Vladimir K. Patchev

3.4k total citations
56 papers, 2.8k citations indexed

About

Vladimir K. Patchev is a scholar working on Behavioral Neuroscience, Social Psychology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Vladimir K. Patchev has authored 56 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Behavioral Neuroscience, 27 papers in Social Psychology and 18 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Vladimir K. Patchev's work include Stress Responses and Cortisol (35 papers), Neuroendocrine regulation and behavior (27 papers) and Estrogen and related hormone effects (14 papers). Vladimir K. Patchev is often cited by papers focused on Stress Responses and Cortisol (35 papers), Neuroendocrine regulation and behavior (27 papers) and Estrogen and related hormone effects (14 papers). Vladimir K. Patchev collaborates with scholars based in Germany, United States and Bulgaria. Vladimir K. Patchev's co-authors include Osborne F. X. Almeida, M. Shoaib, Ali Hassan, Rossitza Konakchieva, Chitose Orikasa, Siegmund S. Wolf, Shinji Hayashi, Philipp von Rosenstiel, Alexandre V. Patchev and D. Fischer and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Neuroscience and SHILAP Revista de lepidopterología.

In The Last Decade

Vladimir K. Patchev

56 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vladimir K. Patchev Germany 31 1.5k 1.0k 571 450 441 56 2.8k
Helen C. Atkinson Australia 29 1.4k 1.0× 846 0.8× 582 1.0× 506 1.1× 148 0.3× 46 2.9k
Luz Torner Mexico 30 1.4k 0.9× 1.8k 1.7× 415 0.7× 583 1.3× 289 0.7× 56 3.3k
P W Gold United States 24 1.8k 1.2× 687 0.7× 826 1.4× 506 1.1× 390 0.9× 33 3.2k
Dimitris Grammatopoulos United Kingdom 36 1.9k 1.3× 706 0.7× 917 1.6× 352 0.8× 484 1.1× 102 4.0k
Themis C. Kamilaris United States 19 1.1k 0.7× 528 0.5× 618 1.1× 237 0.5× 266 0.6× 27 2.3k
Maureen Keller‐Wood United States 25 1.3k 0.9× 694 0.7× 782 1.4× 345 0.8× 135 0.3× 112 2.9k
William C. Engeland United States 31 1.7k 1.2× 897 0.9× 1.0k 1.8× 1.1k 2.4× 386 0.9× 85 3.5k
Gayle Yamamoto United States 11 1.5k 1.0× 598 0.6× 896 1.6× 341 0.8× 370 0.8× 12 2.5k
F. Berkenbosch Netherlands 36 2.0k 1.4× 919 0.9× 561 1.0× 577 1.3× 663 1.5× 69 4.2k
Francesca Spiga United Kingdom 28 1.2k 0.8× 561 0.6× 497 0.9× 566 1.3× 344 0.8× 61 2.3k

Countries citing papers authored by Vladimir K. Patchev

Since Specialization
Citations

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

Fields of papers citing papers by Vladimir K. Patchev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vladimir K. Patchev. 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 Vladimir K. Patchev. The network helps show where Vladimir K. Patchev may publish in the future.

Co-authorship network of co-authors of Vladimir K. Patchev

This figure shows the co-authorship network connecting the top 25 collaborators of Vladimir K. Patchev. A scholar is included among the top collaborators of Vladimir K. Patchev 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 Vladimir K. Patchev. Vladimir K. Patchev 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.
Dmitrieva, Natalia, et al.. (2012). Telemetric Assessment of Referred Vaginal Hyperalgesia and the Effect of Indomethacin in a Rat Model of Endometriosis. Frontiers in Pharmacology. 3. 158–158. 11 indexed citations
2.
Patchev, Vladimir K., С. О. Бачурин, M. Albers, Karl‐Heinrich Fritzemeier, & Vassilios Papadopoulos. (2008). Neurotrophic estrogens: essential profile and endpoints for drug discovery☆. Drug Discovery Today. 13(17-18). 734–747. 1 indexed citations
3.
Meyer, René, et al.. (2007). FoxG1, a member of the forkhead family, is a corepressor of the androgen receptor. The Journal of Steroid Biochemistry and Molecular Biology. 104(3-5). 195–207. 20 indexed citations
4.
Wolf, Siegmund S., et al.. (2007). A novel variant of the putative demethylase gene, s-JMJD1C, is a coactivator of the AR. Archives of Biochemistry and Biophysics. 460(1). 56–66. 57 indexed citations
5.
McPherson, Stephen J., Stuart J. Ellem, Vladimir K. Patchev, Karl‐Heinrich Fritzemeier, & Gail P. Risbridger. (2007). The role of ER[alpha] and ER[beta] in the prostate: insights from genetic models and isoform-selective ligands. 3 indexed citations
6.
McPherson, Stephen J., Stuart J. Ellem, Evan R. Simpson, et al.. (2006). Essential Role for Estrogen Receptor β in Stromal-Epithelial Regulation of Prostatic Hyperplasia. Endocrinology. 148(2). 566–574. 94 indexed citations
7.
Patchev, Alexandre V., D. Fischer, Siegmund S. Wolf, et al.. (2006). Insidious adrenocortical insufficiency underlies neuroendocrine dysregulation in TIF‐2 deficient mice. The FASEB Journal. 21(1). 231–238. 26 indexed citations
9.
Öettel, M., W. Elger, T Gräser, et al.. (1999). The pharmacological profile of dienogest. The European Journal of Contraception & Reproductive Health Care. 4(sup1). 2–13. 58 indexed citations
11.
Almeida, Osborne F. X., et al.. (1997). Activational Effects of Gonadal Steroids on Hypothalamo‐Pituitary‐Adrenal Regulation in the Rat Disclosed by Response to Dexamethasone Suppression. Journal of Neuroendocrinology. 9(2). 129–134. 23 indexed citations
12.
Hassan, Ali, et al.. (1996). Exacerbation of Apoptosis in the Dentate Gyrus of the Aged Rat by Dexamethasone and the Protective Role of Corticosterone. Experimental Neurology. 140(1). 43–52. 157 indexed citations
15.
Patchev, Vladimir K., Shinji Hayashi, Chitose Orikasa, & Osborne F. X. Almeida. (1995). Implications of estrogen‐dependent brain organization for gender differences in hypothalamo‐pituitary‐adrenal regulation. The FASEB Journal. 9(5). 419–423. 166 indexed citations
16.
Castrén, Maija L., et al.. (1995). Regulation of rat mineralocorticoid receptor expression in neurons by progesterone.. Endocrinology. 136(9). 3800–3806. 44 indexed citations
18.
Vamvakopoulos, Nicholas C., Koki Fukuhara, Vladimir K. Patchev, & George P. Chrousos. (1993). Effect of Single and Repeated Immobilization Stress on the Heat Shock Protein 70/90 System of the Rat: Glucocorticoid-Independent, Reversible Reduction of Hsp90 in the Liver and Spleen. Neuroendocrinology. 57(6). 1057–1065. 26 indexed citations
19.
Patchev, Vladimir K., George Mastorakos, Linda S. Brady, et al.. (1993). Increased Arginine Vasopressin Secretion May Participate in the Enhanced Susceptibility of Lewis Rats to Inflammatory Disease. Neuroendocrinology. 58(1). 106–110. 34 indexed citations
20.
Persengiev, Stephan P., et al.. (1991). Steroid hormone receptors in the thymus: A site of immunomodulatory action of melatonin. International Journal of Biochemistry. 23(12). 1483–1485. 22 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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