Mikhail A. Nikiforov

4.0k total citations
69 papers, 2.8k citations indexed

About

Mikhail A. Nikiforov is a scholar working on Molecular Biology, Oncology and Physiology. According to data from OpenAlex, Mikhail A. Nikiforov has authored 69 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Molecular Biology, 14 papers in Oncology and 10 papers in Physiology. Recurrent topics in Mikhail A. Nikiforov's work include Ubiquitin and proteasome pathways (11 papers), Telomeres, Telomerase, and Senescence (9 papers) and Cancer-related Molecular Pathways (8 papers). Mikhail A. Nikiforov is often cited by papers focused on Ubiquitin and proteasome pathways (11 papers), Telomeres, Telomerase, and Senescence (9 papers) and Cancer-related Molecular Pathways (8 papers). Mikhail A. Nikiforov collaborates with scholars based in United States, Russia and Spain. Mikhail A. Nikiforov's co-authors include Sudha Mannava, Michael D. Cole, Marı́a S. Soengas, Andrei V. Gudkov, Emily E. Fink, Vladimir Grachtchouk, Anna Bianchi, Dazhong Zhuang, Joseph A. Wawrzyniak and Brittany C. Lipchick and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Mikhail A. Nikiforov

64 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
Mikhail A. Nikiforov United States 30 2.1k 580 486 376 284 69 2.8k
Duncan L. Smith United Kingdom 28 1.8k 0.9× 490 0.8× 528 1.1× 350 0.9× 107 0.4× 50 2.8k
Martin Mistrík Czechia 30 2.7k 1.3× 1.1k 1.9× 462 1.0× 463 1.2× 168 0.6× 116 3.6k
Cong Liu China 23 1.4k 0.7× 359 0.6× 290 0.6× 214 0.6× 140 0.5× 74 2.1k
Corinne Wendling France 25 1.7k 0.8× 536 0.9× 718 1.5× 542 1.4× 221 0.8× 33 2.9k
Reinout Raijmakers Netherlands 32 3.0k 1.4× 396 0.7× 390 0.8× 253 0.7× 146 0.5× 57 4.3k
Anna Mandinova United States 31 2.5k 1.2× 1.0k 1.8× 531 1.1× 507 1.3× 160 0.6× 61 3.9k
Jing Zhao United States 31 2.3k 1.1× 312 0.5× 315 0.6× 344 0.9× 197 0.7× 107 3.4k
Prathapan Thiru United States 18 2.3k 1.1× 1.0k 1.8× 1.1k 2.3× 342 0.9× 216 0.8× 22 3.7k
Amanda Nourse United States 29 3.5k 1.7× 423 0.7× 220 0.5× 497 1.3× 114 0.4× 53 4.0k
Fei Huang United States 30 2.0k 1.0× 483 0.8× 172 0.4× 230 0.6× 254 0.9× 114 2.9k

Countries citing papers authored by Mikhail A. Nikiforov

Since Specialization
Citations

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

Fields of papers citing papers by Mikhail A. Nikiforov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mikhail A. Nikiforov. 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 Mikhail A. Nikiforov. The network helps show where Mikhail A. Nikiforov may publish in the future.

Co-authorship network of co-authors of Mikhail A. Nikiforov

This figure shows the co-authorship network connecting the top 25 collaborators of Mikhail A. Nikiforov. A scholar is included among the top collaborators of Mikhail A. Nikiforov 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 Mikhail A. Nikiforov. Mikhail A. Nikiforov 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.
Yan, Zhibo, Jun-Qi Lu, Jingyun Lee, et al.. (2025). Targeting ABCD1-ACOX1-MET/IGF1R axis suppresses multiple myeloma. Leukemia. 39(3). 720–733.
2.
Miller, Brandi, Wencheng Li, Sergey A. Krupenko, et al.. (2023). Distinct inflammatory Th17 subsets emerge in autoimmunity and infection. The Journal of Experimental Medicine. 220(10). 16 indexed citations
3.
Wolff, David W., Anna Bianchi, & Mikhail A. Nikiforov. (2022). Compartmentalization and regulation of GTP in control of cellular phenotypes. Trends in Molecular Medicine. 28(9). 758–769. 17 indexed citations
4.
Affronti, Hayley C., Aryn M. Rowsam, Spencer R. Rosario, et al.. (2020). Pharmacological polyamine catabolism upregulation with methionine salvage pathway inhibition as an effective prostate cancer therapy. Nature Communications. 11(1). 52–52. 46 indexed citations
5.
García, Juan Ignacio, Meritxell Sabidó, Mikhail A. Nikiforov, et al.. (2018). The UALE project: a cross-sectional approach for trends in HIV/STI prevalence among key populations attending STI clinics in Guatemala. BMJ Open. 8(9). e022632–e022632. 8 indexed citations
6.
Fink, Emily E., Sudha Moparthy, Archis Bagati, et al.. (2018). XBP1-KLF9 Axis Acts as a Molecular Rheostat to Control the Transition from Adaptive to Cytotoxic Unfolded Protein Response. Cell Reports. 25(1). 212–223.e4. 41 indexed citations
7.
Bianchi, Anna, Mitra S. Rana, Brittany C. Lipchick, et al.. (2017). Internally ratiometric fluorescent sensors for evaluation of intracellular GTP levels and distribution. Nature Methods. 14(10). 1003–1009. 49 indexed citations
8.
Nikiforov, Mikhail A. & Donna S. Shewach. (2016). Detection of Nucleotide Disbalance in Cells Undergoing Oncogene-Induced Senescence. Methods in molecular biology. 1534. 165–173. 1 indexed citations
9.
Bianchi, Anna, Joseph A. Wawrzyniak, Archis Bagati, et al.. (2015). Pharmacological targeting of guanosine monophosphate synthase suppresses melanoma cell invasion and tumorigenicity. Cell Death and Differentiation. 22(11). 1858–1864. 35 indexed citations
10.
Pabona, John Mark P., Frank A. Simmen, Mikhail A. Nikiforov, et al.. (2012). Krüppel-Like Factor 9 and Progesterone Receptor Coregulation of Decidualizing Endometrial Stromal Cells: Implications for the Pathogenesis of Endometriosis. The Journal of Clinical Endocrinology & Metabolism. 97(3). E376–E392. 90 indexed citations
11.
Sabidó, Meritxell, L. Parker Gregg, Xavier Vallès, et al.. (2012). Notification for Sexually Transmitted Infections and HIV Among Sex Workers in Guatemala. Sexually Transmitted Diseases. 39(7). 504–508. 7 indexed citations
12.
Mannava, Sudha, Kalyana Moparthy, Linda J. Wheeler, et al.. (2012). Depletion of Deoxyribonucleotide Pools Is an Endogenous Source of DNA Damage in Cells Undergoing Oncogene-Induced Senescence. American Journal Of Pathology. 182(1). 142–151. 67 indexed citations
13.
Mannava, Sudha, Angela R. Omilian, Joseph A. Wawrzyniak, et al.. (2011). PP2A-B56α controls oncogene-induced senescence in normal and tumor human melanocytic cells. Oncogene. 31(12). 1484–1492. 34 indexed citations
14.
Mannava, Sudha, Vladimir Grachtchouk, Linda J. Wheeler, et al.. (2008). Direct role of nucleotide metabolism in C-MYC-dependent proliferation of melanoma cells. Cell Cycle. 7(15). 2392–2400. 190 indexed citations
15.
Mannava, Sudha, Vladimir Grachtchouk, D. Zhuang, et al.. (2007). c-Myc depletion inhibits proliferation of human tumor cells at various stages of the cell cycle. Oncogene. 27(13). 1905–1915. 137 indexed citations
16.
Denoyelle, Christophe, George A. Abou-Rjaily, Vladimir Bezrookove, et al.. (2006). Anti-oncogenic role of the endoplasmic reticulum differentially activated by mutations in the MAPK pathway. Nature Cell Biology. 8(10). 1053–1063. 269 indexed citations
17.
Nikiforov, Mikhail A., Sanjay Chandriani, Jeong Hyeon Park, et al.. (2002). TRRAP-Dependent and TRRAP-Independent Transcriptional Activation by Myc Family Oncoproteins. Molecular and Cellular Biology. 22(14). 5054–5063. 108 indexed citations
18.
Nikiforov, Mikhail A., Martin A. Gorovsky, & C. David Allis. (2000). A Novel Chromodomain Protein, Pdd3p, Associates with Internal Eliminated Sequences during Macronuclear Development in Tetrahymena thermophila. Molecular and Cellular Biology. 20(11). 4128–4134. 53 indexed citations
19.
Nikiforov, Mikhail A., Serena S. Kwek, James E. Artwohl, et al.. (1997). Suppression of apoptosis by bcl-2 does not prevent p53-mediated control of experimental metastasis and anchorage dependence. Oncogene. 15(25). 3007–3012. 21 indexed citations
20.
Gudkov, Andrei V., et al.. (1992). ART-CH, a new chicken retroviruslike element. Journal of Virology. 66(3). 1726–1736. 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026