Anthea Springbett

1.8k total citations
34 papers, 1.4k citations indexed

About

Anthea Springbett is a scholar working on Genetics, Molecular Biology and Agronomy and Crop Science. According to data from OpenAlex, Anthea Springbett has authored 34 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 14 papers in Molecular Biology and 8 papers in Agronomy and Crop Science. Recurrent topics in Anthea Springbett's work include Reproductive Physiology in Livestock (7 papers), Reproductive Biology and Fertility (6 papers) and Animal Genetics and Reproduction (6 papers). Anthea Springbett is often cited by papers focused on Reproductive Physiology in Livestock (7 papers), Reproductive Biology and Fertility (6 papers) and Animal Genetics and Reproduction (6 papers). Anthea Springbett collaborates with scholars based in United Kingdom, United States and France. Anthea Springbett's co-authors include Richard Lathe, Elizabeth Glass, Susan Craigmile, M McClenaghan, J. Slee, Anthony Clark, Patricia Preston‐Ferrer, Gwen Wilkie, Erol Kirvar and C.G.D. Brown and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Biochemical Journal and Genetics.

In The Last Decade

Anthea Springbett

34 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anthea Springbett United Kingdom 19 594 483 290 229 143 34 1.4k
Eduardo Juan Gimeno Argentina 20 306 0.5× 132 0.3× 250 0.9× 331 1.4× 89 0.6× 116 1.3k
Claus B. Jørgensen Denmark 24 747 1.3× 884 1.8× 108 0.4× 122 0.5× 98 0.7× 75 2.1k
Fuad A. Iraqi Israel 30 1.2k 2.0× 1.0k 2.1× 401 1.4× 49 0.2× 230 1.6× 127 3.0k
E. Redondo Spain 18 159 0.3× 144 0.3× 373 1.3× 178 0.8× 122 0.9× 89 1.1k
A. M. Lawn United Kingdom 27 574 1.0× 320 0.7× 69 0.2× 70 0.3× 135 0.9× 52 1.8k
F. Ehrensperger Switzerland 26 660 1.1× 158 0.3× 111 0.4× 771 3.4× 75 0.5× 94 2.7k
D. O. Rae United States 23 231 0.4× 397 0.8× 101 0.3× 487 2.1× 131 0.9× 72 1.7k
Pierre Lessard United States 20 479 0.8× 63 0.1× 95 0.3× 239 1.0× 124 0.9× 47 1.4k
G. Reed Holyoak United States 18 310 0.5× 161 0.3× 237 0.8× 396 1.7× 10 0.1× 79 1.1k
Tai‐Young Hur South Korea 18 299 0.5× 291 0.6× 100 0.3× 612 2.7× 26 0.2× 102 1.4k

Countries citing papers authored by Anthea Springbett

Since Specialization
Citations

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

Fields of papers citing papers by Anthea Springbett

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anthea Springbett

This figure shows the co-authorship network connecting the top 25 collaborators of Anthea Springbett. A scholar is included among the top collaborators of Anthea Springbett 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 Anthea Springbett. Anthea Springbett 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.
Dougall, Nadine, Paul Lambert, Margaret Maxwell, et al.. (2014). Deaths by suicide and their relationship with general and psychiatric hospital discharge: 30-year record linkage study. The British Journal of Psychiatry. 204(4). 267–273. 28 indexed citations
2.
Unbekandt, Mathieu, et al.. (2011). Evaluation of methods for one-dimensional spatial analysis of two-dimensional patterns in mouse chimaeras. Journal of Anatomy. 219(3). 418–437. 5 indexed citations
3.
4.
Springbett, Anthea, et al.. (2008). Porphyrinuria in childhood autistic disorder is not associated with urinary creatinine deficiency. Pediatrics International. 50(4). 528–532. 11 indexed citations
5.
Glass, Elizabeth, Patricia Preston‐Ferrer, Anthea Springbett, et al.. (2005). Bos taurus and Bos indicus (Sahiwal) calves respond differently to infection with Theileria annulata and produce markedly different levels of acute phase proteins. International Journal for Parasitology. 35(3). 337–347. 109 indexed citations
6.
Manuja, Anju, George C. Russell, Anthea Springbett, et al.. (2004). Quantitative analysis of pro-inflammatory cytokine mRNA expression in Theileria annulata-infected cell lines derived from resistant and susceptible cattle. Veterinary Immunology and Immunopathology. 99(1-2). 87–98. 55 indexed citations
7.
Springbett, Anthea, Katrin Mackenzie, John Woolliams, & S.C. Bishop. (2003). The Contribution of Genetic Diversity to the Spread of Infectious Diseases in Livestock Populations. Genetics. 165(3). 1465–1474. 68 indexed citations
8.
Gasparrini, B., Shaorong Gao, A. Ainslie, et al.. (2003). Cloned Mice Derived from Embryonic Stem Cell Karyoplasts and Activated Cytoplasts Prepared by Induced Enucleation. Biology of Reproduction. 68(4). 1259–1266. 52 indexed citations
9.
Springbett, Anthea, et al.. (2003). Mono-allelic Expression of Variegating Transgene Locus in the Mouse. Transgenic Research. 12(6). 661–669. 5 indexed citations
10.
Glass, Elizabeth, Susan Craigmile, Anthea Springbett, et al.. (2003). The protozoan parasite, Theileria annulata, induces a distinct acute phase protein response in cattle that is associated with pathology. International Journal for Parasitology. 33(12). 1409–1418. 84 indexed citations
11.
McClenaghan, M, Anthea Springbett, Sarah Reid, et al.. (2002). Multiple Effects of Genetic Background on Variegated Transgene Expression in Mice. Genetics. 160(3). 1107–1112. 32 indexed citations
12.
Zhu, Jie, Evelyn E. Telfer, Judy Fletcher, et al.. (2002). Improvement of an Electrical Activation Protocol for Porcine Oocytes1. Biology of Reproduction. 66(3). 635–641. 57 indexed citations
13.
Windl, Otto, Maureen Dempster, J. Peter Estibeiro, et al.. (1996). Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene. Human Genetics. 98(3). 259–264. 164 indexed citations
14.
15.
Whitelaw, Bruce, Anthea Springbett, John Webster, & John A. Clark. (1993). The majority of G0 transgenic mice are derived from mosaic embryos. Transgenic Research. 2(1). 29–32. 50 indexed citations
16.
Webb, R., et al.. (1992). Mechanism controlling ovulation rate in ewes in relation to seasonal anoestrus. Reproduction. 94(1). 143–151. 16 indexed citations
17.
18.
Wilmut, I., Cheryl Ashworth, Anthea Springbett, & D. I. Sales. (1988). Effect of variation in embryo stage on the establishment of pregnancy, and embryo survival and growth in ewes with two embryos. Reproduction. 83(1). 233–237. 10 indexed citations
19.
McNeilly, J. R., et al.. (1988). Changes in the feedback control of gonadotrophin secretion in ewes from lines selected for testis size in the ram lamb. Reproduction. 84(1). 213–221. 17 indexed citations
20.
Webb, R., et al.. (1985). Control of gonadotrophin release in Scottish Blackface and Finnish Landrace ewes during seasonal anoestrus. Reproduction. 73(2). 369–378. 27 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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