Peter Thompson

1.6k total citations
41 papers, 641 citations indexed

About

Peter Thompson is a scholar working on Computer Networks and Communications, Genetics and Economics and Econometrics. According to data from OpenAlex, Peter Thompson has authored 41 papers receiving a total of 641 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Computer Networks and Communications, 8 papers in Genetics and 7 papers in Economics and Econometrics. Recurrent topics in Peter Thompson's work include Genomic variations and chromosomal abnormalities (8 papers), Network Traffic and Congestion Control (6 papers) and Chromosomal and Genetic Variations (6 papers). Peter Thompson is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Network Traffic and Congestion Control (6 papers) and Chromosomal and Genetic Variations (6 papers). Peter Thompson collaborates with scholars based in United Kingdom, United States and Australia. Peter Thompson's co-authors include Elias Dinopoulos, Meena Upadhyaya, S. W. Griffiths, Ian M. Frayling, Susan Roberts, Jeffrey I. Cohen, Elena A. Prikhod’ko, Richard M. Siegel, Marian Major and Meryl Altree and has published in prestigious journals such as Management Science, Human Molecular Genetics and Virology.

In The Last Decade

Peter Thompson

40 papers receiving 595 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter Thompson United Kingdom 12 262 211 83 80 69 41 641
Subhashini Chandrasekharan United States 16 150 0.6× 382 1.8× 19 0.2× 130 1.6× 31 0.4× 29 788
Sara Hamilton United States 12 147 0.6× 137 0.6× 29 0.3× 43 0.5× 20 0.3× 22 453
Guangying Liu China 18 33 0.1× 229 1.1× 72 0.9× 11 0.1× 68 1.0× 56 889
Simon Schneider Germany 19 109 0.4× 456 2.2× 9 0.1× 12 0.1× 43 0.6× 42 907
Malorye Allison United States 12 67 0.3× 205 1.0× 15 0.2× 20 0.3× 21 0.3× 37 584
C. Nissen Denmark 16 46 0.2× 124 0.6× 20 0.2× 35 0.4× 150 2.2× 41 700
Anne Pariser United States 17 229 0.9× 215 1.0× 4 0.0× 79 1.0× 58 0.8× 35 782
Wiebke Werft Germany 12 36 0.1× 295 1.4× 8 0.1× 18 0.2× 34 0.5× 17 580
Sandro Casavilca‐Zambrano Peru 14 23 0.1× 138 0.7× 17 0.2× 42 0.5× 98 1.4× 56 754
Christine E. Napier Australia 14 121 0.5× 514 2.4× 32 0.4× 36 0.5× 24 0.3× 41 802

Countries citing papers authored by Peter Thompson

Since Specialization
Citations

This map shows the geographic impact of Peter Thompson'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 Peter Thompson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Thompson more than expected).

Fields of papers citing papers by Peter Thompson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter Thompson. 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 Peter Thompson. The network helps show where Peter Thompson may publish in the future.

Co-authorship network of co-authors of Peter Thompson

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

All Works

20 of 20 papers shown
1.
Windrum, Paul, Michele Haynes, & Peter Thompson. (2019). “Breaking the mirror”: interface innovation and market capture by Japanese professional camera firms, 1955–1974. Industrial and Corporate Change. 5 indexed citations
2.
Lualdi, Susanna, Barbara Tappino, Marco Di Duca, et al.. (2010). Enigmatic In Vivo iduronate-2-sulfatase (IDS) mutant transcript correction to wild-type in Hunter syndrome. Human Mutation. 31(4). E1261–E1285. 8 indexed citations
3.
Tatton‐Brown, Katrina, Daniela T. Pilz, Karen Helene Ørstavik, et al.. (2009). 15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q. American Journal of Medical Genetics Part A. 149A(2). 147–154. 55 indexed citations
4.
Thompson, Peter. (2007). Founder Quality and Firm Performance: Implications for Local Development Strategies. Australian Economic Review. 40(1). 97–105. 6 indexed citations
5.
Archer, Hayley, Julie Evans, David Millar, et al.. (2006). NTNG1 mutations are a rare cause of Rett syndrome. American Journal of Medical Genetics Part A. 140A(7). 691–694. 38 indexed citations
6.
Pryce, Nat, et al.. (2006). Issues in Developing Ubicomp Applications on Symbian Phones. 51–56. 6 indexed citations
7.
Archer, Hayley, Stuart Enoch, Peter Thompson, et al.. (2005). Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3‐pter. American Journal of Medical Genetics Part A. 136A(1). 38–44. 34 indexed citations
8.
Byrne, Margaret M. & Peter Thompson. (2004). Response to Tabarrok. Econ journal watch. 1(1). 19–25. 2 indexed citations
9.
Prikhod’ko, Elena A., et al.. (2004). The NS3 protein of hepatitis C virus induces caspase-8-mediated apoptosis independent of its protease or helicase activities. Virology. 329(1). 53–67. 62 indexed citations
10.
Upadhyaya, Meena, Peter Thompson, Song Han, & D.N. Cooper. (2004). Neurofibromatosis Type 1: A Common Familial Cancer Syndrome. Humana Press eBooks. 285–310. 4 indexed citations
11.
12.
Thompson, Peter, et al.. (2001). Interstitial deletion 4q32-34 with ulnar deficiency: 4q33 may be the critical region in 4q terminal deletion syndrome. American Journal of Medical Genetics. 99(2). 94–98. 41 indexed citations
13.
Baker, Elizabeth, David F. Callen, Meryl Altree, et al.. (2001). Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies. American Journal of Medical Genetics. 107(4). 285–293. 102 indexed citations
14.
15.
Dinopoulos, Elias & Peter Thompson. (1996). A Contribution to the Empirics of Endogenous Growth. Eastern Economic Journal. 22(4). 389–400. 23 indexed citations
16.
Roberts, Andrew, Sharon D. Whatley, Peter Holmans, et al.. (1995). Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23. Human Molecular Genetics. 4(12). 2387–2390. 48 indexed citations
17.
Thompson, Peter, et al.. (1990). Replication studies in the 16p+ variant. Human Genetics. 84(4). 371–2. 7 indexed citations
18.
Thompson, Peter & Susan Roberts. (1987). A new variant of chromosome 16. Human Genetics. 76(1). 100–1. 21 indexed citations
19.
Birch, John, et al.. (1985). Production of monoclonal antibodies in large-scale cell culture. Biochemical Society Transactions. 13(1). 10–12. 6 indexed citations
20.
Thompson, Peter. (1983). 'Out of this nettle...'.. PubMed. 65(1). 14–7. 3 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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