Nancy R. Forsthoefel

795 total citations
18 papers, 647 citations indexed

About

Nancy R. Forsthoefel is a scholar working on Plant Science, Molecular Biology and Ecology. According to data from OpenAlex, Nancy R. Forsthoefel has authored 18 papers receiving a total of 647 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Plant Science, 11 papers in Molecular Biology and 1 paper in Ecology. Recurrent topics in Nancy R. Forsthoefel's work include Photosynthetic Processes and Mechanisms (10 papers), Plant Molecular Biology Research (7 papers) and Plant Stress Responses and Tolerance (6 papers). Nancy R. Forsthoefel is often cited by papers focused on Photosynthetic Processes and Mechanisms (10 papers), Plant Molecular Biology Research (7 papers) and Plant Stress Responses and Tolerance (6 papers). Nancy R. Forsthoefel collaborates with scholars based in United States and Bangladesh. Nancy R. Forsthoefel's co-authors include Daniel M. Vernon, John C. Cushman, Hans J. Bohnert, Daniel R. Gestaut, Daniel Cushing, Donald E. Nelson, Shailender S. Chauhan, Yong Ran, F. Quigley and S. E. Smith and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and PLANT PHYSIOLOGY.

In The Last Decade

Nancy R. Forsthoefel

18 papers receiving 630 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nancy R. Forsthoefel United States 13 518 374 30 29 16 18 647
Young Myung Kwon South Korea 11 764 1.5× 670 1.8× 29 1.0× 32 1.1× 20 1.3× 30 842
Robin A. P. Stacy Norway 9 327 0.6× 401 1.1× 15 0.5× 21 0.7× 19 1.2× 9 581
Natacha Bies‐Etheve France 9 748 1.4× 481 1.3× 22 0.7× 26 0.9× 9 0.6× 11 853
Sally C. Greenway United Kingdom 4 363 0.7× 274 0.7× 46 1.5× 20 0.7× 14 0.9× 7 482
Jérôme Bove France 7 532 1.0× 408 1.1× 42 1.4× 16 0.6× 28 1.8× 8 663
Karin N. Lohman United States 7 531 1.0× 446 1.2× 16 0.5× 12 0.4× 18 1.1× 8 625
Govinal Badiger Bhaskara Taiwan 11 709 1.4× 353 0.9× 38 1.3× 32 1.1× 20 1.3× 16 808
Fabiola Jaimes‐Miranda Mexico 8 468 0.9× 407 1.1× 24 0.8× 18 0.6× 19 1.2× 16 568
Jiangxin Wan Canada 10 634 1.2× 405 1.1× 18 0.6× 45 1.6× 7 0.4× 10 751
Co‐Shine Wang Taiwan 14 825 1.6× 659 1.8× 60 2.0× 20 0.7× 27 1.7× 30 954

Countries citing papers authored by Nancy R. Forsthoefel

Since Specialization
Citations

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

Fields of papers citing papers by Nancy R. Forsthoefel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nancy R. Forsthoefel

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

All Works

18 of 18 papers shown
1.
Forsthoefel, Nancy R., et al.. (2018). Arabidopsis PIRL6 Is Essential for Male and Female Gametogenesis and Is Regulated by Alternative Splicing. PLANT PHYSIOLOGY. 178(3). 1154–1169. 8 indexed citations
2.
Edger, Patrick P., et al.. (2017). A Whole-Transcriptome Approach to Evaluating Reference Genes for Quantitative Gene Expression Studies: A Case Study in Mimulus. G3 Genes Genomes Genetics. 7(4). 1085–1095. 21 indexed citations
3.
Forsthoefel, Nancy R., et al.. (2013). The Arabidopsis Plant Intracellular Ras-group LRR (PIRL) Family and the Value of Reverse Genetic Analysis for Identifying Genes that Function in Gametophyte Development. SHILAP Revista de lepidopterología. 2(3). 507–520. 12 indexed citations
4.
Chen, Tingsu, Nihar R. Nayak, Jonathan D. Lowenson, et al.. (2010). Substrates of the Arabidopsis thaliana Protein Isoaspartyl Methyltransferase 1 Identified Using Phage Display and Biopanning. Journal of Biological Chemistry. 285(48). 37281–37292. 37 indexed citations
5.
Forsthoefel, Nancy R., Thuy P. Dao, & Daniel M. Vernon. (2010). PIRL1 and PIRL9, encoding members of a novel plant-specific family of leucine-rich repeat proteins, are essential for differentiation of microspores into pollen. Planta. 232(5). 1101–1114. 18 indexed citations
6.
Forsthoefel, Nancy R. & Daniel M. Vernon. (2010). Effect of sporophytic PIRL9 genotype on post-meiotic expression of the Arabidopsis pirl1;pirl9 mutant pollen phenotype. Planta. 233(2). 423–431. 7 indexed citations
7.
Cushing, Daniel, Nancy R. Forsthoefel, Daniel R. Gestaut, & Daniel M. Vernon. (2005). Arabidopsis emb175 and other ppr knockout mutants reveal essential roles for pentatricopeptide repeat (PPR) proteins in plant embryogenesis. Planta. 221(3). 424–436. 125 indexed citations
8.
Forsthoefel, Nancy R., et al.. (2005). PIRLs: A Novel Class of Plant Intracellular Leucine-rich Repeat Proteins. Plant and Cell Physiology. 46(6). 913–922. 39 indexed citations
9.
Vernon, Daniel M., et al.. (2001). An expanded role for the TWN1 gene in embryogenesis: defects in cotyledon pattern and morphology in the  twn1 mutant of Arabidopsis (Brassicaceae). American Journal of Botany. 88(4). 570–582. 27 indexed citations
10.
Chauhan, Sanjay, et al.. (2000). Na+/myo‐inositol symporters and Na+/H+‐antiport in Mesembryanthemum crystallinum. The Plant Journal. 24(4). 511–522. 19 indexed citations
11.
Chauhan, Shailender S., Nancy R. Forsthoefel, Yong Ran, et al.. (2000). Na+/myo-inositol symporters and Na+/H+-antiport in Mesembryanthemum crystallinum. The Plant Journal. 24(4). 511–522. 114 indexed citations
12.
Forsthoefel, Nancy R., Mary Ann Cushman, James A. Ostrem, & John C. Cushman. (1998). Induction of a cysteine protease cDNA from Mesembryanthemum crystallinum leaves by environmental stress and plant growth regulators. Plant Science. 136(2). 195–206. 35 indexed citations
13.
14.
Forsthoefel, Nancy R., Daniel M. Vernon, & John C. Cushman. (1995). A salinity-induced gene from the halophyte M. crystallinum encodes a glycolytic enzyme, cofactor-independent phosphoglyceromutase. Plant Molecular Biology. 29(2). 213–226. 38 indexed citations
15.
Forsthoefel, Nancy R. & John C. Cushman. (1994). Characterization (psbE, psbF, and Acid Metabolism and Expression of Photosystem II Genes psbL) from the Facultative Crassulacean Plant Mesembryanthemum crystallinum'. 1 indexed citations
16.
17.
Forsthoefel, Nancy R., Hans J. Bohnert, & S. E. Smith. (1992). Discordant Inheritance of Mitochondrial and Plastid DNA in Diverse Alfalfa Genotypes. Journal of Heredity. 83(5). 342–345. 29 indexed citations
18.
Yahya, Moyasar T., et al.. (1989). Evaluation of potassium permanganate for inactivation of bacteriophage MS‐2 in water systems. Journal of Environmental Science and Health Part A Environmental Science and Engineering. 24(8). 979–989. 5 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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