W. Keijzer

2.0k citations

33 papers · 1.7k indexed · h-index 20

Impact in

Cancer Research top 2%
- Carcinogens and Genotoxicity Assessment
Molecular Biology top 5%
- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
- DNA and Nucleic Acid Chemistry
- Porphyrin Metabolism and Disorders
- bioluminescence and chemiluminescence research

Papers in

Cancer Research 11
- Carcinogens and Genotoxicity Assessment 11
Molecular Biology 27
- DNA Repair Mechanisms 20
- Glycosylation and Glycoproteins Research 3
- Prion Diseases and Protein Misfolding 3
- CRISPR and Genetic Engineering 3

Co-authors: D. Bootsma E.A. de Weerd-Kastelein C.F. Arlett H. Galjaard Giuseppe Rainaldi Alan R. Lehmann Susan Kirk‐Bell Susan A. Harcourt
Journals: Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis (8 papers)Experimental Cell Research (6 papers)Mutation Research/DNA Repair (1 paper)Journal of Investigative Dermatology (1 paper)Nature (1 paper)
Partner nations: Netherlands Italy United Kingdom

In The Last Decade

W. Keijzer

32 papers receiving 1.5k citations

Peers

Countries citing papers authored by W. Keijzer

Since Specialization

Citations

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

Fields of papers citing papers by W. Keijzer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside W. Keijzer, 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 W. Keijzer Line = papers co-authored together W. Keijzer links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Frequent Occurrence of Activated ras Oncogenes in Seminomas but Not in Nonseminomatous Germ Cell Tumors Recent results in cancer research ·Marlies Mulder, W. Keijzer, T. A. W. Splinter, Johannes L. Bos	1991	4
2	Xeroderma pigmentosum complementation group XP-I withdrawn Mutation Research/DNA Repair ·D. Bootsma, W. Keijzer, E. G. Jung, E. Bohnert	1989	29
3	Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1 Experimental Cell Research ·W. Keijzer, Miria Stefanini, D. Bootsma, Annemieke J.M.H. Verkerk, A.H.M. Geurts van Kessel, J. F. Jongkind, A. Westerveld	1987	8
4	Microinjection of Micrococcus luteus UV-endonuclease restores UV-induced unscheduled DNA synthesis in cells of 9 xeroderma pigmentosum complementation groups Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·R. N. Mukerji, Wim Vermeulen, W. Keijzer, Jan H.J. Hoeijmakers, D. Bootsma	1985	41
5	Interaction of human and chick DNA repair functions in UV-irradiated xeroderma pigmentosum-chick erythrocyte heterokaryons Experimental Cell Research ·D. Bootsma, W. Keijzer, E. van der Veer, Giuseppe Rainaldi, E.A. de Weerd-Kastelein	1982	7
6	Workshop on mapping by somatic cell hybridization. PubMed ·F.H. Ruddle, D. Bootsma, Mariane Martins Araújo Stefani, W. Keijzer, A. Westerveld, N. Van Cong, Dominique Weil, M. C. Hors‐Cayla, Marie‐Sylvie Gross, S. Heuertz, María Cristina Jaquete Pérez, J Frézal, E. Solomon, T.B. Shows, Alan Y. Sakaguchi, Susan L. Naylor	1982	1
7	Differences in the levels of UV repair and in clinical symptoms in two sibs affected by xeroderma pigmentosum Human Genetics ·Miria Stefanini, W. Keijzer, L. Dalpr�, R. Elli, Mariana de Andrade Pranke da Silva, B. Nicoletti, Fiorella Nuzzo	1980	18
8	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, Jia Wang, C.F. Arlett, B. Zelle, Hiraku Takebe, Rochus Hien, D. Bootsma	1979	137
9	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, Shuyu Liu, محمد صنت الحربي, J Boué, A Boué, D. Bootsma	1979	34
10	Induction of sister chromatid exchanges in xeroderma pigmentosum cells after exposure to ultraviolet light Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·E.A. de Weerd-Kastelein, W. Keijzer, Giuseppe Rainaldi, D. Bootsma	1977	103
11	Repair of ultraviolet light damage in a variety of human fibroblast cell strains. PubMed ·Alan R. Lehmann, Susan Kirk‐Bell, C.F. Arlett, Susan A. Harcourt, E.A. de Weerd-Kastelein, W. Keijzer, Sameh I. Hafez	1977	181
12	A xeroderma pigmentosum patient having a high residual activity of unscheduled DNA synthesis after UV is assigned to complementation group A Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·E.A. de Weerd-Kastelein, W. Keijzer, Mohammad Hossein Sabour, Jennifer M. Parrington, D. Bootsma	1976	36
13	Five complementation groups in xeroderma pigmentosum Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·Kenneth H. Kraemer, E.A. de Weerd-Kastelein, J.H. Robbins, W. Keijzer, Susanna F. Barrett, L. Chuhlomina, D. Bootsma	1975	154
14	Different gene mutations in variants of GM1- and GM2-gangliosidosis demonstrated by enzyme analysis of (single) somatic hybrid cells Cytogenetic and Genome Research ·H. Galjaard, A. T. Hoogeveen, W. Keijzer, Jim Henderson, A. J. J. Reuser	1975	0
15	Genetic heterogeneity in inborn errors of metabolism studied by enzyme analysis in single somatic cell hybrids The Histochemical Journal ·H. Galjaard, A. T. Hoogeveen, Jim Henderson, W. Keijzer, A. J. J. Reuser	1975	2
16	A third complementation group in xeroderma pigmentosum Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·E.A. de Weerd-Kastelein, W. Keijzer, D. Bootsma	1974	78
17	Tay-Sachs and Sandhoff's disease: Intergenic complementation after somatic cell hybridization Experimental Cell Research ·H. Galjaard, A. T. Hoogeveen, Jim Henderson, Arnold Reuser, W. Keijzer, A. Westerveld, D. Bootsma	1974	58
18	UV-induced DNA repair synthesis in cells of patients with different forms of xeroderma pigmentosum and of heterozygotes Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·Wim J. Kleijer, E.A. de Weerd-Kastelein, M. Luzzaa, W. Keijzer, Jan de Wit, D. Bootsma	1973	75
19	Repair replication in heterokaryons derived from different repair-deficient xeroderma pigmentosum strains Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·E.A. de Weerd-Kastelein, Wim J. Kleijer, M. Luzzaa, W. Keijzer	1973	24
20	Mammalian cell culture studies OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) ·D. Bootsma, W. Keijzer, Wim J. Kleijer, Yochi Elanda, Joris de Wit, P. Meera Khan, H. van Someren, A. Westerveld	1973	6

About W. Keijzer

W. Keijzer is a scholar working on Cancer Research, Molecular Biology, Clinical Biochemistry, Neurology and Neurology, having authored 33 papers that have together received 1.7k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (20 papers), Carcinogens and Genotoxicity Assessment (11 papers), Glycosylation and Glycoproteins Research (3 papers), Prion Diseases and Protein Misfolding (3 papers), Testicular diseases and treatments (3 papers), Lysosomal Storage Disorders Research (3 papers), Sarcoma Diagnosis and Treatment (3 papers) and CRISPR and Genetic Engineering (3 papers). The work is most often cited by research in Cancer Research (670 citations), Molecular Biology (1.4k citations), Biotechnology (75 citations), Cell Biology (127 citations) and Dermatology (67 citations). W. Keijzer has collaborated with scholars based in Netherlands, Italy and United Kingdom. Frequent co-authors include D. Bootsma, E.A. de Weerd-Kastelein, C.F. Arlett, H. Galjaard, Giuseppe Rainaldi, Alan R. Lehmann, Susan Kirk‐Bell, Susan A. Harcourt, J.H. Robbins and Kenneth H. Kraemer. Their work appears in journals such as Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, Experimental Cell Research, Mutation Research/DNA Repair, Journal of Investigative Dermatology and Nature.

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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