Alan R. Lehmann

25.6k total citations · 5 hit papers
244 papers, 19.9k citations indexed

About

Alan R. Lehmann is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Alan R. Lehmann has authored 244 papers receiving a total of 19.9k indexed citations (citations by other indexed papers that have themselves been cited), including 227 papers in Molecular Biology, 75 papers in Cancer Research and 32 papers in Oncology. Recurrent topics in Alan R. Lehmann's work include DNA Repair Mechanisms (189 papers), Carcinogens and Genotoxicity Assessment (69 papers) and CRISPR and Genetic Engineering (40 papers). Alan R. Lehmann is often cited by papers focused on DNA Repair Mechanisms (189 papers), Carcinogens and Genotoxicity Assessment (69 papers) and CRISPR and Genetic Engineering (40 papers). Alan R. Lehmann collaborates with scholars based in United Kingdom, United States and Netherlands. Alan R. Lehmann's co-authors include Patricia Kannouche, C.F. Arlett, Antony M. Carr, Jonathan Wing, Lynne V. Mayne, Susan A. Harcourt, Robert P. Fuchs, Miria Stefanini, S. Stevens and Susan Kirk‐Bell and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Alan R. Lehmann

243 papers receiving 19.2k citations

Hit Papers

5 papers align trajectories

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.

Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity

1975 798 citations C.F. Arlett, Susan A. Harcourt et al. profile →
Interaction of Human DNA Polymerase η with Monoubiquitinated PCNA

2004 730 citations Patricia Kannouche, Alan R. Lehmann et al. Molecular Cell profile →
Ubiquitin-Binding Domains in Y-Family Polymerases Regulate Translesion Synthesis

2005 587 citations Patricia Kannouche, Alan R. Lehmann et al. profile →
Ku80: product of the XRCC5 gene and its role in DNA repair and V(D)J recombination

1994 555 citations A. Priestley, Alan R. Lehmann et al. profile →
Y-family DNA polymerases and their role in tolerance of cellular DNA damage

2012 528 citations Alan R. Lehmann et al. profile →

Peers

Countries citing papers authored by Alan R. Lehmann

Since Specialization

Citations

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

Fields of papers citing papers by Alan R. Lehmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alan R. Lehmann. 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 Alan R. Lehmann. The network helps show where Alan R. Lehmann may publish in the future.

Co-authorship network of co-authors of Alan R. Lehmann

This figure shows the co-authorship network connecting the top 25 collaborators of Alan R. Lehmann. A scholar is included among the top collaborators of Alan R. Lehmann 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 Alan R. Lehmann. Alan R. Lehmann 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

#	Work	Indexed citations
1	TFIIH-p52ΔC defines a ninth xeroderma pigmentosum complementation–group XP-J and restores TFIIH stability to p8-defective trichothiodystrophy 2025 ·Journal of Clinical Investigation ·Yuka Nakazawa, (unknown), Yasuyoshi Oka, Hironobu Morinaga, (unknown), Mayuko Shimada, (unknown), (unknown), (unknown), Hiva Fassihi, Shehla Mohammed, Alan R. Lehmann, Tomoo Ogi	1
2	Genomic mutation landscape of skin cancers from DNA repair-deficient xeroderma pigmentosum patients 2023 ·Nature Communications ·Andrey A. Yurchenko, (unknown), Tirzah Braz Petta Lajus, Hiva Fassihi, Alan R. Lehmann, Chikako Nishigori, Jinxin Wang, Ismaël Padioleau, Konstantin Gunbin, (unknown), Fanny Morice‐Picard, (unknown), Caroline Robert, Patricia Kannouche, Carlos Frederico Martins Menck, Alain Sarasin, Sergey I. Nikolaev	28
3	Neurological disease in xeroderma pigmentosum: prospective cohort study of its features and progression 2023 ·Brain ·Héctor García‐Moreno, Douglas R. Langbehn, (unknown), (unknown), (unknown), Marta Manes, Ana M. S. Morley, Emma Craythorne, Shehla Mohammed, (unknown), Sally Turner, (unknown), István Bódi, Robert Sarkany, Hiva Fassihi, Alan R. Lehmann, Paola Giunti	10
4	Influence of the live cell DNA marker DRAQ5 on chromatin-associated processes 2010 ·DNA repair ·Pierre‐Olivier Mari, (unknown), Simone Sabbioneda, Audrey M. Gourdin, Nils Wijgers, Christoffel Dinant, Alan R. Lehmann, Wim Vermeulen, Giuseppina Giglia‐Mari	19
5	Inhibitors of the Proteasome Suppress Homologous DNA Recombination in Mammalian Cells 2007 ·Cancer Research ·Yasuhiro Murakawa, Eiichiro Sonoda, Louise J. Barber, Weihua Zeng, Kyoko Yokomori, Hiroshi Kimurâ, Atsuko Niimi, Alan R. Lehmann, Guang Zhao, Helfrid Hochegger, Simon J. Boulton, Shunichi Takeda	88
6	Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome 2006 ·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, (unknown), Carl C. Baker, Kenneth H. Kraemer	98
7	Localisation of human Y-family DNA polymerase κ: relationship to PCNA foci 2004 ·Journal of Cell Science ·Tomoo Ogi, Patricia Kannouche, Alan R. Lehmann	67
8	Co-localization in replication foci and interaction of human Y-family members, DNA polymerase polη and REVl protein 2004 ·DNA repair ·Agnès Tissier, Patricia Kannouche, (unknown), Alan R. Lehmann, Robert P. Fuchs, Agnès Cordonnier	180
9	3 Xeroderma pigmentosum and related disorders: Defects in DNA repair and transcription 2001 ·Advances in genetics ·(unknown), Alan R. Lehmann	155
10	Impaired Translesion Synthesis in Xeroderma Pigmentosum Variant Extracts 1999 ·Molecular and Cellular Biology ·Agnès Cordonnier, Alan R. Lehmann, Robert P. Fuchs	62
11	A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy 1998 ·Molecular Cell ·Jan de Boer, Jan de Wit, Harry van Steeg, Rob J. W. Berg, Hans Morreau, Pim Visser, Alan R. Lehmann, Marinus Durán, (unknown), Geert Weeda	161
12	The rad18 Gene of Schizosaccharomyces pombe Defines a New Subgroup of the SMC Superfamily Involved in DNA Repair 1995 ·Molecular and Cellular Biology ·Alan R. Lehmann, M. Walicka, Dominic J. F. Griffiths, Johanne M. Murray, Felicity Z. Watts, Shirley McCready, Antony M. Carr	182
13	The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH 1995 ·Cell ·Karla A. Henning, Lei Li, Narayan V. Iyer, Lisa D. McDaniel, Michael S. Reagan, Randy J. Legerski, Roger A. Schultz, Miria Stefanini, Alan R. Lehmann, Lynne V. Mayne, Errol C. Friedberg	388
14	Cloning Human DNA Repair Genes 1994 ·International Journal of Radiation Biology ·Penelope A. Jeggo, Antony M. Carr, Alan R. Lehmann	4
15	Three Unusual Repair Deficiencies Associated with Transcription Factor BTF2(TFIIH): Evidence for the Existence of a Transcription Syndrome 1994 ·Cold Spring Harbor Symposia on Quantitative Biology ·Wim Vermeulen, Anneke J. van Vuuren, (unknown), Laurent Schaeffer, Esther Appeldoorn, Geert Weeda, N.G.J. Jaspers, A. Priestley, C.F. Arlett, Alan R. Lehmann, Miria Stefanini, M. Mezzina, (unknown), D. Bootsma, J.M. Egly, Jan H.J. Hoeijmakers	120
16	Workshop on DNA repair 1992 ·Mutation Research/DNA Repair ·Alan R. Lehmann, Jan H.J. Hoeijmakers, A.A. van Zeeland, Claude Backendorf, B.A. Bridges, (unknown), (unknown), Geoffrey P. Margison, Ruggero Montesano, E. Moustacchi, Arvind Natarajan, Miroslav Radman, A Sarasin, Erling Seeberg, Charles A. Smith, Miria Stefanini, L.H. Thompson, G.P. van der Schans, C.A. Weber, M.Z. Zdzienicka	26
17	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
18	Workshop on Ataxia Telangiectasia 1987 ·Cancer Research ·Alan R. Lehmann, N.G.J. Jaspers, R A Gatti	5
19	A Derivative of an Ataxia-telangiectasia (A-T) Cell Line with Normal Radiosensitivity but A-T-like Inhibition of DNA Synthesis 1985 ·International Journal of Radiation Biology and Related Studies in Physics Chemistry and Medicine ·Alan R. Lehmann, C.F. Arlett, J. F. Burke, M.H.L. Green, Michael R. James, J. Lowe	56
20	Effect of Caffeine on DNA Synthesis in Mammalian Cells 1972 ·Biophysical Journal ·Alan R. Lehmann	81

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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