N.G.J. Jaspers

2.0k total citations
26 papers, 1.6k citations indexed

About

N.G.J. Jaspers is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, N.G.J. Jaspers has authored 26 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 12 papers in Cancer Research and 8 papers in Genetics. Recurrent topics in N.G.J. Jaspers's work include DNA Repair Mechanisms (16 papers), Carcinogens and Genotoxicity Assessment (12 papers) and CRISPR and Genetic Engineering (5 papers). N.G.J. Jaspers is often cited by papers focused on DNA Repair Mechanisms (16 papers), Carcinogens and Genotoxicity Assessment (12 papers) and CRISPR and Genetic Engineering (5 papers). N.G.J. Jaspers collaborates with scholars based in Netherlands, United Kingdom and Japan. N.G.J. Jaspers's co-authors include D. Bootsma, Jan H.J. Hoeijmakers, Hanny Odijk, Jan de Wit, Anneke J. van Vuuren, Esther Appeldoorn, Magda Budzowska, Laura J. Niedernhofer, Ellen van Drunen and Roland Kanaar and has published in prestigious journals such as The EMBO Journal, Molecular and Cellular Biology and Brain.

In The Last Decade

N.G.J. Jaspers

26 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
N.G.J. Jaspers Netherlands 18 1.4k 544 294 199 123 26 1.6k
N.G.J. Jaspers Netherlands 15 1.4k 1.0× 487 0.9× 303 1.0× 197 1.0× 146 1.2× 21 1.6k
Maria Fousteri Greece 23 2.4k 1.6× 409 0.8× 348 1.2× 346 1.7× 161 1.3× 36 2.6k
S. Stevens United States 13 974 0.7× 552 1.0× 328 1.1× 78 0.4× 101 0.8× 16 1.4k
Enriqueta Riballo United Kingdom 11 1.7k 1.2× 539 1.0× 664 2.3× 102 0.5× 96 0.8× 14 1.9k
Elena Botta Italy 21 1.4k 1.0× 326 0.6× 153 0.5× 270 1.4× 58 0.5× 30 1.5k
Mitsuo Wakasugi Japan 17 1.5k 1.0× 297 0.5× 276 0.9× 158 0.8× 94 0.8× 31 1.6k
Floyd H. Thompson United States 20 654 0.5× 349 0.6× 360 1.2× 363 1.8× 86 0.7× 28 1.1k
Christine Troelstra Netherlands 14 1.8k 1.3× 369 0.7× 323 1.1× 349 1.8× 194 1.6× 15 2.0k
Valérie Bergoglio France 17 1.0k 0.7× 240 0.4× 272 0.9× 140 0.7× 59 0.5× 30 1.1k
Anastasia Gabriel Australia 7 757 0.5× 156 0.3× 374 1.3× 339 1.7× 66 0.5× 8 1.2k

Countries citing papers authored by N.G.J. Jaspers

Since Specialization
Citations

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

Fields of papers citing papers by N.G.J. Jaspers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by N.G.J. Jaspers. 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 N.G.J. Jaspers. The network helps show where N.G.J. Jaspers may publish in the future.

Co-authorship network of co-authors of N.G.J. Jaspers

This figure shows the co-authorship network connecting the top 25 collaborators of N.G.J. Jaspers. A scholar is included among the top collaborators of N.G.J. Jaspers 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 N.G.J. Jaspers. N.G.J. Jaspers 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.
Jaspers, N.G.J., et al.. (2025). Engineering bacterial cell morphology for the design of robust cell factories. Biochemistry and Biophysics Reports. 43. 102076–102076. 2 indexed citations
2.
Jaakkola, E., Aki Mustonen, Päivi Olsén, et al.. (2010). ERCC6 founder mutation identified in Finnish patients with COFS syndrome. Clinical Genetics. 78(6). 541–547. 17 indexed citations
3.
Rácz, Emöke, Errol P. Prens, Marius Kant, et al.. (2010). Narrowband ultraviolet B inhibits innate cytosolic double-stranded RNA receptors in psoriatic skin and keratinocytes. British Journal of Dermatology. 164(4). 838–847. 16 indexed citations
4.
Anttinen, Anu, Leena Koulu, Eeva Nikoskelainen, et al.. (2008). Neurological symptoms and natural course of xeroderma pigmentosum. Brain. 131(8). 1979–1989. 90 indexed citations
5.
Oh, Kyu‐Seon, Sikandar G. Khan, N.G.J. Jaspers, et al.. (2006). Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome. Human Mutation. 27(11). 1092–1103. 98 indexed citations
6.
Niedernhofer, Laura J., Hanny Odijk, Magda Budzowska, et al.. (2004). The Structure-Specific Endonuclease Ercc1-Xpf Is Required To Resolve DNA Interstrand Cross-Link-Induced Double-Strand Breaks. Molecular and Cellular Biology. 24(13). 5776–5787. 407 indexed citations
7.
Steensel, Maurice A. M. Van, N.G.J. Jaspers, & Peter M. Steijlen. (2001). A case of Rombo syndrome. British Journal of Dermatology. 144(6). 1215–1218. 28 indexed citations
8.
Jaspers, N.G.J.. (1997). DNA Repair: Genes, Enzymes, Patients, and Mouse Models. Recent results in cancer research. 143. 329–335. 1 indexed citations
9.
Vermeulen, Wim, Anneke J. van Vuuren, Laurent Schaeffer, et al.. (1994). Three Unusual Repair Deficiencies Associated with Transcription Factor BTF2(TFIIH): Evidence for the Existence of a Transcription Syndrome. Cold Spring Harbor Symposia on Quantitative Biology. 59(0). 317–329. 120 indexed citations
10.
Verhaegh, Gerald W., N.G.J. Jaspers, P.H.M. Lohman, & Małgorzata Z. Zdzienicka. (1993). Co-dominance of radioresistant DNA synthesis in a group of AT-like Chinese hamster cell mutants. Cytogenetic and Genome Research. 63(3). 176–180. 20 indexed citations
11.
Vuuren, Anneke J. van, Esther Appeldoorn, Hanny Odijk, et al.. (1993). Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.. The EMBO Journal. 12(9). 3693–3701. 154 indexed citations
12.
Roza, Len, Wim Vermeulen, André P. M. Eker, et al.. (1990). Effects of microinjected photoreactivating enzyme on thymine dimer removal and DNA repair synthesis in normal human and xeroderma pigmentosum fibroblasts.. PubMed. 50(6). 1905–10. 23 indexed citations
13.
Amiel, Aliza, et al.. (1989). Ataxia-telangiectasia: a variant with altered in vitro phenotype of fibroblast cells. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 210(2). 211–219. 19 indexed citations
14.
Zdzienicka, Małgorzata Z., N.G.J. Jaspers, G.P. van der Schans, A.T. Natarajan, & J.W.I.M. Simons. (1989). Ataxia-telangiectasia-like Chinese hamster V79 cell mutants with radioresistant DNA synthesis, chromosomal instability, and normal DNA strand break repair.. PubMed. 49(6). 1481–5. 49 indexed citations
15.
Wegner, R.‐D., Marc J. Metzger, F. Hanefeld, et al.. (1988). AT‐related disorder. Clinical Genetics. 33(1). 20–32. 56 indexed citations
16.
Lehmann, Alan R., N.G.J. Jaspers, & R A Gatti. (1987). Workshop on Ataxia Telangiectasia. Cancer Research. 47(17). 4750–4751. 5 indexed citations
17.
18.
Jaspers, N.G.J., et al.. (1981). The rate of DNA synthesis in normal human and ataxia telangiectasia cells after exposure to X-irradiation. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 80(1). 221–226. 97 indexed citations
19.
Keijzer, W., N.G.J. Jaspers, P. J. Abrahams, et al.. (1979). A seventh complementation group in excision-deficient xeroderma pigmentosum. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 62(1). 183–190. 137 indexed citations
20.
Halley, Dicky, W. Keijzer, N.G.J. Jaspers, et al.. (1979). Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair. Clinical Genetics. 16(3). 137–146. 34 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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