Tom Strachan
Impact in
- Genetics top 1%
- Genetic and rare skin diseases.
- Molecular Biology top 1%
- Pluripotent Stem Cells Research
- Genomics and Chromatin Dynamics
- CRISPR and Genetic Engineering
- Muscle Physiology and Disorders
- RNA Research and Splicing
- Renal and related cancers
Papers in
-
- Genomics and Chromatin Dynamics 12
- RNA Research and Splicing 8
- Pluripotent Stem Cells Research 8
- Sexual Differentiation and Disorders 7
- Developmental Biology and Gene Regulation 5
- Genetics 20
- Genetic and rare skin diseases. 6
- Co-authors
- Andrew Read (6 shared papers)Gabriel A. Dover (3 shared papers)Majlinda Lako (11 shared papers)R Harris (6 shared papers)Mayada Tassabehji (3 shared papers)Peter Gruß (2 shared papers)Valerie Newton (2 shared papers)Emma Tonkin (4 shared papers)
- Journals
- Nature Genetics (10 papers)Human Genetics (9 papers)Genomics (5 papers)Human Molecular Genetics (3 papers)Immunogenetics (3 papers)
- Partner nations
- United KingdomUnited StatesFrance
In The Last Decade
Tom Strachan
70 papers receiving 5.7k citations
Tom Strachan's Hit Papers
Peers
Comparison fields: 5 of 145
- Genetics 1.7k
- Molecular Biology 4.1k
- Cell Biology 605
- Sensory Systems 135
- Dermatology 237
Countries citing papers authored by Tom Strachan
This map shows the geographic impact of Tom Strachan'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 Tom Strachan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tom Strachan more than expected).
Fields of papers citing papers by Tom Strachan
This network shows the impact of papers produced by Tom Strachan. 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 Tom Strachan. The network helps show where Tom Strachan may publish in the future.
Co-authors
The 25 scholars most cited alongside Tom Strachan, 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 70 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene Hit paper breakdown → | 1992 | 543 |
| 2 | A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B Hit paper breakdown → | 1998 | 528 |
| 3 | 1999 | 485 | |
| 4 | 2004 | 457 | |
| 5 | 2005 | 297 | |
| 6 | 1982 | 250 | |
| 7 | 1998 | 205 | |
| 8 | 1998 | 190 | |
| 9 | 2005 | 184 | |
| 10 | 1994 | 174 | |
| 11 | 1993 | 168 | |
| 12 | 1985 | 167 | |
| 13 | 2009 | 149 | |
| 14 | 2004 | 130 | |
| 15 | 1995 | 116 | |
| 16 | 2004 | 103 | |
| 17 | 2006 | 90 | |
| 18 | 1985 | 89 | |
| 19 | 2018 | 86 | |
| 20 | 1994 | 78 |
About Tom Strachan
Tom Strachan is a scholar working on Molecular Biology, Genetics, Plant Science, Surgery and Neurology, having authored 70 papers that have together received 5.9k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (12 papers), Chromosomal and Genetic Variations (9 papers), RNA Research and Splicing (8 papers), Pluripotent Stem Cells Research (8 papers), Sexual Differentiation and Disorders (7 papers), Genetic and rare skin diseases. (6 papers), Developmental Biology and Gene Regulation (5 papers) and T-cell and B-cell Immunology (5 papers). The work is most often cited by research in Genetics (1.7k citations), Molecular Biology (4.1k citations), Cell Biology (605 citations), Sensory Systems (135 citations) and Dermatology (237 citations). Tom Strachan has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Andrew Read, Gabriel A. Dover, Majlinda Lako, R Harris, Mayada Tassabehji, Peter Gruß, Valerie Newton, Emma Tonkin, Enrico Coen and Miodrag Stojković. Their work appears in journals such as Nature Genetics, Human Genetics, Genomics, Human Molecular Genetics and Immunogenetics.
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.