David M. Waisman

7.1k total citations
121 papers, 5.7k citations indexed

About

David M. Waisman is a scholar working on Molecular Biology, Cancer Research and Hematology. According to data from OpenAlex, David M. Waisman has authored 121 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 100 papers in Molecular Biology, 36 papers in Cancer Research and 22 papers in Hematology. Recurrent topics in David M. Waisman's work include S100 Proteins and Annexins (58 papers), Protease and Inhibitor Mechanisms (35 papers) and Blood Coagulation and Thrombosis Mechanisms (21 papers). David M. Waisman is often cited by papers focused on S100 Proteins and Annexins (58 papers), Protease and Inhibitor Mechanisms (35 papers) and Blood Coagulation and Thrombosis Mechanisms (21 papers). David M. Waisman collaborates with scholars based in Canada, United States and Portugal. David M. Waisman's co-authors include Nolan R. Filipenko, Jerry H. Wang, Patrícia A. Madureira, Alamelu G. Bharadwaj, Navin Khanna, Sandra L. Fitzpatrick, Alexi P. Surette, Ryan W. Holloway, Kyu‐Sil Choi and Moamen Bydoun and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

David M. Waisman

120 papers receiving 5.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David M. Waisman Canada 45 4.3k 1.6k 927 764 754 121 5.7k
Thomas O. Daniel United States 38 4.6k 1.1× 758 0.5× 1.2k 1.3× 1.0k 1.3× 966 1.3× 58 7.2k
Kathleen Kelly United States 44 3.6k 0.8× 894 0.6× 907 1.0× 270 0.4× 845 1.1× 88 5.9k
Edward V. Prochownik United States 53 6.4k 1.5× 1.8k 1.1× 902 1.0× 645 0.8× 804 1.1× 170 8.6k
Nicholas M. Dean United States 52 6.2k 1.5× 1.5k 0.9× 566 0.6× 288 0.4× 606 0.8× 99 7.8k
Ching-Shih Chen United States 46 3.3k 0.8× 652 0.4× 533 0.6× 381 0.5× 755 1.0× 83 5.3k
Juan Carlos Lacal Spain 54 5.7k 1.3× 1.8k 1.2× 660 0.7× 250 0.3× 1.0k 1.4× 162 8.4k
Luisa Lanfrancone Italy 38 4.9k 1.1× 813 0.5× 1.2k 1.3× 391 0.5× 839 1.1× 95 7.8k
Martijn F.B.G. Gebbink Netherlands 34 2.4k 0.6× 549 0.3× 770 0.8× 506 0.7× 412 0.5× 60 4.0k
Karen Blyth United Kingdom 43 4.7k 1.1× 2.2k 1.4× 939 1.0× 443 0.6× 630 0.8× 134 7.0k
Annik Prat Canada 43 2.8k 0.7× 1.5k 0.9× 1.2k 1.3× 190 0.2× 980 1.3× 101 8.3k

Countries citing papers authored by David M. Waisman

Since Specialization
Citations

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

Fields of papers citing papers by David M. Waisman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David M. Waisman. 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 David M. Waisman. The network helps show where David M. Waisman may publish in the future.

Co-authorship network of co-authors of David M. Waisman

This figure shows the co-authorship network connecting the top 25 collaborators of David M. Waisman. A scholar is included among the top collaborators of David M. Waisman 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 David M. Waisman. David M. Waisman 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.
Bharadwaj, Alamelu G., et al.. (2025). The Role of Extracellular Proteases and Extracellular Matrix Remodeling in the Pre-Metastatic Niche. Biomolecules. 15(12). 1696–1696.
2.
Bharadwaj, Alamelu G., et al.. (2025). Calreticulin—From the Endoplasmic Reticulum to the Plasma Membrane—Adventures of a Wandering Protein. Cancers. 17(2). 288–288. 2 indexed citations
3.
Bharadwaj, Alamelu G., John Woods, Victoria A. Miller, et al.. (2023). Identification and characterization of calreticulin as a novel plasminogen receptor. Journal of Biological Chemistry. 300(1). 105465–105465. 3 indexed citations
4.
Bharadwaj, Alamelu G., Raj Pranap Arun, Brianne M. Cruickshank, et al.. (2023). ALDH1A3 promotes invasion and metastasis in triple‐negative breast cancer by regulating the plasminogen activation pathway. Molecular Oncology. 18(1). 91–112. 4 indexed citations
5.
Bharadwaj, Alamelu G., Ryan W. Holloway, Victoria A. Miller, & David M. Waisman. (2021). Plasmin and Plasminogen System in the Tumor Microenvironment: Implications for Cancer Diagnosis, Prognosis, and Therapy. Cancers. 13(8). 1838–1838. 81 indexed citations
6.
Cruickshank, Brianne M., Cheryl A. Dean, Ryan W. Holloway, et al.. (2020). Decitabine Response in Breast Cancer Requires Efficient Drug Processing and Is Not Limited by Multidrug Resistance. Molecular Cancer Therapeutics. 19(5). 1110–1122. 20 indexed citations
7.
Bharadwaj, Alamelu G., Rong‐Zong Liu, Lynn N. Thomas, et al.. (2020). S100A10 Has a Critical Regulatory Function in Mammary Tumor Growth and Metastasis: Insights Using MMTV-PyMT Oncomice and Clinical Patient Sample Analysis. Cancers. 12(12). 3673–3673. 11 indexed citations
8.
Giacomantonio, Michael, Andra M. Sterea, Youra Kim, et al.. (2019). Quantitative Proteome Responses to Oncolytic Reovirus in GM-CSF- and M-CSF-Differentiated Bone Marrow-Derived Cells. Journal of Proteome Research. 19(2). 708–718. 5 indexed citations
9.
Phipps, Kyle D., Alexi P. Surette, Paul A. O’Connell, & David M. Waisman. (2011). Plasminogen Receptor S100A10 Is Essential for the Migration of Tumor-Promoting Macrophages into Tumor Sites. Cancer Research. 71(21). 6676–6683. 86 indexed citations
10.
O’Connell, Paul A., Alexi P. Surette, Robert Liwski, Per Svenningsson, & David M. Waisman. (2010). S100A10 regulates plasminogen-dependent macrophage invasion. Blood. 116(7). 1136–1146. 119 indexed citations
11.
Hill, Richard, Andrew M. Leidal, Patrícia A. Madureira, et al.. (2008). Chromium-mediated apoptosis: Involvement of DNA-dependent protein kinase (DNA-PK) and differential induction of p53 target genes. DNA repair. 7(9). 1484–1499. 26 indexed citations
12.
Shao, Chenghua, Fuming Zhang, Melissa M. Kemp, et al.. (2006). Crystallographic Analysis of Calcium-dependent Heparin Binding to Annexin A2. Journal of Biological Chemistry. 281(42). 31689–31695. 83 indexed citations
13.
Barabas, A. Z., et al.. (2004). Presence of immunoglobulin M antibodies around the glomerular capillaries and in the mesangium of normal and passive Heymann nephritis rats. International Journal of Experimental Pathology. 85(4). 201–212. 14 indexed citations
14.
Filipenko, Nolan R., et al.. (2004). Annexin A2 Is a Novel RNA-binding Protein. Journal of Biological Chemistry. 279(10). 8723–8731. 115 indexed citations
15.
Kwon, Mijung, et al.. (2003). Phospholipid-associated Annexin A2-S100A10 Heterotetramer and Its Subunits. Journal of Biological Chemistry. 278(28). 25577–25584. 99 indexed citations
16.
Fogg, Darin K., Dave Bridges, Kitty Cheung, et al.. (2002). The p11 Subunit of Annexin II Heterotetramer Is Regulated by Basic Carboxypeptidase. Biochemistry. 41(15). 4953–4961. 30 indexed citations
17.
Kassam, Geetha, Kyu‐Sil Choi, Hyoung-Min Kang, et al.. (1998). The Role of Annexin II Tetramer in the Activation of Plasminogen. Journal of Biological Chemistry. 273(8). 4790–4799. 130 indexed citations
18.
Tokuda, Masaaki, Navin Khanna, & David M. Waisman. (1987). Identification of bovine brain calcium binding proteins. Cell Calcium. 8(3). 229–239. 4 indexed citations
19.
Gimble, Jeffrey M., David M. Waisman, Michael C. Gustin, David B. P. Goodman, & H Rasmussen. (1982). Studies of the Ca2+ transport mechanism of human erythrocyte inside-out membrane vesicles. Evidence for the development of a positive interior membrane potential.. Journal of Biological Chemistry. 257(18). 10781–10788. 15 indexed citations
20.
Srivastava, Ashok K., David M. Waisman, Charles O. Brostrom, & Thomas R. Soderling. (1979). Stimulation of glycogen synthase phosphorylation by calcium-dependent regulator protein.. Journal of Biological Chemistry. 254(3). 583–586. 53 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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