Halina Gabryś

2.9k total citations
62 papers, 2.2k citations indexed

About

Halina Gabryś is a scholar working on Plant Science, Molecular Biology and Oceanography. According to data from OpenAlex, Halina Gabryś has authored 62 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Plant Science, 42 papers in Molecular Biology and 6 papers in Oceanography. Recurrent topics in Halina Gabryś's work include Light effects on plants (44 papers), Photosynthetic Processes and Mechanisms (39 papers) and Plant Molecular Biology Research (25 papers). Halina Gabryś is often cited by papers focused on Light effects on plants (44 papers), Photosynthetic Processes and Mechanisms (39 papers) and Plant Molecular Biology Research (25 papers). Halina Gabryś collaborates with scholars based in Poland, Germany and United States. Halina Gabryś's co-authors include Agnieszka Katarzyna Banaś, Tadeusz Walczak, Paweł Hermanowicz, Justyna Łabuz, Olga Sztatelman, José M. Alonso, Juan Capel, José A. Jarillo, Joseph R. Ecker and Anthony R. Cashmore and has published in prestigious journals such as Nature, PLoS ONE and PLANT PHYSIOLOGY.

In The Last Decade

Halina Gabryś

61 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Halina Gabryś Poland 25 1.6k 1.3k 196 130 109 62 2.2k
Paul A. Davison United Kingdom 23 1.3k 0.8× 1.8k 1.3× 77 0.4× 75 0.6× 21 0.2× 34 2.7k
Allison E. McDonald Canada 21 760 0.5× 1.1k 0.8× 63 0.3× 65 0.5× 46 0.4× 32 1.8k
Fang Huang China 19 473 0.3× 1.3k 0.9× 101 0.5× 133 1.0× 33 0.3× 56 1.8k
Matt Geisler United States 28 2.3k 1.4× 1.8k 1.3× 29 0.1× 195 1.5× 63 0.6× 53 3.4k
J. Romero Spain 28 1.7k 1.0× 1.4k 1.0× 46 0.2× 191 1.5× 89 0.8× 74 2.5k
Robert T. Leonard United States 26 1.3k 0.8× 861 0.6× 68 0.3× 91 0.7× 9 0.1× 42 2.1k
Bernhard Huchzermeyer Germany 21 784 0.5× 455 0.3× 40 0.2× 104 0.8× 23 0.2× 48 1.4k
Hiromichi Morikawa Japan 31 1.7k 1.0× 1.4k 1.0× 19 0.1× 72 0.6× 126 1.2× 129 2.8k
Claire Remacle Belgium 32 356 0.2× 2.2k 1.7× 190 1.0× 71 0.5× 66 0.6× 97 3.0k
A.C. van Aelst Netherlands 23 842 0.5× 671 0.5× 57 0.3× 203 1.6× 65 0.6× 64 1.8k

Countries citing papers authored by Halina Gabryś

Since Specialization
Citations

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

Fields of papers citing papers by Halina Gabryś

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Halina Gabryś

This figure shows the co-authorship network connecting the top 25 collaborators of Halina Gabryś. A scholar is included among the top collaborators of Halina Gabryś 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 Halina Gabryś. Halina Gabryś 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.
Łyczakowski, Jan J., et al.. (2023). Two types of GLR channels cooperate differently in light and dark growth of Arabidopsis seedlings. BMC Plant Biology. 23(1). 358–358. 2 indexed citations
2.
Hebda, Anna, et al.. (2022). Upregulation of GLRs expression by light in Arabidopsis leaves. BMC Plant Biology. 22(1). 197–197. 5 indexed citations
3.
Łabuz, Justyna, Sławomir Samardakiewicz, Paweł Hermanowicz, et al.. (2016). Blue light-dependent changes in loosely bound calcium in Arabidopsis mesophyll cells: an X-ray microanalysis study. Journal of Experimental Botany. 67(13). 3953–3964. 13 indexed citations
4.
Hermanowicz, Paweł, et al.. (2016). Mobilization of storage materials during light-induced germination of tomato ( Solanum lycopersicum ) seeds. Plant Physiology and Biochemistry. 105. 271–281. 14 indexed citations
5.
Sztatelman, Olga, Justyna Łabuz, Paweł Hermanowicz, et al.. (2016). Fine tuning chloroplast movements through physical interactions between phototropins. Journal of Experimental Botany. 67(17). 4963–4978. 23 indexed citations
6.
Łabuz, Justyna, Paweł Hermanowicz, & Halina Gabryś. (2015). The impact of temperature on blue light induced chloroplast movements in Arabidopsis thaliana. Plant Science. 239. 238–249. 32 indexed citations
7.
Banaś, Agnieszka Katarzyna, et al.. (2014). Blue-light-activated phototropin2 trafficking from the cytoplasm to Golgi/post-Golgi vesicles. Journal of Experimental Botany. 65(12). 3263–3276. 25 indexed citations
8.
Łabuz, Justyna, et al.. (2013). Decoding the role of phosphoinositides in phototropin signaling involved in chloroplast movements. Plant Signaling & Behavior. 8(8). e25105–e25105. 5 indexed citations
9.
Strzałka, Wojciech, et al.. (2012). Arabidopsis thaliana proliferating cell nuclear antigen has several potential sumoylation sites. Journal of Experimental Botany. 63(8). 2971–2983. 15 indexed citations
10.
Appenroth, Klaus‐J., et al.. (2011). Light-Induced Degradation of Starch Granules in Turions of Spirodela polyrhiza Studied by Electron Microscopy. Plant and Cell Physiology. 52(2). 384–391. 19 indexed citations
11.
Augustynowicz, Joanna, et al.. (2009). Acquisition of plastid movement responsiveness to light during mesophyll cell differentiation. The International Journal of Developmental Biology. 53(1). 121–127. 6 indexed citations
12.
Anielska-Mazur, Anna, Tytus Bernaś, & Halina Gabryś. (2009). In vivo reorganization of the actin cytoskeleton in leaves of Nicotiana tabacumL. transformed with plastin-GFP. Correlation with light-activated chloroplast responses. BMC Plant Biology. 9(1). 64–64. 29 indexed citations
13.
Latowski, Dariusz, Agnieszka Katarzyna Banaś, Kazimierz Strzałka, & Halina Gabryś. (2006). Amino sugars – new inhibitors of zeaxanthin epoxidase, a violaxanthin cycle enzyme. Journal of Plant Physiology. 164(3). 231–237. 9 indexed citations
14.
Karpiński, Stanisław, Halina Gabryś, Alfonso Mateo, Barbara Karpińska, & Philip M. Mullineaux. (2003). Light perception in plant disease defence signalling. Current Opinion in Plant Biology. 6(4). 390–396. 208 indexed citations
15.
Jarillo, José A., Halina Gabryś, Juan Capel, et al.. (2001). Phototropin-related NPL1 controls chloroplast relocation induced by blue light. Nature. 410(6831). 952–954. 384 indexed citations
16.
Ślesak, Ireneusz & Halina Gabryś. (1996). ROLE OF PHOTOSYNTHESIS IN THE CONTROL OF BLUE LIGHT-INDUCED CHLOROPLAST MOVEMENTS. INHIBITOR STUDY. Acta Physiologiae Plantarum. 18(2). 135–145. 10 indexed citations
17.
Jiang, JinJie, et al.. (1995). Low-Frequency EPR Study of Chromium(V) Formation from Chromium(VI) in Living Plants. Biochemical and Biophysical Research Communications. 206(3). 829–834. 56 indexed citations
18.
Gabryś, Halina. (1985). Chloroplast movement in Mougeotia induced by blue light pulses. Planta. 166(1). 134–140. 29 indexed citations
19.
Gabryś, Halina, Tadeusz Walczak, & Wolfgang Haupt. (1984). Blue-light-induced chloroplast orientation in Mougeotia. Evidence for a separate sensor pigment besides phytochrome. Planta. 160(1). 21–24. 25 indexed citations
20.
Gabryś, Halina, Tadeusz Walczak, & J. Zurzycki. (1981). Chloroplast translocations induced by light pulses. Planta. 152(6). 553–556. 11 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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