Judith L. Roe

2.5k total citations
29 papers, 1.9k citations indexed

About

Judith L. Roe is a scholar working on Plant Science, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Judith L. Roe has authored 29 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Plant Science, 19 papers in Molecular Biology and 4 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Judith L. Roe's work include Plant Molecular Biology Research (15 papers), Plant Reproductive Biology (9 papers) and Photosynthetic Processes and Mechanisms (5 papers). Judith L. Roe is often cited by papers focused on Plant Molecular Biology Research (15 papers), Plant Reproductive Biology (9 papers) and Photosynthetic Processes and Mechanisms (5 papers). Judith L. Roe collaborates with scholars based in United States, Germany and Australia. Judith L. Roe's co-authors include Patricia Zambryski, Jennifer L. Nemhauser, Stephen M. Welch, Zhanshan Dong, Allen Sessions, William J. Lennarz, Kenneth A. Feldmann, Johanna Schmitt, Martha D. Cooper and Amity M. Wilczek and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Judith L. Roe

29 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
Judith L. Roe United States 22 1.4k 1.2k 323 247 98 29 1.9k
Éric Bonnet France 19 1.1k 0.8× 1.6k 1.4× 403 1.2× 243 1.0× 61 0.6× 33 2.7k
Russell L. Malmberg United States 29 2.1k 1.5× 2.4k 2.0× 385 1.2× 307 1.2× 175 1.8× 82 3.2k
Daniel H. Chitwood United States 35 3.3k 2.3× 2.0k 1.7× 368 1.1× 436 1.8× 164 1.7× 79 4.1k
J. Jansen Netherlands 28 1.4k 1.0× 624 0.5× 956 3.0× 184 0.7× 202 2.1× 71 2.5k
Christopher N. Topp United States 25 2.1k 1.5× 902 0.8× 343 1.1× 82 0.3× 113 1.2× 45 2.4k
Jean-Jack M. Riethoven United States 22 733 0.5× 981 0.8× 221 0.7× 64 0.3× 56 0.6× 61 1.8k
Yongfeng Zhou China 23 1.4k 1.0× 933 0.8× 625 1.9× 251 1.0× 153 1.6× 64 2.1k
Glenn Hickey United States 14 348 0.2× 656 0.6× 399 1.2× 77 0.3× 24 0.2× 28 1.0k
Peter M. Rice United States 11 492 0.4× 855 0.7× 223 0.7× 147 0.6× 44 0.4× 17 1.8k
Lieven Sterck Belgium 24 1.0k 0.7× 1.1k 0.9× 306 0.9× 222 0.9× 84 0.9× 41 1.8k

Countries citing papers authored by Judith L. Roe

Since Specialization
Citations

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

Fields of papers citing papers by Judith L. Roe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judith L. Roe. 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 Judith L. Roe. The network helps show where Judith L. Roe may publish in the future.

Co-authorship network of co-authors of Judith L. Roe

This figure shows the co-authorship network connecting the top 25 collaborators of Judith L. Roe. A scholar is included among the top collaborators of Judith L. Roe 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 Judith L. Roe. Judith L. Roe 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.
Fournier‐Level, Alexandre, Mark A. Taylor, Alejandra Martínez‐Berdeja, et al.. (2022). Adaptive significance of flowering time variation across natural seasonal environments in Arabidopsis thaliana. New Phytologist. 234(2). 719–734. 20 indexed citations
2.
Burghardt, Liana T., Daniel E. Runcie, Amity M. Wilczek, et al.. (2015). Fluctuating, warm temperatures decrease the effect of a key floral repressor on flowering time in Arabidopsis thaliana. New Phytologist. 210(2). 564–576. 30 indexed citations
3.
Mandyam, Keerthi, Judith L. Roe, & Ari Jumpponen. (2013). Arabidopsis thaliana model system reveals a continuum of responses to root endophyte colonization. Fungal Biology. 117(4). 250–260. 46 indexed citations
4.
Fournier‐Level, Alexandre, Amity M. Wilczek, Martha D. Cooper, et al.. (2013). Paths to selection on life history loci in different natural environments across the native range of Arabidopsis thaliana. Molecular Ecology. 22(13). 3552–3566. 85 indexed citations
5.
Wilczek, Amity M., Judith L. Roe, Mary Knapp, et al.. (2009). Effects of Genetic Perturbation on Seasonal Life History Plasticity. Science. 323(5916). 930–934. 310 indexed citations
6.
7.
Welch, Stephen M., Zhanshan Dong, Judith L. Roe, & Sanjoy Das. (2005). Flowering time control: gene network modelling and the link to quantitative genetics. Australian Journal of Agricultural Research. 56(9). 919–936. 45 indexed citations
8.
Welch, Stephen M., Judith L. Roe, Sanjoy Das, et al.. (2004). Merging genomic control networks and soil-plant-atmosphere-continuum models. Agricultural Systems. 86(3). 243–274. 15 indexed citations
9.
Ehsan, Hashimul, Jean‐Philippe Reichheld, Tim Durfee, & Judith L. Roe. (2004). TOUSLED Kinase Activity Oscillates during the Cell Cycle and Interacts with Chromatin Regulators. PLANT PHYSIOLOGY. 134(4). 1488–1499. 50 indexed citations
10.
Welch, Stephen M., Zhanshan Dong, & Judith L. Roe. (2004). Modelling gene networks controlling transition to flowering in Arabidopsis. 12 indexed citations
11.
Roe, Judith L., et al.. (2003). Rice Phospholipase D Isoforms Show Differential Cellular Location and Gene Induction. Plant and Cell Physiology. 44(10). 1013–1026. 34 indexed citations
12.
Welch, Stephen M., Judith L. Roe, & Zhanshan Dong. (2003). A Genetic Neural Network Model of Flowering Time Control in Arabidopsis thaliana. Agronomy Journal. 95(1). 71–81. 73 indexed citations
13.
Welch, Stephen M., Judith L. Roe, & Zhanshan Dong. (2003). A Genetic Neural Network Model of Flowering Time Control in. Agronomy Journal. 95(1). 71–71. 63 indexed citations
14.
Durfee, Tim, Judith L. Roe, Carla Inouye, et al.. (2003). The F-box-containing protein UFO and AGAMOUS participate in antagonistic pathways governing early petal development in Arabidopsis. Proceedings of the National Academy of Sciences. 100(14). 8571–8576. 66 indexed citations
15.
Nemhauser, Jennifer L., Patricia Zambryski, & Judith L. Roe. (1998). Auxin signaling in Arabidopsis flower development?. Current Opinion in Plant Biology. 1(6). 531–535. 23 indexed citations
16.
Roe, Judith L., Tim Durfee, John R. Zupan, et al.. (1997). TOUSLED Is a Nuclear Serine/Threonine Protein Kinase That Requires a Coiled-coil Region for Oligomerization and Catalytic Activity. Journal of Biological Chemistry. 272(9). 5838–5845. 46 indexed citations
17.
Roe, Judith L., Jennifer L. Nemhauser, & Patricia Zambryski. (1997). TOUSLED Participates in Apical Tissue Formation during Gynoecium Development in Arabidopsis. The Plant Cell. 9(3). 335–335. 21 indexed citations
18.
Sessions, Allen, et al.. (1997). ETTIN patterns the Arabidopsis floral meristem and reproductive organs. Development. 124(22). 4481–4491. 373 indexed citations
19.
Roe, Judith L., et al.. (1993). The Tousled gene in A. thaliana encodes a protein kinase homolog that is required for leaf and flower development. Cell. 75(5). 939–950. 145 indexed citations
20.
Roe, Judith L., et al.. (1989). Inhibitors of metalloendoproteases block spiculogenesis in sea urchin primary mesenchyme cells. Experimental Cell Research. 181(2). 542–550. 32 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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