Janet Braam

10.2k total citations · 2 hit papers
66 papers, 7.8k citations indexed

About

Janet Braam is a scholar working on Plant Science, Molecular Biology and Materials Chemistry. According to data from OpenAlex, Janet Braam has authored 66 papers receiving a total of 7.8k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Plant Science, 33 papers in Molecular Biology and 6 papers in Materials Chemistry. Recurrent topics in Janet Braam's work include Plant Molecular Biology Research (23 papers), Polysaccharides and Plant Cell Walls (21 papers) and Plant Reproductive Biology (18 papers). Janet Braam is often cited by papers focused on Plant Molecular Biology Research (23 papers), Polysaccharides and Plant Cell Walls (21 papers) and Plant Reproductive Biology (18 papers). Janet Braam collaborates with scholars based in United States, China and United Kingdom. Janet Braam's co-authors include Diana H. Polisensky, Ronald W. Davis, Stephen C. Fry, Elizabeth A. McCormack, E. Wassim Chehab, Yu-Chang Tsai, Mary M. Purugganan, Danuta Maria Antosiewicz, Jocelyn K. C. Rose and Kazuhiko Nishitani and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Janet Braam

66 papers receiving 7.5k citations

Hit Papers

The XTH Family of Enzymes Involved in Xyloglucan Endotran... 1990 2026 2002 2014 2002 1990 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Janet Braam United States 46 6.2k 3.1k 711 607 422 66 7.8k
Jinxing Lin China 52 5.2k 0.8× 4.0k 1.3× 439 0.6× 317 0.5× 220 0.5× 252 8.0k
Michael S. Reid United States 55 6.7k 1.1× 3.3k 1.0× 1.1k 1.6× 574 0.9× 145 0.3× 264 9.7k
Lacey Samuels Canada 52 7.9k 1.3× 5.7k 1.8× 859 1.2× 97 0.2× 192 0.5× 98 10.3k
Simon R. Turner United Kingdom 48 7.5k 1.2× 5.1k 1.6× 1.8k 2.5× 104 0.2× 159 0.4× 83 9.3k
Vincent Bulone Sweden 45 3.6k 0.6× 2.5k 0.8× 1.1k 1.5× 208 0.3× 136 0.3× 179 6.7k
Yupeng Wang China 20 4.0k 0.6× 4.0k 1.3× 363 0.5× 211 0.3× 59 0.1× 60 6.8k
Jocelyn K. C. Rose United States 66 11.8k 1.9× 6.6k 2.1× 778 1.1× 68 0.1× 311 0.7× 148 14.3k
Shinji Kawasaki Japan 43 5.1k 0.8× 3.1k 1.0× 281 0.4× 202 0.3× 42 0.1× 177 7.2k
Lincoln Taiz United States 44 4.0k 0.6× 4.1k 1.3× 233 0.3× 199 0.3× 80 0.2× 94 6.7k
William G. T. Willats Denmark 62 10.7k 1.7× 5.9k 1.9× 1.8k 2.5× 156 0.3× 136 0.3× 196 14.6k

Countries citing papers authored by Janet Braam

Since Specialization
Citations

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

Fields of papers citing papers by Janet Braam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janet Braam

This figure shows the co-authorship network connecting the top 25 collaborators of Janet Braam. A scholar is included among the top collaborators of Janet Braam 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 Janet Braam. Janet Braam 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.
Deng, Bing, Robert A. Carter, Yi Cheng, et al.. (2023). High-temperature electrothermal remediation of multi-pollutants in soil. Nature Communications. 14(1). 6371–6371. 45 indexed citations
2.
Kushwah, Sunita, Alicja Banasiak, Nobuyuki Nishikubo, et al.. (2020). Arabidopsis XTH4 and XTH9 Contribute to Wood Cell Expansion and Secondary Wall Formation. PLANT PHYSIOLOGY. 182(4). 1946–1965. 54 indexed citations
3.
Ogilvie, Huw A., Yuan Liu, Michael Huang, et al.. (2019). Rosette core fungal resistance in Arabidopsis thaliana. Planta. 250(6). 1941–1953. 2 indexed citations
4.
Lei, Jiaxin, G.K. Jayaprakasha, Jashbir Singh, et al.. (2019). CIRCADIAN CLOCK-ASSOCIATED1 Controls Resistance to Aphids by Altering Indole Glucosinolate Production. PLANT PHYSIOLOGY. 181(3). 1344–1359. 42 indexed citations
5.
Martí, María C., Katharine Hubbard, Michael Gardner, et al.. (2018). Circadian oscillations of cytosolic free calcium regulate the Arabidopsis circadian clock. Nature Plants. 4(9). 690–698. 59 indexed citations
6.
Braam, Janet & E. Wassim Chehab. (2017). Thigmomorphogenesis. Current Biology. 27(17). R863–R864. 15 indexed citations
8.
Wang, Jing, Yu Yang, Huiguang Zhu, et al.. (2014). Uptake, Translocation, and Transformation of Quantum Dots with Cationic versus Anionic Coatings byPopulus deltoides×nigraCuttings. Environmental Science & Technology. 48(12). 6754–6762. 44 indexed citations
9.
Goodspeed, Danielle, et al.. (2013). Postharvest Circadian Entrainment Enhances Crop Pest Resistance and Phytochemical Cycling. Current Biology. 23(13). 1235–1241. 60 indexed citations
10.
Goodspeed, Danielle, E. Wassim Chehab, Amelia Min-Venditti, Janet Braam, & Michael F. Covington. (2012). Arabidopsis synchronizes jasmonate-mediated defense with insect circadian behavior. Proceedings of the National Academy of Sciences. 109(12). 4674–4677. 249 indexed citations
11.
Tsai, Yu‐Chang, et al.. (2012). Calmodulin‐related CML 24 interacts with ATG 4b and affects autophagy progression in A rabidopsis. The Plant Journal. 73(2). 325–335. 33 indexed citations
12.
Chehab, E. Wassim, et al.. (2012). Arabidopsis Touch-Induced Morphogenesis Is Jasmonate Mediated and Protects against Pests. Current Biology. 22(8). 701–706. 147 indexed citations
13.
Chehab, E. Wassim, et al.. (2011). Nitric oxide accumulation in Arabidopsis is independent of NOA1 in the presence of sucrose. The Plant Journal. 68(2). 225–233. 46 indexed citations
14.
Ji, Jiabing & Janet Braam. (2010). Restriction Site Extension PCR: A Novel Method for High-Throughput Characterization of Tagged DNA Fragments and Genome Walking. PLoS ONE. 5(5). e10577–e10577. 40 indexed citations
15.
Lee, Chang Woo, Shaily Mahendra, Katherine R. Zodrow, et al.. (2009). Developmental phytotoxicity of metal oxide nanoparticles to Arabidopsis thaliana. Environmental Toxicology and Chemistry. 29(3). 669–675. 359 indexed citations
16.
Chehab, E. Wassim, et al.. (2008). Thigmomorphogenesis: a complex plant response to mechano-stimulation. Journal of Experimental Botany. 60(1). 43–56. 218 indexed citations
17.
Braam, Janet. (2004). In touch: plant responses to mechanical stimuli. New Phytologist. 165(2). 373–389. 483 indexed citations
18.
Braam, Janet, Melissa L. Sistrunk, Diana H. Polisensky, et al.. (1997). Plant responses to environmental stress: regulation and functions of the ArabidopsisTCH genes. Planta. 203(S1). S35–S41. 79 indexed citations
19.
Antosiewicz, Danuta Maria, Diana H. Polisensky, & Janet Braam. (1995). Cellular localization of the Ca2+ binding TCH3 protein of Arabidopsis. The Plant Journal. 8(5). 623–636. 42 indexed citations
20.
Braam, Janet. (1992). Regulation of expression of calmodulin and calmodulin-related genes by environmental stimuli in plants. Cell Calcium. 13(6-7). 457–463. 29 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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