Edward Monosov

2.9k total citations
18 papers, 2.4k citations indexed

About

Edward Monosov is a scholar working on Molecular Biology, Cancer Research and Immunology and Allergy. According to data from OpenAlex, Edward Monosov has authored 18 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Cancer Research and 4 papers in Immunology and Allergy. Recurrent topics in Edward Monosov's work include Cell death mechanisms and regulation (5 papers), Protease and Inhibitor Mechanisms (5 papers) and Cell Adhesion Molecules Research (4 papers). Edward Monosov is often cited by papers focused on Cell death mechanisms and regulation (5 papers), Protease and Inhibitor Mechanisms (5 papers) and Cell Adhesion Molecules Research (4 papers). Edward Monosov collaborates with scholars based in United States, Austria and Russia. Edward Monosov's co-authors include Uğur Özerdem, William B. Stallcup, Kathryn A. Grako, Alex Y. Strongin, Elena I. Deryugina, Boris I. Ratnikov, Jeffrey W. Smith, Richard G. DiScipio, John A. Heyman and Suresh Subramani and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Nature Medicine.

In The Last Decade

Edward Monosov

18 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edward Monosov United States 17 1.4k 584 508 371 286 18 2.4k
Meena Gujrati United States 35 1.5k 1.1× 1.0k 1.8× 652 1.3× 186 0.5× 183 0.6× 87 3.0k
Hsin Chieh Lin United States 18 2.4k 1.8× 555 1.0× 522 1.0× 779 2.1× 245 0.9× 20 3.5k
Graciela B. Sala‐Newby United Kingdom 30 1.5k 1.1× 622 1.1× 282 0.6× 316 0.9× 299 1.0× 61 2.6k
Marina Macı́as-Silva Mexico 23 2.3k 1.7× 322 0.6× 499 1.0× 229 0.6× 220 0.8× 74 3.1k
Fred E. Indig United States 31 2.5k 1.8× 542 0.9× 535 1.1× 550 1.5× 135 0.5× 55 3.5k
Benilde Jiménez Spain 28 2.2k 1.6× 841 1.4× 568 1.1× 396 1.1× 169 0.6× 49 3.1k
Victoria Bolós Spain 10 2.0k 1.5× 535 0.9× 912 1.8× 322 0.9× 205 0.7× 11 2.7k
Steven Swendeman United States 27 1.7k 1.2× 267 0.5× 599 1.2× 283 0.8× 157 0.5× 35 2.6k
Andrew C. Dudley United States 33 1.8k 1.3× 914 1.6× 662 1.3× 322 0.9× 201 0.7× 60 3.2k
Steingrimur Stefansson United States 27 1.4k 1.0× 1.5k 2.6× 559 1.1× 442 1.2× 264 0.9× 48 3.3k

Countries citing papers authored by Edward Monosov

Since Specialization
Citations

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

Fields of papers citing papers by Edward Monosov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edward Monosov

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

All Works

18 of 18 papers shown
1.
Dı́az-Trelles, Ramón, Maria Cecilia Scimia, Paul Bushway, et al.. (2016). Notch-independent RBPJ controls angiogenesis in the adult heart. Nature Communications. 7(1). 12088–12088. 38 indexed citations
2.
Tyrberg, Björn, Philip D.G. Miles, Martin S. Denzel, et al.. (2011). T-cadherin (Cdh13) in association with pancreatic β-cell granules contributes to second phase insulin secretion. Islets. 3(6). 327–337. 27 indexed citations
3.
Scott, Fiona L., Boguslaw Stec, Cristina Pop, et al.. (2008). The Fas–FADD death domain complex structure unravels signalling by receptor clustering. Nature. 457(7232). 1019–1022. 281 indexed citations
4.
Hao, Ergeng, Björn Tyrberg, Pamela Itkin‐Ansari, et al.. (2006). Beta-cell differentiation from nonendocrine epithelial cells of the adult human pancreas. Nature Medicine. 12(3). 310–316. 173 indexed citations
5.
Kim, Hyung‐Ryong, Han–Jung Chae, Michaël Thomas, et al.. (2006). Mammalian dap3 is an essential gene required for mitochondrial homeostasis in vivo and contributing to the extrinsic pathway for apoptosis. The FASEB Journal. 21(1). 188–196. 46 indexed citations
6.
Chen, Emily I., Laurence Florens, Fumiko Axelrod, et al.. (2005). Maspin alters the carcinoma proteome. The FASEB Journal. 19(9). 1123–1124. 27 indexed citations
7.
Chae, Han–Jung, Hyung‐Ryong Kim, Chunyan Xu, et al.. (2004). BI-1 Regulates an Apoptosis Pathway Linked to Endoplasmic Reticulum Stress. Molecular Cell. 15(3). 355–366. 242 indexed citations
8.
Kitada, Shinichi, Edward Monosov, Esther Avery, et al.. (2004). Pro-Apoptotic Effects on CLL (Chronic Lymphocytic Leukemia) of ABT-737, a Novel Fully Synthetic Bcl-2/Bcl-XL Antagonist.. Blood. 104(11). 952–952. 3 indexed citations
9.
Becattini, Barbara, Shinichi Kitada, Marilisa Leone, et al.. (2004). Rational Design and Real Time, In-Cell Detection of the Proapoptotic Activity of a Novel Compound Targeting Bcl-XL. Chemistry & Biology. 11(3). 389–395. 123 indexed citations
10.
Rozanov, Dmitri V., Elena I. Deryugina, Edward Monosov, Natalia Marchenko, & Alex Y. Strongin. (2003). Aberrant, persistent inclusion into lipid rafts limits the tumorigenic function of membrane type-1 matrix metalloproteinase in malignant cells. Experimental Cell Research. 293(1). 81–95. 64 indexed citations
11.
Özerdem, Uğur, Edward Monosov, & William B. Stallcup. (2002). NG2 Proteoglycan Expression by Pericytes in Pathological Microvasculature. Microvascular Research. 63(1). 129–134. 149 indexed citations
12.
Rozanov, Dmitry V., Berhane Ghebrehiwet, Boris I. Ratnikov, et al.. (2002). The cytoplasmic tail peptide sequence of membrane type‐1 matrix metalloproteinase (MT1‐MMP) directly binds to gC1qR, a compartment‐specific chaperone‐like regulatory protein. FEBS Letters. 527(1-3). 51–57. 47 indexed citations
13.
Deryugina, Elena I., Boris I. Ratnikov, Edward Monosov, et al.. (2001). MT1-MMP Initiates Activation of pro-MMP-2 and Integrin αvβ3 Promotes Maturation of MMP-2 in Breast Carcinoma Cells. Experimental Cell Research. 263(2). 209–223. 327 indexed citations
14.
Özerdem, Uğur, et al.. (2001). NG2 proteoglycan is expressed exclusively by mural cells during vascular morphogenesis. Developmental Dynamics. 222(2). 218–227. 487 indexed citations
15.
Rozanov, Dmitry V., Elena I. Deryugina, Boris I. Ratnikov, et al.. (2001). Mutation Analysis of Membrane Type-1 Matrix Metalloproteinase (MT1-MMP). Journal of Biological Chemistry. 276(28). 25705–25714. 146 indexed citations
16.
Monosov, Edward, Thibaut J. Wenzel, Georg H. Lüers, John A. Heyman, & Suresh Subramani. (1996). Labeling of peroxisomes with green fluorescent protein in living P. pastoris cells.. Journal of Histochemistry & Cytochemistry. 44(6). 581–589. 92 indexed citations
17.
Heyman, John A., Edward Monosov, & Suresh Subramani. (1994). Role of the PAS1 gene of Pichia pastoris in peroxisome biogenesis.. The Journal of Cell Biology. 127(5). 1259–1273. 64 indexed citations
18.
Kondratieva, E. N., et al.. (1976). The capacity of phototrophic sulfur bacterium Thiocapsa roseopersicina for chemosynthesis. Archives of Microbiology. 108(3). 287–292. 43 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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