Serge Gangloff

3.5k total citations · 1 hit paper
27 papers, 3.0k citations indexed

About

Serge Gangloff is a scholar working on Molecular Biology, Plant Science and Cancer Research. According to data from OpenAlex, Serge Gangloff has authored 27 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 9 papers in Plant Science and 6 papers in Cancer Research. Recurrent topics in Serge Gangloff's work include DNA Repair Mechanisms (15 papers), Fungal and yeast genetics research (12 papers) and Carcinogens and Genotoxicity Assessment (5 papers). Serge Gangloff is often cited by papers focused on DNA Repair Mechanisms (15 papers), Fungal and yeast genetics research (12 papers) and Carcinogens and Genotoxicity Assessment (5 papers). Serge Gangloff collaborates with scholars based in France, United States and Hungary. Serge Gangloff's co-authors include Rodney Rothstein, Francis Fabre, Christian Bendixen, John P. McDonald, L. Beaudet Arthur, Christine Soustelle, Bénédicte Michel, Kara A. Bernstein, Wolf‐Dietrich Heyer and Guy J.‐M. Lauquin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Serge Gangloff

26 papers receiving 3.0k citations

Hit Papers

The yeast type I topoisomerase Top3 interacts with Sgs1, ... 1994 2026 2004 2015 1994 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Serge Gangloff France 22 2.9k 603 558 335 287 27 3.0k
Steven J. Brill United States 31 3.8k 1.3× 452 0.7× 544 1.0× 445 1.3× 463 1.6× 45 3.9k
Takemi Enomoto Japan 35 3.6k 1.2× 698 1.2× 615 1.1× 473 1.4× 409 1.4× 141 3.9k
Francis Fabre France 29 3.7k 1.3× 885 1.5× 671 1.2× 382 1.1× 450 1.6× 41 3.8k
Albert Pastink Netherlands 30 3.6k 1.2× 681 1.1× 663 1.2× 312 0.9× 551 1.9× 56 3.9k
Miki Shinohara Japan 27 2.5k 0.9× 302 0.5× 380 0.7× 554 1.7× 237 0.8× 62 2.7k
E C Friedberg United States 36 3.9k 1.3× 752 1.2× 470 0.8× 347 1.0× 570 2.0× 72 4.1k
Joshua A. Sommers United States 33 2.6k 0.9× 796 1.3× 436 0.8× 127 0.4× 303 1.1× 57 2.8k
Felicity Z. Watts United Kingdom 30 2.6k 0.9× 220 0.4× 335 0.6× 551 1.6× 261 0.9× 58 2.8k
Matthew J. Neale United Kingdom 21 3.0k 1.0× 386 0.6× 581 1.0× 398 1.2× 304 1.1× 33 3.2k
Ashwini S. Kamath‐Loeb United States 17 1.7k 0.6× 490 0.8× 335 0.6× 134 0.4× 207 0.7× 25 1.8k

Countries citing papers authored by Serge Gangloff

Since Specialization
Citations

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

Fields of papers citing papers by Serge Gangloff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Serge Gangloff

This figure shows the co-authorship network connecting the top 25 collaborators of Serge Gangloff. A scholar is included among the top collaborators of Serge Gangloff 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 Serge Gangloff. Serge Gangloff 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.
Arcangioli, Benoı̂t & Serge Gangloff. (2023). The Fission Yeast Mating-Type Switching Motto: “One-for-Two” and “Two-for-One”. Microbiology and Molecular Biology Reviews. 87(1). e0000821–e0000821. 9 indexed citations
2.
Achaz, Guillaume, Serge Gangloff, & Benoı̂t Arcangioli. (2022). The quiescent X, the replicative Y and the Autosomes. SHILAP Revista de lepidopterología. 2.
3.
Francesconi, Stefania, et al.. (2020). Nitrogen starvation reveals the mitotic potential of mutants in the S/MAPK pathways. Nature Communications. 11(1). 1973–1973. 3 indexed citations
4.
Jagla, Bernd, et al.. (2018). Molecular signature of the imprintosome complex at the mating-type locus in fission yeast. Microbial Cell. 5(4). 169–183. 5 indexed citations
5.
Gangloff, Serge, et al.. (2017). Quiescence unveils a novel mutational force in fission yeast. eLife. 6. 21 indexed citations
6.
Burkovics, Peter, Marek Šebesta, Valéria Szukacsov, et al.. (2013). Srs2 mediates PCNA-SUMO-dependent inhibition of DNA repair synthesis. The EMBO Journal. 32(5). 742–755. 57 indexed citations
7.
Charbonnier, Jean‐Baptiste, et al.. (2010). Stable interactions between DNA polymerase δ catalytic and structural subunits are essential for efficient DNA repair. DNA repair. 9(10). 1098–1111. 24 indexed citations
8.
Bernstein, Kara A., Serge Gangloff, & Rodney Rothstein. (2010). The RecQ DNA Helicases in DNA Repair. Annual Review of Genetics. 44(1). 393–417. 239 indexed citations
9.
Breton, Christophe, P. Dupaigne, Thomas Robert, et al.. (2008). Srs2 removes deadly recombination intermediates independently of its interaction with SUMO-modified PCNA. Nucleic Acids Research. 36(15). 4964–4974. 34 indexed citations
10.
11.
Maloisel, Laurent, Francis Fabre, & Serge Gangloff. (2007). DNA Polymerase δ Is Preferentially Recruited during Homologous Recombination To Promote Heteroduplex DNA Extension. Molecular and Cellular Biology. 28(4). 1373–1382. 92 indexed citations
12.
Robert, Thomas, et al.. (2006). Mrc1 and Srs2 are major actors in the regulation of spontaneous crossover. The EMBO Journal. 25(12). 2837–2846. 84 indexed citations
13.
Fabre, Francis, et al.. (2002). Alternate pathways involving Sgs1/Top3, Mus81/ Mms4, and Srs2 prevent formation of toxic recombination intermediates from single-stranded gaps created by DNA replication. Proceedings of the National Academy of Sciences. 99(26). 16887–16892. 281 indexed citations
14.
Rothstein, Rodney, Bénédicte Michel, & Serge Gangloff. (2000). Replication fork pausing and recombination or “gimme a break”. Genes & Development. 14(1). 1–10. 278 indexed citations
15.
Gangloff, Serge, Christine Soustelle, & Francis Fabre. (2000). Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases. Nature Genetics. 25(2). 192–194. 313 indexed citations
16.
Gangloff, Serge. (1999). The essential role of yeast topoisomerase III in meiosis depends on recombination. The EMBO Journal. 18(6). 1701–1711. 108 indexed citations
17.
Gangloff, Serge, Hui Zou, & Rodney Rothstein. (1996). Gene conversion plays the major role in controlling the stability of large tandem repeats in yeast.. The EMBO Journal. 15(7). 1715–1725. 114 indexed citations
18.
Rothstein, Rodney & Serge Gangloff. (1995). Hyper-recombination and Bloom's syndrome: microbes again provide clues about cancer.. Genome Research. 5(5). 421–426. 38 indexed citations
19.
Bendixen, Christian, Serge Gangloff, & Rodney Rothstein. (1994). A yeast mating-selection scheme for detection of protein – protein interactions. Nucleic Acids Research. 22(9). 1778–1779. 99 indexed citations
20.
Gangloff, Serge, Michael R. Lieber, & Rodney Rothstein. (1994). Transcription, topoisomerases and recombination. Cellular and Molecular Life Sciences. 50(3). 261–269. 39 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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