Che‐Leung Law

6.5k total citations · 1 hit paper
99 papers, 5.0k citations indexed

About

Che‐Leung Law is a scholar working on Radiology, Nuclear Medicine and Imaging, Oncology and Immunology. According to data from OpenAlex, Che‐Leung Law has authored 99 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Radiology, Nuclear Medicine and Imaging, 44 papers in Oncology and 44 papers in Immunology. Recurrent topics in Che‐Leung Law's work include Monoclonal and Polyclonal Antibodies Research (58 papers), HER2/EGFR in Cancer Research (21 papers) and T-cell and B-cell Immunology (20 papers). Che‐Leung Law is often cited by papers focused on Monoclonal and Polyclonal Antibodies Research (58 papers), HER2/EGFR in Cancer Research (21 papers) and T-cell and B-cell Immunology (20 papers). Che‐Leung Law collaborates with scholars based in United States, United Kingdom and Netherlands. Che‐Leung Law's co-authors include Edward A. Clark, Sidorenko Sp, Kristine A. Gordon, Iqbal S. Grewal, Peter D. Senter, Alan F. Wahl, Charles G. Cerveny, Kerry Klussman, Svetlana O. Doronina and Damon L. Meyer and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Che‐Leung Law

98 papers receiving 4.9k citations

Hit Papers

cAC10-vcMMAE, an anti-CD30–monomethyl auristatin E conjug... 2003 2026 2010 2018 2003 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Che‐Leung Law United States 36 2.3k 1.7k 1.6k 1.5k 668 99 5.0k
Rudolf Schmits Germany 25 2.7k 1.2× 1.1k 0.7× 1.4k 0.9× 515 0.3× 798 1.2× 52 4.5k
Kerry Klussman United States 19 1.8k 0.8× 1.4k 0.8× 792 0.5× 938 0.6× 431 0.6× 37 3.4k
Pina M. Cardarelli United States 25 1.1k 0.5× 1.1k 0.6× 1.0k 0.6× 756 0.5× 261 0.4× 66 2.9k
Bahija Jallal United States 47 2.0k 0.9× 1.3k 0.8× 2.6k 1.6× 707 0.5× 465 0.7× 86 5.5k
Kenya Shitara Japan 42 2.8k 1.2× 1.3k 0.8× 5.6k 3.5× 4.3k 2.8× 303 0.5× 86 7.7k
Bryan Irving United States 20 5.5k 2.4× 4.1k 2.4× 1.7k 1.1× 917 0.6× 322 0.5× 44 7.8k
Meike Burger Germany 29 1.8k 0.8× 1.7k 1.0× 1.1k 0.7× 182 0.1× 650 1.0× 46 3.6k
John P. McKearn United States 23 1.4k 0.6× 939 0.5× 1.9k 1.2× 427 0.3× 416 0.6× 56 3.7k
Joaquı́n Teixidó Spain 39 1.3k 0.6× 1.6k 0.9× 2.0k 1.3× 347 0.2× 158 0.2× 71 4.4k
Marcel Spaargaren Netherlands 43 1.2k 0.5× 1.4k 0.8× 3.1k 1.9× 224 0.1× 1.3k 1.9× 98 5.8k

Countries citing papers authored by Che‐Leung Law

Since Specialization
Citations

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

Fields of papers citing papers by Che‐Leung Law

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Che‐Leung Law. 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 Che‐Leung Law. The network helps show where Che‐Leung Law may publish in the future.

Co-authorship network of co-authors of Che‐Leung Law

This figure shows the co-authorship network connecting the top 25 collaborators of Che‐Leung Law. A scholar is included among the top collaborators of Che‐Leung Law 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 Che‐Leung Law. Che‐Leung Law 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.
Austin, Richard J., Bryan D. Lemon, Wade H. Aaron, et al.. (2020). Preclinical Characterization of HPN536, a Trispecific, T-Cell–Activating Protein Construct for the Treatment of Mesothelin-Expressing Solid Tumors. Clinical Cancer Research. 27(5). 1452–1462. 35 indexed citations
2.
Lemon, Bryan D., Wade H. Aaron, Richard J. Austin, et al.. (2018). Abstract 1773: HPN424, a half-life extended, PSMA/CD3-specific TriTAC for the treatment of metastatic prostate cancer. Cancer Research. 78(13_Supplement). 1773–1773. 6 indexed citations
3.
Li, Fu, Michelle Ulrich, Mechthild Jonas, et al.. (2017). Tumor-Associated Macrophages Can Contribute to Antitumor Activity through FcγR-Mediated Processing of Antibody–Drug Conjugates. Molecular Cancer Therapeutics. 16(7). 1347–1354. 53 indexed citations
4.
Fu, Li, Kim K. Emmerton, Mechthild Jonas, et al.. (2016). Intracellular Released Payload Influences Potency and Bystander-Killing Effects of Antibody-Drug Conjugates in Preclinical Models. Cancer Research. 76(9). 2710–2719. 231 indexed citations
5.
Greene, Lloyd A., et al.. (2014). Lack of anti‐factor Xa assay standardization results in significant low molecular weight heparin (enoxaparin) dose variation in neonates and children. Journal of Thrombosis and Haemostasis. 12(9). 1554–1557. 16 indexed citations
6.
Lewis, Timothy S., Kim K. Emmerton, Jeffrey Lau, et al.. (2011). Distinct Apoptotic Signaling Characteristics of the Anti-CD40 Monoclonal Antibody Dacetuzumab and Rituximab Produce Enhanced Antitumor Activity in Non-Hodgkin Lymphoma. Clinical Cancer Research. 17(14). 4672–4681. 27 indexed citations
7.
Sutherland, May Kung, Changpu Yu, Martha E. Anderson, et al.. (2010). 5-Azacytidine enhances the anti-leukemic activity of lintuzumab (SGN-33) in preclinical models of acute myeloid leukemia. mAbs. 2(4). 440–448. 24 indexed citations
8.
Oflazoglu, Ezogelin, Tamar E. Boursalian, Weiping Zeng, et al.. (2009). Blocking of CD27-CD70 Pathway by Anti-CD70 Antibody Ameliorates Joint Disease in Murine Collagen-Induced Arthritis. The Journal of Immunology. 183(6). 3770–3777. 47 indexed citations
9.
Sutherland, May Kung, Changpu Yu, Timothy S. Lewis, et al.. (2009). Anti-leukemic activity of Lintuzumab (SGN-33) in preclinical models of acute myeloid leukemia. mAbs. 1(5). 481–490. 32 indexed citations
10.
McEarchern, Julie A., Leia M. Smith, Charlotte F. McDonagh, et al.. (2008). Preclinical Characterization of SGN-70, a Humanized Antibody Directed against CD70. Clinical Cancer Research. 14(23). 7763–7772. 70 indexed citations
11.
Lewis, Timothy S., Jamie B. Miyamoto, May Kung Sutherland, et al.. (2007). The humanized anti-CD40 monoclonal antibody, SGN-40, signals apoptosis in non-Hodgkin's lymphoma by dual mechanisms. Molecular Cancer Therapeutics. 6. 1 indexed citations
12.
Gerber, Hans‐Peter, Ivan J. Stone, Mechthild Jonas, et al.. (2007). Humanized anti-CD19 auristatin antibody-drug conjugates display potent antitumor activity in preclinical models of B-cell malignancies. Molecular Cancer Therapeutics. 6. 2 indexed citations
13.
Hatjiharissi, Evdoxia, Allen W. Ho, Lian Xu, et al.. (2006). Preclinical In Vitro and In Vivo Evidence Support a Therapeutic Role for the CD70 Directed Monoclonal Antibody (SGN-70) in Waldenstrom’s Macroglobulinemia (WM).. Blood. 108(11). 2490–2490. 2 indexed citations
14.
Law, Che‐Leung, Julie A. McEarchern, Charles G. Cerveny, et al.. (2005). The Humanized Anti-CD40 Monoclonal Antibody SGN-40 Targets Hodgkin’s Disease Cells through Multiple Mechanisms.. Blood. 106(11). 1476–1476. 5 indexed citations
15.
McEarchern, Julie A., Charlotte F. McDonagh, Allen W. Ho, et al.. (2005). A Humanized Anti-CD70 Monoclonal Antibody Targets CD70-Expressing Multiple Myeloma.. Blood. 106(11). 1591–1591. 4 indexed citations
16.
Law, Che‐Leung, et al.. (2002). Expression and characterization of recombinant soluble human CD3 molecules: presentation of antigenic epitopes defined on the native TCR–CD3 complex. International Immunology. 14(4). 389–400. 11 indexed citations
17.
Gibbins, Jonathan M., Judith Asselin, Richard W. Farndale, et al.. (1996). Tyrosine Phosphorylation of the Fc Receptor γ-Chain in Collagen-stimulated Platelets. Journal of Biological Chemistry. 271(30). 18095–18099. 193 indexed citations
18.
Yanaga, Fumi, Alastair W. Poole, Judith Asselin, et al.. (1995). Syk interacts with tyrosine-phosphorylated proteins in human platelets activated by collagen and cross-linking of the Fc γ-IIA receptor. Biochemical Journal. 311(2). 471–478. 127 indexed citations
19.
Law, Che‐Leung, Sidorenko Sp, Kay Draves, et al.. (1994). Molecular cloning of human Syk. A B cell protein-tyrosine kinase associated with the surface immunoglobulin M-B cell receptor complex.. Journal of Biological Chemistry. 269(16). 12310–12319. 126 indexed citations
20.
Villablanca, Judith G., Janet Anderson, Melinda L. Moseley, et al.. (1990). Differentiation of normal human pre-B cells in vitro.. The Journal of Experimental Medicine. 172(1). 325–334. 38 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