Chris Tyler‐Smith
- Genetics top 0.1%
- Molecular Biology top 1%
- Plant Science top 0.5%
- Cancer Research top 2%
- Archeology top 0.5%
- Co-authors
- Yali XueMarc HaberMassimo MezzavillaMatthew E. HurlesQasim AyubCharles LeeStephen W. SchererRichard Redon
- Topics
- Forensic and Genetic Research (41 papers)Chromosomal and Genetic Variations (35 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (27 papers)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
Chris Tyler‐Smith
139 papers receiving 10.0k citations
Hit Papers
Peers
Comparison fields: 5 of 185
- Genetics 6.0k
- Molecular Biology 5.4k
- Plant Science 2.4k
- Cancer Research 917
- Archeology 484
Countries citing papers authored by Chris Tyler‐Smith
This map shows the geographic impact of Chris Tyler‐Smith'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 Chris Tyler‐Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chris Tyler‐Smith more than expected).
Fields of papers citing papers by Chris Tyler‐Smith
This network shows the impact of papers produced by Chris Tyler‐Smith. 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 Chris Tyler‐Smith. The network helps show where Chris Tyler‐Smith may publish in the future.
Co-authorship network of co-authors of Chris Tyler‐Smith
This figure shows the co-authorship network connecting the top 25 collaborators of Chris Tyler‐Smith. A scholar is included among the top collaborators of Chris Tyler‐Smith 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 Chris Tyler‐Smith. Chris Tyler‐Smith is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 15 | |
| 3 | 34 | |
| 4 | 15 | |
| 5 | 54 | |
| 6 | 22 | |
| 7 | 1 | |
| 8 | 23 | |
| 9 | 18 | |
| 10 | 188 | |
| 11 | 92 | |
| 12 | 22 | |
| 13 | 59 | |
| 14 | 6 | |
| 15 | 37 | |
| 16 | Copy number variation: New insights in genome diversitybreakdown → | 592 |
| 17 | 27 | |
| 18 | 98 | |
| 19 | 52 | |
| 20 | 37 |
About Chris Tyler‐Smith
Chris Tyler‐Smith is a scholar working on Genetics, Plant Science and Molecular Biology, having authored 141 papers that have together received 10.2k indexed citations. Recurring topics across this work include Forensic and Genetic Research (41 papers), Chromosomal and Genetic Variations (35 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (27 papers). The work is most often cited by research in Genetics (6.0k citations), Molecular Biology (5.4k citations) and Plant Science (2.4k citations). Chris Tyler‐Smith has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Yali Xue, Marc Haber, Massimo Mezzavilla, Matthew E. Hurles, Qasim Ayub, Charles Lee, Stephen W. Scherer, Richard Redon, Emmanouil T. Dermitzakis and Daniel G. MacArthur. Their work appears in journals such as Science, Cell and Proceedings of the National Academy of Sciences.
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.