Gali Prag

2.1k total citations · 1 hit paper
36 papers, 1.6k citations indexed

About

Gali Prag is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Gali Prag has authored 36 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 13 papers in Cell Biology and 9 papers in Genetics. Recurrent topics in Gali Prag's work include Ubiquitin and proteasome pathways (20 papers), Endoplasmic Reticulum Stress and Disease (7 papers) and Cellular transport and secretion (6 papers). Gali Prag is often cited by papers focused on Ubiquitin and proteasome pathways (20 papers), Endoplasmic Reticulum Stress and Disease (7 papers) and Cellular transport and secretion (6 papers). Gali Prag collaborates with scholars based in Israel, United States and Germany. Gali Prag's co-authors include James H. Hurley, Sangho Lee, Amos B. Oppenheim, Constantinos E. Vorgias, Kyriacos Petratos, Y. Papanikolau, Rodolfo Ghirlando, Bruce Horazdovsky, Saurav Misra and Brian A. Davies and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Gali Prag

34 papers receiving 1.6k citations

Hit Papers

Ubiquitin-binding domains 2006 2026 2012 2019 2006 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gali Prag Israel 17 1.4k 472 264 238 155 36 1.6k
Andrea Scrima Germany 17 1.4k 1.1× 285 0.6× 208 0.8× 109 0.5× 224 1.4× 31 1.8k
Alexander Fish Netherlands 27 1.5k 1.1× 306 0.6× 328 1.2× 147 0.6× 188 1.2× 43 1.9k
Alison V. Nairn United States 21 2.1k 1.6× 513 1.1× 155 0.6× 104 0.4× 130 0.8× 33 2.5k
Jean Spence United States 10 1.1k 0.8× 189 0.4× 232 0.9× 152 0.6× 263 1.7× 14 1.3k
Alexander Y. Amerik United States 15 1.8k 1.3× 676 1.4× 479 1.8× 438 1.8× 225 1.5× 22 2.1k
Shunji Natsuka Japan 24 1.6k 1.2× 411 0.9× 284 1.1× 144 0.6× 89 0.6× 68 2.4k
Christian U. Stirnimann Switzerland 15 1.3k 1.0× 301 0.6× 472 1.8× 92 0.4× 175 1.1× 17 2.0k
Ilana Berlin Netherlands 24 1.5k 1.1× 643 1.4× 360 1.4× 380 1.6× 137 0.9× 33 2.3k
Daniel J. Kelleher United States 18 1.8k 1.3× 504 1.1× 129 0.5× 209 0.9× 113 0.7× 19 2.2k
Yves Nominé France 22 1.0k 0.8× 256 0.5× 237 0.9× 392 1.6× 210 1.4× 51 1.4k

Countries citing papers authored by Gali Prag

Since Specialization
Citations

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

Fields of papers citing papers by Gali Prag

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gali Prag

This figure shows the co-authorship network connecting the top 25 collaborators of Gali Prag. A scholar is included among the top collaborators of Gali Prag 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 Gali Prag. Gali Prag 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.
Steklov, Mikhail, Hyunbum Jang, Raj Nayan Sewduth, et al.. (2024). K128 ubiquitination constrains RAS activity by expanding its binding interface with GAP proteins. The EMBO Journal. 43(14). 2862–2877. 8 indexed citations
2.
Ben-Moshe, Zohar, Joel Reiter, Talya Dor, et al.. (2024). A deleterious variant of INTS1 leads to disrupted sleep–wake cycles. Disease Models & Mechanisms. 17(8).
3.
Berdichevsky, Yevgeny, Itzhak Braverman, Sergiu C. Blumen, et al.. (2024). Disease-associated polyalanine expansion mutations impair UBA6-dependent ubiquitination. The EMBO Journal. 43(2). 250–276. 3 indexed citations
4.
Prag, Gali, et al.. (2024). CRL4DCAF1ubiquitin ligase regulates PLK4 protein levels to prevent premature centriole duplication. Life Science Alliance. 7(6). e202402668–e202402668. 2 indexed citations
5.
Lodeiro, Carlos, Gali Prag, Emanuele Micaglio, et al.. (2024). Dithiothreitol-based protein equalisation in the context of multiple myeloma: Enhancing proteomic analysis and therapeutic insights. Talanta. 279. 126589–126589.
6.
Hensel, Göetz, Christian Kappel, Gali Prag, et al.. (2024). RING/U-box E3 protein BIR1 interacts with and ubiquitinates barley growth repressor BROAD LEAF1. PLANT PHYSIOLOGY. 196(1). 228–243. 2 indexed citations
8.
Berdichevsky, Yevgeny, et al.. (2021). Deubiquitylating enzymes in neuronal health and disease. Cell Death and Disease. 12(1). 120–120. 17 indexed citations
9.
Li, Chuanyin, Rong Guo, Peng Chen, et al.. (2020). An Integrative Synthetic Biology Approach to Interrogating Cellular Ubiquitin and Ufm Signaling. International Journal of Molecular Sciences. 21(12). 4231–4231. 19 indexed citations
10.
Keren‐Kaplan, Tal, et al.. (2018). E. coli-Based Selection and Expression Systems for Discovery, Characterization, and Purification of Ubiquitylated Proteins. Methods in molecular biology. 1844. 155–166. 1 indexed citations
11.
Attali, Ilan, William S. Tobelaim, Avinash K. Persaud, et al.. (2017). Ubiquitylation‐dependent oligomerization regulates activity of Nedd4 ligases. The EMBO Journal. 36(4). 425–440. 40 indexed citations
12.
Attali, Ilan, Tal Keren‐Kaplan, Shay Artzi, et al.. (2016). A bacterial genetic selection system for ubiquitylation cascade discovery. Nature Methods. 13(11). 945–952. 19 indexed citations
13.
Keren‐Kaplan, Tal, Ilan Attali, Lillian S. Kuo, et al.. (2013). Structure‐based in silico identification of ubiquitin‐binding domains provides insights into the ALIX‐V:ubiquitin complex and retrovirus budding. The EMBO Journal. 32(4). 538–551. 54 indexed citations
14.
Prag, Gali, et al.. (2012). Purification and crystallization of yeast Ent1 ENTH domain. Acta Crystallographica Section F Structural Biology and Crystallization Communications. 68(7). 820–823. 3 indexed citations
15.
Moldavski, Ofer, et al.. (2012). The Hetero-Hexameric Nature of a Chloroplast AAA+ FtsH Protease Contributes to Its Thermodynamic Stability. PLoS ONE. 7(4). e36008–e36008. 25 indexed citations
16.
Keren‐Kaplan, Tal & Gali Prag. (2012). Purification and crystallization of mono-ubiquitylated ubiquitin receptor Rpn10. Acta Crystallographica Section F Structural Biology and Crystallization Communications. 68(9). 1120–1123. 8 indexed citations
17.
Prag, Gali, Hadiya A. Watson, Bridgette M. Beach, et al.. (2007). The Vps27/Hse1 Complex Is a GAT Domain-Based Scaffold for Ubiquitin-Dependent Sorting. Developmental Cell. 12(6). 973–986. 63 indexed citations
18.
Hurley, James H., Sangho Lee, & Gali Prag. (2006). Ubiquitin-binding domains. Biochemical Journal. 399(3). 361–372. 515 indexed citations breakdown →
20.
Giladi, Hilla, et al.. (1998). Participation of IHF and a distant UP element in the stimulation of the phage λ PL promoter. Molecular Microbiology. 30(2). 443–451. 37 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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