Anna A. Dobritsa

2.1k total citations
28 papers, 1.5k citations indexed

About

Anna A. Dobritsa is a scholar working on Molecular Biology, Plant Science and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Anna A. Dobritsa has authored 28 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 21 papers in Plant Science and 7 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Anna A. Dobritsa's work include Plant Reproductive Biology (23 papers), Plant Molecular Biology Research (20 papers) and Photosynthetic Processes and Mechanisms (14 papers). Anna A. Dobritsa is often cited by papers focused on Plant Reproductive Biology (23 papers), Plant Molecular Biology Research (20 papers) and Photosynthetic Processes and Mechanisms (14 papers). Anna A. Dobritsa collaborates with scholars based in United States, Russia and France. Anna A. Dobritsa's co-authors include John R. Carlson, Wynand van der Goes van Naters, Coral G. Warr, R. A. Steinbrecht, Daphne Preuss, Robert Swanson, Jay Shrestha, Lloyd W. Sumner, Ewa Urbańczyk-Wochniak and Michiyo Matsuno and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neuron and The Plant Cell.

In The Last Decade

Anna A. Dobritsa

27 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna A. Dobritsa United States 16 998 839 467 343 293 28 1.5k
Martine Schorderet Switzerland 15 505 0.5× 983 1.2× 217 0.5× 116 0.3× 120 0.4× 20 1.3k
Veit Grabe Germany 18 308 0.3× 301 0.4× 890 1.9× 450 1.3× 602 2.1× 42 1.6k
Joaquı́n Cañizares Spain 27 1.3k 1.3× 1.7k 2.1× 214 0.5× 124 0.4× 713 2.4× 52 2.6k
Sylwester Chyb United States 14 391 0.4× 231 0.3× 801 1.7× 126 0.4× 133 0.5× 20 1.2k
Xiangyu Song United States 10 414 0.4× 268 0.3× 438 0.9× 109 0.3× 170 0.6× 10 1.0k
Takahiro Shiotsuki Japan 24 782 0.8× 192 0.2× 791 1.7× 229 0.7× 454 1.5× 90 1.6k
Marion J. Healy Australia 15 358 0.4× 198 0.2× 321 0.7× 118 0.3× 246 0.8× 29 786
Alessia Para United States 12 551 0.6× 728 0.9× 195 0.4× 66 0.2× 105 0.4× 18 1.1k
Allard A. Cossé United States 25 186 0.2× 439 0.5× 299 0.6× 462 1.3× 361 1.2× 70 1.8k
Youssef Dewer Egypt 22 467 0.5× 326 0.4× 778 1.7× 141 0.4× 506 1.7× 81 1.4k

Countries citing papers authored by Anna A. Dobritsa

Since Specialization
Citations

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

Fields of papers citing papers by Anna A. Dobritsa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna A. Dobritsa. 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 Anna A. Dobritsa. The network helps show where Anna A. Dobritsa may publish in the future.

Co-authorship network of co-authors of Anna A. Dobritsa

This figure shows the co-authorship network connecting the top 25 collaborators of Anna A. Dobritsa. A scholar is included among the top collaborators of Anna A. Dobritsa 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 Anna A. Dobritsa. Anna A. Dobritsa 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.
Zhou, Yuan & Anna A. Dobritsa. (2025). Molecular mechanisms of pollen aperture formation in Arabidopsis and rice. Journal of Experimental Botany. 76(22). 6674–6682.
2.
Zhou, Yuan & Anna A. Dobritsa. (2025). Forging the pollen fortress: Cell biological mechanisms of exine formation. Current Opinion in Plant Biology. 86. 102742–102742. 2 indexed citations
3.
Zhou, Yuan & Anna A. Dobritsa. (2023). Putting the brakes on pollen wall development: A conserved negative feedback loop regulates pollen exine formation in flowering plants. Molecular Plant. 16(9). 1376–1378. 2 indexed citations
4.
5.
Lee, Byung Ha, Rui Wang, Michelle H. Tan, et al.. (2021). A species-specific functional module controls formation of pollen apertures. Nature Plants. 7(7). 966–978. 9 indexed citations
6.
Honys, David, et al.. (2021). The Role of INAPERTURATE POLLEN1 as a Pollen Aperture Factor Is Conserved in the Basal Eudicot Eschscholzia californica (Papaveraceae). Frontiers in Plant Science. 12. 701286–701286. 9 indexed citations
7.
Wang, Rui & Anna A. Dobritsa. (2021). Loss ofTHIN EXINE2disrupts multiple processes in the mechanism of pollen exine formation. PLANT PHYSIOLOGY. 187(1). 133–157. 17 indexed citations
8.
Zhou, Yuan & Anna A. Dobritsa. (2019). Formation of aperture sites on the pollen surface as a model for development of distinct cellular domains. Plant Science. 288. 110222–110222. 13 indexed citations
9.
10.
Weber, Zachary, Melina Zourelidou, Brigitte T. Hofmeister, et al.. (2018). Arabidopsis Protein Kinase D6PKL3 Is Involved in the Formation of Distinct Plasma Membrane Aperture Domains on the Pollen Surface. The Plant Cell. 30(9). 2038–2056. 25 indexed citations
11.
Li, Peng, et al.. (2017). INP1 involvement in pollen aperture formation is evolutionarily conserved and may require species-specific partners. Journal of Experimental Botany. 69(5). 983–996. 24 indexed citations
12.
Albert, Béatrice, Adrienne Ressayre, Christine Dillmann, et al.. (2017). Effect of aperture number on pollen germination, survival and reproductive success in Arabidopsis thaliana. Annals of Botany. 121(4). 733–740. 27 indexed citations
13.
Lee, Byung Ha, et al.. (2016). A Ploidy-Sensitive Mechanism Regulates Aperture Formation on the Arabidopsis Pollen Surface and Guides Localization of the Aperture Factor INP1. PLoS Genetics. 12(5). e1006060–e1006060. 21 indexed citations
14.
Prieu, Charlotte, Alexis Matamoro‐Vidal, Christian Raquin, et al.. (2016). Aperture number influences pollen survival in Arabidopsis mutants. American Journal of Botany. 103(3). 452–459. 29 indexed citations
15.
Dobritsa, Anna A., Zhentian Lei, Shuh‐ichi Nishikawa, et al.. (2010). LAP5 and LAP6 Encode Anther-Specific Proteins with Similarity to Chalcone Synthase Essential for Pollen Exine Development in Arabidopsis. PLANT PHYSIOLOGY. 153(3). 937–955. 182 indexed citations
16.
Dobritsa, Anna A., Shuh‐ichi Nishikawa, Daphne Preuss, et al.. (2009). LAP3, a novel plant protein required for pollen development, is essential for proper exine formation. Sexual Plant Reproduction. 22(3). 167–177. 57 indexed citations
17.
Dobritsa, Anna A., Wynand van der Goes van Naters, Coral G. Warr, R. A. Steinbrecht, & John R. Carlson. (2003). Integrating the Molecular and Cellular Basis of Odor Coding in the Drosophila Antenna. Neuron. 37(5). 827–841. 434 indexed citations
18.
Kalmykova, Alla, Yuri Y. Shevelyov, Oksana Polesskaya, et al.. (2002). CK2βtes gene encodes a testis‐specific isoform of the regulatory subunit of casein kinase 2 in Drosophila melanogaster. European Journal of Biochemistry. 269(5). 1418–1427. 12 indexed citations
19.
Kalmykova, Alla, Anna A. Dobritsa, & В. А. Гвоздев. (1998). Su(Ste) Diverged Tandem Repeats in a Y Chromosome of Drosophila melanogaster Are Transcribed and Variously Processed. Genetics. 148(1). 243–249. 24 indexed citations
20.
Kalmykova, Alla, Anna A. Dobritsa, & В. А. Гвоздев. (1997). The Su(Ste) repeat in the Y chromosome and βCK2tes gene encode predicted isoforms of regulatory β‐subunit of protein kinase CK2 in Drosophila melanogaster. FEBS Letters. 416(2). 164–166. 12 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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