Emmanuel A. Asante

3.3k total citations
40 papers, 2.4k citations indexed

About

Emmanuel A. Asante is a scholar working on Molecular Biology, Neurology and Nutrition and Dietetics. According to data from OpenAlex, Emmanuel A. Asante has authored 40 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 19 papers in Neurology and 8 papers in Nutrition and Dietetics. Recurrent topics in Emmanuel A. Asante's work include Prion Diseases and Protein Misfolding (33 papers), Neurological diseases and metabolism (19 papers) and Trace Elements in Health (8 papers). Emmanuel A. Asante is often cited by papers focused on Prion Diseases and Protein Misfolding (33 papers), Neurological diseases and metabolism (19 papers) and Trace Elements in Health (8 papers). Emmanuel A. Asante collaborates with scholars based in United Kingdom, United States and Germany. Emmanuel A. Asante's co-authors include John Collinge, Jacqueline M. Linehan, Ian Gowland, Jonathan D. F. Wadsworth, Sebastian Brandner, Andrew F. Hill, John G. R. Jefferys, Stéphanie Ratté, Susan Joiner and Giovanna R. Mallucci and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Emmanuel A. Asante

39 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emmanuel A. Asante United Kingdom 23 2.2k 1.1k 673 494 160 40 2.4k
Katie Sidle United Kingdom 17 3.2k 1.5× 1.9k 1.7× 1.1k 1.6× 375 0.8× 783 4.9× 25 3.8k
Dallas Foster United States 13 2.5k 1.2× 1.6k 1.4× 1.1k 1.6× 203 0.4× 94 0.6× 17 2.8k
Wen‐Quan Zou United States 29 2.8k 1.3× 1.6k 1.4× 944 1.4× 552 1.1× 693 4.3× 99 3.4k
Anna Ladogana Italy 31 2.6k 1.2× 1.3k 1.1× 512 0.8× 519 1.1× 1.0k 6.3× 67 3.2k
J. Hope United Kingdom 23 1.8k 0.8× 876 0.8× 839 1.2× 137 0.3× 38 0.2× 39 2.3k
Bradley R. Groveman United States 28 1.7k 0.8× 855 0.8× 382 0.6× 566 1.1× 765 4.8× 60 2.5k
Christina D. Orrú United States 31 2.5k 1.2× 1.2k 1.1× 532 0.8× 818 1.7× 1.4k 8.6× 58 3.7k
Constanze Riemer Germany 17 822 0.4× 358 0.3× 252 0.4× 288 0.6× 134 0.8× 23 1.1k
Franco Cardone Italy 22 1.5k 0.7× 702 0.6× 453 0.7× 153 0.3× 209 1.3× 52 1.6k
Tamaki Muramoto Japan 21 1.6k 0.7× 936 0.8× 630 0.9× 168 0.3× 167 1.0× 28 1.7k

Countries citing papers authored by Emmanuel A. Asante

Since Specialization
Citations

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

Fields of papers citing papers by Emmanuel A. Asante

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emmanuel A. Asante

This figure shows the co-authorship network connecting the top 25 collaborators of Emmanuel A. Asante. A scholar is included among the top collaborators of Emmanuel A. Asante 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 Emmanuel A. Asante. Emmanuel A. Asante 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.
Jones, Emma, Elizabeth Hill, Jacqueline M. Linehan, et al.. (2023). Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6. Neurobiology of Disease. 190. 106363–106363. 3 indexed citations
2.
Asante, Emmanuel A., Jacqueline M. Linehan, Andrew Tomlinson, et al.. (2020). Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS. PLoS Biology. 18(6). e3000725–e3000725. 13 indexed citations
3.
Joiner, Susan, Emmanuel A. Asante, Jacqueline M. Linehan, et al.. (2017). Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein. Journal of the Neurological Sciences. 386. 4–11. 7 indexed citations
4.
Asante, Emmanuel A., Andrew Tomlinson, Caroline Powell, et al.. (2015). Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS. PLoS Pathogens. 11(7). e1004953–e1004953. 24 indexed citations
5.
Clayton, Emma L., Sarah Mizielinska, James R. Edgar, et al.. (2015). Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathology. Acta Neuropathologica. 130(4). 511–523. 74 indexed citations
6.
Asante, Emmanuel A., Richard Houghton, Andrew Tomlinson, et al.. (2015). A naturally occurring variant of the human prion protein completely prevents prion disease. Nature. 522(7557). 478–481. 129 indexed citations
7.
Asante, Emmanuel A., Jacqueline M. Linehan, Andrew Tomlinson, et al.. (2013). Inherited Prion Disease A117V Is Not Simply a Proteinopathy but Produces Prions Transmissible to Transgenic Mice Expressing Homologous Prion Protein. PLoS Pathogens. 9(9). e1003643–e1003643. 42 indexed citations
8.
Ghazi‐Noori, Shabnam, Kristina E. Froud, Sarah Mizielinska, et al.. (2012). Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic mice. Brain. 135(3). 819–832. 80 indexed citations
9.
Ratté, Stéphanie, Martin Vreugdenhil, Jessica K.R. Boult, et al.. (2011). Threshold for epileptiform activity is elevated in prion knockout mice. Neuroscience. 179. 56–61. 17 indexed citations
10.
Sandberg, Malin, Huda Al-Doujaily, Christina J. Sigurdson, et al.. (2010). Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein. Journal of General Virology. 91(10). 2651–2657. 82 indexed citations
11.
Wadsworth, Jonathan D. F., Susan Joiner, Jacqueline M. Linehan, et al.. (2010). Effect of fixation on brain and lymphoreticular vCJD prions and bioassay of key positive specimens from a retrospective vCJD prevalence study. The Journal of Pathology. 223(4). 511–518. 19 indexed citations
12.
Wadsworth, Jonathan D. F., Emmanuel A. Asante, Melanie Desbruslais, et al.. (2004). Human Prion Protein with Valine 129 Prevents Expression of Variant CJD Phenotype. Science. 306(5702). 1793–1796. 197 indexed citations
13.
Asante, Emmanuel A., et al.. (2004). Pathogenic human prion protein rescues PrP null phenotype in transgenic mice. Neuroscience Letters. 360(1-2). 33–36. 15 indexed citations
14.
Asante, Emmanuel A.. (2002). BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein. The EMBO Journal. 21(23). 6358–6366. 281 indexed citations
15.
Asante, Emmanuel A., Ian Gowland, Jackie Linehan, Sukhvir P. Mahal, & John Collinge. (2002). Expression Pattern of a Mini Human PrP Gene Promoter in Transgenic Mice. Neurobiology of Disease. 10(1). 1–7. 15 indexed citations
16.
Mahal, Sukhvir P., Emmanuel A. Asante, Michael Antoniou, & John Collinge. (2001). Isolation and functional characterisation of the promoter region of the human prion protein gene. Gene. 268(1-2). 105–114. 36 indexed citations
17.
Collinge, John, Andrew F. Hill, Ian Gowland, et al.. (1997). Unaltered susceptibility to BSE in transgenic mice expressing human prion protein (vol 378, pg 779, 1995). UCL Discovery (University College London). 5 indexed citations
18.
Collinge, John, Mark S. Palmer, Andrew F. Hill, et al.. (1995). Unaltered susceptibility to BSE in transgenic mice expressing human prion protein. Nature. 378(6559). 779–783. 141 indexed citations
19.
Asante, Emmanuel A., et al.. (1994). Tissue specific expression of an α-skeletal actin-lacZ fusion gene during development in transgenic mice. Transgenic Research. 3(1). 59–66. 13 indexed citations
20.
Asante, Emmanuel A., William G. Hill, & Grahame Bulfield. (1991). Analysis of lines of mice selected for fat content: 3. Flux through thede novolipid synthesis pathway. Genetics Research. 58(2). 123–127. 4 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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