Francis Fabre

4.5k total citations
41 papers, 3.8k citations indexed

About

Francis Fabre is a scholar working on Molecular Biology, Plant Science and Cancer Research. According to data from OpenAlex, Francis Fabre has authored 41 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 12 papers in Plant Science and 5 papers in Cancer Research. Recurrent topics in Francis Fabre's work include DNA Repair Mechanisms (32 papers), Fungal and yeast genetics research (27 papers) and CRISPR and Genetic Engineering (12 papers). Francis Fabre is often cited by papers focused on DNA Repair Mechanisms (32 papers), Fungal and yeast genetics research (27 papers) and CRISPR and Genetic Engineering (12 papers). Francis Fabre collaborates with scholars based in France, United States and Russia. Francis Fabre's co-authors include Serge Gangloff, R. Chanet, Christine Soustelle, Xavier Veaute, Éric Le Cam, Abdelilah Aboussekhra, Josette Jeusset, E L Ivanov, Herschel Roman and M. Heude and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Francis Fabre

41 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Francis Fabre France 29 3.7k 885 671 450 382 41 3.8k
E C Friedberg United States 36 3.9k 1.1× 752 0.8× 470 0.7× 570 1.3× 347 0.9× 72 4.1k
Serge Gangloff France 22 2.9k 0.8× 603 0.7× 558 0.8× 287 0.6× 335 0.9× 27 3.0k
Steven J. Brill United States 31 3.8k 1.0× 452 0.5× 544 0.8× 463 1.0× 445 1.2× 45 3.9k
Carol S. Newlon United States 41 4.7k 1.3× 256 0.3× 815 1.2× 768 1.7× 700 1.8× 72 4.9k
John P. McDonald United States 28 3.4k 0.9× 828 0.9× 432 0.6× 765 1.7× 230 0.6× 55 3.6k
Neal Sugawara United States 26 3.3k 0.9× 499 0.6× 617 0.9× 320 0.7× 302 0.8× 32 3.5k
John C. Game United States 28 2.6k 0.7× 339 0.4× 439 0.7× 276 0.6× 161 0.4× 49 2.8k
José Antonio Tercero Spain 19 2.4k 0.6× 415 0.5× 213 0.3× 318 0.7× 581 1.5× 33 2.5k
Miki Shinohara Japan 27 2.5k 0.7× 302 0.3× 380 0.6× 237 0.5× 554 1.5× 62 2.7k
Nancy M. Hollingsworth United States 32 4.0k 1.1× 353 0.4× 631 0.9× 309 0.7× 1.2k 3.3× 50 4.2k

Countries citing papers authored by Francis Fabre

Since Specialization
Citations

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

Fields of papers citing papers by Francis Fabre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francis Fabre

This figure shows the co-authorship network connecting the top 25 collaborators of Francis Fabre. A scholar is included among the top collaborators of Francis Fabre 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 Francis Fabre. Francis Fabre 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.
Liu, Jie, Ludovic Renault, Xavier Veaute, et al.. (2011). Rad51 paralogues Rad55–Rad57 balance the antirecombinase Srs2 in Rad51 filament formation. Nature. 479(7372). 245–248. 155 indexed citations
2.
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
3.
4.
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
5.
Soustelle, Christine, Laurence Vernis, Karine Fréon, et al.. (2004). A New Saccharomyces cerevisiae Strain with a Mutant Smt3-Deconjugating Ulp1 Protein Is Affected in DNA Replication and Requires Srs2 and Homologous Recombination for Its Viability. Molecular and Cellular Biology. 24(12). 5130–5143. 33 indexed citations
6.
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
7.
Chanet, R., M. Heude, Adouda Adjiri, Laurent Maloisel, & Francis Fabre. (1996). Semidominant Mutations in the Yeast Rad51 Protein and Their Relationships with the Srs2 Helicase. Molecular and Cellular Biology. 16(9). 4782–4789. 70 indexed citations
8.
Aboussekhra, Abdelilah, et al.. (1996). A novel role for the budding yeast RAD9 checkpoint gene in DNA damage-dependent transcription.. The EMBO Journal. 15(15). 3912–3922. 102 indexed citations
9.
Heude, M., R. Chanet, & Francis Fabre. (1995). Regulation of theSaccharomyces cerevisiae Srs2 helicase during the mitotic cell cycle, meiosis and after irradiation. Molecular and General Genetics MGG. 248(1). 59–68. 35 indexed citations
10.
Ivanov, E L, Neal Sugawara, Charles I. White, Francis Fabre, & James E. Haber. (1994). Mutations in XRS2 and RAD50 Delay but Do Not Prevent Mating-Type Switching in Saccharomyces cerevisiae. Molecular and Cellular Biology. 14(5). 3414–3425. 200 indexed citations
11.
Adjiri, Adouda, R. Chanet, Christine Mézard, & Francis Fabre. (1994). Sequence comparison of the ARG4 chromosomal regions from the two related yeasts, Saccharomyces cerevisiae and Saccharomyces douglasii. Yeast. 10(3). 309–317. 19 indexed citations
12.
Fabre, Francis, et al.. (1994). Efficient UV stimulation of yeast integrative transformation requires damage on both plasmid strands. Molecular and General Genetics MGG. 243(3). 308–314. 4 indexed citations
13.
Jang, Yeun Kyu, Yong Hwan Jin, Eun Mi Kim, et al.. (1994). Cloning and sequence analysis of rhp51+, a Schizosaccharomyces pombe homolog of the Saccharomyces cerevisiae RAD51 gene. Gene. 142(2). 207–211. 39 indexed citations
14.
Cassier‐Chauvat, Corinne & Francis Fabre. (1991). A similar defect in UV-induced mutagenesis conferred by the rad6 and rad18 mutations of Saccharomyces cerevisiae. Mutation Research/DNA Repair. 254(3). 247–253. 56 indexed citations
15.
Zgaga, Zoran, R. Chanet, Miroslav Radman, & Francis Fabre. (1991). Mismatch-stimulated plasmid integration in yeast. Current Genetics. 19(4). 329–332. 10 indexed citations
16.
Fabre, Francis, Annick Boulet, & Gérard Faye. (1991). Possible involvement of the yeast POLIII DNA polymerase in induced gene conversion. Molecular and General Genetics MGG. 229(3). 353–356. 20 indexed citations
17.
Fabre, Francis, Nieve Magaña‐Schwencke, & R. Chanet. (1989). Isolation of the RAD18 gene of Saccharomyces cerevisiae and construction of rad18 deletion mutants. Molecular and General Genetics MGG. 215(3). 425–430. 19 indexed citations
18.
Fabre, Francis & Herschel Roman. (1977). Genetic evidence for inducibility of recombination competence in yeast.. Proceedings of the National Academy of Sciences. 74(4). 1667–1671. 90 indexed citations
19.
20.
Fabre, Francis. (1971). A UV-supersensitive mutant in the yeast Schizosaccharomyces pombe. Molecular and General Genetics MGG. 110(2). 134–143. 31 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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