Julian E. Sale

8.2k total citations · 2 hit papers
96 papers, 5.8k citations indexed

About

Julian E. Sale is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Julian E. Sale has authored 96 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 20 papers in Cancer Research and 13 papers in Oncology. Recurrent topics in Julian E. Sale's work include DNA Repair Mechanisms (53 papers), CRISPR and Genetic Engineering (22 papers) and Genomics and Chromatin Dynamics (20 papers). Julian E. Sale is often cited by papers focused on DNA Repair Mechanisms (53 papers), CRISPR and Genetic Engineering (22 papers) and Genomics and Chromatin Dynamics (20 papers). Julian E. Sale collaborates with scholars based in United Kingdom, Japan and United States. Julian E. Sale's co-authors include Michael S. Neuberger, Laura J. Simpson, Alan R. Lehmann, Roger Woodgate, Peter Sarkies, Guillaume Guilbaud, Shunichi Takeda, Michael R. Stratton, Ludmil B. Alexandrov and Pierre Murat and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Julian E. Sale

95 papers receiving 5.8k citations

Hit Papers

Clock-like mutational processes in human somatic cells 2012 2026 2016 2021 2015 2012 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julian E. Sale United Kingdom 39 4.9k 1.4k 935 725 641 96 5.8k
Michael J. Difilippantonio United States 33 3.4k 0.7× 1.1k 0.8× 1.4k 1.5× 1.4k 1.9× 775 1.2× 61 5.5k
Dale A. Ramsden United States 47 6.5k 1.3× 1.1k 0.8× 1.7k 1.9× 1.6k 2.3× 727 1.1× 106 7.7k
Eric A. Hendrickson United States 44 4.6k 0.9× 735 0.5× 1.5k 1.6× 541 0.7× 538 0.8× 105 5.4k
Nicola Crosetto Sweden 30 3.7k 0.8× 1.0k 0.7× 1.0k 1.1× 294 0.4× 428 0.7× 72 4.6k
Katheryn Meek United States 43 4.6k 0.9× 877 0.6× 1.8k 1.9× 928 1.3× 382 0.6× 83 5.6k
Alberto Ciccia United States 28 6.6k 1.3× 1.1k 0.8× 2.2k 2.3× 427 0.6× 844 1.3× 45 7.5k
Elsa Callén United States 33 4.0k 0.8× 592 0.4× 1.4k 1.5× 738 1.0× 481 0.8× 44 4.8k
Alessandro A. Sartori Switzerland 31 3.9k 0.8× 649 0.5× 1.5k 1.6× 301 0.4× 459 0.7× 54 4.5k
Masamichi Ishiai Japan 36 2.7k 0.5× 714 0.5× 679 0.7× 928 1.3× 469 0.7× 67 3.7k
Matthias Dobbelstein Germany 44 4.7k 1.0× 1.3k 0.9× 2.7k 2.9× 515 0.7× 996 1.6× 129 6.1k

Countries citing papers authored by Julian E. Sale

Since Specialization
Citations

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

Fields of papers citing papers by Julian E. Sale

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julian E. Sale. 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 Julian E. Sale. The network helps show where Julian E. Sale may publish in the future.

Co-authorship network of co-authors of Julian E. Sale

This figure shows the co-authorship network connecting the top 25 collaborators of Julian E. Sale. A scholar is included among the top collaborators of Julian E. Sale 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 Julian E. Sale. Julian E. Sale 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.
Petris, Gianluca, Pierre Murat, Kim C. Liu, et al.. (2025). High-fidelity human chromosome transfer and elimination. Science. 390(6777). 1038–1043. 1 indexed citations
2.
Gillis, Alexander, et al.. (2024). CRL3ARMC5 ubiquitin ligase and Integrator phosphatase form parallel mechanisms to control early stages of RNA Pol II transcription. Molecular Cell. 84(24). 4808–4823.e13. 6 indexed citations
3.
Murat, Pierre, Guillaume Guilbaud, & Julian E. Sale. (2024). DNA replication initiation drives focal mutagenesis and rearrangements in human cancers. Nature Communications. 15(1). 10850–10850. 3 indexed citations
4.
Alcón, Pablo, Artur Kaczmarczyk, Guillaume Guilbaud, et al.. (2024). FANCD2–FANCI surveys DNA and recognizes double- to single-stranded junctions. Nature. 632(8027). 1165–1173. 11 indexed citations
5.
Kleefeldt, Askar A., Louise F. H. Funke, Jakob Birnbaum, et al.. (2023). Continuous synthesis of E. coli genome sections and Mb-scale human DNA assembly. Nature. 619(7970). 555–562. 30 indexed citations
6.
Šviković, Saša, et al.. (2023). PRIMPOL ensures robust handoff between on-the-fly and post-replicative DNA lesion bypass. Nucleic Acids Research. 52(1). 243–258. 10 indexed citations
7.
Guilbaud, Guillaume, et al.. (2022). Determination of human DNA replication origin position and efficiency reveals principles of initiation zone organisation. Nucleic Acids Research. 50(13). 7436–7450. 36 indexed citations
8.
Sale, Julian E.. (2022). Focus and persistence: how Pol IV unblocks stalled DNA synthesis. Nature Structural & Molecular Biology. 29(9). 846–847. 2 indexed citations
9.
Petljak, Mia, Alexandra Dananberg, Kevan Chu, et al.. (2022). Mechanisms of APOBEC3 mutagenesis in human cancer cells. Nature. 607(7920). 799–807. 123 indexed citations
10.
Murat, Pierre, et al.. (2022). DNA replication initiation shapes the mutational landscape and expression of the human genome. Science Advances. 8(45). eadd3686–eadd3686. 13 indexed citations
11.
Bonnin, Sarah, Carlos Martínez, Talía Velasco-Hernández, et al.. (2021). Distinct roles for PARP-1 and PARP-2 in c-Myc–driven B-cell lymphoma in mice. Blood. 139(2). 228–239. 24 indexed citations
12.
Šviković, Saša, et al.. (2021). The intersection of DNA replication with antisense 3' RNA processing in Arabidopsis FLC chromatin silencing.. Apollo (University of Cambridge). 2 indexed citations
13.
Šviković, Saša, et al.. (2021). The intersection of DNA replication with antisense 3′ RNA processing in Arabidopsis FLC chromatin silencing. Proceedings of the National Academy of Sciences. 118(28). 12 indexed citations
14.
Lerner, Letícia Koch, M.L. Kilkenny, Saša Šviković, et al.. (2020). Timeless couples G‐quadruplex detection with processing by DDX 11 helicase during DNA replication. The EMBO Journal. 39(18). e104185–e104185. 55 indexed citations
15.
Schiavone, Davide, et al.. (2016). Histone H3.3 promotes IgV gene diversification by enhancing formation of AID ‐accessible single‐stranded DNA. The EMBO Journal. 35(13). 1452–1464. 23 indexed citations
16.
Alexandrov, Ludmil B., Philip H. Jones, David C. Wedge, et al.. (2015). Clock-like mutational processes in human somatic cells. Nature Genetics. 47(12). 1402–1407. 569 indexed citations breakdown →
17.
Williams, Gareth T., et al.. (2015). Directed evolution of human scFvs in DT40 cells. Protein Engineering Design and Selection. 29(2). 39–48. 6 indexed citations
18.
Schiavone, Davide, Guillaume Guilbaud, Pierre Murat, et al.. (2014). Determinants of G quadruplex‐induced epigenetic instability in REV 1‐deficient cells. The EMBO Journal. 33(21). 2507–2520. 103 indexed citations
19.
Listovsky, Tamar, et al.. (2014). Histone H3.3 Is Required to Maintain Replication Fork Progression after UV Damage. Current Biology. 24(18). 2195–2201. 48 indexed citations
20.
Harris, Reuben S., Julian E. Sale, Svend K. Petersen‐Mahrt, & Michael S. Neuberger. (2002). AID Is Essential for Immunoglobulin V Gene Conversion in a Cultured B Cell Line. Current Biology. 12(5). 435–438. 191 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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