Elisar Barbar

3.1k total citations
86 papers, 2.1k citations indexed

About

Elisar Barbar is a scholar working on Molecular Biology, Cell Biology and Materials Chemistry. According to data from OpenAlex, Elisar Barbar has authored 86 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Molecular Biology, 39 papers in Cell Biology and 10 papers in Materials Chemistry. Recurrent topics in Elisar Barbar's work include Microtubule and mitosis dynamics (35 papers), Protein Structure and Dynamics (30 papers) and Photosynthetic Processes and Mechanisms (25 papers). Elisar Barbar is often cited by papers focused on Microtubule and mitosis dynamics (35 papers), Protein Structure and Dynamics (30 papers) and Photosynthetic Processes and Mechanisms (25 papers). Elisar Barbar collaborates with scholars based in United States, Germany and France. Elisar Barbar's co-authors include Afua Nyarko, P. Andrew Karplus, Michael Hare, Gregory Benison, Thomas S. Hays, Clare Woodward, Yujuan Song, George Bárány, J. Perry Hall and Mingang Li and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Cell Biology and Journal of Molecular Biology.

In The Last Decade

Elisar Barbar

83 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
Elisar Barbar United States 30 1.7k 833 265 190 142 86 2.1k
Michael Davey Canada 13 2.0k 1.2× 530 0.6× 183 0.7× 163 0.9× 378 2.7× 22 2.3k
Ágnes Tantos Hungary 16 1.6k 0.9× 365 0.4× 361 1.4× 94 0.5× 150 1.1× 45 2.0k
Rina Rosenzweig Israel 22 2.2k 1.3× 604 0.7× 406 1.5× 81 0.4× 165 1.2× 35 2.6k
Elizabeth H. Kellogg United States 19 2.3k 1.4× 764 0.9× 360 1.4× 149 0.8× 308 2.2× 31 2.9k
Stephen W. Michnick Canada 26 2.6k 1.5× 608 0.7× 149 0.6× 153 0.8× 210 1.5× 41 3.1k
F. Jon Kull United States 27 2.0k 1.1× 1.5k 1.8× 159 0.6× 203 1.1× 248 1.7× 74 3.1k
Elisabeth Bragado‐Nilsson Spain 11 1.7k 1.0× 351 0.4× 131 0.5× 153 0.8× 119 0.8× 16 2.0k
Rosemary Williams United States 14 2.4k 1.4× 405 0.5× 241 0.9× 108 0.6× 133 0.9× 18 2.7k
Bálint Mészáros Hungary 20 2.8k 1.6× 322 0.4× 561 2.1× 171 0.9× 246 1.7× 33 3.3k
Tzviya Zeev‐Ben‐Mordehai United Kingdom 20 1.1k 0.7× 242 0.3× 196 0.7× 128 0.7× 232 1.6× 34 1.8k

Countries citing papers authored by Elisar Barbar

Since Specialization
Citations

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

Fields of papers citing papers by Elisar Barbar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisar Barbar

This figure shows the co-authorship network connecting the top 25 collaborators of Elisar Barbar. A scholar is included among the top collaborators of Elisar Barbar 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 Elisar Barbar. Elisar Barbar 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.
Reardon, Patrick N., et al.. (2025). LC8 enhances 53BP1 foci through heterogeneous bridging of 53BP1 oligomers. eLife. 14.
2.
Barbar, Elisar, et al.. (2025). Dynamic interactions of dimeric hub proteins underlie their diverse functions and structures: A comparative analysis of 14-3-3 and LC8. Journal of Biological Chemistry. 301(4). 108416–108416. 2 indexed citations
3.
Barbar, Elisar. (2025). The BPTI Story: From the Slow Exchange Core to Intrinsically Disordered Proteins. International Journal of Peptide Research and Therapeutics. 31(3).
4.
Yu, Zhentao, et al.. (2023). RNA structure and multiple weak interactions balance the interplay between RNA binding and phase separation of SARS-CoV-2 nucleocapsid. PNAS Nexus. 2(10). pgad333–pgad333. 13 indexed citations
5.
Rolland, Amber D., et al.. (2023). Linker Length Drives Heterogeneity of Multivalent Complexes of Hub Protein LC8 and Transcription Factor ASCIZ. Biomolecules. 13(3). 404–404. 5 indexed citations
6.
Barbar, Elisar, et al.. (2023). Quantifying cooperative multisite binding in the hub protein LC8 through Bayesian inference. PLoS Computational Biology. 19(4). e1011059–e1011059. 8 indexed citations
7.
Eastwood, Evelyn L., Susanne Bornelöv, Marzia Munafò, et al.. (2021). Dimerisation of the PICTS complex via LC8/Cut-up drives co-transcriptional transposon silencing in Drosophila. eLife. 10. 30 indexed citations
8.
Reardon, Patrick N., et al.. (2021). Multivalent binding of the partially disordered SARS-CoV-2 nucleocapsid phosphoprotein dimer to RNA. Biophysical Journal. 120(14). 2890–2901. 28 indexed citations
9.
Barbar, Elisar, et al.. (2020). Emerging Features of Linear Motif-Binding Hub Proteins. Trends in Biochemical Sciences. 45(5). 375–384. 29 indexed citations
10.
Barbar, Elisar, et al.. (2020). Emerging Features of Linear Motif-Binding Hub Proteins. Biophysical Journal. 118(3). 341a–341a. 2 indexed citations
11.
Mickolajczyk, Keith J., et al.. (2020). The Tail of Kinesin-14a in Giardia Is a Dual Regulator of Motility. Current Biology. 30(18). 3664–3671.e4. 5 indexed citations
12.
Davey, Norman E., Cecilia Blikstad, Anna Akhmanova, et al.. (2019). Systematic identification of recognition motifs for the hub protein LC8. Life Science Alliance. 2(4). e201900366–e201900366. 24 indexed citations
13.
Jensen, Malene Ringkjøbing, et al.. (2017). The LC8 Recognition Motif Preferentially Samples Polyproline II Structure in Its Free State. Biochemistry. 56(35). 4656–4666. 7 indexed citations
14.
Barbar, Elisar & Afua Nyarko. (2014). Polybivalency and disordered proteins in ordering macromolecular assemblies. Seminars in Cell and Developmental Biology. 37. 20–25. 32 indexed citations
15.
16.
Nyarko, Afua, J. Perry Hall, Andrea Hall, et al.. (2011). Conformational dynamics promote binding diversity of dynein light chain LC8. Biophysical Chemistry. 159(1). 41–47. 14 indexed citations
17.
Hall, J. Perry, P. Andrew Karplus, & Elisar Barbar. (2009). Multivalency in the Assembly of Intrinsically Disordered Dynein Intermediate Chain. Journal of Biological Chemistry. 284(48). 33115–33121. 63 indexed citations
18.
Deeb, Ruba S., Gang Hao, Steven S. Gross, et al.. (2006). Heme catalyzes tyrosine 385 nitration and inactivation of prostaglandin H2 synthase-1 by peroxynitrite. Journal of Lipid Research. 47(5). 898–911. 47 indexed citations
19.
Barbar, Elisar, et al.. (1995). Extensive nonrandom structure in reduced and unfolded bovine pancreatic trypsin inhibitor. Biochemistry. 34(43). 13974–13981. 42 indexed citations
20.
Breslow, Esther, Vinod Sardana, Ruba S. Deeb, Elisar Barbar, & David H. Peyton. (1995). NMR Behavior of the Aromatic Protons of Bovine Neurophysin-I and Its Peptide Complexes: Implications for Solution Structure and for Function. Biochemistry. 34(7). 2137–2147. 10 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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