Bernard C. Broughton

2.8k total citations
29 papers, 2.3k citations indexed

About

Bernard C. Broughton is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Bernard C. Broughton has authored 29 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 14 papers in Cancer Research and 4 papers in Oncology. Recurrent topics in Bernard C. Broughton's work include DNA Repair Mechanisms (25 papers), Carcinogens and Genotoxicity Assessment (13 papers) and Plant Genetic and Mutation Studies (3 papers). Bernard C. Broughton is often cited by papers focused on DNA Repair Mechanisms (25 papers), Carcinogens and Genotoxicity Assessment (13 papers) and Plant Genetic and Mutation Studies (3 papers). Bernard C. Broughton collaborates with scholars based in United Kingdom, United States and Netherlands. Bernard C. Broughton's co-authors include Alan R. Lehmann, C.F. Arlett, Susan A. Harcourt, Miria Stefanini, Herdis Steingrimsdottir, Elena Botta, Alain Sarasin, Fumio Hanaoka, Marcel Volker and Patricia Kannouche and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Genes & Development.

In The Last Decade

Bernard C. Broughton

29 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bernard C. Broughton United Kingdom	22	2.2k	804	442	269	180	29	2.3k
KumKum Khanna Australia	16	1.4k 0.7×	485 0.6×	607 1.4×	239 0.9×	197 1.1×	21	1.7k
Cordula U. Kirchgessner United States	8	2.1k 1.0×	575 0.7×	733 1.7×	232 0.9×	152 0.8×	8	2.4k
N.G.J. Jaspers Netherlands	18	1.4k 0.7×	544 0.7×	294 0.7×	199 0.7×	103 0.6×	26	1.6k
Jean-Marie Buerstedde Japan	17	1.9k 0.9×	547 0.7×	373 0.8×	206 0.8×	169 0.9×	18	2.1k
John Sgouros United Kingdom	11	1.4k 0.7×	370 0.5×	346 0.8×	251 0.9×	163 0.9×	18	1.8k
Torsten Krude United Kingdom	27	2.3k 1.0×	459 0.6×	360 0.8×	184 0.7×	219 1.2×	52	2.5k
N.G.J. Jaspers Netherlands	15	1.4k 0.7×	487 0.6×	303 0.7×	197 0.7×	76 0.4×	21	1.6k
Juhani E. Syväoja Finland	23	1.7k 0.8×	334 0.4×	421 1.0×	274 1.0×	175 1.0×	46	1.9k
Irina I. Dianova United Kingdom	23	1.7k 0.8×	375 0.5×	653 1.5×	172 0.6×	133 0.7×	25	1.9k

Countries citing papers authored by Bernard C. Broughton

Since Specialization

Citations

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

Fields of papers citing papers by Bernard C. Broughton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bernard C. Broughton. 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 Bernard C. Broughton. The network helps show where Bernard C. Broughton may publish in the future.

Co-authorship network of co-authors of Bernard C. Broughton

This figure shows the co-authorship network connecting the top 25 collaborators of Bernard C. Broughton. A scholar is included among the top collaborators of Bernard C. Broughton 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 Bernard C. Broughton. Bernard C. Broughton is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Broughton, Bernard C.. (2001). Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene. Human Molecular Genetics. 10(22). 2539–2547. 77 indexed citations

Kannouche, Patricia, Bernard C. Broughton, Marcel Volker, et al.. (2001). Domain structure, localization, and function of DNA polymerase η, defective in xeroderma pigmentosum variant cells. Genes & Development. 15(2). 158–172. 237 indexed citations

McDonald, John P., Vesna Rapić-Otrin, Jonathan A. Epstein, et al.. (1999). Novel Human and Mouse Homologs of Saccharomyces cerevisiae DNA Polymerase η. Genomics. 60(1). 20–30. 159 indexed citations

Critchlow, Susan E., Soo‐Hwang Teo, Aidan J. Doherty, et al.. (1999). Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient. Current Biology. 9(13). 699–S2. 312 indexed citations

Botta, Elena, Tiziana Nardò, Bernard C. Broughton, et al.. (1998). Analysis of Mutations in the XPD Gene in Italian Patients with Trichothiodystrophy: Site of Mutation Correlates with Repair Deficiency, but Gene Dosage Appears to Determine Clinical Severity. The American Journal of Human Genetics. 63(4). 1036–1048. 91 indexed citations

Taylor, Elaine M., Bernard C. Broughton, Elena Botta, et al.. (1997). Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD ( ERCC 2) repair/transcription gene. Proceedings of the National Academy of Sciences. 94(16). 8658–8663. 213 indexed citations

Broughton, Bernard C., Herdis Steingrimsdottir, & Alan R. Lehmann. (1996). Five polymorphisms in the coding sequence of the xeroderma pigmentosum group D gene. Mutation Research/DNA Repair. 362(2). 209–211. 53 indexed citations

Moriwaki, Shinichi, Jan H.J. Hoeijmakers, Jay H. Robbins, et al.. (1996). DNA Repair and Ultraviolet Mutagenesis in Cells From a New Patient With Xeroderma Pigmentosum Group G and Cockayne Syndrome Resemble Xeroderma Pigmentosum Cells. Journal of Investigative Dermatology. 107(4). 647–653. 45 indexed citations

Broughton, Bernard C., Susan A. Harcourt, Wim Vermeulen, et al.. (1995). Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome.. PubMed. 56(1). 167–74. 97 indexed citations

10.

Broughton, Bernard C., Herdis Steingrimsdottir, Christine A. Weber, & Alan R. Lehmann. (1994). Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy. Nature Genetics. 7(2). 189–194. 109 indexed citations

11.

Jeggo, Penny A., Majid Hafezparast, Bernard C. Broughton, et al.. (1992). Localization of a DNA repair gene (XRCC5) involved in double-strand-break rejoining to human chromosome 2.. Proceedings of the National Academy of Sciences. 89(14). 6423–6427. 58 indexed citations

12.

Broughton, Bernard C., Johanne M. Murray, Felicity Z. Watts, et al.. (1991). Assignment of ten DNA repair genes from Schizosaccharomyces pombe to chromosomal NotI restriction fragments. Molecular and General Genetics MGG. 228(3). 470–472. 6 indexed citations

13.

Broughton, Bernard C., Alan R. Lehmann, Susan A. Harcourt, et al.. (1990). Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: Studies using cells from patients with trichothiodystrophy. Mutation Research/DNA Repair. 235(1). 33–40. 64 indexed citations

14.

Lamb, John R., Corinne Petit-Frère, Bernard C. Broughton, Alan R. Lehmann, & M.H.L. Green. (1989). Inhibition of DNA Replication by Ionizing Radiation is Mediated by aTrans-acting Factor. International Journal of Radiation Biology. 56(2). 125–130. 40 indexed citations

15.

Lehmann, Alan R., Anne E. Willis, Bernard C. Broughton, et al.. (1988). Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndrome.. PubMed. 48(22). 6343–7. 55 indexed citations

16.

Heddle, John A., et al.. (1984). Genetic effects of specific DNA lesions in mammalian cells. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 127(2). 139–147. 19 indexed citations

17.

Lehmann, Alan R. & Bernard C. Broughton. (1984). Poly(ADP-ribosylation) reduces the steady-state level of breaks in DNA following treatment of human cells with alkylating agents. Carcinogenesis. 5(1). 117–119. 21 indexed citations

18.

Mayne, Lynne V., Bernard C. Broughton, & Alan R. Lehmann. (1984). The ultraviolet sensitivity of Cockayne syndrome cells is not a consequence of reduced cellular NAD content.. PubMed. 36(2). 311–9. 4 indexed citations

19.

Teo, Ian, C.F. Arlett, Susan A. Harcourt, A. Priestley, & Bernard C. Broughton. (1983). Multiple hypersensitivity to mutagens in a cell strain (46BR) derived from a patient with immuno-deficiencies. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 107(2). 371–386. 50 indexed citations

20.

Arlett, C.F., Susan A. Harcourt, & Bernard C. Broughton. (1975). The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet-light irradiation. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 33(2-3). 341–346. 119 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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