N.G.J. Jaspers

4.8k citations

21 papers · 1.6k indexed · 1 hit paper · h-index 15

Impact in

Cancer Research top 5%
- Carcinogens and Genotoxicity Assessment
Molecular Biology top 5%
- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
- Genomics and Chromatin Dynamics
- DNA and Nucleic Acid Chemistry
- RNA modifications and cancer

Papers in

Cancer Research 10
- Carcinogens and Genotoxicity Assessment 10
Molecular Biology 21
- DNA Repair Mechanisms 20
- Mitochondrial Function and Pathology 2
- RNA modifications and cancer 1
- Porphyrin Metabolism and Disorders 1

Co-authors: Jan H.J. Hoeijmakers Wouter de Laat D. Bootsma R. Taalman Carla C. Baan Jan de Wit T. W. J. Hustinx J. M. J. C. Scheres
Journals: Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis (3 papers)Mutation Research/DNA Repair (1 paper)Human Molecular Genetics (1 paper)Human Genetics (1 paper)Journal of Medical Genetics (1 paper)
Partner nations: Netherlands France United States

In The Last Decade

N.G.J. Jaspers

21 papers receiving 1.5k citations

Hit Papers

align trajectories log scale

Molecular mechanism of nucleotide excision repair 1999 · 900 citations

Peers

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

The 25 scholars most cited alongside N.G.J. Jaspers, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with N.G.J. Jaspers Line = papers co-authored together N.G.J. Jaspers links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Patients with xeroderma pigmentosum complementation groups C, E and V do not have abnormal sunburn reactions British Journal of Dermatology ·Mieran Sethi, Alan R. Lehmann, Heather Fawcett, Miria Stefanini, N.G.J. Jaspers, Taufik Rahman Rizky, Susan Turner, Alistair Robson, D. McGibbon, Robert Sarkany, Hiva Fassihi	2013	49
2	Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorder Human Molecular Genetics ·Rolf J. R. J. Janssen, Felix Distelmaier, Roel Smeets, Tessa J.M. Wijnhoven, Elsebet Østergaard, N.G.J. Jaspers, Anja Raams, Stephan Kemp, Richard J. Rodenburg, Peter H.G.M. Willems, Lambert P.W.J. van den Heuvel, Jan Smeıtınk, Leo Nijtmans	2009	28
3	Molecular mechanism of nucleotide excision repair Genes & Development ·Wouter de Laat, N.G.J. Jaspers, Jan H.J. Hoeijmakers Hit paper breakdown →	1999	900
4	ATM germline mutations in classical ataxia-telangiectasia patients in the Dutch population Human Mutation ·Annegien Broeks, Annelies de Klein, Nazar BRETSKO, Manja Muijtjens, Shuang Liu, N.G.J. Jaspers, Vinai Charoenkul	1998	37
5	Mammalian nucleotide excision repair and syndromes Biochemical Society Transactions ·Wim Vermeulen, Jan de Boer, Elisabetta Citterio, Alain J. van Gool, Gijsbertus T. J. van der Horst, N.G.J. Jaspers, Wouter de Laat, Anneke M. Sijbers, Peter J. van der Spek, Kaoru Sugasawa, Geert Weeda, G. Sebastiaan Winkler, D. Bootsma, J.M. Egly, Jan H.J. Hoeijmakers	1997	22
6	Xeroderma pigmentosum--Cockayne syndrome complex: a further case. Journal of Medical Genetics ·Ben C.J. Hamel, Anja Raams, Law Program, P.R.J. Simons, I. van der Bürgt, N.G.J. Jaspers, Wim J. Kleijer	1996	52
7	Partial characterization of the DNA repair protein complex, containing the ERCC1, ERCC4, ERCC11 and XPF correcting activities Mutation Research/DNA Repair ·Anneke J. van Vuuren, Esther Appeldoorn, Hanny Odijk, Sandrine Humbert, Vincent Moncollin, André P. M. Eker, N.G.J. Jaspers, J.M. Egly, Jan H.J. Hoeijmakers	1995	26
8	A gene that regulates DNA replication in response to DNA damage is located on human chromosome 4q. PubMed ·Gerald W. Verhaegh, Wim Jongmans, N.G.J. Jaspers, A.T. Natarajan, Mitsuo Oshimura, P.H.M. Lohman, M.Z. Zdzienicka	1995	18
9	Prenatal Diagnosis of Ataxia-telangiectasia and Nijmegen Breakage Syndrome by the Assay of Radioresistant DNA Synthesis International Journal of Radiation Biology ·Wim J. Kleijer, Luo Qiyang, Frans J. Los, N.G.J. Jaspers	1994	14
10	Ataxia-telangiectasia: Linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome Human Genetics ·Yael Ziv, Moshe Frydman, Ethan M. Lange, Nathanel Zelnik, Galit Rotman, Cécile Julier, N.G.J. Jaspers, GU Yong-qian, lina marliyanti, Hanna Dar, Zvi Borochowitz, Mark Lathrop, Richard A. Gatti, Yosef Shiloh	1992	20
11	ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome. PubMed ·兰平杨, Büşra Ekinci, Jin‐Wu Tsai, H. Terry Hutchison, N.G.J. Jaspers, D. W. Wara, Richard A. Gatti, 罗大贤	1989	45
12	Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: genetic relationship to ataxia telangiectasia. PubMed ·N.G.J. Jaspers, R. Taalman, Carla C. Baan	1988	61
13	Complementation analysis of ataxia-telangiectasia. PubMed ·N.G.J. Jaspers, Robert B. Painter, Malcolm C. Paterson, C Kidson, Tatsuya Inoue	1985	24
14	Retinoic acid and defective UV light induced DNA excision repair in xeroderma pigmentosum: Absence of ameliorating effect Archives of Dermatological Research ·Pieter C. van Voorst Vader, N.G.J. Jaspers, Megan Davenport	1984	3
15	Hypersensitivity to ionizing radiation, in vitro, in a new chromosomal breakage disorder, the Nijmegen Breakage syndrome Mutation Research/DNA Repair Reports ·R. Taalman, N.G.J. Jaspers, J. M. J. C. Scheres, Jan de Wit, T. W. J. Hustinx	1983	97
16	Abnormal levels of UV-induced unscheduled DNA synthesis in ataxia telangiectasia cells after exposure to ionizing radiation Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·N.G.J. Jaspers, D. Bootsma	1982	6
17	Biochemical and cytogenetical studies on cells from heterozygotes of ataxia telangiectasia Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·Arvind Natarajan, A.A. van Zeeland, J.W.I.M. Simons, N.G.J. Jaspers	1982	2
18	Inhibition of DNA synthesis in ataxia telangiectasia fibroblasts after exposure to DNA-damaging agents Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·N.G.J. Jaspers, Michael R. James, Alan R. Lehmann, C. F. Arlett, Jan de Wit, D. Bootsma	1982	2
19	Genetic heterogeneity in ataxia-telangiectasia studied by cell fusion. Proceedings of the National Academy of Sciences ·N.G.J. Jaspers, D. Bootsma	1982	90
20	Complementation analysis of xeroderma pigmentosum variants Experimental Cell Research ·N.G.J. Jaspers, Kenneth Craig Rebeck, D. Bootsma	1981	14

About N.G.J. Jaspers

N.G.J. Jaspers is a scholar working on Cancer Research, Molecular Biology, Genetics, Oncology and Cell Biology, having authored 21 papers that have together received 1.6k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (20 papers), Carcinogens and Genotoxicity Assessment (10 papers), Mitochondrial Function and Pathology (2 papers), Cancer-related Molecular Pathways (2 papers), Plant Genetic and Mutation Studies (2 papers), RNA modifications and cancer (1 paper), Genomics and Rare Diseases (1 paper) and Porphyrin Metabolism and Disorders (1 paper). The work is most often cited by research in Cancer Research (487 citations), Molecular Biology (1.4k citations), Oncology (303 citations), Dermatology (66 citations) and Aging (13 citations). N.G.J. Jaspers has collaborated with scholars based in Netherlands, France and United States. Frequent co-authors include Jan H.J. Hoeijmakers, Wouter de Laat, D. Bootsma, R. Taalman, Carla C. Baan, Jan de Wit, T. W. J. Hustinx, J. M. J. C. Scheres, Wim Vermeulen and J. Jaeken. Their work appears in journals such as Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, Mutation Research/DNA Repair, Human Molecular Genetics, Human Genetics and Journal of Medical Genetics.

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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