Natalya Nersesian

578 total citations
13 papers, 414 citations indexed

About

Natalya Nersesian is a scholar working on Plant Science, Molecular Biology and Cell Biology. According to data from OpenAlex, Natalya Nersesian has authored 13 papers receiving a total of 414 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Plant Science, 8 papers in Molecular Biology and 2 papers in Cell Biology. Recurrent topics in Natalya Nersesian's work include Plant nutrient uptake and metabolism (3 papers), Plant responses to elevated CO2 (2 papers) and Photosynthetic Processes and Mechanisms (2 papers). Natalya Nersesian is often cited by papers focused on Plant nutrient uptake and metabolism (3 papers), Plant responses to elevated CO2 (2 papers) and Photosynthetic Processes and Mechanisms (2 papers). Natalya Nersesian collaborates with scholars based in United States, Austria and Canada. Natalya Nersesian's co-authors include Thomas E. Clemente, Shirley Sato, Truyen Quach, Tom Clemente, Zhengxiang Ge, Xin Li, Gary J. Muehlbauer, Shane Heinen, Susan P. McCormick and Ismail Dweikat and has published in prestigious journals such as Journal of Experimental Botany, Frontiers in Plant Science and Planta.

In The Last Decade

Natalya Nersesian

13 papers receiving 407 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Natalya Nersesian United States	9	340	120	69	58	30	13	414
Miaoping Zhou China	12	545 1.6×	248 2.1×	121 1.8×	57 1.0×	54 1.8×	24	624
Hilde-Gunn Opsahl-Sorteberg Norway	10	449 1.3×	370 3.1×	53 0.8×	14 0.2×	41 1.4×	15	596
Judy Cheong Australia	13	605 1.8×	60 0.5×	91 1.3×	152 2.6×	24 0.8×	25	643
Shashank K. Pandey South Korea	13	666 2.0×	326 2.7×	51 0.7×	30 0.5×	19 0.6×	21	744
Luís M. Muñiz Spain	13	593 1.7×	449 3.7×	27 0.4×	30 0.5×	30 1.0×	20	732
I. Kars Netherlands	7	667 2.0×	164 1.4×	117 1.7×	8 0.1×	20 0.7×	8	687
Gábor Giczey Hungary	9	670 2.0×	75 0.6×	223 3.2×	90 1.6×	32 1.1×	11	706
Shane Heinen United States	10	569 1.7×	194 1.6×	220 3.2×	20 0.3×	59 2.0×	14	606
Kandasamy Ulaganathan India	13	323 0.9×	228 1.9×	43 0.6×	7 0.1×	33 1.1×	51	438
Melanie Craze United Kingdom	14	744 2.2×	332 2.8×	68 1.0×	75 1.3×	45 1.5×	21	799

Countries citing papers authored by Natalya Nersesian

Since Specialization

Citations

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

Fields of papers citing papers by Natalya Nersesian

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natalya Nersesian

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

All Works

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13 of 13 papers shown

Jaikumar, Nikhil S., Truyen Quach, Zhengxiang Ge, et al.. (2025). Constitutive down‐regulation of liguleless alleles in sorghum drives increased productivity and water use efficiency. Plant Biotechnology Journal. 23(8). 3401–3413. 1 indexed citations

Quach, Truyen, Ming Guo, Tara J. Nazarenus, et al.. (2025). In‐context promoter bashing of the Sorghum bicolor gene models functionally annotated as bundle sheath cell preferred expressing phosphoenolpyruvate carboxykinase and alanine aminotransferase. Crop Science. 65(2). 1 indexed citations

Ferguson, John N., Truyen Quach, Zhengxiang Ge, et al.. (2024). Reducing stomatal density by expression of a synthetic epidermal patterning factor increases leaf intrinsic water use efficiency and reduces plant water use in a C4 crop. Journal of Experimental Botany. 75(21). 6823–6836. 20 indexed citations

Funnell‐Harris, Deanna L., et al.. (2023). Effects of Altering Three Steps of Monolignol Biosynthesis on Sorghum Responses to Stalk Pathogens and Water Deficit. Plant Disease. 107(12). 3984–3995. 2 indexed citations

Sandhu, Jaspreet, Shirley Sato, Natalya Nersesian, et al.. (2020). The LATERAL ROOT DENSITY gene regulates root growth during water stress in wheat. Plant Biotechnology Journal. 18(9). 1955–1968. 59 indexed citations

Satyanarayana, T., Shirley Sato, Natalya Nersesian, et al.. (2019). Transgenic Wheat Harboring an RNAi Element Confers Dual Resistance Against Synergistically Interacting Wheat Streak Mosaic Virus and Triticum Mosaic Virus. Molecular Plant-Microbe Interactions. 33(1). 108–122. 8 indexed citations

Quach, Truyen, Shirley Sato, Zhengxiang Ge, et al.. (2017). Molecular and phenotypic characterization of transgenic wheat and sorghum events expressing the barley alanine aminotransferase. Planta. 246(6). 1097–1107. 20 indexed citations

Quach, Truyen, Shirley Sato, Zhengxiang Ge, et al.. (2017). Expression of the Maize Dof1 Transcription Factor in Wheat and Sorghum. Frontiers in Plant Science. 8. 434–434. 43 indexed citations

Kaur, Jagdeep, John P. Fellers, Alok Adholeya, et al.. (2016). Expression of apoplast-targeted plant defensin MtDef4.2 confers resistance to leaf rust pathogen Puccinia triticina but does not affect mycorrhizal symbiosis in transgenic wheat. Transgenic Research. 26(1). 37–49. 44 indexed citations

10.

Li, Xin, Sanghyun Shin, Shane Heinen, et al.. (2015). Transgenic Wheat Expressing a Barley UDP-Glucosyltransferase Detoxifies Deoxynivalenol and Provides High Levels of Resistance to Fusarium graminearum. Molecular Plant-Microbe Interactions. 28(11). 1237–1246. 105 indexed citations

11.

Dweikat, Ismail, Shirley Sato, Zhengxiang Ge, et al.. (2012). Modulation of kernel storage proteins in grain sorghum (Sorghum bicolor (L.) Moench). Plant Biotechnology Journal. 10(5). 533–544. 49 indexed citations

12.

Fu, Jianming, Ivana Momčilović, Thomas E. Clemente, et al.. (2008). Heterologous expression of a plastid EF-Tu reduces protein thermal aggregation and enhances CO2 fixation in wheat (Triticum aestivum) following heat stress. Plant Molecular Biology. 68(3). 277–288. 59 indexed citations

13.

Zhang, Hong, Sheila K. Jacobi, Katherine Cianflone, et al.. (2002). Purification and characterization of acylation stimulating protein from porcine serum. Protein Expression and Purification. 25(2). 348–352. 3 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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