T Strachan
- Neurology top 1%
- Neurofibromatosis and Schwannoma Cases 14
- Neuroblastoma Research and Treatments 4
- Vascular Malformations Diagnosis and Treatment 4
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Molecular Biology top 5%
- Sexual Differentiation and Disorders 8
- Cell Biology top 5%
- Epidemiology top 5%
- Meningioma and schwannoma management 11
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- Bone Tumor Diagnosis and Treatments 5
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- Metabolism and Genetic Disorders 3
- Co-authors
- D. Gareth EvansR HarrisDavid I. WilsonValerie NewtonSusan HusonAndrew J. WallaceDian DonnaiW Neary
- Cited by
- NeurologyGeneticsMolecular Biology
- Journals
- Journal of Medical Genetics (8 papers)Human Molecular Genetics (4 papers)The American Journal of Human Genetics (4 papers)
- Partner nations
- United KingdomUnited StatesSouth Africa
In The Last Decade
T Strachan
49 papers receiving 3.3k citations
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 1 | |
| 2 | A novel gene is disrupted by a Cornelia de Lange-associated translocation breakpoint at 3q26.3 | 2001 | 2 |
| 3 | Mapping gene expression domains and neuronal cell differentiation during human embryonic forebrain development | 1999 | 2 |
| 4 | 1999 | 104 | |
| 5 | 1999 | 134 | |
| 6 | 1999 | 15 | |
| 7 | 1999 | 41 | |
| 8 | 1998 | 96 | |
| 9 | Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familybreakdown → | 1997 | 667 |
| 10 | Molecular Genetics of Early Human Development | 1997 | 62 |
| 11 | 1996 | 3 | |
| 12 | 1995 | 242 | |
| 13 | 1995 | 19 | |
| 14 | 1994 | 4 | |
| 15 | 1994 | 6 | |
| 16 | Transcription of HLA-G transgenes commences shortly after implantation during embryonic development in mice. | 1994 | 8 |
| 17 | 1993 | 9 | |
| 18 | 1992 | 8 | |
| 19 | 1992 | 122 | |
| 20 | 1988 | 7 |
About T Strachan
T Strachan is a scholar working on Neurology, Urology, Clinical Biochemistry, 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), Neuroblastoma Research and Treatments (4 papers), Vascular Malformations Diagnosis and Treatment (4 papers) and Metabolism and Genetic Disorders (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, United States and South Africa. 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.