Gerald S. Pullman

2.8k total citations
67 papers, 2.0k citations indexed

About

Gerald S. Pullman is a scholar working on Plant Science, Molecular Biology and Nature and Landscape Conservation. According to data from OpenAlex, Gerald S. Pullman has authored 67 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Plant Science, 49 papers in Molecular Biology and 13 papers in Nature and Landscape Conservation. Recurrent topics in Gerald S. Pullman's work include Plant tissue culture and regeneration (37 papers), Seed Germination and Physiology (33 papers) and Plant Reproductive Biology (17 papers). Gerald S. Pullman is often cited by papers focused on Plant tissue culture and regeneration (37 papers), Seed Germination and Physiology (33 papers) and Plant Reproductive Biology (17 papers). Gerald S. Pullman collaborates with scholars based in United States, Slovakia and Sweden. Gerald S. Pullman's co-authors include John Cairney, Shannon L. Johnson, Anna Aleksandrovna Skryabina, David T. Webb, Ross Whetten, Nanfei Xu, Allan Wenck, Heike Sederoff, Roger Timmis and Thomas J. Oh and has published in prestigious journals such as Nature Biotechnology, PLANT PHYSIOLOGY and New Phytologist.

In The Last Decade

Gerald S. Pullman

67 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gerald S. Pullman United States 29 1.8k 1.5k 257 234 211 67 2.0k
Luc Harvengt France 24 858 0.5× 844 0.6× 108 0.4× 144 0.6× 84 0.4× 33 1.3k
Celia María Gonzalo Miguel Portugal 22 1.1k 0.7× 1.2k 0.8× 57 0.2× 102 0.4× 139 0.7× 90 1.6k
Ulrika Egertsdotter Sweden 24 1.2k 0.7× 1.2k 0.8× 114 0.4× 111 0.5× 55 0.3× 62 1.6k
R. T. Sherwood United States 17 1.3k 0.8× 431 0.3× 98 0.4× 414 1.8× 386 1.8× 39 1.8k
Malin Elfstrand Sweden 24 1.2k 0.7× 488 0.3× 87 0.3× 171 0.7× 283 1.3× 66 1.6k
Jarmo Schrader Sweden 14 1.7k 1.0× 1.5k 1.0× 90 0.4× 60 0.3× 133 0.6× 16 2.1k
Sharon Regan Canada 21 1.5k 0.9× 1.3k 0.9× 45 0.2× 112 0.5× 67 0.3× 37 1.9k
Victor Busov United States 28 2.3k 1.3× 1.8k 1.2× 103 0.4× 89 0.4× 50 0.2× 52 2.6k
Gerd Bossinger Australia 20 1.0k 0.6× 946 0.6× 110 0.4× 172 0.7× 150 0.7× 51 1.4k
Natalia Requena Germany 28 2.7k 1.5× 509 0.3× 131 0.5× 281 1.2× 326 1.5× 47 3.0k

Countries citing papers authored by Gerald S. Pullman

Since Specialization
Citations

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

Fields of papers citing papers by Gerald S. Pullman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gerald S. Pullman. 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 Gerald S. Pullman. The network helps show where Gerald S. Pullman may publish in the future.

Co-authorship network of co-authors of Gerald S. Pullman

This figure shows the co-authorship network connecting the top 25 collaborators of Gerald S. Pullman. A scholar is included among the top collaborators of Gerald S. Pullman 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 Gerald S. Pullman. Gerald S. Pullman 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
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Pullman, Gerald S., et al.. (2019). Seed cryopreservation and micropropagation of the federally threatened species, Price’s potato-bean (Apios priceana B.L. Robins.). In Vitro Cellular & Developmental Biology - Plant. 55(5). 558–568. 6 indexed citations
3.
Pullman, Gerald S., et al.. (2015). Conifer somatic embryogenesis: improvements by supplementation of medium with oxidation-reduction agents. Tree Physiology. 35(2). 209–224. 33 indexed citations
4.
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Johnson, S. S., et al.. (2009). Survey of bacterial populations present in US-produced linerboard with high recycle content. Journal of Applied Microbiology. 108(2). 416–427. 6 indexed citations
7.
Pullman, Gerald S. & Shannon L. Johnson. (2009). Osmotic measurements in whole megagametophytes and embryos of loblolly pine (Pinus taeda) during seed development. Tree Physiology. 29(6). 819–827. 11 indexed citations
8.
Pullman, Gerald S. & Shannon L. Johnson. (2009). Loblolly pine (Pinus taeda) female gametophyte and embryo pH changes during seed development. Tree Physiology. 29(6). 829–836. 6 indexed citations
9.
Pullman, Gerald S., et al.. (2008). Conifer embryogenic tissue initiation: improvements by supplementation of medium with D-xylose and D-chiro-inositol. Tree Physiology. 29(1). 147–156. 20 indexed citations
10.
Pullman, Gerald S. & Michael R. Buchanan. (2008). Identification and quantitative analysis of stage-specific carbohydrates in loblolly pine (Pinus taeda) zygotic embryo and female gametophyte tissues. Tree Physiology. 28(7). 985–996. 31 indexed citations
11.
Oh, Thomas J., Roger M. Wartell, John Cairney, & Gerald S. Pullman. (2008). Evidence for stage‐specific modulation of specific microRNAs (miRNAs) and miRNA processing components in zygotic embryo and female gametophyte of loblolly pine (Pinus taeda). New Phytologist. 179(1). 67–80. 66 indexed citations
12.
Skryabina, Anna Aleksandrovna, M. Cameron Sullards, Di Wu, et al.. (2007). Isolation and characterization of a molecule stimulatory to growth of somatic embryos from early stage female gametophyte tissue of loblolly pine. Plant Cell Reports. 27(4). 633–646. 10 indexed citations
13.
Cairney, John, Zheng Li, Joseph Hsiao, et al.. (2006). Expressed Sequence Tags from loblolly pine embryos reveal similarities with angiosperm embryogenesis. Plant Molecular Biology. 62(4-5). 485–501. 62 indexed citations
14.
Vales, Teresa R., Xiaorong Feng, Nanfei Xu, et al.. (2006). Improved somatic embryo maturation in loblolly pine by monitoring ABA-responsive gene expression. Plant Cell Reports. 26(2). 133–143. 28 indexed citations
15.
Pullman, Gerald S., et al.. (2004). Gibberellin inhibitors improve embryogenic tissue initiation in conifers. Plant Cell Reports. 23(9). 596–605. 34 indexed citations
16.
Johnson, Shannon L., et al.. (2003). The impact of Gelrite and activated carbon on the elemental composition of two conifer embryogenic tissue initiation media. Plant Cell Reports. 21(12). 1175–1182. 46 indexed citations
17.
Pullman, Gerald S., et al.. (2003). Brassinolide improves embryogenic tissue initiation in conifers and rice. Plant Cell Reports. 22(2). 96–104. 76 indexed citations
18.
Wenck, Allan, et al.. (1999). High-efficiency Agrobacterium-mediated transformation of Norway spruce (Picea abies) and loblolly pine (Pinus taeda). Plant Molecular Biology. 39(3). 407–416. 113 indexed citations
19.
Dimmel, Donald R., et al.. (1997). Teak extract as a catalyst for the pulping of loblolly pine. TAPPI Journal. 81(5). 237–240. 6 indexed citations
20.
Pullman, Gerald S. & J. E. DeVay. (1981). Effect of soil flooding and paddy rice culture on the survival of Verticillium dahliae and incidence of Verticillium wilt in cotton.. Phytopathology. 71(12). 1285–1289. 26 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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