James C.‐H. Mao

762 citations
20 papers · 616 indexed · h-index 13
Topics
RNA and protein synthesis mechanisms (6 papers)Chemical Synthesis and Analysis (3 papers)Cancer therapeutics and mechanisms (3 papers)

In The Last Decade

James C.‐H. Mao

20 papers receiving 532 citations

Peers

James C.‐H. Mao
Comparison fields: 5 of 80
  • Molecular Biology 375
  • Epidemiology 144
  • Genetics 129
  • Organic Chemistry 113
  • Pharmacology 92
Replace W E Kohlbrenner with:
W E Kohlbrenner United States
Hiroomi Watabe Japan
Karlheinz Tovar Germany
S. Valisena Italy
Martin Stieger Switzerland
József Aszódi France
F Jacob Belgium
S.C. Mosimann Canada
Kelly S.E. Tanaka United States
Hsu‐Tso Ho United States
James C.‐H. Mao relative to W E Kohlbrenner United States W E Kohlbrenner's profile →
Citations per field
00.5×1.5×2.4×
W E Kohlbrenner · 1×
Citations per year

Countries citing papers authored by James C.‐H. Mao

Since Specialization
Citations

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

Fields of papers citing papers by James C.‐H. Mao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James C.‐H. Mao. 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 James C.‐H. Mao. The network helps show where James C.‐H. Mao may publish in the future.

Co-authorship network of co-authors of James C.‐H. Mao

This figure shows the co-authorship network connecting the top 25 collaborators of James C.‐H. Mao. A scholar is included among the top collaborators of James C.‐H. Mao 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 James C.‐H. Mao. James C.‐H. Mao 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
#WorkIndexed citations
1 10
2 18
3 29
4 21
5 5
6 6
7 29
8 120
9 8
10 4
11 37
12 9
13 46
14 9
15 79
16 41
17 51
18 24
19 39
20 31

About James C.‐H. Mao

James C.‐H. Mao is a scholar working on Toxicology, Sensory Systems and Molecular Biology, having authored 20 papers that have together received 616 indexed citations. Recurring topics across this work include RNA and protein synthesis mechanisms (6 papers), Chemical Synthesis and Analysis (3 papers) and Cancer therapeutics and mechanisms (3 papers). The work is most often cited by research in Molecular Medicine (51 citations), Molecular Biology (375 citations) and Pharmacology (92 citations). James C.‐H. Mao has collaborated with scholars based in United Kingdom, United States and Japan. Frequent co-authors include Ronald G. Wiegand, Thomas Herrin, André G. Pernet, N. L. Shipkowitz, Robert R. Bower, Linus L. Shen, Terry Rosen, Prabhavathi Fernandes, Mary Marovich and Thomas J. Perun. Their work appears in journals such as Journal of Molecular Biology, Biochemistry and Biochemical and Biophysical Research Communications.

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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