Tibor van Welsem

2.3k total citations
34 papers, 1.7k citations indexed

About

Tibor van Welsem is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Tibor van Welsem has authored 34 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Epidemiology. Recurrent topics in Tibor van Welsem's work include Epigenetics and DNA Methylation (16 papers), Genomics and Chromatin Dynamics (15 papers) and Cancer-related gene regulation (9 papers). Tibor van Welsem is often cited by papers focused on Epigenetics and DNA Methylation (16 papers), Genomics and Chromatin Dynamics (15 papers) and Cancer-related gene regulation (9 papers). Tibor van Welsem collaborates with scholars based in Netherlands, United States and United Kingdom. Tibor van Welsem's co-authors include Fred van Leeuwen, Petra M. Nederlof, Laura J. van’t Veer, Kitty F. Verzijlbergen, Lodewyk F.A. Wessels, Floor Frederiks, George Q. Daley, Els C. Robanus-Maandag, Petra Kristel and Maarten van Lohuizen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Tibor van Welsem

33 papers receiving 1.6k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Tibor van Welsem Netherlands 19 1.4k 431 236 220 128 34 1.7k
Ondřej Gojiš United Kingdom 11 1.2k 0.9× 296 0.7× 279 1.2× 298 1.4× 112 0.9× 18 1.6k
Céline Vallot France 19 1.3k 0.9× 334 0.8× 267 1.1× 494 2.2× 71 0.6× 35 1.7k
Mark A. Brenneman United States 18 1.6k 1.2× 223 0.5× 389 1.6× 339 1.5× 195 1.5× 22 1.7k
José F. Ruiz Spain 17 1.0k 0.7× 158 0.4× 171 0.7× 377 1.7× 108 0.8× 29 1.4k
Sabrina A. Stratton United States 21 1.7k 1.3× 200 0.5× 354 1.5× 350 1.6× 109 0.9× 23 1.9k
Dan Hasson United States 20 1.4k 1.0× 247 0.6× 176 0.7× 184 0.8× 404 3.2× 38 1.6k
Beatrice Rondinelli United States 6 1.5k 1.1× 214 0.5× 585 2.5× 202 0.9× 147 1.1× 6 1.6k
Peyton Greenside United States 11 1.3k 1.0× 208 0.5× 238 1.0× 312 1.4× 83 0.6× 13 1.6k
Josée Guirouilh‐Barbat France 24 1.5k 1.1× 158 0.4× 534 2.3× 269 1.2× 167 1.3× 40 1.7k

Countries citing papers authored by Tibor van Welsem

Since Specialization
Citations

This map shows the geographic impact of Tibor van Welsem's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Tibor van Welsem with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tibor van Welsem more than expected).

Fields of papers citing papers by Tibor van Welsem

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tibor van Welsem. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Tibor van Welsem. The network helps show where Tibor van Welsem may publish in the future.

Co-authorship network of co-authors of Tibor van Welsem

This figure shows the co-authorship network connecting the top 25 collaborators of Tibor van Welsem. A scholar is included among the top collaborators of Tibor van Welsem based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Tibor van Welsem. Tibor van Welsem is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Aslam, Muhammad Assad, Teun van den Brand, Bram van den Broek, et al.. (2025). Histone methyltransferase DOT1L maintains cell state and restricts cytotoxic potential of CD8 T cells. Science Advances. 11(50). eadw1289–eadw1289.
2.
Kruijsbergen, Ila van, Chitvan Mittal, Cor Lieftink, et al.. (2023). Locus-specific proteome decoding reveals Fpt1 as a chromatin-associated negative regulator of RNA polymerase III assembly. Molecular Cell. 83(23). 4205–4221.e9. 4 indexed citations
3.
Silva, Joana, Ning Qing Liu, Judith H.I. Haarhuis, et al.. (2022). The histone methyltransferase SETD2 negatively regulates cell size. Journal of Cell Science. 135(19). 2 indexed citations
4.
Welsem, Tibor van, Remco van Doorn, Maarten H. Vermeer, et al.. (2022). DOT1L inhibition does not modify the sensitivity of cutaneous T cell lymphoma to pan-HDAC inhibitors in vitro. Frontiers in Genetics. 13. 1032958–1032958. 2 indexed citations
5.
Aslam, Muhammad Assad, Mir Farshid Alemdehy, Teun van den Brand, et al.. (2020). The histone methyltransferase DOT1L prevents antigen-independent differentiation and safeguards epigenetic identity of CD8 + T cells. Proceedings of the National Academy of Sciences. 117(34). 20706–20716. 32 indexed citations
6.
Cucinotta, Christine E., Ila van Kruijsbergen, Tibor van Welsem, et al.. (2020). Inhibition of transcription leads to rewiring of locus-specific chromatin proteomes. Genome Research. 30(4). 635–646. 7 indexed citations
7.
Kruijsbergen, Ila van, Monique P. C. Mulder, Michael Uckelmann, et al.. (2020). Strategy for Development of Site-Specific Ubiquitin Antibodies. Frontiers in Chemistry. 8. 111–111. 9 indexed citations
8.
Welsem, Tibor van, Reggy Ekkebus, Su Ming Sun, et al.. (2018). Dot1 promotes H2B ubiquitination by a methyltransferase-independent mechanism. Nucleic Acids Research. 46(21). 11251–11261. 26 indexed citations
9.
Kruijsbergen, Ila van, et al.. (2018). Decoding the chromatin proteome of a single genomic locus by DNA sequencing. PLoS Biology. 16(7). e2005542–e2005542. 12 indexed citations
10.
Huseinovic, Angelina, Jolanda van Leeuwen, Tibor van Welsem, et al.. (2017). The effect of acetaminophen on ubiquitin homeostasis in Saccharomyces cerevisiae. PLoS ONE. 12(3). e0173573–e0173573. 6 indexed citations
11.
Stulemeijer, I.J.E., Dirk De Vos, Onkar Joshi, et al.. (2015). Dot1 histone methyltransferases share a distributive mechanism but have highly diverged catalytic properties. Scientific Reports. 5(1). 9824–9824. 15 indexed citations
12.
Vlaming, Hanneke, Tibor van Welsem, Erik L. de Graaf, et al.. (2014). Flexibility in crosstalk between H2B ubiquitination and H3 methylation in vivo. EMBO Reports. 15(11). 1220–1221. 4 indexed citations
13.
Vlaming, Hanneke, Tibor van Welsem, Erik L. de Graaf, et al.. (2014). Flexibility in crosstalk between H2B ubiquitination and H3 methylation in vivo. EMBO Reports. 15(10). 1077–1084. 33 indexed citations
14.
Bemmel, Joke G. van, Guillaume J. Filion, Wendy Talhout, et al.. (2013). A Network Model of the Molecular Organization of Chromatin in Drosophila. Molecular Cell. 49(4). 759–771. 43 indexed citations
15.
Srivas, Rohith, Thomas Costelloe, Anne‐Ruxandra Carvunis, et al.. (2013). A UV-Induced Genetic Network Links the RSC Complex to Nucleotide Excision Repair and Shows Dose-Dependent Rewiring. Cell Reports. 5(6). 1714–1724. 18 indexed citations
16.
Radman‐Livaja, Marta, Lourdes Valenzuela, Jennifer A. Armstrong, et al.. (2012). A Key Role for Chd1 in Histone H3 Dynamics at the 3′ Ends of Long Genes in Yeast. PLoS Genetics. 8(7). e1002811–e1002811. 52 indexed citations
17.
Verzijlbergen, Kitty F., Tibor van Welsem, Daoud Sie, et al.. (2011). A Barcode Screen for Epigenetic Regulators Reveals a Role for the NuB4/HAT-B Histone Acetyltransferase Complex in Histone Turnover. PLoS Genetics. 7(10). e1002284–e1002284. 22 indexed citations
18.
Stulemeijer, I.J.E., Brietta L. Pike, Alex W. Faber, et al.. (2011). Dot1 binding induces chromatin rearrangements by histone methylation-dependent and -independent mechanisms. Epigenetics & Chromatin. 4(1). 2–2. 26 indexed citations
19.
Welsem, Tibor van, Floor Frederiks, Kitty F. Verzijlbergen, et al.. (2008). Synthetic Lethal Screens Identify Gene Silencing Processes in Yeast and Implicate the Acetylated Amino Terminus of Sir3 in Recognition of the Nucleosome Core. Molecular and Cellular Biology. 28(11). 3861–3872. 49 indexed citations
20.
Jacobs, Jacqueline J.L., Els C. Robanus-Maandag, Petra Kristel, et al.. (2000). Senescence bypass screen identifies TBX2, which represses Cdkn2a (p19ARF) and is amplified in a subset of human breast cancers. Nature Genetics. 26(3). 291–299. 318 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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