C.C. Rohena

587 total citations
18 papers, 474 citations indexed

About

C.C. Rohena is a scholar working on Molecular Biology, Cell Biology and Organic Chemistry. According to data from OpenAlex, C.C. Rohena has authored 18 papers receiving a total of 474 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Cell Biology and 5 papers in Organic Chemistry. Recurrent topics in C.C. Rohena's work include Microtubule and mitosis dynamics (6 papers), Synthesis and biological activity (4 papers) and Quinazolinone synthesis and applications (3 papers). C.C. Rohena is often cited by papers focused on Microtubule and mitosis dynamics (6 papers), Synthesis and biological activity (4 papers) and Quinazolinone synthesis and applications (3 papers). C.C. Rohena collaborates with scholars based in United States, Thailand and Canada. C.C. Rohena's co-authors include Susan L. Mooberry, Pradipta Ghosh, Jiangnan Peng, Aleem Gangjee, Ernest Hamel, J. Li, Sandra Diaz, Ismael Secundino, Victor Nizet and Ross Corriden and has published in prestigious journals such as Blood, Cancer Research and Journal of Cell Science.

In The Last Decade

C.C. Rohena

18 papers receiving 470 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C.C. Rohena United States 11 284 151 112 104 67 18 474
Audrey Restouin France 12 295 1.0× 83 0.5× 45 0.4× 61 0.6× 66 1.0× 20 462
Jean M. Lockyer United States 8 209 0.7× 105 0.7× 121 1.1× 55 0.5× 102 1.5× 12 445
Róbert Alföldi Hungary 11 205 0.7× 50 0.3× 41 0.4× 48 0.5× 59 0.9× 15 364
Vladimı́r Čermák Czechia 12 322 1.1× 98 0.6× 151 1.3× 172 1.7× 42 0.6× 18 631
Staci N. Keller United States 10 742 2.6× 76 0.5× 290 2.6× 91 0.9× 102 1.5× 15 844
Kazuo Kamemura Japan 12 540 1.9× 183 1.2× 62 0.6× 45 0.4× 202 3.0× 32 628
Ki‐Ling Suen United States 12 428 1.5× 108 0.7× 45 0.4× 91 0.9× 133 2.0× 14 678
Koichi Koseki Japan 11 679 2.4× 120 0.8× 140 1.3× 38 0.4× 203 3.0× 15 814
Suk‐Kyeong Jung South Korea 13 504 1.8× 92 0.6× 53 0.5× 68 0.7× 94 1.4× 19 643
Rósula García‐Navas Spain 12 223 0.8× 99 0.7× 39 0.3× 99 1.0× 65 1.0× 20 443

Countries citing papers authored by C.C. Rohena

Since Specialization
Citations

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

Fields of papers citing papers by C.C. Rohena

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C.C. Rohena

This figure shows the co-authorship network connecting the top 25 collaborators of C.C. Rohena. A scholar is included among the top collaborators of C.C. Rohena 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 C.C. Rohena. C.C. Rohena 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.
Castillo, Vanessa, Gajanan D. Katkar, Inmaculada López-Sánchez, et al.. (2021). GIV/Girdin, a non-receptor modulator for Gαi/s, regulates spatiotemporal signaling during sperm capacitation and is required for male fertility. eLife. 10. 4 indexed citations
2.
Rohena, C.C., et al.. (2020). GIV/Girdin and Exo70 Collaboratively Regulate the Mammalian Polarized Exocytic Machinery. iScience. 23(7). 101246–101246. 1 indexed citations
3.
Rohena, C.C., Nicholas A. Kalogriopoulos, Suchismita Roy, et al.. (2020). GIV•Kindlin Interaction Is Required for Kindlin-Mediated Integrin Recognition and Activation. iScience. 23(6). 101209–101209. 8 indexed citations
4.
Midde, Krishna, et al.. (2018). Single-Cell Imaging of Metastatic Potential of Cancer Cells. iScience. 10. 53–65. 15 indexed citations
5.
Lizcano, Anel, Ismael Secundino, Simon Döhrmann, et al.. (2017). Erythrocyte sialoglycoproteins engage Siglec-9 on neutrophils to suppress activation. Blood. 129(23). 3100–3110. 83 indexed citations
6.
Rohena, C.C., April L. Risinger, Nicholas F. Dybdal‐Hargreaves, et al.. (2016). Janus Compounds, 5-Chloro-N4-methyl-N4-aryl-9H-pyrimido[4,5-b]indole-2,4-diamines, Cause Both Microtubule Depolymerizing and Stabilizing Effects. Molecules. 21(12). 1661–1661. 7 indexed citations
7.
Rogers, Stephen L., et al.. (2016). Drosophila Ringmaker regulates microtubule stabilization and axonal extension during embryonic development. Journal of Cell Science. 129(17). 3282–3294. 12 indexed citations
8.
Aznar, Nicolas, C.C. Rohena, Ying Dunkel, et al.. (2016). AMP-activated protein kinase fortifies epithelial tight junctions during energetic stress via its effector GIV/Girdin. eLife. 5. 39 indexed citations
9.
Ghosh, Pradipta, Nicolas Aznar, Inmaculada López-Sánchez, et al.. (2016). Biochemical, Biophysical and Cellular Techniques to Study the Guanine Nucleotide Exchange Factor, GIV/Girdin. PubMed. 8(4). 265–298. 4 indexed citations
10.
Namjoshi, Ojas A., Shruti Choudhary, Ernest Hamel, et al.. (2016). Design, Synthesis, and Preclinical Evaluation of 4-Substituted-5-methyl-furo[2,3-d]pyrimidines as Microtubule Targeting Agents That Are Effective against Multidrug Resistant Cancer Cells. Journal of Medicinal Chemistry. 59(12). 5752–5765. 31 indexed citations
11.
Rohena, C.C., April L. Risinger, James A. Sikorski, et al.. (2015). Biological Characterization of an Improved Pyrrole-Based Colchicine Site Agent Identified through Structure-Based Design. Molecular Pharmacology. 89(2). 287–296. 7 indexed citations
12.
Zhang, Xin, Sudhir Raghavan, Michael A. Ihnat, et al.. (2014). The design and discovery of water soluble 4-substituted-2,6-dimethylfuro[2,3-d]pyrimidines as multitargeted receptor tyrosine kinase inhibitors and microtubule targeting antitumor agents. Bioorganic & Medicinal Chemistry. 22(14). 3753–3772. 43 indexed citations
13.
Rohena, C.C. & Susan L. Mooberry. (2014). Recent progress with microtubule stabilizers: new compounds, binding modes and cellular activities. Natural Product Reports. 31(3). 335–355. 105 indexed citations
14.
Rohena, C.C., et al.. (2014). Antiproliferative Effects of 12-Oxoheteronemin vs Heteronemin. Natural Product Communications. 9(3). 359–60. 5 indexed citations
15.
Li, J., et al.. (2013). Taccalonolide Binding to Tubulin Imparts Microtubule Stability and Potent In Vivo Activity. Cancer Research. 73(22). 6780–6792. 53 indexed citations
16.
Rohena, C.C., Jiangnan Peng, Tyler A. Johnson, Phillip Crews, & Susan L. Mooberry. (2013). Chemically diverse microtubule stabilizing agents initiate distinct mitotic defects and dysregulated expression of key mitotic kinases. Biochemical Pharmacology. 85(8). 1104–1114. 16 indexed citations
18.
Risinger, April L., et al.. (2013). The Bat Flower: A Source of Microtubule-Destabilizing and -Stabilizing Compounds with Synergistic Antiproliferative Actions. Journal of Natural Products. 76(10). 1923–1929. 17 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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