T. D. Willis
Impact in
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
- Genetics top 5%
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genomic variations and chromosomal abnormalities
Papers in
-
- Gene expression and cancer classification 3
- Advanced biosensing and bioanalysis techniques 2
-
- Genetic factors in colorectal cancer 4
- Co-authors
- Paul Hardenbol (6 shared papers)Ronald W. Davis (6 shared papers)Martin Moorhead (7 shared papers)Malek Faham (8 shared papers)Eugeni Namsaraev (4 shared papers)Maneesh Jain (3 shared papers)Hossein Fakhrai-Rad (3 shared papers)George Karlin‐Neumann (2 shared papers)
- Journals
- Genome Research (4 papers)PLoS Genetics (2 papers)The Astrophysical Journal (2 papers)Proceedings of the National Academy of Sciences (2 papers)Nature Genetics (1 paper)
- Partner nations
- United StatesUnited KingdomSweden
In The Last Decade
T. D. Willis
27 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 124
- Cancer Research 270
- Genetics 472
- Pathology and Forensic Medicine 276
- Molecular Biology 589
- Genetics 72
Countries citing papers authored by T. D. Willis
This map shows the geographic impact of T. D. Willis'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 T. D. Willis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. D. Willis more than expected).
Fields of papers citing papers by T. D. Willis
This network shows the impact of papers produced by T. D. Willis. 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 T. D. Willis. The network helps show where T. D. Willis may publish in the future.
Co-authors
The 25 scholars most cited alongside T. D. Willis, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 393 | |
| 2 | 2005 | 354 | |
| 3 | 2015 | 307 | |
| 4 | The London practice of physick | 1973 | 105 |
| 5 | 1996 | 68 | |
| 6 | 2005 | 39 | |
| 7 | 2005 | 25 | |
| 8 | 2004 | 22 | |
| 9 | 2005 | 21 | |
| 10 | 2008 | 20 | |
| 11 | 1999 | 19 | |
| 12 | 2001 | 16 | |
| 13 | 1997 | 14 | |
| 14 | 2001 | 11 | |
| 15 | 1999 | 11 | |
| 16 | 2005 | 11 | |
| 17 | Cerebri anatome : cui accessit nervorum descripto et usus | 1973 | 9 |
| 18 | 1975 | 5 | |
| 19 | 1993 | 3 | |
| 20 | 1994 | 3 |
About T. D. Willis
T. D. Willis is a scholar working on Molecular Biology, Pathology and Forensic Medicine, Genetics, Astronomy and Astrophysics and Atomic and Molecular Physics, and Optics, having authored 28 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (4 papers), Genetic Associations and Epidemiology (4 papers), Astrophysics and Cosmic Phenomena (3 papers), Cancer Genomics and Diagnostics (3 papers), Solar and Space Plasma Dynamics (3 papers), Gene expression and cancer classification (3 papers), Advanced biosensing and bioanalysis techniques (2 papers) and Innovative Microfluidic and Catalytic Techniques Innovation (2 papers). The work is most often cited by research in Cancer Research (270 citations), Genetics (472 citations), Pathology and Forensic Medicine (276 citations), Molecular Biology (589 citations) and Genetics (72 citations). T. D. Willis has collaborated with scholars based in United States, United Kingdom and Sweden. Frequent co-authors include Paul Hardenbol, Ronald W. Davis, Martin Moorhead, Malek Faham, Eugeni Namsaraev, Maneesh Jain, Hossein Fakhrai-Rad, George Karlin‐Neumann, Mostafa Ronaghi and Ulf Landegren. Their work appears in journals such as Genome Research, PLoS Genetics, The Astrophysical Journal, Proceedings of the National Academy of Sciences and Nature Genetics.
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.