T Strachan

4.8k total citations · 1 hit paper
50 papers, 3.4k citations indexed

About

T Strachan is a scholar working on Molecular Biology, Neurology and Epidemiology. According to data from OpenAlex, T Strachan has authored 50 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 16 papers in Neurology and 13 papers in Epidemiology. Recurrent topics in T Strachan's work include Neurofibromatosis and Schwannoma Cases (14 papers), Meningioma and schwannoma management (11 papers) and Sexual Differentiation and Disorders (8 papers). T Strachan is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (14 papers), Meningioma and schwannoma management (11 papers) and Sexual Differentiation and Disorders (8 papers). T Strachan collaborates with scholars based in United Kingdom, United States and South Africa. T Strachan's 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 and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

T Strachan

49 papers receiving 3.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

1997 667 citations David I. Wilson, Thomas C. Gebuhr et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
T Strachan United Kingdom	25	1.9k	933	932	930	444	50	3.4k
Sigrid Tinschert Germany	31	1.3k 0.7×	351 0.4×	985 1.1×	860 0.9×	232 0.5×	94	3.1k
R L Martuza United States	21	1.3k 0.7×	1.1k 1.2×	1.5k 1.6×	646 0.7×	101 0.2×	27	3.0k
Lisa Garrett‐Beal United States	15	2.4k 1.3×	418 0.4×	709 0.8×	226 0.2×	310 0.7×	17	3.5k
K. Schwechheimer Germany	27	1.1k 0.6×	482 0.5×	178 0.2×	585 0.6×	449 1.0×	70	2.8k
Hildegard Kehrer‐Sawatzki Germany	37	2.3k 1.2×	345 0.4×	1.9k 2.0×	1.6k 1.8×	152 0.3×	126	4.6k
B S Emanuel United States	30	1.8k 0.9×	368 0.4×	1.1k 1.2×	290 0.3×	101 0.2×	44	2.9k
James Dalton United States	27	2.3k 1.2×	313 0.3×	268 0.3×	677 0.7×	443 1.0×	44	5.2k
Antje Bornemann Germany	28	1.5k 0.7×	520 0.6×	173 0.2×	850 0.9×	405 0.9×	88	3.3k
Radhika P. Atit United States	25	1.3k 0.7×	239 0.3×	339 0.4×	219 0.2×	472 1.1×	44	2.5k
Meena Upadhyaya United Kingdom	44	2.5k 1.3×	934 1.0×	837 0.9×	3.7k 3.9×	310 0.7×	166	6.7k

Countries citing papers authored by T Strachan

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of T Strachan

This figure shows the co-authorship network connecting the top 25 collaborators of T Strachan. A scholar is included among the top collaborators of T Strachan 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 T Strachan. T Strachan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Strachan, T, et al.. (2024). Disseminated TB associated with acute severe malnutrition in a Roma child. SHILAP Revista de lepidopterología. 1(12). 571–574. 1 indexed citations

Tonkin, Emma, Moyra Smith, Pieter J.A. Eichhorn, et al.. (2001). A novel gene is disrupted by a Cornelia de Lange-associated translocation breakpoint at 3q26.3. The American Journal of Human Genetics. 2 indexed citations

Lisgo, Steven, T Strachan, Duncan Davidson, et al.. (1999). Mapping gene expression domains and neuronal cell differentiation during human embryonic forebrain development. The American Journal of Human Genetics. 2 indexed citations

Ruiz‐Pérez, Víctor L., Eugene Healy, C. Todd, et al.. (1999). ATP2A2 Mutations in Darier's Disease: Variant Cutaneous Phenotypes Are Associated with Missense Mutations, But Neuropsychiatry Features Are Independent of Mutation Class. Human Molecular Genetics. 8(9). 1621–1630. 104 indexed citations

Hanley, Neil A., Steve Ball, Mark Clement-Jones, et al.. (1999). Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination. Mechanisms of Development. 87(1-2). 175–180. 134 indexed citations

Rankin, Julia, T Strachan, Majlinda Lako, & Susan Lindsay. (1999). Partial cloning and assignment<footref rid="foot01"><sup>1</sup></footref> of WNT6 to human chromosome band 2q35 by in situ hybridization. Cytogenetic and Genome Research. 84(1-2). 50–52. 15 indexed citations

Evans, D. Gareth, R. H. Lye, W Neary, et al.. (1999). Probability of bilateral disease in people presenting with a unilateral vestibular schwannoma. Journal of Neurology Neurosurgery & Psychiatry. 66(6). 764–767. 41 indexed citations

Lako, Majlinda, et al.. (1998). Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lung. Gene. 219(1-2). 101–110. 96 indexed citations

Wilson, David I., Thomas C. Gebuhr, T Strachan, et al.. (1997). Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family. Nature Genetics. 15(1). 21–29. 667 indexed citations breakdown →

10.

Strachan, T, et al.. (1997). Molecular Genetics of Early Human Development. Medical Entomology and Zoology. 62 indexed citations

11.

Bushby, Kate, R. Bashir, Sharon Keers, et al.. (1996). The molecular biology of LGMD2B — Towards the identification of the LGMD gene on chromosome 2p13. Neuromuscular Disorders. 6(6). 491–492. 3 indexed citations

12.

McLean, W.H. Irwin, E.L. Rugg, Declan P. Lunny, et al.. (1995). Keratin 16 and keratin 17 mutations cause pachyonychia congenita. Nature Genetics. 9(3). 273–278. 242 indexed citations

13.

Sainio, Markku, T Strachan, Göran Blomstedt, et al.. (1995). Presymptomatic DNA and MRI diagnosis of neurofibromatosis 2 with mild clinical course in an extended pedigree. Neurology. 45(7). 1314–1322. 19 indexed citations

14.

Bourn, David & T Strachan. (1994). Dinucleotide repeat polymorphism at the NF2 gene. Human Molecular Genetics. 3(10). 1914–1914. 4 indexed citations

15.

Rogers, Lisa R., Meredith A. Weinstein, Melinda L. Estes, J. Gregory Cairncross, & T Strachan. (1994). Diffuse bilateral cerebral astrocytomas with atypical neuroimaging studies. Journal of neurosurgery. 81(6). 817–821. 6 indexed citations

16.

Horuzsko, Anatolij, Peter Tomlinson, T Strachan, & Andrew L. Mellor. (1994). Transcription of HLA-G transgenes commences shortly after implantation during embryonic development in mice.. PubMed. 83(2). 324–8. 8 indexed citations

17.

Neary, W, Valerie Newton, R. T. Ramsden, et al.. (1993). A clinical, genetic and audiological study of patients and families with bilateral acoustic neurofibromatosis. The Journal of Laryngology & Otology. 107(1). 6–11. 9 indexed citations

18.

Collier, Simon, May Tassabehji, & T Strachan. (1992). A method for specific amplification and PCR sequencing of individual members of multigene families: application to the study of steroid 21-hydroxylase deficiency.. Genome Research. 1(3). 181–186. 8 indexed citations

19.

Evans, D. Gareth, Susan Huson, Dian Donnai, et al.. (1992). A genetic study of type 2 neurofibromatosis in the United Kingdom. II. Guidelines for genetic counselling.. Journal of Medical Genetics. 29(12). 847–852. 122 indexed citations

20.

Stern, Peter L., A. G. Morris, Janet M. Risk, et al.. (1988). MHC class I expression by developmental tumors: Teratocarcinoma stem cells are TCA positive. Human Immunology. 22(4). 247–261. 7 indexed citations

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.

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