Mark D. TrailSmith

8 papers receiving 438 citations

Peers

Mark D. TrailSmith
Comparison fields: 5 of 65
  • Immunology 153
  • Biotechnology 59
  • Urology 33
  • Oncology 117
  • Genetics 28
Replace Lu Qiao with:
Lu Qiao China
Geoff Strutton Australia
Juan Luis Callejas‐Valera United States
Sylvie Mathieu France
Olga Hahn Germany
Jung Yoon Bae South Korea
Paul D. Robbins United States
Andrea Stoler United States
Sabrina Kellouche France
Kalle Sipilä Finland
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Citations per year

Countries citing papers authored by Mark D. TrailSmith

Since Specialization
Citations

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

Fields of papers citing papers by Mark D. TrailSmith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Mark D. TrailSmith, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mark D. TrailSmith Line = papers co-authored together Mark D. TrailSmith links everyone, so they are left out of the graph.

All Works

8 of 8 papers shown
#Work
1 1999152
2 199681
3 200159
4 199256
5
Effect of linker variation on the stability, potency, and efficacy of carcinoma-reactive BR64-doxorubicin immunoconjugates.
199745
6
Enhanced antitumor activity of paclitaxel in combination with the anticarcinoma immunoconjugate BR96-doxorubicin.
199932
7 200224
8 20005

About Mark D. TrailSmith

Mark D. TrailSmith is a scholar working on Molecular Biology, Oncology, Genetics, Endocrinology, Diabetes and Metabolism and Organic Chemistry, having authored 8 papers that have together received 454 indexed citations. Recurring topics across this work include Virus-based gene therapy research (2 papers), Peptidase Inhibition and Analysis (2 papers), Cancer Treatment and Pharmacology (1 paper), Lymphoma Diagnosis and Treatment (1 paper), Nanoplatforms for cancer theranostics (1 paper), Bone health and osteoporosis research (1 paper), Pharmacological Effects and Toxicity Studies (1 paper) and Cancer Research and Treatments (1 paper). The work is most often cited by research in Immunology (153 citations), Biotechnology (59 citations), Urology (33 citations), Oncology (117 citations) and Genetics (28 citations). Mark D. TrailSmith has collaborated with scholars based in United States, Germany and Switzerland. Frequent co-authors include Kerry Klussman, Robert S. Mittler, Michael K. Hoffmann, Peter V.N. Bodine, Barry S. Komm, Marc Charette, R. Bruce Rutherford, Maria Ryan, Xiaobo Luo and Trung Bao Le. Their work appears in journals such as Journal of Medicinal Chemistry, The Journal of Experimental Medicine, Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics, Archives of Oral Biology and Journal of Bone and Mineral Research.

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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