T Strachan
Impact in
Papers in
-
- Sexual Differentiation and Disorders 8
- Congenital heart defects research 3
- Neurology 16
- Neurofibromatosis and Schwannoma Cases 14
- Vascular Malformations Diagnosis and Treatment 4
- Neuroblastoma Research and Treatments 4
- Co-authors
- D. Gareth Evans (12 shared papers)R Harris (9 shared papers)David I. Wilson (5 shared papers)Valerie Newton (5 shared papers)Susan Huson (3 shared papers)Andrew J. Wallace (5 shared papers)Dian Donnai (3 shared papers)W Neary (5 shared papers)
- Journals
- Journal of Medical Genetics (8 papers)Human Molecular Genetics (4 papers)The American Journal of Human Genetics (4 papers)The Journal of Laryngology & Otology (3 papers)Nature Genetics (2 papers)
- Partner nations
- United KingdomSouth AfricaUnited States
In The Last Decade
T Strachan
49 papers receiving 3.3k citations
T Strachan's Hit Papers
Peers
Comparison fields: 5 of 96
- Neurology 930
- Genetics 932
- Molecular Biology 1.9k
- Cell Biology 444
- Epidemiology 933
Countries citing papers authored by T Strachan
This map shows the geographic impact of T 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 T Strachan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T Strachan more than expected).
Fields of papers citing papers by T Strachan
This network shows the impact of papers produced by T 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 T Strachan. The network helps show where T Strachan may publish in the future.
Co-authors
The 25 scholars most cited alongside T 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family Hit paper breakdown → | 1997 | 667 |
| 2 | 1992 | 336 | |
| 3 | 1995 | 242 | |
| 4 | 2000 | 211 | |
| 5 | 1998 | 142 | |
| 6 | 1994 | 141 | |
| 7 | 1984 | 140 | |
| 8 | 1999 | 134 | |
| 9 | 1992 | 122 | |
| 10 | 1999 | 104 | |
| 11 | 1998 | 98 | |
| 12 | 1998 | 96 | |
| 13 | 1994 | 94 | |
| 14 | 1989 | 94 | |
| 15 | 1994 | 86 | |
| 16 | Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndrome. | 1993 | 65 |
| 17 | 1997 | 64 | |
| 18 | Molecular Genetics of Early Human Development | 1997 | 62 |
| 19 | 1990 | 56 | |
| 20 | A mutation in the neurofibromatosis type 2 tumor-suppressor gene, giving rise to widely different clinical phenotypes in two unrelated individuals. | 1994 | 55 |
About T Strachan
T Strachan is a scholar working on Molecular Biology, Neurology, Epidemiology, Genetics and Rheumatology, having authored 50 papers that have together received 3.4k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (14 papers), Meningioma and schwannoma management (11 papers), Sexual Differentiation and Disorders (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Bone Tumor Diagnosis and Treatments (5 papers), Vascular Malformations Diagnosis and Treatment (4 papers), Neuroblastoma Research and Treatments (4 papers) and Congenital heart defects research (3 papers). The work is most often cited by research in Neurology (930 citations), Genetics (932 citations), Molecular Biology (1.9k citations), Cell Biology (444 citations) and Epidemiology (933 citations). T Strachan has collaborated with scholars based in United Kingdom, South Africa and United States. Frequent co-authors include D. Gareth Evans, R Harris, David I. Wilson, Valerie Newton, Susan Huson, Andrew J. Wallace, Dian Donnai, W Neary, V Blair and Susan Lindsay. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, The American Journal of Human Genetics, The Journal of Laryngology & Otology 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.