D. Bootsma

21.2k total citations · 7 hit papers
167 papers, 16.9k citations indexed

About

D. Bootsma is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, D. Bootsma has authored 167 papers receiving a total of 16.9k indexed citations (citations by other indexed papers that have themselves been cited), including 133 papers in Molecular Biology, 38 papers in Cancer Research and 27 papers in Genetics. Recurrent topics in D. Bootsma's work include DNA Repair Mechanisms (99 papers), Carcinogens and Genotoxicity Assessment (38 papers) and CRISPR and Genetic Engineering (35 papers). D. Bootsma is often cited by papers focused on DNA Repair Mechanisms (99 papers), Carcinogens and Genotoxicity Assessment (38 papers) and CRISPR and Genetic Engineering (35 papers). D. Bootsma collaborates with scholars based in Netherlands, Japan and United Kingdom. D. Bootsma's co-authors include Jan H.J. Hoeijmakers, Jan de Wit, W. Keijzer, E.A. de Weerd-Kastelein, Wim Vermeulen, A. Westerveld, Christine Troelstra, Gerard C. Grosveld, Nora Heisterkamp and John Groffen and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

D. Bootsma

166 papers receiving 16.1k citations

Hit Papers

DNA repair and mutagenesis 1975 2026 1992 2009 1996 1999 1982 1998 1992 500 1000 1.5k
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. DNA repair and mutagenesis
    1996 1.9k citations D. Bootsma, Jan H.J. Hoeijmakers profile →
  2. Mammalian Cry1 and Cry2 are essential for maintenance of circadian rhythms
    1999 1.1k citations Jan de Wit, André P. M. Eker et al. profile →
  3. A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia
    1982 1.1k citations Anne Hagemeijer, D. Bootsma et al. profile →
  4. Xeroderma Pigmentosum Group C Protein Complex Is the Initiator of Global Genome Nucleotide Excision Repair
    1998 728 citations Kaoru Sugasawa, Jessica M.Y. Ng et al. profile →
  5. ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes
    1992 608 citations Christine Troelstra, Jan de Wit et al. Cell profile →
  6. Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia
    1983 551 citations Anne Hagemeijer, D. Bootsma et al. profile →
  7. Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation.
    1975 487 citations P.H.M. Lohman, D. Bootsma et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D. Bootsma Netherlands 62 12.7k 3.5k 2.6k 2.1k 1.8k 167 16.9k
Richard Treisman United Kingdom 70 19.1k 1.5× 2.5k 0.7× 3.2k 1.2× 3.8k 1.8× 1.5k 0.8× 116 25.1k
George Thomas Switzerland 83 18.4k 1.4× 1.8k 0.5× 1.4k 0.6× 3.0k 1.4× 1.1k 0.6× 162 24.4k
Johji Inazawa Japan 75 13.1k 1.0× 4.8k 1.4× 2.8k 1.1× 4.2k 2.0× 487 0.3× 410 20.6k
Robert N. Eisenman United States 82 25.2k 2.0× 2.9k 0.8× 5.1k 2.0× 5.8k 2.8× 1.5k 0.8× 204 30.7k
Peter J. Parker United Kingdom 95 25.3k 2.0× 2.0k 0.6× 1.5k 0.6× 3.9k 1.9× 820 0.5× 406 33.7k
A. Ullrich Germany 92 22.5k 1.8× 2.6k 0.8× 2.6k 1.0× 9.0k 4.3× 346 0.2× 193 33.0k
Eric W.‐F. Lam United Kingdom 87 15.3k 1.2× 4.0k 1.2× 1.7k 0.7× 5.4k 2.6× 1.2k 0.7× 298 23.1k
Michael F. Seldin United States 73 8.3k 0.7× 1.6k 0.5× 4.0k 1.6× 1.9k 0.9× 437 0.2× 281 17.6k
Shunsuke Ishii Japan 69 12.8k 1.0× 1.4k 0.4× 2.6k 1.0× 3.1k 1.5× 1.3k 0.7× 278 16.7k
Andrew J. Bannister United Kingdom 52 20.1k 1.6× 2.3k 0.7× 2.8k 1.1× 2.6k 1.3× 2.1k 1.2× 84 23.5k

Countries citing papers authored by D. Bootsma

Since Specialization
Citations

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

Fields of papers citing papers by D. Bootsma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D. Bootsma

This figure shows the co-authorship network connecting the top 25 collaborators of D. Bootsma. A scholar is included among the top collaborators of D. Bootsma 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 D. Bootsma. D. Bootsma 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.
Sugasawa, Kaoru, Jessica M.Y. Ng, Chikahide Masutani, et al.. (1997). Two Human Homologs of Rad23 Are Functionally Interchangeable in Complex Formation and Stimulation of XPC Repair Activity. Molecular and Cellular Biology. 17(12). 6924–6931. 110 indexed citations
2.
Masutani, Chikahide, Marito Araki, Kaoru Sugasawa, et al.. (1997). Identification and Characterization of XPC-Binding Domain of hHR23B. Molecular and Cellular Biology. 17(12). 6915–6923. 89 indexed citations
3.
Roest, Henk P., Jan de Wit, Marcel Koken, et al.. (1996). Inactivation of the HR6B Ubiquitin-Conjugating DNA Repair Enzyme in Mice Causes Male Sterility Associated with Chromatin Modification. Cell. 86(5). 799–810. 325 indexed citations
4.
Sugasawa, Kaoru, Chikahide Masutani, Akio Uchida, et al.. (1996). HHR23B, a Human Rad23 Homolog, Stimulates XPC Protein in Nucleotide Excision Repair In Vitro. Molecular and Cellular Biology. 16(9). 4852–4861. 141 indexed citations
5.
McKay, Michael J., Christine Troelstra, Peter J. van der Spek, et al.. (1996). Sequence Conservation of therad21 Schizosaccharomyces pombeDNA Double-Strand Break Repair Gene in Human and Mouse. Genomics. 36(2). 305–315. 70 indexed citations
6.
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
7.
Koken, Marcel, Paul R. Reynolds, Louise Prakash, et al.. (1991). Structural and functional conservation of two human homologs of the yeast DNA repair gene RAD6.. Proceedings of the National Academy of Sciences. 88(20). 8865–8869. 213 indexed citations
8.
Troelstra, Christine, Hanny Odijk, Jan de Wit, et al.. (1990). Molecular Cloning of the Human DNA Excision Repair Gene ERCC-6. Molecular and Cellular Biology. 10(11). 5806–5813. 27 indexed citations
9.
Duin, Marcel van, Lynne V. Mayne, Hanny Odijk, et al.. (1989). The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I.. Data Archiving and Networked Services (DANS). 64 indexed citations
10.
Khan, P. Meera, et al.. (1976). Assignment of <i>inosine triphosphatase</i> gene to gorilla chromosome 13 and to human chromosome 20 in primate-rodent somatic cell hybrids. Cytogenetic and Genome Research. 16(1-5). 420–421. 16 indexed citations
11.
Wullems, G. J., et al.. (1976). Transfer of the human X chromosome to human-Chinese hamster cell hybrids via isolated HeLa metaphase chromosomes. Somatic Cell and Molecular Genetics. 2(4). 359–371. 22 indexed citations
12.
Bootsma, D., et al.. (1975). Human gene mapping 2 : Rotterdam Conference (1974). S. Karger eBooks. 2 indexed citations
13.
Wit, Jan de, D. Bootsma, P. Pearson, & A. Westerveld. (1975). Regional mapping of the human No. 1 and X chromosome in interspecific cell hybrids using an X/1 translocation. Cytogenetic and Genome Research. 15(3). 129–137. 3 indexed citations
14.
Khan, P. Meera, et al.. (1975). α-Galactosidase in man-Chinese hamster somatic cell hybrids. Cytogenetic and Genome Research. 14(3-6). 375–380. 12 indexed citations
15.
Cleaver, James E. & D. Bootsma. (1975). XERODERMA PIGMENTOSUM: BIOCHEMICAL AND GENETIC CHARACTERISTICS. Annual Review of Genetics. 9(1). 19–38. 321 indexed citations
16.
Pearson, P., et al.. (1974). Genetical Studies on the Multiple Forms of Human Guanylate Kinase in Man-Chinese Hamster Somatic Cell Hybrids. Human Heredity. 24(5-6). 415–423. 13 indexed citations
17.
Someren, H. van, et al.. (1974). Synteny of the human loci for fumarate hydratase and UDPG pyrophosphorylase with chromosome 1 markers in somatic cell hybrids. Cytogenetic and Genome Research. 13(6). 551–557. 14 indexed citations
18.
Bootsma, D., et al.. (1970). Different inherited levels of DNA repair replication in xeroderma pigmentosum cell strains after exposure to ultraviolet irradiation. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 9(5). 507–516. 130 indexed citations
19.
Kleijer, Wim J., P.H.M. Lohman, Marlies Mulder, & D. Bootsma. (1970). Repair of X-ray damage in DNA of cultivated cells from patients having xeroderma pigmentosum. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 9(5). 517–523. 61 indexed citations
20.
Bootsma, D. & Ronald M. Humphrey. (1968). The progression of mammalian cells through the division cycle following ultraviolet irradiation. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 5(2). 289–298. 43 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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