Susan R. McCouch

46.9k total citations · 13 hit papers
238 papers, 32.4k citations indexed

About

Susan R. McCouch is a scholar working on Plant Science, Genetics and Molecular Biology. According to data from OpenAlex, Susan R. McCouch has authored 238 papers receiving a total of 32.4k indexed citations (citations by other indexed papers that have themselves been cited), including 222 papers in Plant Science, 154 papers in Genetics and 45 papers in Molecular Biology. Recurrent topics in Susan R. McCouch's work include Genetic Mapping and Diversity in Plants and Animals (151 papers), Rice Cultivation and Yield Improvement (98 papers) and GABA and Rice Research (61 papers). Susan R. McCouch is often cited by papers focused on Genetic Mapping and Diversity in Plants and Animals (151 papers), Rice Cultivation and Yield Improvement (98 papers) and GABA and Rice Research (61 papers). Susan R. McCouch collaborates with scholars based in United States, Philippines and South Korea. Susan R. McCouch's co-authors include Steven D. Tanksley, Svetlana V. Temnykh, Olivier Panaud, Megan Sweeney, Yunbi Xu, Michael J. Thomson, Leonard Lipovich, Genevieve DeClerck, Melissa Fitzgerald and Samuel W. Cartinhour and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Susan R. McCouch

236 papers receiving 30.5k citations

Hit Papers

Seed Banks and Molecular ... 1988 2026 2000 2013 1997 2002 2001 2011 1988 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Susan R. McCouch United States 91 28.8k 17.4k 6.4k 1.3k 1.0k 238 32.4k
Mark E. Sorrells United States 86 23.2k 0.8× 13.0k 0.7× 3.9k 0.6× 1.1k 0.9× 2.3k 2.2× 289 26.7k
Masahiro Yano Japan 99 31.4k 1.1× 13.7k 0.8× 8.5k 1.3× 666 0.5× 1.3k 1.3× 288 33.7k
John Doebley United States 71 19.9k 0.7× 13.6k 0.8× 7.9k 1.2× 2.5k 1.9× 1.9k 1.8× 153 25.6k
Qifa Zhang China 84 22.3k 0.8× 11.5k 0.7× 8.7k 1.4× 567 0.4× 769 0.7× 241 25.3k
Rajeev K. Varshney India 99 33.7k 1.2× 8.5k 0.5× 9.0k 1.4× 2.6k 2.0× 2.3k 2.2× 878 40.3k
Steven D. Tanksley United States 94 29.7k 1.0× 11.3k 0.6× 12.4k 1.9× 2.1k 1.7× 816 0.8× 236 33.7k
W. Powell United Kingdom 74 15.5k 0.5× 8.7k 0.5× 5.9k 0.9× 2.9k 2.2× 1.1k 1.0× 278 21.2k
Robbie Waugh United Kingdom 76 15.8k 0.5× 5.9k 0.3× 4.7k 0.7× 1.0k 0.8× 1.1k 1.0× 282 18.2k
G. S. Khush Philippines 63 18.5k 0.6× 7.3k 0.4× 5.1k 0.8× 1.9k 1.5× 1.3k 1.2× 264 20.9k
Andrew H. Paterson United States 90 26.2k 0.9× 9.8k 0.6× 12.3k 1.9× 2.5k 1.9× 2.2k 2.1× 419 32.7k

Countries citing papers authored by Susan R. McCouch

Since Specialization
Citations

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

Fields of papers citing papers by Susan R. McCouch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Susan R. McCouch. 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 Susan R. McCouch. The network helps show where Susan R. McCouch may publish in the future.

Co-authorship network of co-authors of Susan R. McCouch

This figure shows the co-authorship network connecting the top 25 collaborators of Susan R. McCouch. A scholar is included among the top collaborators of Susan R. McCouch 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 Susan R. McCouch. Susan R. McCouch 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.
Liao, Chuan, Jenny Kao‐Kniffin, Matthew C. Reid, et al.. (2025). Rice farming for climate change adaptation in the Northeastern United States. Proceedings of the National Academy of Sciences. 122(49). e2402181122–e2402181122. 1 indexed citations
2.
Waqas, Muhammad, Susan R. McCouch, Davide Francioli, et al.. (2025). Blueprints for sustainable plant production through the utilization of crop wild relatives and their microbiomes. Nature Communications. 16(1). 6364–6364. 5 indexed citations
3.
Bessho‐Uehara, Kanako, Diane Wang, Rosalyn B. Angeles‐Shim, et al.. (2023). Regulator of Awn Elongation 3 , an E3 ubiquitin ligase, is responsible for loss of awns during African rice domestication. Proceedings of the National Academy of Sciences. 120(4). e2207105120–e2207105120. 13 indexed citations
4.
Riewe, David, et al.. (2022). Can biochemical traits bridge the gap between genomics and plant performance? A study in rice under drought. PLANT PHYSIOLOGY. 189(2). 1139–1152. 8 indexed citations
5.
Reynolds, Matthew, Owen K. Atkin, Malcolm J. Bennett, et al.. (2021). Addressing Research Bottlenecks to Crop Productivity. Trends in Plant Science. 26(6). 607–630. 90 indexed citations
6.
Li, Nana, Ping Li, Jennifer Spindel, et al.. (2021). Genetic mapping identifies a rice naringenin O‐glucosyltransferase that influences insect resistance. The Plant Journal. 106(5). 1401–1413. 21 indexed citations
7.
Greenberg, Anthony J., Luz Stella Barrero, Lyza Maron, et al.. (2020). Low Additive Genetic Variation in a Trait Under Selection in Domesticated Rice. G3 Genes Genomes Genetics. 10(7). 2435–2443. 10 indexed citations
8.
9.
Wang, Diane, Francisco Agosto-Perez, Dmytro Chebotarov, et al.. (2018). An imputation platform to enhance integration of rice genetic resources. Nature Communications. 9(1). 3519–3519. 56 indexed citations
10.
Uga, Yusaku, Yuka Kitomi, Brandon Larson, et al.. (2018). Genomic regions responsible for seminal and crown root lengths identified by 2D & 3D root system image analysis. BMC Genomics. 19(1). 273–273. 11 indexed citations
11.
Daygon, Venea Dara, Mariafe Calingacion, James J. De Voss, et al.. (2017). Metabolomics and genomics combine to unravel the pathway for the presence of fragrance in rice. Scientific Reports. 7(1). 8767–8767. 44 indexed citations
12.
Piñeros, Miguel A., Brandon Larson, Jon E. Shaff, et al.. (2015). Evolving technologies for growing, imaging and analyzing 3D root system architecture of crop plants. Journal of Integrative Plant Biology. 58(3). 230–241. 38 indexed citations
13.
Yan, Jian, Takako Aboshi, Masayoshi Teraishi, et al.. (2015). The Tyrosine Aminomutase TAM1 Is Required for β-Tyrosine Biosynthesis in Rice. The Plant Cell. 27(4). 1265–1278. 31 indexed citations
14.
Schatz, Michael C., Lyza Maron, Joshua C. Stein, et al.. (2014). Whole genome de novo assemblies of three divergent strains of rice, Oryza sativa, document novel gene space of aus and indica. Genome biology. 15(11). 506–506. 188 indexed citations
15.
Li, Jianyong, Jiping Liu, Dekun Dong, et al.. (2014). Natural variation underlies alterations in Nramp aluminum transporter ( NRAT1 ) expression and function that play a key role in rice aluminum tolerance. Proceedings of the National Academy of Sciences. 111(17). 6503–6508. 126 indexed citations
16.
Cardoso, Catarina, Yanxia Zhang, Muhammad Jamil, et al.. (2014). Natural variation of rice strigolactone biosynthesis is associated with the deletion of two MAX1 orthologs. Proceedings of the National Academy of Sciences. 111(6). 2379–2384. 110 indexed citations
17.
Kovach, Michael J., Mariafe Calingacion, Melissa Fitzgerald, & Susan R. McCouch. (2009). The origin and evolution of fragrance in rice ( Oryza sativa L.). Proceedings of the National Academy of Sciences. 106(34). 14444–14449. 241 indexed citations
18.
Woo, Mi‐Ok, Tae‐Ho Ham, Hyeonso Ji, et al.. (2008). Inactivation of the UGPase1 gene causes genic male sterility and endosperm chalkiness in rice (Oryza sativa L.). The Plant Journal. 54(2). 190–204. 87 indexed citations
19.
Sweeney, Megan, Michael J. Thomson, Bernard E. Pfeil, & Susan R. McCouch. (2006). Caught Red-Handed:RcEncodes a Basic Helix-Loop-Helix Protein Conditioning Red Pericarp in Rice. The Plant Cell. 18(2). 283–294. 414 indexed citations
20.
Septiningsih, Endang M., Kurniawan Rudi Trijatmiko, Sugiono Moeljopawiro, & Susan R. McCouch. (2003). Identification of quantitative trait loci for grain quality in an advanced backcross population derived from the Oryza sativa variety IR64 and the wild relative O. rufipogon. Theoretical and Applied Genetics. 107(8). 1433–1441. 151 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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