Wolfgang Moeder

4.5k total citations
49 papers, 3.4k citations indexed

About

Wolfgang Moeder is a scholar working on Plant Science, Molecular Biology and Physiology. According to data from OpenAlex, Wolfgang Moeder has authored 49 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Plant Science, 17 papers in Molecular Biology and 3 papers in Physiology. Recurrent topics in Wolfgang Moeder's work include Plant Stress Responses and Tolerance (26 papers), Plant-Microbe Interactions and Immunity (26 papers) and Plant Parasitism and Resistance (11 papers). Wolfgang Moeder is often cited by papers focused on Plant Stress Responses and Tolerance (26 papers), Plant-Microbe Interactions and Immunity (26 papers) and Plant Parasitism and Resistance (11 papers). Wolfgang Moeder collaborates with scholars based in Canada, United States and Japan. Wolfgang Moeder's co-authors include Keiko Yoshioka, Daniel F. Klessig, Christian Langebartels, Heinrich Sandermann, Wim Van Camp, Dirk Inzé, Thomas A. DeFalco, Kimberley Chin, W. E. S. Urquhart and Patricia L. Conklin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Angewandte Chemie International Edition and PLoS ONE.

In The Last Decade

Wolfgang Moeder

48 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wolfgang Moeder Canada 31 3.0k 1.3k 220 109 100 49 3.4k
José Marı́a Bellés Spain 34 2.6k 0.9× 1.7k 1.3× 169 0.8× 174 1.6× 117 1.2× 63 3.5k
Kirk Overmyer Finland 23 2.7k 0.9× 1.4k 1.0× 163 0.7× 158 1.4× 96 1.0× 48 3.0k
Nam‐Soo Jwa South Korea 35 2.6k 0.9× 1.5k 1.1× 266 1.2× 269 2.5× 93 0.9× 68 3.2k
David E. Hanke United Kingdom 26 1.7k 0.6× 1.1k 0.8× 145 0.7× 91 0.8× 76 0.8× 66 2.2k
Jyan-Chyun Jang United States 25 3.5k 1.2× 2.2k 1.7× 80 0.4× 36 0.3× 83 0.8× 34 3.9k
Youko Oono Japan 21 3.9k 1.3× 2.5k 1.9× 192 0.9× 57 0.5× 112 1.1× 39 4.7k
Guillaume Tena United States 9 4.1k 1.4× 2.3k 1.7× 230 1.0× 130 1.2× 72 0.7× 31 4.5k
Christine Rustérucci France 15 2.5k 0.8× 1.5k 1.2× 143 0.7× 283 2.6× 142 1.4× 21 3.2k
Elena Baena–González Portugal 28 5.4k 1.8× 3.4k 2.6× 100 0.5× 79 0.7× 186 1.9× 42 6.4k
Julie M. Stone United States 25 3.5k 1.2× 2.2k 1.7× 280 1.3× 91 0.8× 145 1.4× 39 4.2k

Countries citing papers authored by Wolfgang Moeder

Since Specialization
Citations

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

Fields of papers citing papers by Wolfgang Moeder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wolfgang Moeder

This figure shows the co-authorship network connecting the top 25 collaborators of Wolfgang Moeder. A scholar is included among the top collaborators of Wolfgang Moeder 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 Wolfgang Moeder. Wolfgang Moeder 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.
Jia, Yifan, et al.. (2025). Single‐Cell Force Spectroscopy Uncovers Root Zone‐ and Bacteria‐Specific Interactions. Angewandte Chemie International Edition. 64(19). e202419510–e202419510.
2.
Wang, Ren, Ellie Himschoot, Matteo Grenzi, et al.. (2022). Auxin analog-induced Ca2+ signaling is independent of inhibition of endosomal aggregation in Arabidopsis roots. Journal of Experimental Botany. 73(8). 2308–2319. 5 indexed citations
3.
Wang, Limin, Jian Sun, Katie A. Wilkins, et al.. (2022). Arabidopsis thaliana CYCLIC NUCLEOTIDE‐GATED CHANNEL2 mediates extracellular ATP signal transduction in root epidermis. New Phytologist. 234(2). 412–421. 22 indexed citations
4.
Toyota, Masatsugu, Wolfgang Moeder, Kimberley Chin, et al.. (2021). CYCLIC NUCLEOTIDE-GATED ION CHANNEL 2 modulates auxin homeostasis and signaling. PLANT PHYSIOLOGY. 187(3). 1690–1703. 29 indexed citations
5.
Cao, Feng, Thomas A. DeFalco, Wolfgang Moeder, et al.. (2018). Arabidopsis ETHYLENE RESPONSE FACTOR 8 (ERF8) has dual functions in ABA signaling and immunity. BMC Plant Biology. 18(1). 211–211. 53 indexed citations
6.
DeFalco, Thomas A., et al.. (2017). Using GCaMP3 to Study Ca2+ Signaling in Nicotiana Species. Plant and Cell Physiology. 58(7). 1173–1184. 35 indexed citations
7.
DeFalco, Thomas A., Christopher B. Marshall, Kim Munro, et al.. (2016). Multiple Calmodulin-binding Sites Positively and Negatively Regulate Arabidopsis CYCLIC NUCLEOTIDE-GATED CHANNEL12. The Plant Cell. 28(7). tpc.00870.2015–tpc.00870.2015. 84 indexed citations
8.
DeFalco, Thomas A., Wolfgang Moeder, & Keiko Yoshioka. (2016). Opening the Gates: Insights into Cyclic Nucleotide-Gated Channel-Mediated Signaling. Trends in Plant Science. 21(11). 903–906. 69 indexed citations
9.
Lee, Jihyun, et al.. (2015). Crossroads of stress responses, development and flowering regulation—the multiple roles of Cyclic Nucleotide Gated Ion Channel 2. Plant Signaling & Behavior. 10(3). e989758–e989758. 24 indexed citations
10.
Chin, Kimberley, Thomas A. DeFalco, Wolfgang Moeder, & Keiko Yoshioka. (2013). The Arabidopsis Cyclic Nucleotide-Gated Ion Channels AtCNGC2 and AtCNGC4 Work in the Same Signaling Pathway to Regulate Pathogen Defense and Floral Transition   . PLANT PHYSIOLOGY. 163(2). 611–624. 118 indexed citations
11.
Urquhart, W. E. S., et al.. (2011). The cyclic nucleotide-gated channels AtCNGC11 and 12 are involved in multiple Ca2+-dependent physiological responses and act in a synergistic manner. Journal of Experimental Botany. 62(10). 3671–3682. 37 indexed citations
12.
Yoshioka, Keiko, et al.. (2011). Altered Germination and Subcellular Localization Patterns for PUB44/SAUL1 in Response to Stress and Phytohormone Treatments. PLoS ONE. 6(6). e21321–e21321. 44 indexed citations
13.
Moeder, Wolfgang, et al.. (2011). The Role of Cyclic Nucleotide-Gated Ion Channels in Plant Immunity. Molecular Plant. 4(3). 442–452. 105 indexed citations
14.
Moeder, Wolfgang, et al.. (2010). SA-ABA antagonism in defense responses. Plant Signaling & Behavior. 5(10). 1231–1233. 42 indexed citations
15.
16.
Carviel, Jessie, et al.. (2009). Forward and reverse genetics to identify genes involved in the age‐related resistance response in Arabidopsis thaliana. Molecular Plant Pathology. 10(5). 621–634. 36 indexed citations
17.
Moeder, Wolfgang, W. E. S. Urquhart, Dea Shahinas, et al.. (2008). Identification of a functionally essential amino acid for Arabidopsis cyclic nucleotide gated ion channels using the chimeric AtCNGC11/12 gene. The Plant Journal. 56(3). 457–469. 33 indexed citations
18.
Moeder, Wolfgang & Keiko Yoshioka. (2008). Lesion mimic mutants. Plant Signaling & Behavior. 3(10). 764–767. 78 indexed citations
19.
Nandi, Ashis Kumar, Wolfgang Moeder, Pradeep Kachroo, Daniel F. Klessig, & Jyoti Shah. (2005). Arabidopsis ssi2-Conferred Susceptibility to Botrytis cinerea Is Dependent on EDS5 and PAD4. Molecular Plant-Microbe Interactions. 18(4). 363–370. 44 indexed citations
20.
Schraudner, M., et al.. (1998). Ozone-induced oxidative burst in the ozone biomonitor plant, tobacco Bel W3. HAL (Le Centre pour la Communication Scientifique Directe). 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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