Robert M. Stupar

7.3k total citations · 1 hit paper
93 papers, 4.3k citations indexed

About

Robert M. Stupar is a scholar working on Plant Science, Molecular Biology and Genetics. According to data from OpenAlex, Robert M. Stupar has authored 93 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 88 papers in Plant Science, 24 papers in Molecular Biology and 11 papers in Genetics. Recurrent topics in Robert M. Stupar's work include Soybean genetics and cultivation (36 papers), Legume Nitrogen Fixing Symbiosis (33 papers) and Plant Virus Research Studies (21 papers). Robert M. Stupar is often cited by papers focused on Soybean genetics and cultivation (36 papers), Legume Nitrogen Fixing Symbiosis (33 papers) and Plant Virus Research Studies (21 papers). Robert M. Stupar collaborates with scholars based in United States, Canada and China. Robert M. Stupar's co-authors include Nathan M. Springer, Shaun J. Curtin, Jiming Jiang, William J. Haun, Jean‐Michel Michno, Daniel F. Voytas, C. Robin Buell, Adrian O. Stec, Thomas J. Y. Kono and Benjamin W. Campbell and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Plant Cell and PLANT PHYSIOLOGY.

In The Last Decade

Robert M. Stupar

89 papers receiving 4.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Soybean2035: A decadal vision for soybean functional genomics and breeding

2025 19 citations Robert M. Stupar, Jianxin Ma et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Robert M. Stupar United States	38	3.6k	2.0k	1000	221	153	93	4.3k
Axel Himmelbach Germany	39	4.0k 1.1×	2.2k 1.1×	709 0.7×	255 1.2×	230 1.5×	107	4.7k
Candice N. Hirsch United States	30	3.2k 0.9×	1.8k 0.9×	1.3k 1.3×	209 0.9×	158 1.0×	71	4.0k
Frank M. You Canada	36	3.5k 1.0×	1.3k 0.7×	1.2k 1.2×	333 1.5×	223 1.5×	105	4.4k
Martin Trick United Kingdom	37	4.2k 1.2×	3.4k 1.7×	1.0k 1.0×	235 1.1×	356 2.3×	66	5.5k
Brande B. H. Wulff United Kingdom	28	3.7k 1.0×	1.1k 0.6×	714 0.7×	205 0.9×	61 0.4×	61	4.0k
Gerard R. Lazo United States	31	2.6k 0.7×	1.6k 0.8×	602 0.6×	231 1.0×	222 1.5×	52	3.5k
M. Motto Italy	33	2.8k 0.8×	1.3k 0.7×	1.0k 1.0×	245 1.1×	109 0.7×	94	3.3k
Boulos Chalhoub France	34	4.8k 1.3×	2.8k 1.4×	793 0.8×	132 0.6×	246 1.6×	60	5.4k
Christine Camilleri France	28	3.7k 1.0×	2.7k 1.4×	748 0.7×	79 0.4×	228 1.5×	53	4.4k
Eduard Akhunov United States	39	4.4k 1.2×	1.3k 0.6×	1.6k 1.6×	441 2.0×	167 1.1×	91	4.8k

Countries citing papers authored by Robert M. Stupar

Since Specialization

Citations

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

Fields of papers citing papers by Robert M. Stupar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert M. Stupar. 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 Robert M. Stupar. The network helps show where Robert M. Stupar may publish in the future.

Co-authorship network of co-authors of Robert M. Stupar

This figure shows the co-authorship network connecting the top 25 collaborators of Robert M. Stupar. A scholar is included among the top collaborators of Robert M. Stupar 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 Robert M. Stupar. Robert M. Stupar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Devkar, Vikas, Yi Chen, Kaushik Ghose, et al.. (2025). Cell‐type‐specific response to silicon treatment in soybean leaves revealed by single‐nucleus RNA sequencing and targeted gene editing. The Plant Journal. 123(1). e70309–e70309. 1 indexed citations

Kumar, Ritesh, Rahul Mahadev Shelake, Doug K. Allen, et al.. (2025). Targets and strategies to design soybean seed composition traits. The Plant Genome. 18(4). e70115–e70115.

Wang, Longlong, Wentao Shao, Duo Zhao, et al.. (2025). GmSop20 Functions as a Key Coordinator of the Oil‐To‐Protein Ratio in Soybean Seeds. Advanced Science. 12(38). e05181–e05181. 2 indexed citations

Lovell, John T., Jerry Jenkins, Shengqiang Shu, et al.. (2024). Assembly, comparative analysis, and utilization of a single haplotype reference genome for soybean. The Plant Journal. 120(3). 1221–1235. 10 indexed citations

Gilbert, Erin, et al.. (2023). A genome‐wide analysis of the USDA Soybean Isoline Collection. The Plant Genome. 16(2). e20310–e20310. 2 indexed citations

Rosso, M. Luciana, Bo Zhang, Robert M. Stupar, et al.. (2023). A chromosome 16 deletion conferring a high sucrose phenotype in soybean. Theoretical and Applied Genetics. 136(5). 109–109. 3 indexed citations

Diers, Brian W., James E. Specht, George L. Graef, et al.. (2023). Genetic architecture of protein and oil content in soybean seed and meal. The Plant Genome. 16(1). e20308–e20308. 6 indexed citations

Lorenz, Aaron J., et al.. (2022). Development of a controlled-environment assay to induce iron deficiency chlorosis in soybean by adjusting calcium carbonates, pH, and nodulation. Plant Methods. 18(1). 36–36. 9 indexed citations

McAssey, Edward V., Priscilla S. Redd, Hanh Nguyen, et al.. (2021). Development of mPing ‐based activation tags for crop insertional mutagenesis. Plant Direct. 5(1). e00300–e00300. 8 indexed citations

10.

Lakhssassi, Naoufal, Gunvant Patil, Tri D. Vuong, et al.. (2021). Dissecting nematode resistance regions in soybean revealed pleiotropic effect of soybean cyst and reniform nematode resistance genes. The Plant Genome. 14(2). e20083–e20083. 11 indexed citations

11.

Patil, Gunvant, David M. Bubeck, Raymond C. Dobert, et al.. (2020). Plant Genome Editing and the Relevance of Off-Target Changes(1)([OPEN]). Default journal. 1453–1471. 1 indexed citations

12.

Michno, Jean‐Michel, Kamaldeep S. Virdi, Adrian O. Stec, et al.. (2020). Integration, abundance, and transmission of mutations and transgenes in a series of CRISPR/Cas9 soybean lines. BMC Biotechnology. 20(1). 10–10. 19 indexed citations

13.

Moll, Karen, Peng Zhou, Thiruvarangan Ramaraj, et al.. (2017). Strategies for optimizing BioNano and Dovetail explored through a second reference quality assembly for the legume model, Medicago truncatula. BMC Genomics. 18(1). 578–578. 39 indexed citations

14.

Bandillo, Nonoy, Justin Anderson, Michael B. Kantar, et al.. (2017). Dissecting the Genetic Basis of Local Adaptation in Soybean. Scientific Reports. 7(1). 17195–17195. 42 indexed citations

15.

Campbell, Benjamin W., Suma Sreekanta, Fengli Fu, et al.. (2016). Fast neutron-induced structural rearrangements at a soybean NAP1 locus result in gnarled trichomes. Theoretical and Applied Genetics. 129(9). 1725–1738. 36 indexed citations

16.

Curtin, Shaun J., Justin Anderson, Colby G. Starker, et al.. (2013). Targeted Mutagenesis for Functional Analysis of Gene Duplication in Legumes. Methods in molecular biology. 1069. 25–42. 17 indexed citations

17.

Stec, Adrian O., Pudota B. Bhaskar, Yung‐Tsi Bolon, et al.. (2013). Genomic Heterogeneity and Structural Variation in Soybean Near Isogenic Lines. Frontiers in Plant Science. 4. 104–104. 11 indexed citations

18.

O’Rourke, Jamie A., L. Iñiguez, Bruna Bucciarelli, et al.. (2013). A re-sequencing based assessment of genomic heterogeneity and fast neutron-induced deletions in a common bean cultivar. Frontiers in Plant Science. 4. 210–210. 12 indexed citations

19.

Kantar, Michael B., Kevin J. Betts, Brent S. Hulke, Robert M. Stupar, & Donald L. Wyse. (2012). Breaking Tuber Dormancy in Helianthus tuberosus L. and Interspecific Hybrids of Helianthus annuus L. × Helianthus tuberosus. HortScience. 47(9). 1342–1346. 7 indexed citations

20.

Chaudhary, Bhupendra, Lex Flagel, Robert M. Stupar, et al.. (2009). Reciprocal Silencing, Transcriptional Bias and Functional Divergence of Homeologs in Polyploid Cotton (Gossypium). Genetics. 182(2). 503–517. 181 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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