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Sandrine van Hees‐Stuivenberg

Observed names: Sandrine Stuivenberg, Sandrine Stuivenberg-van Hees, Sandrine van Hees, Sandrine van Hees-Stuivenberg, Sandrine van Hees-Stuivenberg
OpenAlex ID: A5007843296
Effect of nucleotide excision repair on hprt gene mutations in rodent cells exposed to DNA ethylating agents
1997 · Christel W.Op het Veld, Sandrine van Hees-Stuivenberg, et al. · Mutagenesis · 49
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A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants
2011 · Mark Drost, José B.M. Zonneveld, et al. · Human Mutation · 48
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Temporally distinct translesion synthesis pathways for ultraviolet light-induced photoproducts in the mammalian genome
2012 · Piya Temviriyanukul, Sandrine van Hees-Stuivenberg, et al. · DNA repair · 41
Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome
2020 · Mark Drost, Yvonne Tiersma, et al. · Genetics in Medicine · 27
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Stress response induced by DNA damage leads to specific, delayed and untargeted mutations
1992 · Jan J. B. Boesen, Sandrine Stuivenberg, et al. · Molecular and General Genetics MGG · 27
Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome
2013 · Mark Drost, Anne Lützen, et al. · Proceedings of the National Academy of Sciences · 22
Different Sets of Translesion Synthesis DNA Polymerases Protect From Genome Instability Induced by Distinct Food-Derived Genotoxins
2012 · Piya Temviriyanukul, Matty Meijers, et al. · Toxicological Sciences · 21
DNA mismatch repair mediates protection from mutagenesis induced by short-wave ultraviolet light
2006 · Viola Borgdorff, Bea Pauw, et al. · DNA repair · 21
Excision of translesion synthesis errors orchestrates responses to helix-distorting DNA lesions
2015 · Anastasia Tsaalbi-Shtylik, Cristina Ferrás, et al. · The Journal of Cell Biology · 19
Spontaneous and mutagen-induced loss of DNA mismatch repair in Msh2-heterozygous mammalian cells
2005 · Viola Borgdorff, Sandrine van Hees-Stuivenberg, et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 19
Enhanced UV-induced mutagenesis in the UV61 cell line, the Chinese hamster homologue of Cockayne's syndrome B, is associated with defective transcription coupled repair of cyclobutane pyrimidine dimers
1998 · Maaike P.G. Vreeswijk, Miep W.J.I. Overkamp, et al. · Mutation Research/DNA Repair · 16
Unexpected moves: a conformational change in MutSα enables high-affinity DNA mismatch binding
2023 · Susanne R Bruekner, Wietske Pieters, et al. · Nucleic Acids Research · 11
Predictive functional assay‐based classification of PMS2 variants in Lynch syndrome
2022 · Emily Rayner, Yvonne Tiersma, et al. · Human Mutation · 11
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Induction of mismatch repair deficiency, compromised DNA damage signaling and compound hypermutagenesis by a dietary mutagen in a cell-based model for Lynch syndrome
2021 · Robbert Ijsselsteijn, Sandrine van Hees, et al. · Carcinogenesis · 6
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Mechanisms and biomarkers of genotoxicity. Molecular dosimetry of chemical mutagens
1995 · Albert A. van Zeeland, Jacob G. Jansen, et al. · Toxicology Letters · 4
Clastogenesis by low densities of nucleotide lesions requires the completion of two cell cycles
2026 · Niels de Wind, Jacob G Jansen, et al. · Research Square
Functional assay-based classification of PMS2 variants in Lynch Syndrome
2021 · Emily Rayner, Yvonne Tiersma, et al.
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Works count: 17
Citation count: 342
H-index: 11
I10-index: 13
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