Mark S. Dillingham

7.0k total citations · 2 hit papers
76 papers, 5.4k citations indexed

About

Mark S. Dillingham is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Mark S. Dillingham has authored 76 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Molecular Biology, 37 papers in Genetics and 8 papers in Ecology. Recurrent topics in Mark S. Dillingham's work include DNA Repair Mechanisms (54 papers), DNA and Nucleic Acid Chemistry (37 papers) and Bacterial Genetics and Biotechnology (36 papers). Mark S. Dillingham is often cited by papers focused on DNA Repair Mechanisms (54 papers), DNA and Nucleic Acid Chemistry (37 papers) and Bacterial Genetics and Biotechnology (36 papers). Mark S. Dillingham collaborates with scholars based in United Kingdom, Spain and United States. Mark S. Dillingham's co-authors include Dale B. Wigley, Stephen C. Kowalczykowski, Martin R. Singleton, Panos Soultanas, Martin R. Webb, Sameer Velankar, Hosahalli S. Subramanya, Joseph T.P. Yeeles, Maria Spies and Fernando Moreno‐Herrero and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Mark S. Dillingham

75 papers receiving 5.4k citations

Hit Papers

Structure and Mechanism of Helicases and Nucleic Acid Tra... 1999 2026 2008 2017 2007 1999 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark S. Dillingham United Kingdom 37 4.8k 2.0k 583 462 336 76 5.4k
James L. Keck United States 38 3.8k 0.8× 1.6k 0.8× 438 0.8× 363 0.8× 358 1.1× 103 4.3k
Marat Yusupov France 40 7.9k 1.7× 1.5k 0.7× 639 1.1× 334 0.7× 561 1.7× 118 8.7k
G. Yusupova France 36 7.0k 1.5× 1.3k 0.6× 537 0.9× 284 0.6× 423 1.3× 67 7.6k
Xiong Yu United States 41 4.1k 0.9× 1.4k 0.7× 562 1.0× 377 0.8× 302 0.9× 78 5.0k
Phoebe A. Rice United States 35 4.6k 0.9× 1.5k 0.7× 944 1.6× 478 1.0× 350 1.0× 86 5.5k
Alfred Pingoud Germany 44 5.7k 1.2× 1.7k 0.9× 778 1.3× 327 0.7× 500 1.5× 186 6.6k
C.M.T. Spahn Germany 48 6.4k 1.3× 1.3k 0.6× 436 0.7× 415 0.9× 555 1.7× 103 7.6k
Otto Berninghausen Germany 58 7.0k 1.5× 1.3k 0.6× 579 1.0× 262 0.6× 346 1.0× 101 8.6k
Dmitry G. Vassylyev United States 44 6.2k 1.3× 2.6k 1.3× 1.2k 2.0× 279 0.6× 619 1.8× 87 7.1k
S C Kowalczykowski United States 31 4.0k 0.8× 2.0k 1.0× 338 0.6× 319 0.7× 165 0.5× 39 4.3k

Countries citing papers authored by Mark S. Dillingham

Since Specialization
Citations

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

Fields of papers citing papers by Mark S. Dillingham

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark S. Dillingham. 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 Mark S. Dillingham. The network helps show where Mark S. Dillingham may publish in the future.

Co-authorship network of co-authors of Mark S. Dillingham

This figure shows the co-authorship network connecting the top 25 collaborators of Mark S. Dillingham. A scholar is included among the top collaborators of Mark S. Dillingham 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 Mark S. Dillingham. Mark S. Dillingham 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.
Sio, Chiara De, A. Chambers, Mark S. Dillingham, et al.. (2024). Simulation of cell cycle effects on DNA strand break induction due to α-particles. Physica Medica. 129. 104871–104871.
2.
Aulicino, Francesco, Christine Toelzer, Julien Capin, et al.. (2022). Highly efficient CRISPR-mediated large DNA docking and multiplexed prime editing using a single baculovirus. Nucleic Acids Research. 50(13). 7783–7799. 35 indexed citations
4.
Hormeño, Silvia, et al.. (2022). Human HELB is a processive motor protein that catalyzes RPA clearance from single-stranded DNA. Proceedings of the National Academy of Sciences. 119(15). e2112376119–e2112376119. 18 indexed citations
6.
Wojtaszek, Jessica L., Sara Przetocka, Dawid Zyla, et al.. (2021). A stapled peptide mimetic of the CtIP tetramerization motif interferes with double-strand break repair and replication fork protection. Science Advances. 7(8). 9 indexed citations
7.
Hormeño, Silvia, et al.. (2018). Force determination in lateral magnetic tweezers combined with TIRF microscopy. Nanoscale. 10(9). 4579–4590. 19 indexed citations
8.
Carrasco, Carolina, et al.. (2016). Chi hotspots trigger a conformational change in the helicase-like domain of AddAB to activate homologous recombination. Nucleic Acids Research. 44(6). 2727–2741. 6 indexed citations
9.
Carrasco, Carolina, Mark S. Dillingham, & Fernando Moreno‐Herrero. (2014). Single molecule approaches to monitor the recognition and resection of double-stranded DNA breaks during homologous recombination. DNA repair. 20. 119–129. 10 indexed citations
10.
Smith, Abigail J., et al.. (2013). The Conserved C-Terminus of the PcrA/UvrD Helicase Interacts Directly with RNA Polymerase. PLoS ONE. 8(10). e78141–e78141. 38 indexed citations
11.
Fuentes-Perez, Maria Eugenia, Mark S. Dillingham, & Fernando Moreno‐Herrero. (2013). AFM volumetric methods for the characterization of proteins and nucleic acids. Methods. 60(2). 113–121. 45 indexed citations
12.
Yeeles, Joseph T.P., Kara van Aelst, Mark S. Dillingham, & Fernando Moreno‐Herrero. (2011). Recombination Hotspots and Single-Stranded DNA Binding Proteins Couple DNA Translocation to DNA Unwinding by the AddAB Helicase-Nuclease. Molecular Cell. 42(6). 806–816. 35 indexed citations
13.
Yeeles, Joseph T.P. & Mark S. Dillingham. (2010). The processing of double-stranded DNA breaks for recombinational repair by helicase–nuclease complexes. DNA repair. 9(3). 276–285. 69 indexed citations
14.
Fili, Natalia, Gregory I. Mashanov, Christopher P. Toseland, et al.. (2010). Visualizing helicases unwinding DNA at the single molecule level. Nucleic Acids Research. 38(13). 4448–4457. 46 indexed citations
15.
Dillingham, Mark S., et al.. (2008). Fluorescent Single-Stranded DNA Binding Protein as a Probe for Sensitive, Real-Time Assays of Helicase Activity. Biophysical Journal. 95(7). 3330–3339. 53 indexed citations
16.
Dillingham, Mark S.. (2006). Replicative Helicases: A Staircase with a Twist. Current Biology. 16(19). R844–R847. 2 indexed citations
17.
Dillingham, Mark S., Martin R. Webb, & Stephen C. Kowalczykowski. (2005). Bipolar DNA Translocation Contributes to Highly Processive DNA Unwinding by RecBCD Enzyme. Journal of Biological Chemistry. 280(44). 37069–37077. 41 indexed citations
18.
Dillingham, Mark S. & Stephen C. Kowalczykowski. (2001). A Step Backward in Advancing DNA Replication. Molecular Cell. 8(4). 734–736. 16 indexed citations
19.
Velankar, Sameer, Panos Soultanas, Mark S. Dillingham, Hosahalli S. Subramanya, & Dale B. Wigley. (1999). Crystal Structures of Complexes of PcrA DNA Helicase with a DNA Substrate Indicate an Inchworm Mechanism. Cell. 97(1). 75–84. 666 indexed citations breakdown →
20.
Soultanas, Panos, Mark S. Dillingham, & Dale B. Wigley. (1998). Escherichia coli ribosomal protein L3 stimulates the helicase activity of the Bacillus stearothermophilus PcrA helicase. Nucleic Acids Research. 26(10). 2374–2379. 20 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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