Sergey Mareninov

1.8k total citations
25 papers, 1.1k citations indexed

About

Sergey Mareninov is a scholar working on Radiology, Nuclear Medicine and Imaging, Molecular Biology and Genetics. According to data from OpenAlex, Sergey Mareninov has authored 25 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Radiology, Nuclear Medicine and Imaging, 8 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Sergey Mareninov's work include Glioma Diagnosis and Treatment (5 papers), Retinal and Macular Surgery (5 papers) and Molecular Biology Techniques and Applications (4 papers). Sergey Mareninov is often cited by papers focused on Glioma Diagnosis and Treatment (5 papers), Retinal and Macular Surgery (5 papers) and Molecular Biology Techniques and Applications (4 papers). Sergey Mareninov collaborates with scholars based in United States, Japan and Canada. Sergey Mareninov's co-authors include William H. Yong, Kyuseok Im, Miguel F. Diaz, Lynn K. Gordon, Timothy F. Cloughesy, Bowen Wei, Maryam Shabihkhani, Jerry J. Lou, Gregory M. Lucey and Elyse J. Singer and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

In The Last Decade

Sergey Mareninov

25 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sergey Mareninov United States 17 504 167 149 135 113 25 1.1k
P. Sirigu Italy 18 391 0.8× 210 1.3× 93 0.6× 83 0.6× 67 0.6× 64 1.1k
Tetiana Zaichuk United States 10 752 1.5× 72 0.4× 217 1.5× 96 0.7× 24 0.2× 11 1.1k
Stephanie H. Kim United States 22 630 1.3× 99 0.6× 160 1.1× 85 0.6× 47 0.4× 35 1.4k
Show‐Li Chen Taiwan 26 799 1.6× 145 0.9× 116 0.8× 282 2.1× 39 0.3× 66 1.5k
Patricia Parsons‐Wingerter United States 17 390 0.8× 229 1.4× 167 1.1× 35 0.3× 25 0.2× 30 1.1k
Hiroshi Ichikawa Japan 26 672 1.3× 77 0.5× 272 1.8× 151 1.1× 34 0.3× 142 1.9k
Lorita Dudus United States 16 1.3k 2.5× 107 0.6× 87 0.6× 201 1.5× 45 0.4× 19 2.0k
Changwon Kang South Korea 27 1.4k 2.7× 172 1.0× 239 1.6× 79 0.6× 87 0.8× 91 2.5k
Christopher Campbell United States 12 710 1.4× 61 0.4× 130 0.9× 58 0.4× 23 0.2× 50 1.0k
Zhonghao Wang China 19 334 0.7× 209 1.3× 162 1.1× 163 1.2× 14 0.1× 75 928

Countries citing papers authored by Sergey Mareninov

Since Specialization
Citations

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

Fields of papers citing papers by Sergey Mareninov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sergey Mareninov

This figure shows the co-authorship network connecting the top 25 collaborators of Sergey Mareninov. A scholar is included among the top collaborators of Sergey Mareninov 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 Sergey Mareninov. Sergey Mareninov 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.
Hagiwara, Akifumi, Hiroyuki Tatekawa, Jingwen Yao, et al.. (2022). Visualization of tumor heterogeneity and prediction of isocitrate dehydrogenase mutation status for human gliomas using multiparametric physiologic and metabolic MRI. Scientific Reports. 12(1). 1078–1078. 16 indexed citations
2.
Magaki, Shino, Harry V. Vinters, Christopher Kwesi O. Williams, et al.. (2022). Neuropathologic Findings in Elderly HIV-Positive Individuals. Journal of Neuropathology & Experimental Neurology. 81(7). 565–576. 3 indexed citations
3.
Hagiwara, Akifumi, Jingwen Yao, Catalina Raymond, et al.. (2021). “Aerobic glycolytic imaging” of human gliomas using combined pH-, oxygen-, and perfusion-weighted magnetic resonance imaging. NeuroImage Clinical. 32. 102882–102882. 8 indexed citations
4.
Hagiwara, Akifumi, Talia C. Oughourlian, Nicholas S. Cho, et al.. (2021). Diffusion MRI is an early biomarker of overall survival benefit in IDH wild-type recurrent glioblastoma treated with immune checkpoint inhibitors. Neuro-Oncology. 24(6). 1020–1028. 19 indexed citations
5.
Voth, Brittany, Panayiotis E. Pelargos, Natalie E. Barnette, et al.. (2020). Intratumor injection of CCL21-coupled vault nanoparticles is associated with reduction in tumor volume in an in vivo model of glioma. Journal of Neuro-Oncology. 147(3). 599–605. 21 indexed citations
6.
Im, Kyuseok, Sergey Mareninov, Miguel F. Diaz, & William H. Yong. (2018). An Introduction to Performing Immunofluorescence Staining. Methods in molecular biology. 299–311. 288 indexed citations
7.
Yong, William H., Maryam Shabihkhani, Donatello Telesca, et al.. (2015). Ribosomal Proteins RPS11 and RPS20, Two Stress-Response Markers of Glioblastoma Stem Cells, Are Novel Predictors of Poor Prognosis in Glioblastoma Patients. PLoS ONE. 10(10). e0141334–e0141334. 53 indexed citations
8.
Shabihkhani, Maryam, Gregory M. Lucey, Bowen Wei, et al.. (2014). The procurement, storage, and quality assurance of frozen blood and tissue biospecimens in pathology, biorepository, and biobank settings. Clinical Biochemistry. 47(4-5). 258–266. 189 indexed citations
9.
Mareninov, Sergey, Desiree E. Sanchez, Ivan Babić, et al.. (2013). Lyophilized brain tumor specimens can be used for histologic, nucleic acid, and protein analyses after 1 year of room temperature storage. Journal of Neuro-Oncology. 113(3). 365–373. 25 indexed citations
10.
Lou, Jerry J., Leili Mirsadraei, Desiree E. Sanchez, et al.. (2013). A review of room temperature storage of biospecimen tissue and nucleic acids for anatomic pathology laboratories and biorepositories. Clinical Biochemistry. 47(4-5). 267–273. 58 indexed citations
11.
Telander, David G., Sergey Mareninov, Ágnes Nagy, et al.. (2012). Anti-EMP2 diabody blocks epithelial membrane protein 2 (EMP2) and FAK mediated collagen gel contraction in ARPE-19 cells. Experimental Eye Research. 102. 10–16. 14 indexed citations
12.
Mareninov, Sergey, et al.. (2011). Considerations for uniform and accurate biospecimen labelling in a biorepository and research environment. Journal of Clinical Pathology. 64(7). 634–636. 8 indexed citations
13.
Telander, David G., et al.. (2011). Epithelial Membrane Protein-2 (EMP2) and Experimental Proliferative Vitreoretinopathy (PVR). Current Eye Research. 36(6). 546–552. 19 indexed citations
15.
Chen, Ling, Ann M. Chan, Loise M. Francisco, et al.. (2009). Role of the Immune Modulator Programmed Cell Death-1 during Development and Apoptosis of Mouse Retinal Ganglion Cells. Investigative Ophthalmology & Visual Science. 50(10). 4941–4941. 15 indexed citations
16.
Chan, Ann M., Raymond J. Moniz, Madhuri Wadehra, et al.. (2009). Blockade of epithelial membrane protein 2 (EMP2) abrogates infection ofChlamydia muridarummurine genital infection model. FEMS Immunology & Medical Microbiology. 55(2). 240–249. 10 indexed citations
17.
Kim, Seok‐Hwan, Yasunari Munemasa, Jacky M. K. Kwong, et al.. (2008). Activation of autophagy in retinal ganglion cells. Journal of Neuroscience Research. 86(13). 2943–2951. 69 indexed citations
18.
Lepin, Eric J., Bo Wei, Ágnes Nagy, et al.. (2008). Diabodies Targeting Epithelial Membrane Protein 2 Reduce Tumorigenicity of Human Endometrial Cancer Cell Lines. Clinical Cancer Research. 14(22). 7367–7377. 28 indexed citations
19.
Mareninov, Sergey, et al.. (2007). Collagen gel contraction by ARPE-19 cells is mediated by a FAK-Src dependent pathway. Experimental Eye Research. 85(6). 790–798. 28 indexed citations
20.
Kwong, Jacky M. K., Maziar Lalezary, Christine Yang, et al.. (2006). Co-expression of heat shock transcription factors 1 and 2 in rat retinal ganglion cells. Neuroscience Letters. 405(3). 191–195. 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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