Publications by authors named "Sander Boymans"

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The genome-wide mutational consequences of DNA hypomethylation.
Nicolle Besselink, Janneke Keijer, Carlo Vermeulen, Sander Boymans, Jeroen de Ridder

Sci Rep· April 2023

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Precancerous liver diseases do not cause increased mutagenesis in liver stem cells.
Luan Nguyen, Myrthe Jager, Ruby Lieshout, Petra E de Ruiter, Mauro D Locati, Sander Boymans

Commun Biol· November 2021

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Reconstructing single-cell karyotype alterations in colorectal cancer identifies punctuated and gradual diversification patterns.
Yannik Bollen, Ellen Stelloo, Petra van Leenen, Myrna van den Bos, Bas Ponsioen, Sander Boymans

Nat Genet· August 2021

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Publisher Correction: The mutational impact of culturing human pluripotent and adult stem cells.
Ewart Kuijk, Myrthe Jager, Bastiaan van der Roest, Mauro D Locati, Arne Van Hoeck, Sander Boymans

Nat Commun· August 2020

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The mutational impact of culturing human pluripotent and adult stem cells.
Ewart Kuijk, Myrthe Jager, Bastiaan van der Roest, Mauro D Locati, Arne Van Hoeck, Sander Boymans

Nat Commun· May 2020

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Sperm DNA damage causes genomic instability in early embryonic development.
Sjors Middelkamp, Helena T A van Tol, Diana C J Spierings, Sander Boymans, Victor Guryev

Sci Adv· April 2020

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Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variants.
Sjors Middelkamp, Judith M Vlaar, Jacques Giltay, Jerome Korzelius, Nicolle Besselink, Sander Boymans

Genome Med· December 2019

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5-Fluorouracil treatment induces characteristic T>G mutations in human cancer.
Sharon Christensen, Bastiaan Van der Roest, Nicolle Besselink, Roel Janssen, Sander Boymans

Nat Commun· October 2019

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Deficiency of nucleotide excision repair is associated with mutational signature observed in cancer.
Myrthe Jager, Francis Blokzijl, Ewart Kuijk, Johanna Bertl, Maria Vougioukalaki, Sander Boymans

Genome Res· July 2019

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Early divergence of mutational processes in human fetal tissues.
Ewart Kuijk, Francis Blokzijl, Myrthe Jager, Nicolle Besselink, Sander Boymans

Sci Adv· May 2019

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Integrative Functional Annotation of 52 Genetic Loci Influencing Myocardial Mass Identifies Candidate Regulatory Variants and Target Genes.
Daiane Hemerich, Jiayi Pei, Magdalena Harakalova, Jessica van Setten, Sander Boymans

Circ Genom Precis Med· February 2019

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Measuring mutation accumulation in single human adult stem cells by whole-genome sequencing of organoid cultures.
Myrthe Jager, Francis Blokzijl, Valentina Sasselli, Sander Boymans, Roel Janssen

Nat Protoc· January 2018

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Tissue-specific mutation accumulation in human adult stem cells during life.
Francis Blokzijl, Joep de Ligt, Myrthe Jager, Valentina Sasselli, Sophie Roerink, Sander Boymans

Nature· October 2016

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Genomic landscape of rat strain and substrain variation.
Roel Hermsen, Joep de Ligt, Wim Spee, Francis Blokzijl, Sebastian Schäfer, Sander Boymans

BMC Genomics· May 2015

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Genomic and functional overlap between somatic and germline chromosomal rearrangements.
Sebastiaan van Heesch, Marieke Simonis, Markus J van Roosmalen, Vamsee Pillalamarri, Harrison Brand, Sander Boymans

Cell Rep· December 2014

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Extensive localization of long noncoding RNAs to the cytosol and mono- and polyribosomal complexes.
Sebastiaan van Heesch, Maarten van Iterson, Jetse Jacobi, Sander Boymans, Paul B Essers

Genome Biol· January 2014

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Fast selection of miRNA candidates based on large-scale pre-computed MFE sets of randomized sequences.
Sven Warris, Sander Boymans, Iwe Muiser, Michiel Noback, Wim Krijnen

BMC Res Notes· January 2014

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Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients.
Gerald Schwank, Bon-Kyoung Koo, Valentina Sasselli, Johanna F Dekkers, Inha Heo, Sander Boymans

Cell Stem Cell· December 2013

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