Edward J. Louis

18.3k total citations · 1 hit paper
116 papers, 11.0k citations indexed

About

Edward J. Louis is a scholar working on Molecular Biology, Food Science and Plant Science. According to data from OpenAlex, Edward J. Louis has authored 116 papers receiving a total of 11.0k indexed citations (citations by other indexed papers that have themselves been cited), including 89 papers in Molecular Biology, 38 papers in Food Science and 33 papers in Plant Science. Recurrent topics in Edward J. Louis's work include Fungal and yeast genetics research (55 papers), Fermentation and Sensory Analysis (38 papers) and DNA Repair Mechanisms (19 papers). Edward J. Louis is often cited by papers focused on Fungal and yeast genetics research (55 papers), Fermentation and Sensory Analysis (38 papers) and DNA Repair Mechanisms (19 papers). Edward J. Louis collaborates with scholars based in United Kingdom, United States and France. Edward J. Louis's co-authors include Rhona H. Borts, Gianni Liti, Stephen G. Oliver, James E. Haber, Bernard Dujon, Ian D. Hickson, B. G. Barrell, Hervé Tettelin, Horst Feldmann and Yasufumi Murakami and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Edward J. Louis

115 papers receiving 10.7k citations

Hit Papers

Life with 6000 Genes 1996 2026 2006 2016 1996 500 1000 1.5k 2.0k 2.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edward J. Louis United Kingdom 48 8.8k 3.3k 2.6k 1.7k 952 116 11.0k
Bernard Dujon France 58 13.7k 1.6× 3.3k 1.0× 1.4k 0.5× 2.0k 1.2× 210 0.2× 174 15.5k
James R. Broach United States 70 16.0k 1.8× 2.7k 0.8× 687 0.3× 1.7k 1.0× 395 0.4× 224 18.2k
Howard Bussey Canada 60 12.3k 1.4× 4.0k 1.2× 1.2k 0.5× 1.0k 0.6× 229 0.2× 141 14.8k
R. Daniel Gietz Canada 29 12.3k 1.4× 2.9k 0.9× 724 0.3× 979 0.6× 272 0.3× 44 14.5k
Jasper Rine United States 68 14.1k 1.6× 2.5k 0.8× 419 0.2× 2.0k 1.2× 599 0.6× 203 16.8k
Peter Philippsen Switzerland 51 17.4k 2.0× 3.7k 1.1× 1.0k 0.4× 1.1k 0.7× 420 0.4× 102 19.0k
Jürg Bähler United Kingdom 59 14.2k 1.6× 2.7k 0.8× 359 0.1× 1.2k 0.7× 365 0.4× 194 16.3k
Aron Marchler‐Bauer United States 29 8.6k 1.0× 3.5k 1.1× 451 0.2× 1.4k 0.8× 169 0.2× 50 12.9k
‎Berend Snel Netherlands 51 9.9k 1.1× 2.4k 0.7× 686 0.3× 1.6k 1.0× 198 0.2× 116 12.2k
Rodney Rothstein United States 64 21.6k 2.4× 3.5k 1.1× 388 0.1× 2.7k 1.6× 609 0.6× 158 22.9k

Countries citing papers authored by Edward J. Louis

Since Specialization
Citations

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

Fields of papers citing papers by Edward J. Louis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edward J. Louis. 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 Edward J. Louis. The network helps show where Edward J. Louis may publish in the future.

Co-authorship network of co-authors of Edward J. Louis

This figure shows the co-authorship network connecting the top 25 collaborators of Edward J. Louis. A scholar is included among the top collaborators of Edward J. Louis 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 Edward J. Louis. Edward J. Louis 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.
Hu, Yue, et al.. (2024). Impact of inter-species hybridisation on antifungal drug response in the Saccharomyces genus. BMC Genomics. 25(1). 1165–1165. 1 indexed citations
3.
Branduardi, Paola, et al.. (2022). Molecular Tools for Leveraging the Potential of the Acid-Tolerant Yeast Zygosaccharomyces bailii as Cell Factory. Methods in molecular biology. 2513. 179–204. 2 indexed citations
4.
Boekhout, Teun, M. Catherine Aime, Dominik Begerow, et al.. (2021). The evolving species concepts used for yeasts: from phenotypes and genomes to speciation networks. Fungal Diversity. 109(1). 27–55. 39 indexed citations
5.
Naseeb, Samina, Yue Hu, Thomas Walsh, et al.. (2021). Restoring fertility in yeast hybrids: Breeding and quantitative genetics of beneficial traits. Proceedings of the National Academy of Sciences. 118(38). 26 indexed citations
6.
Barton, David B. H., et al.. (2018). PHENOS: a high-throughput and flexible tool for microorganism growth phenotyping on solid media. BMC Microbiology. 18(1). 9–9. 12 indexed citations
7.
Zaky, Abdelrahman Saleh, Darren Greetham, Edward J. Louis, Gregory A. Tucker, & Chenyu Du. (2016). A New Isolation and Evaluation Method for Marine-Derived Yeast spp. with Potential Applications in Industrial Biotechnology. Journal of Microbiology and Biotechnology. 26(11). 1891–1907. 33 indexed citations
8.
Salinas, F., Francisco A. Cubillos, Verónica García, et al.. (2012). The Genetic Basis of Natural Variation in Oenological Traits in Saccharomyces cerevisiae. PLoS ONE. 7(11). e49640–e49640. 66 indexed citations
9.
Louis, Edward J.. (2011). Population genomics and speciation in yeasts. Fungal Biology Reviews. 25(3). 136–142. 20 indexed citations
10.
Reed, Simon H., et al.. (2010). Silenced yeast chromatin is maintained by Sir2 in preference to permitting histone acetylations for efficient NER. Nucleic Acids Research. 38(14). 4675–4686. 11 indexed citations
11.
Dunham, Maitreya J. & Edward J. Louis. (2010). Yeast evolution and ecology meet genomics. EMBO Reports. 12(1). 8–10. 3 indexed citations
12.
Inglis, Peter W., Sarah Sharp, Fiona Pryde, et al.. (2009). Repressive and non-repressive chromatin at native telomeres in Saccharomyces cerevisiae. Epigenetics & Chromatin. 2(1). 18–18. 25 indexed citations
14.
Louis, Edward J. & Rhona H. Borts. (2003). Meiotic Recombination: Too Much of a Good Thing?. Current Biology. 13(24). R953–R955. 11 indexed citations
15.
Delneri, Daniela, Isabelle Colson, Sofia Grammenoudi, et al.. (2003). Engineering evolution to study speciation in yeasts. Nature. 422(6927). 68–72. 189 indexed citations
16.
Greig, Duncan, Edward J. Louis, Rhona H. Borts, & Michael Travisano. (2002). Hybrid Speciation in Experimental Populations of Yeast. Science. 298(5599). 1773–1775. 132 indexed citations
17.
Huang, Pei‐Hsiu, et al.. (2001). SGS1 is required for telomere elongation in the absence of telomerase. Current Biology. 11(2). 125–129. 157 indexed citations
18.
Wang, Xinwang, Paul M. Watt, Rhona H. Borts, Edward J. Louis, & Ian D. Hickson. (1999). The topoisomerase II-associated protein, Pat1p, is required for maintenance of rDNA locus stability in Saccharomyces cerevisiae. Molecular and General Genetics MGG. 261(4-5). 831–840. 14 indexed citations
19.
Louis, Edward J.. (1995). The chromosome ends of Saccharomyces cerevisiae. Yeast. 11(16). 1553–1573. 182 indexed citations
20.
Наумова, Е. С., et al.. (1992). Genetic homology between Saccharomyces cerevisiae and its sibling species S. paradoxus and S. bayanus: Electrophoretic karyotypes. Yeast. 8(8). 599–612. 152 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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