Bernard C. Broughton

2.8k citations

29 papers · 2.3k indexed · h-index 22

Molecular Biology top 5%
Cancer Research top 2%
Oncology top 10%
Genetics top 10%
Cell Biology top 10%

Co-authors: Alan R. Lehmann C.F. Arlett Susan A. Harcourt Miria Stefanini Herdis Steingrimsdottir Elena Botta Alain Sarasin Fumio Hanaoka
Topics: DNA Repair Mechanisms (25 papers)Carcinogens and Genotoxicity Assessment (13 papers)Plant Genetic and Mutation Studies (3 papers)
Cited by: Cancer Research Molecular Biology Oncology
Journals: Proceedings of the National Academy of Sciences Nature Genetics Genes & Development
Partner nations: United Kingdom United States Netherlands

In The Last Decade

Bernard C. Broughton

29 papers receiving 2.3k citations

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene 2001 ·Human Molecular Genetics ·Bernard C. Broughton	77
2	Domain structure, localization, and function of DNA polymerase η, defective in xeroderma pigmentosum variant cells 2001 ·Genes & Development ·Patricia Kannouche,Bernard C. Broughton,Marcel Volker,Fumio Hanaoka,Leon H.F. Mullenders,Alan R. Lehmann	237
3	Novel Human and Mouse Homologs of Saccharomyces cerevisiae DNA Polymerase η 1999 ·Genomics ·John P. McDonald,Vesna Rapić-Otrin,Jonathan A. Epstein,Bernard C. Broughton,Xiangyuan Wang,(unknown),Debra J. Wolgemuth,Roger Woodgate	159
4	Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient 1999 ·Current Biology ·(unknown),Susan E. Critchlow,Soo‐Hwang Teo,Aidan J. Doherty,A. Priestley,Bernard C. Broughton,Boris Kysela,Heather Beamish,Nicholas Plowman,C.F. Arlett,A. Lehmann,Stephen P. Jackson,Penny A. Jeggo	312
5	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 1998 ·The American Journal of Human Genetics ·Elena Botta,Tiziana Nardò,Bernard C. Broughton,S. Marinoni,Alan R. Lehmann,Miria Stefanini	91
6	Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD ( ERCC 2) repair/transcription gene 1997 ·Proceedings of the National Academy of Sciences ·Elaine M. Taylor,Bernard C. Broughton,Elena Botta,Miria Stefanini,Alain Sarasin,Nicolaas G.J. Jaspers,Heather Fawcett,Susan A. Harcourt,C.F. Arlett,Alan R. Lehmann	213
7	Five polymorphisms in the coding sequence of the xeroderma pigmentosum group D gene 1996 ·Mutation Research/DNA Repair ·Bernard C. Broughton,Herdis Steingrimsdottir,Alan R. Lehmann	53
8	DNA Repair and Ultraviolet Mutagenesis in Cells From a New Patient With Xeroderma Pigmentosum Group G and Cockayne Syndrome Resemble Xeroderma Pigmentosum Cells 1996 ·Journal of Investigative Dermatology ·Shinichi Moriwaki,(unknown),(unknown),Jan H.J. Hoeijmakers,Jay H. Robbins,I. Rapin,Elena Botta,(unknown),Wim Vermeulen,Bernard C. Broughton,Kenneth H. Kraemer	45
9	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. 1995 ·Europe PMC (PubMed Central) ·Bernard C. Broughton,(unknown),Susan A. Harcourt,Wim Vermeulen,Jan H.J. Hoeijmakers,Elena Botta,Miria Stefanini,(unknown),C.A. Weber,Jane Cole	97
10	Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy 1994 ·Nature Genetics ·Bernard C. Broughton,Herdis Steingrimsdottir,Christine A. Weber,Alan R. Lehmann	109
11	Localization of a DNA repair gene (XRCC5) involved in double-strand-break rejoining to human chromosome 2. 1992 ·Proceedings of the National Academy of Sciences ·Penny A. Jeggo,Majid Hafezparast,(unknown),Bernard C. Broughton,Gagandeep Kaur,Małgorzata Z. Zdzienicka,R. S. Athwal	58
12	Assignment of ten DNA repair genes from Schizosaccharomyces pombe to chromosomal NotI restriction fragments 1991 ·Molecular and General Genetics MGG ·Bernard C. Broughton,(unknown),Johanne M. Murray,Felicity Z. Watts,Marcel Koken,Alan R. Lehmann,Antony M. Carr	6
13	Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: Studies using cells from patients with trichothiodystrophy 1990 ·Mutation Research/DNA Repair ·Bernard C. Broughton,Alan R. Lehmann,Susan A. Harcourt,C.F. Arlett,Alain Sarasin,(unknown),F. A. Beemer,(unknown),David L. Mitchell	64
14	Inhibition of DNA Replication by Ionizing Radiation is Mediated by aTrans-acting Factor 1989 ·International Journal of Radiation Biology ·John R. Lamb,Corinne Petit-Frère,Bernard C. Broughton,Alan R. Lehmann,M.H.L. Green	40
15	Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndrome. 1988 ·PubMed ·Alan R. Lehmann,Anne E. Willis,Bernard C. Broughton,Michael R. James,Herdis Steingrimsdottir,Susan A. Harcourt,C.F. Arlett,Tomas Lindahl	55
16	Genetic effects of specific DNA lesions in mammalian cells 1984 ·Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·(unknown),John A. Heddle,C.F. Arlett,Bernard C. Broughton	19
17	Poly(ADP-ribosylation) reduces the steady-state level of breaks in DNA following treatment of human cells with alkylating agents 1984 ·Carcinogenesis ·Alan R. Lehmann,Bernard C. Broughton	21
18	The ultraviolet sensitivity of Cockayne syndrome cells is not a consequence of reduced cellular NAD content. 1984 ·PubMed ·Lynne V. Mayne,Bernard C. Broughton,Alan R. Lehmann	4
19	Multiple hypersensitivity to mutagens in a cell strain (46BR) derived from a patient with immuno-deficiencies 1983 ·Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·Ian Teo,C.F. Arlett,Susan A. Harcourt,A. Priestley,Bernard C. Broughton	50
20	The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet-light irradiation 1975 ·Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·C.F. Arlett,Susan A. Harcourt,Bernard C. Broughton	119

About Bernard C. Broughton

Bernard C. Broughton is a scholar working on Cancer Research, Molecular Biology and Cell Biology, having authored 29 papers that have together received 2.3k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (25 papers), Carcinogens and Genotoxicity Assessment (13 papers) and Plant Genetic and Mutation Studies (3 papers). The work is most often cited by research in Cancer Research (804 citations), Molecular Biology (2.2k citations) and Oncology (442 citations). Bernard C. Broughton has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Genes & Development.

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