Maarten van Lohuizen

25.4k total citations · 7 hit papers
143 papers, 20.4k citations indexed

About

Maarten van Lohuizen is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Maarten van Lohuizen has authored 143 papers receiving a total of 20.4k indexed citations (citations by other indexed papers that have themselves been cited), including 135 papers in Molecular Biology, 25 papers in Genetics and 20 papers in Oncology. Recurrent topics in Maarten van Lohuizen's work include Epigenetics and DNA Methylation (79 papers), Genomics and Chromatin Dynamics (42 papers) and Cancer-related gene regulation (32 papers). Maarten van Lohuizen is often cited by papers focused on Epigenetics and DNA Methylation (79 papers), Genomics and Chromatin Dynamics (42 papers) and Cancer-related gene regulation (32 papers). Maarten van Lohuizen collaborates with scholars based in Netherlands, United States and United Kingdom. Maarten van Lohuizen's co-authors include Jacqueline J.L. Jacobs, Anton Berns, Anke Sparmann, Anders H. Lund, Silvia Marino, Sophia W.M. Bruggeman, Ronald A. DePinho, Jan Willem Voncken, Ellen Wientjens and Ellen Tanger and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Maarten van Lohuizen

143 papers receiving 20.2k citations

Hit Papers

The oncogene and Polycomb... 1991 2026 2002 2014 1999 2006 1999 2010 1994 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maarten van Lohuizen Netherlands 73 17.4k 4.0k 2.6k 2.4k 1.4k 143 20.4k
John G. Doench United States 51 15.7k 0.9× 3.2k 0.8× 2.1k 0.8× 3.8k 1.6× 2.6k 1.9× 145 20.0k
Martin Eilers Germany 77 16.1k 0.9× 6.9k 1.7× 1.7k 0.7× 3.1k 1.3× 2.2k 1.6× 193 20.6k
Robert Benezra United States 63 14.6k 0.8× 5.2k 1.3× 1.7k 0.7× 3.8k 1.6× 1.9k 1.4× 118 19.3k
Peggy Farnham United States 77 17.5k 1.0× 3.6k 0.9× 3.7k 1.4× 4.7k 2.0× 1.8k 1.3× 184 21.1k
Peter Marynen Belgium 67 6.8k 0.4× 2.3k 0.6× 3.1k 1.2× 2.0k 0.9× 2.0k 1.5× 289 14.9k
David A. Largaespada United States 57 7.8k 0.4× 1.9k 0.5× 2.6k 1.0× 1.6k 0.7× 2.1k 1.5× 213 11.8k
Ad Geurts van Kessel Netherlands 63 8.0k 0.5× 2.0k 0.5× 4.8k 1.8× 1.9k 0.8× 1.2k 0.9× 256 15.6k
Thomas W. Glover United States 60 10.3k 0.6× 3.6k 0.9× 4.5k 1.7× 1.8k 0.8× 352 0.3× 159 15.8k
Frank Speleman Belgium 60 7.9k 0.5× 2.2k 0.6× 2.1k 0.8× 4.6k 1.9× 732 0.5× 285 12.9k
Toru Nakano Japan 68 12.9k 0.7× 1.8k 0.4× 2.7k 1.0× 1.8k 0.8× 4.6k 3.3× 208 18.9k

Countries citing papers authored by Maarten van Lohuizen

Since Specialization
Citations

This map shows the geographic impact of Maarten van Lohuizen'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 Maarten van Lohuizen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maarten van Lohuizen more than expected).

Fields of papers citing papers by Maarten van Lohuizen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maarten van Lohuizen. 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 Maarten van Lohuizen. The network helps show where Maarten van Lohuizen may publish in the future.

Co-authorship network of co-authors of Maarten van Lohuizen

This figure shows the co-authorship network connecting the top 25 collaborators of Maarten van Lohuizen. A scholar is included among the top collaborators of Maarten van Lohuizen 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 Maarten van Lohuizen. Maarten van Lohuizen 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.
Hulsman, Danielle, et al.. (2024). Combination of EZH2 and ATM inhibition in BAP1-deficient mesothelioma. British Journal of Cancer. 130(11). 1855–1865. 6 indexed citations
2.
Badhai, Jitendra, Gaurav Kumar Pandey, Ji‐Ying Song, et al.. (2023). Combined Inhibition of EZH2 and FGFR is Synergistic in BAP1-deficient Malignant Mesothelioma. Cancer Research Communications. 4(1). 18–27. 5 indexed citations
3.
Berk, Paul van den, Cesare Lancini, Michela Serresi, et al.. (2020). USP15 Deubiquitinase Safeguards Hematopoiesis and Genome Integrity in Hematopoietic Stem Cells and Leukemia Cells. Cell Reports. 33(13). 108533–108533. 17 indexed citations
4.
Kato, Yuko, Satoru Miyagi, Eriko Nitta, et al.. (2019). Bmi1 restricts the adipogenic differentiation of bone marrow stromal cells to maintain the integrity of the hematopoietic stem cell niche. Experimental Hematology. 76. 24–37. 9 indexed citations
5.
Koppens, Martijn, Ellen Tanger, Karim Nacerddine, et al.. (2016). A new transgenic mouse model for conditional overexpression of the Polycomb Group protein EZH2. Transgenic Research. 26(2). 187–196. 7 indexed citations
6.
Koppens, Martijn, Gergana Bounova, Paulien Cornelissen‐Steijger, et al.. (2016). Large variety in a panel of human colon cancer organoids in response to EZH2 inhibition. Oncotarget. 7(43). 69816–69828. 21 indexed citations
7.
Pósfai, Eszter, Vincent Brochard, Juliette Salvaing, et al.. (2012). Polycomb function during oogenesis is required for mouse embryonic development. Genes & Development. 26(9). 920–932. 107 indexed citations
8.
Smith, Lan‐Lan, Jenny Yeung, Bernd B. Zeisig, et al.. (2011). Functional Crosstalk between Bmi1 and MLL/Hoxa9 Axis in Establishment of Normal Hematopoietic and Leukemic Stem Cells. Cell stem cell. 8(6). 649–662. 89 indexed citations
9.
Vries, Nienke A. de, Sophia W.M. Bruggeman, Danielle Hulsman, et al.. (2010). Rapid and Robust Transgenic High-Grade Glioma Mouse Models for Therapy Intervention Studies. Clinical Cancer Research. 16(13). 3431–3441. 40 indexed citations
10.
Kool, Jaap, Anthony G. Uren, Jeroen de Ridder, et al.. (2010). Novel Candidate Cancer Genes Identified by a Large-Scale Cross-Species Comparative Oncogenomics Approach. Cancer Research. 70(3). 883–895. 34 indexed citations
11.
Kool, Jaap, Anthony G. Uren, Daoud Sie, et al.. (2010). Insertional Mutagenesis in Mice Deficient for p15Ink4b, p16Ink4a, p21Cip1 , and p27Kip1 Reveals Cancer Gene Interactions and Correlations with Tumor Phenotypes. Cancer Research. 70(2). 520–531. 25 indexed citations
12.
Uren, Anthony G., Harald Mikkers, Jaap Kool, et al.. (2009). A high-throughput splinkerette-PCR method for the isolation and sequencing of retroviral insertion sites. Nature Protocols. 4(5). 789–798. 129 indexed citations
13.
Miyazaki, Masaki, Kazuko Miyazaki, Manami Itoi, et al.. (2008). Thymocyte Proliferation Induced by Pre-T Cell Receptor Signaling Is Maintained through Polycomb Gene Product Bmi-1-Mediated Cdkn2a Repression. Immunity. 28(2). 231–245. 55 indexed citations
14.
Crippa, Sylvain V., Ellen Tanger, Daniel F. Schorderet, et al.. (2007). Bmi1 Loss Delays Photoreceptor Degeneration in Rd1 Mice. Advances in experimental medicine and biology. 572. 209–215. 3 indexed citations
15.
Hosokawa, Hiroyuki, Motoko Y. Kimura, Ryo Shinnakasu, et al.. (2006). Regulation of Th2 Cell Development by Polycomb Group Gene bmi-1 through the Stabilization of GATA3. The Journal of Immunology. 177(11). 7656–7664. 47 indexed citations
16.
Bruggeman, Sophia W.M., Jacqueline J.L. Jacobs, Ellen Tanger, et al.. (2005). Ink4a and Arf differentially affect cell proliferation and neural stem cell self-renewal in Bmi1-deficient mice. Genes & Development. 19(12). 1438–1443. 260 indexed citations
17.
Smith, Kevin S., Sumit K. Chanda, Douglas T. Ross, et al.. (2003). Bmi-1 Regulation of INK4A-ARF Is a Downstream Requirement for Transformation of Hematopoietic Progenitors by E2a-Pbx1. Molecular Cell. 12(2). 393–400. 75 indexed citations
18.
Jacobs, Jacqueline J.L. & Maarten van Lohuizen. (2002). Polycomb repression: from cellular memory to cellular proliferation and cancer. Biochimica et Biophysica Acta (BBA) - Reviews on Cancer. 1602(2). 151–161. 178 indexed citations
19.
Itahana, Koji, Ying Zou, Yoko Itahana, et al.. (2002). Control of the Replicative Life Span of Human Fibroblasts by p16 and the Polycomb Protein Bmi-1. Molecular and Cellular Biology. 23(1). 389–401. 340 indexed citations
20.
Nusse, Roel, et al.. (1985). Retroviral insertional mutagenesis in murine mammary cancer. Proceedings of the Royal Society of London. Series B, Biological sciences. 226(1242). 3–13. 14 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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