D. A. HOPKINSON

11.2k total citations · 4 hit papers
177 papers, 9.5k citations indexed

About

D. A. HOPKINSON is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, D. A. HOPKINSON has authored 177 papers receiving a total of 9.5k indexed citations (citations by other indexed papers that have themselves been cited), including 99 papers in Molecular Biology, 39 papers in Genetics and 28 papers in Surgery. Recurrent topics in D. A. HOPKINSON's work include Biochemical and Molecular Research (23 papers), Pancreatic function and diabetes (22 papers) and Erythrocyte Function and Pathophysiology (19 papers). D. A. HOPKINSON is often cited by papers focused on Biochemical and Molecular Research (23 papers), Pancreatic function and diabetes (22 papers) and Erythrocyte Function and Pathophysiology (19 papers). D. A. HOPKINSON collaborates with scholars based in United Kingdom, United States and Australia. D. A. HOPKINSON's co-authors include Harry Harris, N. Sṕencer, Yvonne H. Edwards, Moyra Smith, H Harris, H. Harris, S. Povey, Moacyr Antônio Mestriner, J A Cortner and P.J.L. Cook and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

D. A. HOPKINSON

175 papers receiving 8.3k citations

Hit Papers

Handbook of enzyme electrophoresis in human genetics 1964 2026 1984 2005 1976 1964 1968 1973 500 1000 1.5k 2.0k
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.

  1. Handbook of enzyme electrophoresis in human genetics
    1976 2.0k citations D. A. HOPKINSON et al. profile →
  2. Phosphoglucomutase Polymorphism in Man
    1964 530 citations D. A. HOPKINSON et al. profile →
  3. Adenosine deaminase polymorphism in man
    1968 408 citations D. A. HOPKINSON et al. Annals of Human Genetics profile →
  4. Esterase D: a new human polymorphism
    1973 348 citations D. A. HOPKINSON et al. Annals of Human Genetics profile →

Peers

D. A. HOPKINSON
Harry Harris United Kingdom
Ruth Sager United States
Kenneth Paigen United States
Alan Tunnacliffe United Kingdom
John L. VandeBerg United States
David L. Garbers United States
Lars Bolund Denmark
Avery A. Sandberg United States
Joseph Martial Belgium
A. Bowcock United States
Harry Harris United Kingdom
D. A. HOPKINSON
Citations per year, relative to D. A. HOPKINSON D. A. HOPKINSON (= 1×) peers Harry Harris

Countries citing papers authored by D. A. HOPKINSON

Since Specialization
Citations

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

Fields of papers citing papers by D. A. HOPKINSON

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. A. HOPKINSON. 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 D. A. HOPKINSON. The network helps show where D. A. HOPKINSON may publish in the future.

Co-authorship network of co-authors of D. A. HOPKINSON

This figure shows the co-authorship network connecting the top 25 collaborators of D. A. HOPKINSON. A scholar is included among the top collaborators of D. A. HOPKINSON 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 D. A. HOPKINSON. D. A. HOPKINSON 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.
Ferrari, Jill, D. A. HOPKINSON, & Alf D. Linney. (2004). Size and Shape Differences Between Male and Female Foot Bones. Journal of the American Podiatric Medical Association. 94(5). 434–452. 49 indexed citations
2.
Jones, Rhiannon, A. J. Shorthouse, R. S. Vaughan, et al.. (2003). Testosterone-induced vasodilatation of isolated human mesenteric and pulmonary resistance arteries is independent of the vascular endothelium. 3 indexed citations
3.
Dissing, J., Mariann Thymann, & D. A. HOPKINSON. (2003). Simultaneous Detection of ACP1 and GC Genotypes Using PCR/SSCP. Annals of Human Genetics. 67(1). 81–85. 3 indexed citations
4.
HOPKINSON, D. A. & P. E. G. Baird. (2002). An interferometric test of time reversal invariance in atoms. Journal of Physics B Atomic Molecular and Optical Physics. 35(5). 1307–1327. 4 indexed citations
5.
Whitehouse, David, Janine Tomkins, J. U. Lovegrove, D. A. HOPKINSON, & W. Owen McMillan. (1998). A phylogenetic approach to the identification of phosphoglucomutase genes. Molecular Biology and Evolution. 15(4). 456–462. 39 indexed citations
6.
Tomkins, Janine, M. Fox, J. U. Lovegrove, et al.. (1997). Molecular and cytological investigations of phosphoglucomutase (PGM1) in the K562 cell line. Annals of Human Genetics. 61(2). 99–108. 3 indexed citations
7.
Edwards, Yvonne H., W. Putt, David I. Stott, et al.. (1996). The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27.. Genome Research. 6(3). 226–233. 66 indexed citations
8.
Fisher, Rosemary A., Philip H. Johnson, S. Povey, D. A. HOPKINSON, & SylviaD. Lawler. (1993). ABO Genotyping of Complete Hydatidiform Moles. Disease Markers. 11(4). 179–185. 1 indexed citations
9.
Hollyoake, Martine, et al.. (1993). Genetic polymorphism in the 3‘ ntranslated region of human phosphoglucomutase‐1. Annals of Human Genetics. 57(1). 1–8. 4 indexed citations
10.
Drago, G.A., et al.. (1991). Antigenic analysis of the major human phosphoglucomutase isozymes:PGM1, PGM2, PGM3 and PGM4. Annals of Human Genetics. 55(4). 263–271. 6 indexed citations
11.
Doherty, Derek G., Peter T. Donaldson, David Whitehouse, et al.. (1990). Hla Phenotypes and Gene Polymorphisms in Juvenile Liver Disease Associated With α1–Antitrypsin Deficiency. Hepatology. 12(2). 218–223. 17 indexed citations
12.
Whitehouse, David, J. U. Lovegrove, & D. A. HOPKINSON. (1989). Variation in alpha-1-antitrypsin phenotypes associated with penicillamine therapy. Clinica Chimica Acta. 179(1). 109–115. 15 indexed citations
13.
Whitehouse, David, et al.. (1989). Immunological detection of human phosphoglucomutase (PGM 1) subtypes. Forensic Science International. 41(1-2). 25–34. 4 indexed citations
14.
Arredondo-Vega, F X, et al.. (1989). Isozyme and DNA analysis of human S‐adenosyl‐L‐homocysteine hydrolase (AHCY).. Annals of Human Genetics. 53(2). 157–167. 11 indexed citations
15.
Reeders, Stephen T., M.H. Breuning, G. CORNEY, et al.. (1986). Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16.. BMJ. 292(6524). 851–853. 74 indexed citations
16.
Edwards, Yvonne H., et al.. (1982). Isozyme patterns and protein profiles in neuromuscular disorders.. Journal of Medical Genetics. 19(3). 175–183. 4 indexed citations
17.
Edwards, Yvonne H., et al.. (1979). A comparison of the biochemical properties of the human diaphorase (DIA3) isozymes determined by the common alleles DIA13, DIA23 and DIA33. Annals of Human Genetics. 42(3). 293–302. 7 indexed citations
18.
Williams, Larry G. & D. A. HOPKINSON. (1975). Further Data on the Incidence and Segregation of Genetically Determined Electrophoretic Variants of Human Red Cell NADH Diaphorase. Human Heredity. 25(3). 161–171. 6 indexed citations
19.
20.
Geerdink, R. A., et al.. (1974). Phosphoglucomutase (PGM<sub>2</sub>) variants in Trio Indians from Surinam. Human Heredity. 24(1). 40–44. 9 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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