Irit Orr

1.0k total citations
28 papers, 811 citations indexed

About

Irit Orr is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Irit Orr has authored 28 papers receiving a total of 811 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 12 papers in Cardiology and Cardiovascular Medicine and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Irit Orr's work include Ion channel regulation and function (18 papers), Cardiac electrophysiology and arrhythmias (11 papers) and Neuroscience and Neuropharmacology Research (4 papers). Irit Orr is often cited by papers focused on Ion channel regulation and function (18 papers), Cardiac electrophysiology and arrhythmias (11 papers) and Neuroscience and Neuropharmacology Research (4 papers). Irit Orr collaborates with scholars based in Israel, Germany and United States. Irit Orr's co-authors include Varda Shoshan‐Barmatz, Ofer Yifrach, Ludwig M.G. Heilmeyer, Magdolna Varsányi, Orly Reiner, Tamar Sapir, Wei Feng, Sven Bergmann, Gregor Eichele and Talia Levy and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Irit Orr

28 papers receiving 801 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Irit Orr Israel 16 539 155 117 116 112 28 811
Timothy J. Manning United States 11 599 1.1× 178 1.1× 61 0.5× 176 1.5× 45 0.4× 13 934
Akiko Yanagiya Canada 19 1.1k 2.0× 126 0.8× 75 0.6× 67 0.6× 85 0.8× 31 1.5k
Fujiko Tsukahara Japan 17 608 1.1× 90 0.6× 143 1.2× 101 0.9× 66 0.6× 49 1.0k
Alex Sobko Russia 15 781 1.4× 251 1.6× 105 0.9× 78 0.7× 127 1.1× 21 965
Nieves Ibarrola Spain 18 595 1.1× 142 0.9× 95 0.8× 68 0.6× 27 0.2× 33 1.2k
Katrin Hayeß Germany 16 1.0k 1.9× 163 1.1× 79 0.7× 293 2.5× 354 3.2× 25 1.4k
Miwako Iwai Japan 17 829 1.5× 192 1.2× 71 0.6× 241 2.1× 59 0.5× 38 1.2k
Silas Maniatis United States 7 558 1.0× 66 0.4× 137 1.2× 42 0.4× 35 0.3× 7 990
Valentina A. Valova Australia 16 810 1.5× 207 1.3× 54 0.5× 483 4.2× 129 1.2× 21 1.1k
Minh M. Nguyen United States 14 467 0.9× 151 1.0× 84 0.7× 143 1.2× 47 0.4× 25 765

Countries citing papers authored by Irit Orr

Since Specialization
Citations

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

Fields of papers citing papers by Irit Orr

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Irit Orr

This figure shows the co-authorship network connecting the top 25 collaborators of Irit Orr. A scholar is included among the top collaborators of Irit Orr 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 Irit Orr. Irit Orr 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.
Orr, Irit, et al.. (2023). Regulating Shaker Kv channel clustering by hetero-oligomerization. Frontiers in Molecular Biosciences. 9. 1050942–1050942. 1 indexed citations
2.
Yahalom-Ronen, Yfat, Hadas Tamir, Sharon Melamed, et al.. (2023). VSV-ΔG-Spike Candidate Vaccine Induces Protective Immunity and Protects K18-hACE2 Mice against SARS-CoV-2 Variants. Viruses. 15(6). 1364–1364. 2 indexed citations
3.
Hadad, Uzi, et al.. (2020). Molecular and cellular correlates in Kv channel clustering: entropy-based regulation of cluster ion channel density. Scientific Reports. 10(1). 11304–11304. 7 indexed citations
4.
Lewinsky, Hadas, Matthias P. Kramer, Lihi Radomir, et al.. (2018). CD84 regulates PD-1/PD-L1 expression and function in chronic lymphocytic leukemia. Journal of Clinical Investigation. 128(12). 5465–5478. 55 indexed citations
5.
Abdu, Uri, et al.. (2018). Direct Evidence for a Similar Molecular Mechanism Underlying Shaker Kv Channel Fast Inactivation and Clustering. Journal of Molecular Biology. 431(3). 542–556. 4 indexed citations
6.
Ben‐Dor, Shifra, et al.. (2018). Genomic profiling of bovine corpus luteum maturation. PLoS ONE. 13(3). e0194456–e0194456. 31 indexed citations
7.
Zinoviev, Alexandra, et al.. (2015). The eIF3 complex ofLeishmania—subunit composition and mode of recruitment to different cap-binding complexes. Nucleic Acids Research. 43(13). 6222–6235. 22 indexed citations
8.
Marciano, Shir, et al.. (2015). Alternative splicing modulates Kv channel clustering through a molecular ball and chain mechanism. Nature Communications. 6(1). 6488–6488. 17 indexed citations
9.
Marciano, Shir, et al.. (2013). The Intrinsically Disordered Tail of the Shaker Kv Channel is an Entropic Clock that Times its Binding to Scaffold Proteins. Biophysical Journal. 104(2). 466a–466a. 1 indexed citations
11.
Orr, Irit, et al.. (2011). Probing the Transition State of the Allosteric Pathway of the SHAKER Kv Channel Pore by Linear Free Energy Relations. Biophysical Journal. 100(3). 29a–29a. 7 indexed citations
12.
Orr, Irit, et al.. (2010). Probing the Transition State of the Allosteric Pathway of the Shaker Kv Channel Pore by Linear Free-Energy Relations. Journal of Molecular Biology. 403(2). 167–173. 7 indexed citations
14.
Shmueli, Anat, Tamar Sapir, Ryouhei Tsutsumi, et al.. (2009). Ndel1 palmitoylation: a new mean to regulate cytoplasmic dynein activity. The EMBO Journal. 29(1). 107–119. 44 indexed citations
15.
Coquelle, Frédéric M., Talia Levy, Sven Bergmann, et al.. (2006). The DCX Superfamily 1: Common and Divergent Roles for Members of the Mouse DCX Superfamily. Cell Cycle. 5(9). 976–983. 58 indexed citations
16.
Reiner, Orly, Frédéric M. Coquelle, Bastian Peter, et al.. (2006). The evolving doublecortin (DCX) superfamily. BMC Genomics. 7(1). 188–188. 96 indexed citations
17.
Shoshan‐Barmatz, Varda, Irit Orr, Cécile Martin, & Noga Vardi. (2005). Novel ryanodine-binding properties in mammalian retina. The International Journal of Biochemistry & Cell Biology. 37(8). 1681–1695. 12 indexed citations
18.
Shoshan‐Barmatz, Varda, Irit Orr, Simy Weil, et al.. (1996). The identification of the phosphorylated 150/160-kDa proteins of sarcoplasmic reticulum, their kinase and their association with the ryanodine receptor. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1283(1). 89–100. 43 indexed citations
19.
Orr, Irit & Varda Shoshan‐Barmatz. (1996). Modulation of the skeletal muscle ryanodine receptor by endogenous phosphorylation of 160/150-kDa proteins of the sarcoplasmic reticulum. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1283(1). 80–88. 29 indexed citations
20.
Shoshan‐Barmatz, Varda, et al.. (1996). VDAC/porin is present in sarcoplasmic reticulum from skeletal muscle. FEBS Letters. 386(2-3). 205–210. 116 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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