Alexander Johnson

2.2k total citations
74 papers, 1.1k citations indexed

About

Alexander Johnson is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Alexander Johnson has authored 74 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 13 papers in Cell Biology and 9 papers in Plant Science. Recurrent topics in Alexander Johnson's work include Cellular transport and secretion (11 papers), Photosynthetic Processes and Mechanisms (8 papers) and Plant Molecular Biology Research (8 papers). Alexander Johnson is often cited by papers focused on Cellular transport and secretion (11 papers), Photosynthetic Processes and Mechanisms (8 papers) and Plant Molecular Biology Research (8 papers). Alexander Johnson collaborates with scholars based in Austria, United States and France. Alexander Johnson's co-authors include Martin Raff, Bruce Alberts, Julian Lewis, Grégory Vert, Peter Walter, Keith Roberts, Jiřı́ Friml, Keith Roberts, Shutang Tan and Walter A. Kaufmann and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and The EMBO Journal.

In The Last Decade

Alexander Johnson

73 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexander Johnson Austria 20 674 471 232 76 54 74 1.1k
Xiangdong Luo China 22 537 0.8× 619 1.3× 141 0.6× 96 1.3× 21 0.4× 59 1.3k
Xiangxiang Zhang China 17 511 0.8× 389 0.8× 99 0.4× 103 1.4× 37 0.7× 56 1.0k
Jamie Senft United States 6 500 0.7× 153 0.3× 97 0.4× 119 1.6× 56 1.0× 9 1.1k
Jeffrey G. Ault United States 23 959 1.4× 348 0.7× 682 2.9× 40 0.5× 92 1.7× 38 1.5k
Rolf Stucka Germany 24 1.1k 1.6× 217 0.5× 287 1.2× 121 1.6× 56 1.0× 45 1.4k
Silvère Pagant United States 17 587 0.9× 581 1.2× 321 1.4× 113 1.5× 129 2.4× 25 1.2k
Nathan Reed United States 15 811 1.2× 117 0.2× 545 2.3× 123 1.6× 85 1.6× 21 1.5k
Ines Müller Germany 21 582 0.9× 197 0.4× 71 0.3× 48 0.6× 47 0.9× 34 1.3k
Patrick McNutt United States 21 446 0.7× 178 0.4× 124 0.5× 46 0.6× 42 0.8× 57 1.2k
Janet L. Paluh United States 20 1.1k 1.6× 200 0.4× 320 1.4× 114 1.5× 39 0.7× 54 1.4k

Countries citing papers authored by Alexander Johnson

Since Specialization
Citations

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

Fields of papers citing papers by Alexander Johnson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander Johnson

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander Johnson. A scholar is included among the top collaborators of Alexander Johnson 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 Alexander Johnson. Alexander Johnson 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.
Gallei, Michelle, Sven Truckenbrodt, Caroline Kreuzinger, et al.. (2025). Super-resolution expansion microscopy in plant roots. The Plant Cell. 37(4). 6 indexed citations
2.
Johnson, Alexander. (2024). Mechanistic divergences of endocytic clathrin-coated vesicle formation in mammals, yeasts and plants. Journal of Cell Science. 137(16). 5 indexed citations
3.
Reynolds, Gregory D., Jessica Cardenas, Dominique Eeckhout, et al.. (2022). Proteomic characterization of isolated Arabidopsis clathrin-coated vesicles reveals evolutionarily conserved and plant-specific components. The Plant Cell. 34(6). 2150–2173. 34 indexed citations
4.
Johnson, Alexander, Walter A. Kaufmann, Christoph Sommer, et al.. (2022). Three-dimensional visualization of planta clathrin-coated vesicles at ultrastructural resolution. Molecular Plant. 15(10). 1533–1542. 4 indexed citations
5.
Ötvös, Krisztina, M. Marconi, Andrea Vega, et al.. (2021). Modulation of plant root growth by nitrogen source‐defined regulation of polar auxin transport. The EMBO Journal. 40(3). e106862–e106862. 68 indexed citations
6.
Johnson, Alexander, Walter A. Kaufmann, Vanessa Zheden, et al.. (2021). The TPLATE complex mediates membrane bending during plant clathrin–mediated endocytosis. Proceedings of the National Academy of Sciences. 118(51). 27 indexed citations
7.
Glanc, Matouš, Kasper van Gelderen, Lukas Hoermayer, et al.. (2021). AGC kinases and MAB4/MEL proteins maintain PIN polarity by limiting lateral diffusion in plant cells. Current Biology. 31(9). 1918–1930.e5. 34 indexed citations
8.
Narasimhan, Madhumitha, Michelle Gallei, Shutang Tan, et al.. (2021). Systematic analysis of specific and nonspecific auxin effects on endocytosis and trafficking. PLANT PHYSIOLOGY. 186(2). 1122–1142. 30 indexed citations
9.
Wang, Jie, Alexander Johnson, Geert De Jaeger, et al.. (2020). High Temporal Resolution Reveals Simultaneous Plasma Membrane Recruitment of TPLATE Complex Subunits. PLANT PHYSIOLOGY. 183(3). 986–997. 25 indexed citations
10.
Antoniadi, Ioanna, Ondřej Novák, Zuzana Gelová, et al.. (2020). Cell-surface receptors enable perception of extracellular cytokinins. Nature Communications. 11(1). 4284–4284. 51 indexed citations
11.
Liu, Derui, Rahul Kumar, Lucas Alves Neubus Claus, et al.. (2020). Endocytosis of BRASSINOSTEROID INSENSITIVE1 Is Partly Driven by a Canonical Tyr-Based Motif. The Plant Cell. 32(11). 3598–3612. 27 indexed citations
12.
Spanova, Miroslava, et al.. (2018). Isolation of synaptic vesicles from genetically engineered cultured neurons. Journal of Neuroscience Methods. 312. 114–121. 1 indexed citations
13.
Johnson, Alexander & Grégory Vert. (2017). Single Event Resolution of Plant Plasma Membrane Protein Endocytosis by TIRF Microscopy. Frontiers in Plant Science. 8. 612–612. 32 indexed citations
14.
Johnson, Alexander & Grégory Vert. (2016). Unraveling K63 Polyubiquitination Networks by Sensor-Based Proteomics. PLANT PHYSIOLOGY. 171(3). 1808–1820. 51 indexed citations
15.
Martins, Sara, Esther M.N. Dohmann, Anne Cayrel, et al.. (2015). Internalization and vacuolar targeting of the brassinosteroid hormone receptor BRI1 are regulated by ubiquitination. Nature Communications. 6(1). 6151–6151. 123 indexed citations
16.
Johnson, Alexander. (2011). I Should Be Included in the Census. Schizophrenia Bulletin. 38(2). 207–208. 5 indexed citations
17.
Alberts, Bruce, Alexander Johnson, Julian Lewis, et al.. (2002). The Extracellular Matrix of Animals. Organic Letters. 4(21). 3695–8. 56 indexed citations
18.
Alberts, Bruce, Alexander Johnson, Julian Lewis, et al.. (2002). An Overview of the Cell Cycle. Frontiers in Sociology. 5. 50–50. 6 indexed citations
19.
Alberts, Bruce, et al.. (2002). Genesis, Modulation, and Regeneration of Skeletal Muscle. Radiologic Clinics of North America. 2. 167–83. 7 indexed citations
20.
Alberts, Bruce, Alexander Johnson, Julian Lewis, et al.. (2002). Extracellular Control of Cell Division, Cell Growth, and Apoptosis. Korean Journal for Food Science of Animal Resources. 35(4). 486–93. 9 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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