N.G.J. Jaspers

2.0k citations
26 papers · 1.6k · h-index 18

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
    • Cancer therapeutics and mechanisms
    • RNA modifications and cancer

Papers in

  • Molecular Biology 23
    • DNA Repair Mechanisms 16
    • CRISPR and Genetic Engineering 5
    • Prion Diseases and Protein Misfolding 2
    • Viral Infectious Diseases and Gene Expression in Insects 2
  • Cancer Research 12
    • Carcinogens and Genotoxicity Assessment 12
Co-authors
D. Bootsma (7 shared papers)Jan H.J. Hoeijmakers (5 shared papers)Hanny Odijk (2 shared papers)Jan de Wit (2 shared papers)Anneke J. van Vuuren (3 shared papers)Esther Appeldoorn (3 shared papers)Roland Kanaar (1 shared paper)Ellen van Drunen (1 shared paper)
Journals
Clinical Genetics (3 papers)British Journal of Dermatology (2 papers)The EMBO Journal (2 papers)International Journal of Radiation Biology (2 papers)Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis (2 papers)
Partner nations
NetherlandsUnited KingdomJapan

In The Last Decade

N.G.J. Jaspers

26 papers receiving 1.6k citations

Peers

N.G.J. Jaspers
Comparison fields: 5 of 88
  • Cancer Research 544
  • Molecular Biology 1.4k
  • Oncology 294
  • Aging 18
  • Genetics 199
Replace N.G.J. Jaspers with:
N.G.J. Jaspers Netherlands
Elena Botta Italy
Christine Troelstra Netherlands
Mitsuo Wakasugi Japan
Maria Fousteri Greece
S. Stevens United States
Claire Attwooll United States
Thomas Trimarchi United States
Elisabetta Citterio Netherlands
Euan M. Slorach United States
N.G.J. Jaspers relative to N.G.J. Jaspers Netherlands N.G.J. Jaspers's profile →
Citations per field
00.5×1.5×
N.G.J. Jaspers · 1×
Citations per year

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-authors

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

20 of 20 papers shown

Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.

#Work
1
The Structure-Specific Endonuclease Ercc1-Xpf Is Required To Resolve DNA Interstrand Cross-Link-Induced Double-Strand Breaks
Molecular and Cellular Biology ·Laura J. Niedernhofer, Hanny Odijk, Magda Budzowska, Ellen van Drunen, Alex Maas, Arjan F. Theil, Jan de Wit, N.G.J. Jaspers, H. Berna Beverloo, Jan H.J. Hoeijmakers, Roland Kanaar
2004407
2
Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.
The EMBO Journal ·Anneke J. van Vuuren, Esther Appeldoorn, Hanny Odijk, Akira Yasui, N.G.J. Jaspers, D. Bootsma, Jan H.J. Hoeijmakers
1993154
3
A seventh complementation group in excision-deficient xeroderma pigmentosum
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·W. Keijzer, N.G.J. Jaspers, P. J. Abrahams, A. M. R. Taylor, C.F. Arlett, B. Zelle, Hiraku Takebe, P.D.S. Kinmont, D. Bootsma
1979137
4
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 ·Wim Vermeulen, Anneke J. van Vuuren, M. Chipoulet, Laurent Schaeffer, Esther Appeldoorn, Geert Weeda, N.G.J. Jaspers, A. Priestley, C.F. Arlett, Alan R. Lehmann, Miria Stefanini, M. Mezzina, A. Sarasin, D. Bootsma, J.M. Egly, Jan H.J. Hoeijmakers
1994120
5
Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome
Human Mutation ·Kyu‐Seon Oh, Sikandar G. Khan, N.G.J. Jaspers, Anja Raams, Takahiro Ueda, Alan R. Lehmann, Peter S. Friedmann, Steffen Emmert, Alexei Gratchev, Katherine Lachlan, Anneke Lucassan, Carl C. Baker, Kenneth H. Kraemer
200698
6
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 ·J. de Witt, N.G.J. Jaspers, D. Bootsma
198197
7
Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH).
The EMBO Journal ·Anneke J. van Vuuren, Wim Vermeulen, Lanping Ma, Geert Weeda, Esther Appeldoorn, N.G.J. Jaspers, A.J. van der Eb, D. Bootsma, Jan H.J. Hoeijmakers, Sandrine Humbert
199497
8
Neurological symptoms and natural course of xeroderma pigmentosum
Brain ·Anu Anttinen, Leena Koulu, Eeva Nikoskelainen, Raija Portin, Timo Kurki, M. Erkinjuntti, N.G.J. Jaspers, Anja Raams, Michael H.L. Green, Alan R. Lehmann, Jonathan Wing, C.F. Arlett, R. J. Marttila
200890
9
Abnormal regulation of DNA replication and increased lethality in ataxia telangiectasia cells exposed to carcinogenic agents.
PubMed ·N.G.J. Jaspers, Jan de Wit, Michael Regulski, D. Bootsma
198270
10
AT‐related disorder
Clinical Genetics ·R.‐D. Wegner, Marc J. Metzger, F. Hanefeld, N.G.J. Jaspers, Carla C. Baan, K. Magdorf, J. Kunze, Karl Sperling
198856
11
Ataxia-telangiectasia-like Chinese hamster V79 cell mutants with radioresistant DNA synthesis, chromosomal instability, and normal DNA strand break repair.
PubMed ·Małgorzata Z. Zdzienicka, N.G.J. Jaspers, G.P. van der Schans, A.T. Natarajan, J.W.I.M. Simons
198949
12
Cellular and molecular characteristics of an immortalized ataxia-telangiectasia (group AB) cell line.
PubMed ·Yael Ziv, N.G.J. Jaspers, Sara Etkin, Tsafi Danieli, L. Trakhtenbrot, Aliza Amiel, Yehoshua Ravia, Y. Shiloh
198942
13
Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair
Clinical Genetics ·Dicky Halley, W. Keijzer, N.G.J. Jaspers, M. F. Niermeuer, W. J. Rleijer, J Boué, A Boué, D. Bootsma
197934
14
A case of Rombo syndrome
British Journal of Dermatology ·Maurice A. M. Van Steensel, N.G.J. Jaspers, Peter M. Steijlen
200128
15
Effects of microinjected photoreactivating enzyme on thymine dimer removal and DNA repair synthesis in normal human and xeroderma pigmentosum fibroblasts.
PubMed ·Len Roza, Wim Vermeulen, J B Bergen Henegouwen, André P. M. Eker, N.G.J. Jaspers, P.H.M. Lohman, Jan H.J. Hoeijmakers
199023
16
Sister chromatid exchanges, hyperdiploidy and chromosomal rearrangements studied in cells from melanoma-prone individuals belonging to families with the dysplastic nevus syndrome
Cancer Genetics and Cytogenetics ·N.G.J. Jaspers, Elly J.M. Roza-De Jongh, I. G. Donselaar, J.T.M. Van Velzen-Tillemans, J. O. Van Hemel, P Rümke, A.W.M. van der Kamp
198721
17
Co-dominance of radioresistant DNA synthesis in a group of AT-like Chinese hamster cell mutants
Cytogenetic and Genome Research ·Gerald W. Verhaegh, N.G.J. Jaspers, P.H.M. Lohman, Małgorzata Z. Zdzienicka
199320
18
Ataxia-telangiectasia: a variant with altered in vitro phenotype of fibroblast cells
Mutation research. Fundamental and molecular mechanisms of mutagenesis ·U. Ziv, Aliza Amiel, N.G.J. Jaspers, A.I. van Berkel, Yosef Shiloh
198919
19
ERCC6 founder mutation identified in Finnish patients with COFS syndrome
Clinical Genetics ·E. Jaakkola, Aki Mustonen, Päivi Olsén, S. Miettinen, T Savuoja, Anja Raams, N.G.J. Jaspers, Hong Shao, BL Wu, Jaakko Ignatius
201017
20
Narrowband ultraviolet B inhibits innate cytosolic double-stranded RNA receptors in psoriatic skin and keratinocytes
British Journal of Dermatology ·Emöke Rácz, Errol P. Prens, Marius Kant, Edwin F. Florencia, N.G.J. Jaspers, Jon D. Laman, Dick de Ridder, Leslie van der Fits
201016

About N.G.J. Jaspers

N.G.J. Jaspers is a scholar working on Molecular Biology, Cancer Research, Genetics, Pathology and Forensic Medicine and Dermatology, having authored 26 papers that have together received 1.6k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (16 papers), Carcinogens and Genotoxicity Assessment (12 papers), CRISPR and Genetic Engineering (5 papers), Animal Genetics and Reproduction (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Prion Diseases and Protein Misfolding (2 papers), Viral Infectious Diseases and Gene Expression in Insects (2 papers) and Genetic and rare skin diseases. (2 papers). The work is most often cited by research in Cancer Research (544 citations), Molecular Biology (1.4k citations), Oncology (294 citations), Aging (18 citations) and Genetics (199 citations). N.G.J. Jaspers has collaborated with scholars based in Netherlands, United Kingdom and Japan. Frequent co-authors include D. Bootsma, Jan H.J. Hoeijmakers, Hanny Odijk, Jan de Wit, Anneke J. van Vuuren, Esther Appeldoorn, Roland Kanaar, Ellen van Drunen, H. Berna Beverloo and Arjan F. Theil. Their work appears in journals such as Clinical Genetics, British Journal of Dermatology, The EMBO Journal, International Journal of Radiation Biology and Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by N.G.J. JaspersBreakdown of academic impact, for papers by Elena BottaBreakdown of academic impact, for papers by Christine TroelstraBreakdown of academic impact, for papers by Mitsuo WakasugiBreakdown of academic impact, for papers by Maria FousteriBreakdown of academic impact, for papers by S. StevensBreakdown of academic impact, for papers by Claire AttwoollBreakdown of academic impact, for papers by Thomas TrimarchiBreakdown of academic impact, for papers by Elisabetta CitterioBreakdown of academic impact, for papers by Euan M. Slorach