Martin Digweed

5.9k citations

76 papers · 4.1k indexed · 1 hit paper · h-index 28

Impact in

Cancer Research top 1%
- Carcinogens and Genotoxicity Assessment
Molecular Biology top 2%
- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
- Genomics and Chromatin Dynamics

Papers in

Cancer Research 31
- Carcinogens and Genotoxicity Assessment 29
Molecular Biology 72
- DNA Repair Mechanisms 52
- CRISPR and Genetic Engineering 13
- RNA and protein synthesis mechanisms 12
- RNA modifications and cancer 9
- Genomics and Phylogenetic Studies 6

Co-authors: Karl Sperling Ilja Demuth André Reis Krystyńa Chrzańowska Zhao‐Qi Wang Raymonda Varon E Seemanová Patrick Concannon
Journals: Nucleic Acids Research (6 papers)Gene (4 papers)European Journal of Biochemistry (4 papers)Human Genetics (4 papers)Human Molecular Genetics (3 papers)
Partner nations: Germany United States Poland

In The Last Decade

Martin Digweed

76 papers receiving 4.0k citations

Hit Papers

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Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome 1998 · 811 citations

Peers

Countries citing papers authored by Martin Digweed

Since Specialization

Citations

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

Fields of papers citing papers by Martin Digweed

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Deficiency of the DNA repair protein nibrin increases the basal but not the radiation induced mutation frequency in vivo Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Caroline Teulier, Jan Vijg, André Nussenzweig, Martin Digweed	2014	6
2	Nijmegen breakage syndrome (NBS) Orphanet Journal of Rare Diseases ·Krystyńa Chrzańowska, Hanna Gregorek, Bożenna Dembowska–Bagińska, Maria Kalina, Martin Digweed	2012	165
3	Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotype Human Mutation ·Manisha Khatkar, Ilja Demuth, Ulrich Baumann, Detlev Schindler, Abbas Khadidja, Heidemarie Neitzel, Gabriele Gillessen-Kaesbach, 西田憲史, De Vries Jk, 秀晴柳下, Gudrun Nürnberg, Peter Nürnberg, Keng Wee Teik, Revathy Nallusamy, André Reis, Zumaira Refni, Martin Digweed, Raymonda Varon	2010	22
4	Nijmegen Breakage Syndrome Protein (NBN) Causes Resistance to Methylating Anticancer Drugs Such as Temozolomide Molecular Pharmacology ·Marcus Eich, Wynand P. Roos, Grigory L. Dianov, Martin Digweed, Bernd Kaina	2010	16
5	Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita Proceedings of the National Academy of Sciences ·Tom Vulliamy, Richard Beswick, Michael Kirwan, Anna Marrone, Martin Digweed, Amanda J. Walne, Inderjeet Dokal	2008	235
6	The Fanconi anemia group A protein modulates homologous repair of DNA double-strand breaks in mammalian cells Carcinogenesis ·Yun‐Gui Yang, Zdenko Herceg, Koji Nakanishi, Ilja Demuth, C. Piccoli, Jocelyne Michelon, J. Vermeiden, Maria Jasin, Martin Digweed, Zhao‐Qi Wang	2005	63
7	Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability Journal of Medical Genetics ·E Seemanová, Zumaira Refni, Heidemarie Neitzel, Raymonda Varon, Jan Hadač, Dietmar Wiedemann, Evelin Schröck, Pavel Seeman, Martin Digweed	2005	37
8	Response to environmental carcinogens in DNA-repair-deficient disorders Toxicology ·Martin Digweed	2003	8
9	Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia Carcinogenesis ·Martin Digweed	2002	71
10	Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene The American Journal of Human Genetics ·Johan P. de Winter, France Léveillé, Carola G.M. van Berkel, Martin A. Rooimans, Laura van der Weel, Jûrgen Steltenpool, Ilja Demuth, Neil V. Morgan, Noa Alon, Lucine Bosnoyan-Collins, Jeff Lightfoot, Peter A. J. Leegwater, Quinten Waisfisz, Kenshi Komatsu, Fré Arwert, Jan C. Pronk, Christopher G. Mathew, Martin Digweed, Manuel Buchwald, Hans Joenje	2000	175
11	The Fanconi Anemia Group E Gene, FANCE, Maps to Chromosome 6p The American Journal of Human Genetics ·Quinten Waisfisz, Çiğdem Altay, Peter A. J. Leegwater, Johan P. de Winter, Kenshi Komatsu, D. Gareth Evans, Rolf‐Dieter Wegner, André Reis, Hans Joenje, Fré Arwert, Christopher G. Mathew, Jan C. Pronk, Kathrin Saar, Neil V. Morgan, Martin Digweed	1999	41
12	Molekulare Grundlagen der Fanconi-Anämie Klinische Pädiatrie ·Martin Digweed	1999	6
13	Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome Cell ·Raymonda Varon, Christine Vissinga, Matthias Platzer, Karen Cerosaletti, Krystyńa Chrzańowska, Kathrin Saar, Georg Beckmann, E Seemanová, Paul R. Cooper, Norma J. Nowak, Markus Stümm, Corry M.R. Weemaes, Richard A. Gatti, Richard K. Wilson, Martin Digweed, André Rosenthal, Karl Sperling, Patrick Concannon, André Reis Hit paper breakdown →	1998	811
14	Localisation of a Fanconi anaemia gene to chromosome 9p European Journal of Human Genetics ·Kathrin Saar, Detlev Schindler, Rolf‐Dieter Wegner, André Reis, Thomas F. Wienker, Holger Hoehn, Hans Joenje, Karl Sperling, Martin Digweed	1998	17
15	Genomic organization of a potential human DNA-crosslink repair gene, KIAA0086 Mutation Research/DNA Repair ·Ilja Demuth, Martin Digweed	1998	9
16	Retroviral gene transfer for the assignment of Fanconi anemia (FA) patients to a FA complementation group Human Genetics ·Wanting Chen, Shirley del Carmen Molina Campoverde, 伊藤東, Martin Digweed, Johnson M. Liu, Christopher Walsh	1998	8
17	Sequence variations in the Fanconi anaemia gene, FAC : pathogenicity of 1806insA and R548X and recognition of D195V as a polymorphic variant Human Genetics ·Jerome R. Lo Ten Foe, Martine T. Barel, Shirley del Carmen Molina Campoverde, Martin Digweed, Fré Arwert, Hans Joenje	1996	18
18	Routine applications of DNA fingerprinting with the oligonucleotide probe (CAC)₅/(GTG)₅ Clinical Genetics ·Heidemarie Neitzel, Martin Digweed, Peter Nürnberg, Fernando Velez, Cornelia Schmidt, Sigrid Tinschert, Karl Sperling	1991	7
19	Identification of a HeLa mRNA fraction which can correct the DNA-repair defect in Fanconi anaemia fibroblasts Mutation Research/DNA Repair ·Martin Digweed, Karl Sperling	1989	9
20	Fanconi's anaemia: correlation of genetic complementation group with psoralen/UVA response Human Genetics ·Martin Digweed, Luiz Sergio de Almeida Camargo, Karl Sperling	1988	25

About Martin Digweed

Martin Digweed is a scholar working on Cancer Research, Molecular Biology, Aging, Oncology and Genetics, having authored 76 papers that have together received 4.1k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (52 papers), Carcinogens and Genotoxicity Assessment (29 papers), CRISPR and Genetic Engineering (13 papers), RNA and protein synthesis mechanisms (12 papers), Plant Genetic and Mutation Studies (10 papers), RNA modifications and cancer (9 papers), Cancer-related Molecular Pathways (9 papers) and Genomics and Phylogenetic Studies (6 papers). The work is most often cited by research in Cancer Research (1.2k citations), Molecular Biology (3.6k citations), Oncology (848 citations), Aging (51 citations) and Cell Biology (454 citations). Martin Digweed has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Karl Sperling, Ilja Demuth, André Reis, Krystyńa Chrzańowska, Zhao‐Qi Wang, Raymonda Varon, E Seemanová, Patrick Concannon, Kathrin Saar and Alan D. D’Andrea. Their work appears in journals such as Nucleic Acids Research, Gene, European Journal of Biochemistry, Human Genetics and Human Molecular Genetics.

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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