Anat Nussbaum‐Shochat

603 total citations
18 papers, 462 citations indexed

About

Anat Nussbaum‐Shochat is a scholar working on Molecular Biology, Genetics and Materials Chemistry. According to data from OpenAlex, Anat Nussbaum‐Shochat has authored 18 papers receiving a total of 462 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 17 papers in Genetics and 4 papers in Materials Chemistry. Recurrent topics in Anat Nussbaum‐Shochat's work include Bacterial Genetics and Biotechnology (17 papers), RNA and protein synthesis mechanisms (12 papers) and Protein Structure and Dynamics (4 papers). Anat Nussbaum‐Shochat is often cited by papers focused on Bacterial Genetics and Biotechnology (17 papers), RNA and protein synthesis mechanisms (12 papers) and Protein Structure and Dynamics (4 papers). Anat Nussbaum‐Shochat collaborates with scholars based in Israel, United States and India. Anat Nussbaum‐Shochat's co-authors include Orna Amster‐Choder, Keren Nevo‐Dinur, Sigal Ben‐Yehuda, Andrew Wright, Liat Fux, Sutharsan Govindarajan, Qing Chen, Ora Schueler‐Furman, Emmanuel D. Levy and E. Sirotkin and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Anat Nussbaum‐Shochat

17 papers receiving 459 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anat Nussbaum‐Shochat Israel 10 393 281 131 51 22 18 462
Caryn S. Wadler United States 5 322 0.8× 207 0.7× 128 1.0× 27 0.5× 28 1.3× 6 387
Françoise Vannier France 12 461 1.2× 315 1.1× 93 0.7× 71 1.4× 22 1.0× 16 521
Venu Kamarthapu India 10 509 1.3× 256 0.9× 65 0.5× 73 1.4× 17 0.8× 13 569
Jonathan A. Stead United Kingdom 11 566 1.4× 256 0.9× 135 1.0× 39 0.8× 11 0.5× 11 635
Tomofumi Negishi Japan 7 334 0.8× 176 0.6× 58 0.4× 45 0.9× 7 0.3× 13 360
Lætitia My France 9 227 0.6× 137 0.5× 58 0.4× 28 0.5× 48 2.2× 17 311
Jisha Chalissery India 10 336 0.9× 232 0.8× 124 0.9× 32 0.6× 15 0.7× 16 381
Rajendran Harinarayanan India 9 281 0.7× 202 0.7× 78 0.6× 33 0.6× 18 0.8× 13 331
Claire M.L. Barrett United Kingdom 9 507 1.3× 442 1.6× 376 2.9× 28 0.5× 12 0.5× 9 592
Kai Virumäe Estonia 8 417 1.1× 153 0.5× 73 0.6× 16 0.3× 13 0.6× 9 446

Countries citing papers authored by Anat Nussbaum‐Shochat

Since Specialization
Citations

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

Fields of papers citing papers by Anat Nussbaum‐Shochat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anat Nussbaum‐Shochat. 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 Anat Nussbaum‐Shochat. The network helps show where Anat Nussbaum‐Shochat may publish in the future.

Co-authorship network of co-authors of Anat Nussbaum‐Shochat

This figure shows the co-authorship network connecting the top 25 collaborators of Anat Nussbaum‐Shochat. A scholar is included among the top collaborators of Anat Nussbaum‐Shochat 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 Anat Nussbaum‐Shochat. Anat Nussbaum‐Shochat is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Heidenreich, Meta, E. Sirotkin, Anat Nussbaum‐Shochat, et al.. (2025). Uncovering the mechanism for polar sequestration of the major bacterial sugar regulator by high-throughput screens and 3D interaction modeling. Cell Reports. 44(3). 115436–115436.
2.
Alam, Nawsad, Georgina D. Barnabas, Yair Pozniak, et al.. (2024). MinD-RNase E interplay controls localization of polar mRNAs in E. coli. The EMBO Journal. 43(4). 637–662. 4 indexed citations
3.
Dezorella, Nili, et al.. (2023). Regulation of major bacterial survival strategies by transcripts sequestration in a membraneless organelle. Cell Reports. 42(11). 113393–113393. 3 indexed citations
4.
Nussbaum‐Shochat, Anat, et al.. (2022). Heterotypic phase separation of Hfq is linked to its roles as an RNA chaperone. Cell Reports. 41(13). 111881–111881. 26 indexed citations
5.
Nussbaum‐Shochat, Anat, et al.. (2021). Evolutionarily conserved mechanism for membrane recognition from bacteria to mitochondria. FEBS Letters. 595(22). 2805–2815. 3 indexed citations
6.
Govindarajan, Sutharsan, et al.. (2020). Tyrosine phosphorylation-dependent localization of TmaR that controls activity of a major bacterial sugar regulator by polar sequestration. Proceedings of the National Academy of Sciences. 118(2). 13 indexed citations
7.
Govindarajan, Sutharsan, et al.. (2018). Phenotypic Heterogeneity in Sugar Utilization by E. coli Is Generated by Stochastic Dispersal of the General PTS Protein EI from Polar Clusters. Frontiers in Microbiology. 8. 2695–2695. 10 indexed citations
8.
Gordon, Noa, et al.. (2015). A Search for Ribonucleic Antiterminator Sites in Bacterial Genomes: Not Only Antitermination. Microbial Physiology. 25(2-3). 143–153. 2 indexed citations
9.
Nevo‐Dinur, Keren, Anat Nussbaum‐Shochat, Sigal Ben‐Yehuda, & Orna Amster‐Choder. (2011). Translation-Independent Localization of mRNA in E. coli. Science. 331(6020). 1081–1084. 215 indexed citations
10.
Nussbaum‐Shochat, Anat, et al.. (2010). Spatial and temporal organization of the E. coli PTS components. The EMBO Journal. 29(21). 3630–3645. 39 indexed citations
11.
Nussbaum‐Shochat, Anat, et al.. (2009). Modulation of transcription antitermination in the bgl operon of Escherichia coli by the PTS. Proceedings of the National Academy of Sciences. 106(32). 13523–13528. 19 indexed citations
12.
Fux, Liat, et al.. (2004). Modulation of Monomer Conformation of the BglG Transcriptional Antiterminator from Escherichia coli. Journal of Bacteriology. 186(20). 6775–6781. 6 indexed citations
13.
Nussbaum‐Shochat, Anat, et al.. (2003). The BglF sensor recruits the BglG transcription regulator to the membrane and releases it on stimulation. Proceedings of the National Academy of Sciences. 100(12). 7099–7104. 41 indexed citations
14.
Fux, Liat, Anat Nussbaum‐Shochat, & Orna Amster‐Choder. (2003). A Fraction of the BglG Transcriptional Antiterminator from Escherichia coli Exists as a Compact Monomer. Journal of Biological Chemistry. 278(51). 50978–50984. 8 indexed citations
15.
Fux, Liat, Anat Nussbaum‐Shochat, & Orna Amster‐Choder. (2003). Interactions between the PTS Regulation domains of the BglG Transcriptional Antiterminator from Escherichia coli. Journal of Biological Chemistry. 278(47). 46203–46209. 15 indexed citations
16.
Chen, Qing, Anat Nussbaum‐Shochat, & Orna Amster‐Choder. (2001). A Novel Sugar-stimulated Covalent Switch in a Sugar Sensor. Journal of Biological Chemistry. 276(48). 44751–44756. 7 indexed citations
17.
Nussbaum‐Shochat, Anat & Orna Amster‐Choder. (1999). BglG, the transcriptional antiterminator of the bgl system, interacts with the β′ subunit of the Escherichia coli RNA polymerase. Proceedings of the National Academy of Sciences. 96(8). 4336–4341. 25 indexed citations
18.
Nussbaum‐Shochat, Anat, et al.. (1999). Characterization of the Dimerization Domain in BglG, an RNA-Binding Transcriptional Antiterminator from Escherichia coli. Journal of Bacteriology. 181(6). 1755–1766. 26 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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