Prenatal Exposure to Chemotherapy Increases the Mutation Burden in Human Neonatal Hematopoietic Stem CellsIlana Struys, Carolina Velázquez, Joske Ubels, et al.
Nature Communications|March 29, 2024
Mitochondrial H2O2 release does not directly cause damage to chromosomal DNADaan M K van Soest, Paulien E Polderman, Wytze T F den Toom, et al.
Haematologica|April 9, 2026
UV-induced mutations accumulate during early clonal expansion in aneuploid subtypes of pediatric B-cell precursor acute lymphoblastic leukemiaLianne C Suurenbroek, Cédric G Van der Ham, Judith M Boer, et al.
Genome Biology|October 22, 2011
Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancerWigard P Kloosterman, Marlous Hoogstraat, Oscar Paling, et al.
Nature Communications|November 8, 2017
Mapping and phasing of structural variation in patient genomes using nanopore sequencingMircea Cretu Stancu, Markus J van Roosmalen, Ivo Renkens, et al.
Nature Communications|July 17, 2024
Selective pressures of platinum compounds shape the evolution of therapy-related myeloid neoplasmsEline J M Bertrums, Jurrian K de Kanter, Lucca L M Derks, et al.
Genome Medicine|January 28, 2017
Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cellsSjors Middelkamp, Sebastiaan van Heesch, A Koen Braat, et al.
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