Alexander V. Medvedev

4.1k total citations
38 papers, 2.9k citations indexed

About

Alexander V. Medvedev is a scholar working on Molecular Biology, Physiology and Health, Toxicology and Mutagenesis. According to data from OpenAlex, Alexander V. Medvedev has authored 38 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 10 papers in Physiology and 8 papers in Health, Toxicology and Mutagenesis. Recurrent topics in Alexander V. Medvedev's work include Effects and risks of endocrine disrupting chemicals (8 papers), Adipose Tissue and Metabolism (8 papers) and Nuclear Receptors and Signaling (7 papers). Alexander V. Medvedev is often cited by papers focused on Effects and risks of endocrine disrupting chemicals (8 papers), Adipose Tissue and Metabolism (8 papers) and Nuclear Receptors and Signaling (7 papers). Alexander V. Medvedev collaborates with scholars based in United States, Japan and France. Alexander V. Medvedev's co-authors include Sheila Collins, Kiefer W. Daniel, Wenhong Cao, Anton M. Jetten, Jacques Robidoux, Xu Bai, Sergei S. Makarov, Bruce M. Spiegelman, Pere Puigserver and Takahisa Hirose 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

Alexander V. Medvedev

37 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alexander V. Medvedev United States	24	1.2k	1.2k	547	371	318	38	2.9k
Taira Wada Japan	25	945 0.8×	1.1k 0.9×	588 1.1×	247 0.7×	182 0.6×	34	3.1k
Christopher J.B. Nicol Canada	32	901 0.7×	2.4k 2.1×	668 1.2×	243 0.7×	229 0.7×	75	4.0k
Yu Luo United States	35	744 0.6×	1.5k 1.3×	494 0.9×	153 0.4×	290 0.9×	95	3.3k
Zunji Ke China	38	451 0.4×	1.3k 1.1×	432 0.8×	229 0.6×	151 0.5×	98	3.5k
Pamela A. Lucchesi United States	38	614 0.5×	1.9k 1.6×	235 0.4×	219 0.6×	161 0.5×	86	3.8k
Hidetaka Morinaga Japan	28	1.2k 1.0×	2.5k 2.2×	1.0k 1.9×	619 1.7×	314 1.0×	46	5.4k
Junxiang Wan United States	31	1.6k 1.3×	1.8k 1.5×	217 0.4×	337 0.9×	206 0.6×	68	3.7k
Tong Lü United States	35	1.4k 1.1×	1.5k 1.3×	970 1.8×	207 0.6×	69 0.2×	91	4.0k
Mercy M. Davidson United States	42	652 0.5×	3.6k 3.1×	463 0.8×	177 0.5×	174 0.5×	73	5.1k
Utpal Sen United States	38	637 0.5×	1.1k 1.0×	278 0.5×	269 0.7×	113 0.4×	118	3.8k

Countries citing papers authored by Alexander V. Medvedev

Since Specialization

Citations

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

Fields of papers citing papers by Alexander V. Medvedev

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexander V. Medvedev. 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 Alexander V. Medvedev. The network helps show where Alexander V. Medvedev may publish in the future.

Co-authorship network of co-authors of Alexander V. Medvedev

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander V. Medvedev. A scholar is included among the top collaborators of Alexander V. Medvedev 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 Alexander V. Medvedev. Alexander V. Medvedev is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

James, Bryan D., Alexander V. Medvedev, Sergei S. Makarov, et al.. (2024). Moldable Plastics (Polycaprolactone) can be Acutely Toxic to Developing Zebrafish and Activate Nuclear Receptors in Mammalian Cells. ACS Biomaterials Science & Engineering. 10(8). 5237–5251. 6 indexed citations

James, Bryan D., Alexander V. Medvedev, E. S. Martsen, et al.. (2024). Burnt Plastic (Pyroplastic) from the M/V X-Press Pearl Ship Fire and Plastic Spill Contain Compounds That Activate Endocrine and Metabolism-Related Human and Fish Transcription Factors. Environment & Health. 3(1). 91–101. 1 indexed citations

Medvedev, Alexander V., Matt Moeser, E. S. Martsen, et al.. (2022). Comprehensive assessment of NR ligand polypharmacology by a multiplex reporter NR assay. Scientific Reports. 12(1). 3115–3115. 8 indexed citations

Houck, Keith A., Grace Patlewicz, Ann M. Richard, et al.. (2021). Bioactivity profiling of per- and polyfluoroalkyl substances (PFAS) identifies potential toxicity pathways related to molecular structure. Toxicology. 457. 152789–152789. 89 indexed citations

Houck, Keith A., Audrey J. Bone, Jon A. Doering, et al.. (2020). Evaluation of a multiplexed, multispecies nuclear receptor assay for chemical hazard assessment. Toxicology in Vitro. 72. 105016–105016. 10 indexed citations

Blackwell, Brett R., Gerald T. Ankley, Paul M. Bradley, et al.. (2018). Potential Toxicity of Complex Mixtures in Surface Waters from a Nationwide Survey of United States Streams: Identifying in Vitro Bioactivities and Causative Chemicals. Environmental Science & Technology. 53(2). 973–983. 89 indexed citations

Medvedev, Alexander V., Matt Moeser, E. S. Martsen, et al.. (2018). Evaluating biological activity of compounds by transcription factor activity profiling. Science Advances. 4(9). eaar4666–eaar4666. 23 indexed citations

Burdick, Andrew D., Simone Sciabola, Srinivasa R. Mantena, et al.. (2014). Sequence motifs associated with hepatotoxicity of locked nucleic acid—modified antisense oligonucleotides. Nucleic Acids Research. 42(8). 4882–4891. 114 indexed citations

Varghese, Sabu, Fei Yang, Víctor Pacheco, et al.. (2013). Expression, Purification, and Solid-State NMR Characterization of the Membrane Binding Heme Protein Nitrophorin 7 in Two Electronic Spin States. Biochemistry. 52(40). 7031–7040. 1 indexed citations

10.

Tchivileva, Inna E., Kai Soo Tan, Andrea G. Nackley, et al.. (2009). Signaling pathways mediating β3-adrenergic receptor-induced production of interleukin-6 in adipocytes. Molecular Immunology. 46(11-12). 2256–2266. 32 indexed citations

11.

Wang, Haibo, Yuan Zhang, Einav Yehuda‐Shnaidman, et al.. (2008). Liver X Receptor α Is a Transcriptional Repressor of the Uncoupling Protein 1 Gene and the Brown Fat Phenotype. Molecular and Cellular Biology. 28(7). 2187–2200. 85 indexed citations

12.

Medvedev, Alexander V., et al.. (2001). Transcriptional Regulation of the Mouse Uncoupling Protein-2 Gene. Journal of Biological Chemistry. 276(14). 10817–10823. 97 indexed citations

13.

Cao, Wenhong, Alexander V. Medvedev, Kiefer W. Daniel, & Sheila Collins. (2001). β-Adrenergic Activation of p38 MAP Kinase in Adipocytes. Journal of Biological Chemistry. 276(29). 27077–27082. 259 indexed citations

14.

Collins, Sheila, Wenhong Cao, Kiefer W. Daniel, et al.. (2001). Adrenoceptors, Uncoupling Proteins, and Energy Expenditure. Experimental Biology and Medicine. 226(11). 982–990. 23 indexed citations

15.

Cao, Wenhong, Louis M. Luttrell, Alexander V. Medvedev, et al.. (2000). Direct Binding of Activated c-Src to the β3-Adrenergic Receptor Is Required for MAP Kinase Activation. Journal of Biological Chemistry. 275(49). 38131–38134. 167 indexed citations

16.

Bernacki, Susan H., et al.. (1998). Suppression of relaxin gene expression by retinoids in squamous differentiated rabbit tracheal epithelial cells. Molecular and Cellular Endocrinology. 138(1-2). 115–125. 3 indexed citations

17.

Yan, Zhong, et al.. (1998). Regulation of Peroxisome Proliferator-activated Receptor α-Induced Transactivation by the Nuclear Orphan Receptor TAK1/TR4. Journal of Biological Chemistry. 273(18). 10948–10957. 59 indexed citations

18.

Medvedev, Alexander V., et al.. (1998). Induction of the nuclear orphan receptor RORgamma during adipocyte differentiation of D1 and 3T3-L1 cells.. PubMed. 9(3). 267–76. 45 indexed citations

19.

Yan, Zhong, Alexander V. Medvedev, Takahisa Hirose, Hideo Gotoh, & Anton M. Jetten. (1997). Characterization of the Response Element and DNA Binding Properties of the Nuclear Orphan Receptor Germ Cell Nuclear Factor/Retinoid Receptor-related Testis-associated Receptor. Journal of Biological Chemistry. 272(16). 10565–10572. 77 indexed citations

20.

Medvedev, Alexander V., et al.. (1990). [The characteristics of the transformed phenotype and the expression of indicator plasmids in the cells of rat embryonic fibroblasts immortalized by oncogene E1Aad5 and transformed by oncogenes E1Aad5+c-Ha-ras].. PubMed. 32(2). 148–55. 6 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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