Michael D. Losiewicz

1.2k total citations
15 papers, 1.0k citations indexed

About

Michael D. Losiewicz is a scholar working on Molecular Biology, Environmental Chemistry and Oncology. According to data from OpenAlex, Michael D. Losiewicz has authored 15 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Environmental Chemistry and 5 papers in Oncology. Recurrent topics in Michael D. Losiewicz's work include Aquatic Ecosystems and Phytoplankton Dynamics (6 papers), Cancer-related Molecular Pathways (3 papers) and Biomedical Research and Pathophysiology (2 papers). Michael D. Losiewicz is often cited by papers focused on Aquatic Ecosystems and Phytoplankton Dynamics (6 papers), Cancer-related Molecular Pathways (3 papers) and Biomedical Research and Pathophysiology (2 papers). Michael D. Losiewicz collaborates with scholars based in United States, China and Ukraine. Michael D. Losiewicz's co-authors include Edward A. Sausville, Peter J. Worland, Gurmeet Kaur, Adrian M. Senderowicz, Haohao Liu, Xinghai Chen, Huizhen Zhang, Xingde Du, Tsunehiro Shimizu and Ramachandra Naik and has published in prestigious journals such as Blood, Cancer Research and Journal of Hazardous Materials.

In The Last Decade

Michael D. Losiewicz

14 papers receiving 973 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael D. Losiewicz United States 12 499 495 179 178 158 15 1.0k
Katalin Szabó Hungary 20 595 1.2× 939 1.9× 90 0.5× 147 0.8× 129 0.8× 31 1.6k
Yali Kong China 24 853 1.7× 354 0.7× 75 0.4× 335 1.9× 71 0.4× 54 2.1k
James P. Perras United States 18 363 0.7× 395 0.8× 52 0.3× 133 0.7× 129 0.8× 48 1.1k
Shigeru Yoshizawa Japan 15 240 0.5× 184 0.4× 33 0.2× 133 0.7× 311 2.0× 37 1.1k
Héctor R. Contreras Chile 24 528 1.1× 349 0.7× 159 0.9× 343 1.9× 131 0.8× 69 1.3k
Weida Gong United States 23 1.5k 3.0× 371 0.7× 173 1.0× 129 0.7× 42 0.3× 42 2.0k
Peter S. Harris United States 24 1.1k 2.2× 195 0.4× 157 0.9× 98 0.6× 23 0.1× 55 1.8k
Marion P. Boland United Kingdom 14 548 1.1× 228 0.5× 49 0.3× 33 0.2× 179 1.1× 17 1.0k
Cheng Zeng China 15 401 0.8× 132 0.3× 52 0.3× 63 0.4× 71 0.4× 39 745
Francesco Esposito Italy 33 1.6k 3.2× 226 0.5× 61 0.3× 219 1.2× 228 1.4× 83 2.7k

Countries citing papers authored by Michael D. Losiewicz

Since Specialization
Citations

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

Fields of papers citing papers by Michael D. Losiewicz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael D. Losiewicz. 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 Michael D. Losiewicz. The network helps show where Michael D. Losiewicz may publish in the future.

Co-authorship network of co-authors of Michael D. Losiewicz

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

All Works

15 of 15 papers shown
1.
Hou, Jian, Wenqian Huo, Xiao Liang, et al.. (2025). The role of aging biomarkers and reproductive hormones in the association between microcystin-LR exposure and semen quality. Journal of Hazardous Materials. 499. 140075–140075.
2.
Liu, Haohao, Xingde Du, Zongxin Zhang, et al.. (2024). Co-exposure of microcystin and nitrite enhanced spermatogenic disorders: The role of mtROS-mediated pyroptosis and apoptosis. Environment International. 188. 108771–108771. 11 indexed citations
3.
Liu, Haohao, Xin Zeng, MA Ya, et al.. (2022). Long-term exposure to low concentrations of MC-LR induces blood-testis barrier damage through the RhoA/ROCK pathway. Ecotoxicology and Environmental Safety. 236. 113454–113454. 28 indexed citations
4.
Liu, Haohao, Xin Zeng, Yueqin Wang, et al.. (2022). Chronic Exposure to Environmentally Relevant Concentrations of Microcystin-Leucine Arginine Causes Lung Barrier Damage through PP2A Activity Inhibition and Claudin1 Ubiquitination. Journal of Agricultural and Food Chemistry. 70(35). 10907–10918. 20 indexed citations
5.
Tian, Zhihui, Haohao Liu, Xinghai Chen, et al.. (2021). The activated ATM/p53 pathway promotes autophagy in response to oxidative stress-mediated DNA damage induced by Microcystin-LR in male germ cells. Ecotoxicology and Environmental Safety. 227. 112919–112919. 34 indexed citations
6.
Wang, Rui, Xiaohui Liu, Jinxia Wu, et al.. (2020). Role of microRNA‐122 in microcystin‐leucine arginine‐induced dysregulation of hepatic iron homeostasis in mice. Environmental Toxicology. 35(8). 822–830. 6 indexed citations
7.
Wu, Jinxia, Haohao Liu, Hui Huang, et al.. (2019). p53‐Dependent pathway and the opening of mPTP mediate the apoptosis of co‐cultured Sertoli‐germ cells induced by microcystin‐LR. Environmental Toxicology. 34(10). 1074–1084. 12 indexed citations
8.
Du, Xingde, Haohao Liu, Le Yuan, et al.. (2019). The Diversity of Cyanobacterial Toxins on Structural Characterization, Distribution and Identification: A Systematic Review. Toxins. 11(9). 530–530. 133 indexed citations
9.
Zhao, Zhenze, Xiuye Ma, Spencer D. Shelton, et al.. (2016). A combined gene expression and functional study reveals the crosstalk between N-Myc and differentiation-inducing microRNAs in neuroblastoma cells. Oncotarget. 7(48). 79372–79387. 22 indexed citations
10.
Woynarowska, Barbara, et al.. (2005). Targeting of redox-controlling proteins of the thioredoxin family by oxaliplatin. Cancer Research. 65. 550–551. 1 indexed citations
11.
Losiewicz, Michael D., Gurjeet Kaur, & Edward A. Sausville. (1999). Different early effects of tyrphostin AG957 and geldanamycins on mitogen-activated protein kinase and p120cbl phosphorylation in anti CD-3-stimulated T-lymphoblasts. Biochemical Pharmacology. 57(3). 281–289. 13 indexed citations
12.
Kaur, Gurmeet, Wilberto Nieves‐Neira, Mohammed Taimi, et al.. (1998). Early Induction of Apoptosis in Hematopoietic Cell Lines After Exposure to Flavopiridol. Blood. 91(2). 458–465. 13 indexed citations
13.
Kaur, Gurmeet, Wilberto Nieves‐Neira, Mohammed Taimi, et al.. (1998). Early Induction of Apoptosis in Hematopoietic Cell Lines After Exposure to Flavopiridol. Blood. 91(2). 458–465. 193 indexed citations
14.
Sedlacek, H.H., Jörg Czech, Ramachandra Naik, et al.. (1996). Flavopiridol (L86 8275; NSC 649890), a new kinase inhibitor for tumor therapy. International Journal of Oncology. 231 indexed citations
15.
Losiewicz, Michael D., et al.. (1994). Potent Inhibition of Cdc2 Kinase Activity by the Flavonoid L86-8275. Biochemical and Biophysical Research Communications. 201(2). 589–595. 285 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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