Jûrgen Steltenpool

2.5k total citations
12 papers, 1.7k citations indexed

About

Jûrgen Steltenpool is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Jûrgen Steltenpool has authored 12 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 4 papers in Cancer Research and 2 papers in Genetics. Recurrent topics in Jûrgen Steltenpool's work include DNA Repair Mechanisms (12 papers), Carcinogens and Genotoxicity Assessment (4 papers) and CRISPR and Genetic Engineering (4 papers). Jûrgen Steltenpool is often cited by papers focused on DNA Repair Mechanisms (12 papers), Carcinogens and Genotoxicity Assessment (4 papers) and CRISPR and Genetic Engineering (4 papers). Jûrgen Steltenpool collaborates with scholars based in Netherlands, United Kingdom and United States. Jûrgen Steltenpool's co-authors include Johan P. de Winter, Hans Joenje, Martin A. Rooimans, Christopher G. Mathew, Quinten Waisfisz, Fré Arwert, Anneke B. Oostra, Maureen E. Hoatlin, Marieke Levitus and Amom Ruhikanta Meetei and has published in prestigious journals such as Nature Genetics, Blood and PLoS ONE.

In The Last Decade

Jûrgen Steltenpool

12 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jûrgen Steltenpool Netherlands 11 1.7k 508 432 214 193 12 1.7k
Annette L. Medhurst United States 15 1.7k 1.0× 557 1.1× 353 0.8× 197 0.9× 253 1.3× 15 1.8k
Reinhard Kalb Germany 16 1.9k 1.1× 451 0.9× 527 1.2× 163 0.8× 125 0.6× 25 2.1k
Christine Troelstra Netherlands 14 1.8k 1.1× 369 0.7× 349 0.8× 194 0.9× 101 0.5× 15 2.0k
Mark A. Brenneman United States 18 1.6k 1.0× 339 0.7× 223 0.5× 195 0.9× 103 0.5× 22 1.7k
Kelly M. Trujillo United States 15 1.9k 1.2× 381 0.8× 214 0.5× 200 0.9× 173 0.9× 19 2.0k
David Ciccone United States 10 1.9k 1.1× 329 0.6× 297 0.7× 161 0.8× 104 0.5× 20 2.1k
Marina A. Bellani United States 18 1.3k 0.8× 225 0.4× 194 0.4× 172 0.8× 128 0.7× 30 1.4k
Joel E. Straughen United States 6 1.2k 0.7× 322 0.6× 238 0.6× 227 1.1× 88 0.5× 9 1.4k
Wojciech Niedźwiedź United Kingdom 21 1.9k 1.1× 422 0.8× 257 0.6× 166 0.8× 334 1.7× 35 2.0k
Magda Budzowska Netherlands 11 1.7k 1.0× 401 0.8× 176 0.4× 164 0.8× 268 1.4× 12 1.8k

Countries citing papers authored by Jûrgen Steltenpool

Since Specialization
Citations

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

Fields of papers citing papers by Jûrgen Steltenpool

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jûrgen Steltenpool. 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 Jûrgen Steltenpool. The network helps show where Jûrgen Steltenpool may publish in the future.

Co-authorship network of co-authors of Jûrgen Steltenpool

This figure shows the co-authorship network connecting the top 25 collaborators of Jûrgen Steltenpool. A scholar is included among the top collaborators of Jûrgen Steltenpool 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 Jûrgen Steltenpool. Jûrgen Steltenpool is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Stoepker, Chantal, Beatrice Schuster, Yvonne Hilhorst‐Hofstee, et al.. (2011). SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype. Nature Genetics. 43(2). 138–141. 233 indexed citations
2.
Singh, Thiyam Ramsing, Sietske T. Bakker, Sheba Agarwal, et al.. (2009). Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M. Blood. 114(1). 174–180. 100 indexed citations
3.
Bakker, Sietske T., Henri J. van de Vrugt, Martin A. Rooimans, et al.. (2009). Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M. Human Molecular Genetics. 18(18). 3484–3495. 108 indexed citations
4.
Lelij, Petra van der, Barbara C. Godthelp, Wouter van Zon, et al.. (2009). The Cellular Phenotype of Roberts Syndrome Fibroblasts as Revealed by Ectopic Expression of ESCO2. PLoS ONE. 4(9). e6936–e6936. 59 indexed citations
5.
Dorsman, Josephine C., Marieke Levitus, Davy Rockx, et al.. (2007). Identification of the Fanconi Anemia Complementation Group I Gene, FANCI. Analytical Cellular Pathology. 29(3). 211–218. 101 indexed citations
6.
Léveillé, France, Miriam Ferrer, Annette L. Medhurst, et al.. (2006). The nuclear accumulation of the Fanconi anemia protein FANCE depends on FANCC. DNA repair. 5(5). 556–565. 20 indexed citations
7.
Medhurst, Annette L., El Houari Laghmani, Jûrgen Steltenpool, et al.. (2006). Evidence for subcomplexes in the Fanconi anemia pathway. Blood. 108(6). 2072–2080. 75 indexed citations
8.
Levitus, Marieke, Quinten Waisfisz, Barbara C. Godthelp, et al.. (2005). The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J. Nature Genetics. 37(9). 934–935. 338 indexed citations
9.
Meetei, Amom Ruhikanta, Annette L. Medhurst, Ling Chen, et al.. (2005). A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M. Nature Genetics. 37(9). 958–963. 351 indexed citations
10.
Levitus, Marieke, Martin A. Rooimans, Jûrgen Steltenpool, et al.. (2003). Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes. Blood. 103(7). 2498–2503. 177 indexed citations
11.
Winter, Johan P. de, France Léveillé, Carola G.M. van Berkel, et al.. (2000). Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene. The American Journal of Human Genetics. 67(5). 1306–1308. 175 indexed citations
12.
Winter, Johan P. de, Carola G.M. van Berkel, Martin A. Rooimans, et al.. (2000). Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene. The American Journal of Human Genetics. 67(5). 1306–1308. 9 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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