Alex Y. Strongin

15.9k total citations · 3 hit papers
204 papers, 13.3k citations indexed

About

Alex Y. Strongin is a scholar working on Cancer Research, Oncology and Molecular Biology. According to data from OpenAlex, Alex Y. Strongin has authored 204 papers receiving a total of 13.3k indexed citations (citations by other indexed papers that have themselves been cited), including 97 papers in Cancer Research, 83 papers in Oncology and 78 papers in Molecular Biology. Recurrent topics in Alex Y. Strongin's work include Protease and Inhibitor Mechanisms (92 papers), Peptidase Inhibition and Analysis (81 papers) and Cell Adhesion Molecules Research (35 papers). Alex Y. Strongin is often cited by papers focused on Protease and Inhibitor Mechanisms (92 papers), Peptidase Inhibition and Analysis (81 papers) and Cell Adhesion Molecules Research (35 papers). Alex Y. Strongin collaborates with scholars based in United States, Russia and Canada. Alex Y. Strongin's co-authors include Elena I. Deryugina, Barry L. Marmer, Ivan E. Collier, Boris I. Ratnikov, Gregory I. Goldberg, Sergey A. Shiryaev, Jeffrey W. Smith, Dmitri V. Rozanov, G. A. Bannikov and Gregory A. Grant 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

Alex Y. Strongin

203 papers receiving 13.0k citations

Hit Papers

Mechanism Of Cell Surface Activation Of 72-kDa Type IV Co... 1995 2026 2005 2015 1995 2003 2002 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alex Y. Strongin United States 60 6.2k 5.1k 4.6k 2.2k 2.0k 204 13.3k
Dieter Brömme Canada 66 4.7k 0.8× 7.3k 1.4× 3.2k 0.7× 1.1k 0.5× 955 0.5× 196 13.6k
Jay L. Degen United States 66 3.5k 0.6× 3.8k 0.7× 2.0k 0.4× 1.2k 0.6× 4.8k 2.3× 151 15.3k
Thomas Bugge United States 62 2.4k 0.4× 4.5k 0.9× 1.9k 0.4× 1.5k 0.7× 2.0k 1.0× 165 11.2k
James P. Quigley United States 54 4.9k 0.8× 5.5k 1.1× 3.8k 0.8× 2.1k 1.0× 1.5k 0.8× 119 12.5k
Roy A. Black United States 50 2.6k 0.4× 7.3k 1.4× 3.8k 0.8× 2.7k 1.2× 947 0.5× 95 14.8k
Carl Blobel United States 72 2.7k 0.4× 8.0k 1.6× 5.6k 1.2× 4.4k 2.0× 909 0.4× 148 16.2k
Duanqing Pei China 65 3.4k 0.6× 9.0k 1.8× 3.0k 0.7× 782 0.4× 1.2k 0.6× 259 14.2k
Francesco Blasi Italy 79 11.7k 1.9× 9.5k 1.9× 4.6k 1.0× 3.7k 1.7× 6.0k 3.0× 281 20.7k
Mathew A. Vadas Australia 69 3.7k 0.6× 9.2k 1.8× 2.2k 0.5× 1.9k 0.9× 1.1k 0.5× 207 17.4k
Dominique Belin Switzerland 52 4.2k 0.7× 8.0k 1.6× 1.3k 0.3× 1.2k 0.5× 2.6k 1.3× 114 15.0k

Countries citing papers authored by Alex Y. Strongin

Since Specialization
Citations

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

Fields of papers citing papers by Alex Y. Strongin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alex Y. Strongin. 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 Alex Y. Strongin. The network helps show where Alex Y. Strongin may publish in the future.

Co-authorship network of co-authors of Alex Y. Strongin

This figure shows the co-authorship network connecting the top 25 collaborators of Alex Y. Strongin. A scholar is included among the top collaborators of Alex Y. Strongin 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 Alex Y. Strongin. Alex Y. Strongin 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.
Dolkas, Jennifer, Andrei V. Chernov, Tony L. Yaksh, et al.. (2024). Cholesterol-dependent LXR transcription factor activity represses pronociceptive effects of estrogen in sensory neurons and pain induced by myelin basic protein fragments. Brain Behavior & Immunity - Health. 38. 100757–100757. 1 indexed citations
2.
Chernov, Andrei V., Kelly A. Eddinger, Jennifer Dolkas, et al.. (2020). A myelin basic protein fragment induces sexually dimorphic transcriptome signatures of neuropathic pain in mice. Journal of Biological Chemistry. 295(31). 10807–10821. 20 indexed citations
3.
Barile, Elisa, Carlo Baggio, Luca Gambini, et al.. (2020). Potential Therapeutic Targeting of Coronavirus Spike Glycoprotein Priming. Molecules. 25(10). 2424–2424. 17 indexed citations
4.
Remacle, Albert G., Jennifer Dolkas, Mila Angert, et al.. (2018). Acute- and late-phase matrix metalloproteinase (MMP)-9 activity is comparable in female and male rats after peripheral nerve injury. Journal of Neuroinflammation. 15(1). 89–89. 28 indexed citations
5.
Qin, Peng, Shaoying Lu, Yuxin Shi, et al.. (2018). Coordinated histone modifications and chromatin reorganization in a single cell revealed by FRET biosensors. Proceedings of the National Academy of Sciences. 115(50). E11681–E11690. 45 indexed citations
6.
Limsakul, Praopim, Peng Qin, Yiqian Wu, et al.. (2018). Directed Evolution to Engineer Monobody for FRET Biosensor Assembly and Imaging at Live-Cell Surface. Cell chemical biology. 25(4). 370–379.e4. 20 indexed citations
7.
Remacle, Albert G., Vladislav S. Golubkov, Sergey A. Shiryaev, et al.. (2012). Novel MT1-MMP Small-Molecule Inhibitors Based on Insights into Hemopexin Domain Function in Tumor Growth. Cancer Research. 72(9). 2339–2349. 110 indexed citations
8.
Chernov, Andrei V. & Alex Y. Strongin. (2011). Epigenetic regulation of matrix metalloproteinases and their collagen substrates in cancer. BioMolecular Concepts. 2(3). 135–147. 55 indexed citations
9.
Golubkov, Vladislav S., Alexander E. Aleshin, & Alex Y. Strongin. (2011). Potential Relation of Aberrant Proteolysis of Human Protein Tyrosine Kinase 7 (PTK7) chuzhoi by Membrane Type 1 Matrix Metalloproteinase (MT1-MMP) to Congenital Defects. Journal of Biological Chemistry. 286(23). 20970–20976. 23 indexed citations
10.
Ouyang, Mingxing, He Huang, Nathan C. Shaner, et al.. (2010). Simultaneous Visualization of Protumorigenic Src and MT1-MMP Activities with Fluorescence Resonance Energy Transfer. Cancer Research. 70(6). 2204–2212. 91 indexed citations
11.
Shiryaev, Sergey A., Anton Cheltsov, Katarzyna Gawlik, Boris I. Ratnikov, & Alex Y. Strongin. (2010). Virtual Ligand Screening of the National Cancer Institute (NCI) Compound Library Leads to the Allosteric Inhibitory Scaffolds of the West Nile Virus NS3 Proteinase. Assay and Drug Development Technologies. 9(1). 69–78. 40 indexed citations
12.
Shiryaev, Sergey A., et al.. (2009). NS4A regulates the ATPase activity of the NS3 helicase: a novel cofactor role of the non-structural protein NS4A from West Nile virus. Journal of General Virology. 90(9). 2081–2085. 61 indexed citations
13.
Rozanov, Dmitri V., Alexei Y. Savinov, Roy Williams, et al.. (2008). Molecular Signature of MT1-MMP: Transactivation of the Downstream Universal Gene Network in Cancer. Cancer Research. 68(11). 4086–4096. 54 indexed citations
14.
Johnston, Paul A., Jennifer Phillips, Tong Ying Shun, et al.. (2007). HTS Identifies Novel and Specific Uncompetitive Inhibitors of the Two-Component NS2B-NS3 Proteinase of West Nile Virus. Assay and Drug Development Technologies. 5(6). 737–750. 85 indexed citations
15.
Golubkov, Vladislav S., et al.. (2006). Membrane Type-1 Matrix Metalloproteinase Confers Aneuploidy and Tumorigenicity on Mammary Epithelial Cells. Cancer Research. 66(21). 10460–10465. 33 indexed citations
16.
Strongin, Alex Y.. (2006). Mislocalization and unconventional functions of cellular MMPs in cancer. Cancer and Metastasis Reviews. 25(1). 87–98. 75 indexed citations
17.
Marchenko, Natalia, Г. Н. Марченко, Robert N. Weinreb, et al.. (2004). β-Catenin regulates the gene of MMP-26, a novel matrix metalloproteinase expressed both in carcinomas and normal epithelial cells. The International Journal of Biochemistry & Cell Biology. 36(5). 942–956. 80 indexed citations
18.
Rozanov, Dmitri V. & Alex Y. Strongin. (2003). Membrane Type-1 Matrix Metalloproteinase Functions as a Proprotein Self-convertase. Journal of Biological Chemistry. 278(10). 8257–8260. 43 indexed citations
19.
Ratnikov, Boris I., Elena I. Deryugina, & Alex Y. Strongin. (2002). Gelatin Zymography and Substrate Cleavage Assays of Matrix Metalloproteinase-2 in Breast Carcinoma Cells Overexpressing Membrane Type-1 Matrix Metalloproteinase. Laboratory Investigation. 82(11). 1583–1590. 37 indexed citations
20.
Strongin, Alex Y., et al.. (1990). Chemical modification of the recombinant human αA- and β-interferons. Biochemical and Biophysical Research Communications. 167(1). 74–80. 2 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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