Eric M. Nicholson

2.0k total citations
81 papers, 1.2k citations indexed

About

Eric M. Nicholson is a scholar working on Molecular Biology, Neurology and Nutrition and Dietetics. According to data from OpenAlex, Eric M. Nicholson has authored 81 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 36 papers in Neurology and 32 papers in Nutrition and Dietetics. Recurrent topics in Eric M. Nicholson's work include Prion Diseases and Protein Misfolding (52 papers), Neurological diseases and metabolism (35 papers) and Trace Elements in Health (32 papers). Eric M. Nicholson is often cited by papers focused on Prion Diseases and Protein Misfolding (52 papers), Neurological diseases and metabolism (35 papers) and Trace Elements in Health (32 papers). Eric M. Nicholson collaborates with scholars based in United States, Canada and Germany. Eric M. Nicholson's co-authors include Justin J. Greenlee, J. Martin Scholtz, Amir N. Hamir, Robert A. Kunkle, Jüergen A. Richt, M. Heather West Greenlee, Brian W. Brunelle, Jodi D. Smith, Jürgen A. Richt and Catherine E. Vrentas and has published in prestigious journals such as Nature, PLoS ONE and Journal of Molecular Biology.

In The Last Decade

Eric M. Nicholson

78 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eric M. Nicholson United States 22 944 422 353 138 69 81 1.2k
Luca Ferretti Italy 25 965 1.0× 175 0.4× 176 0.5× 67 0.5× 109 1.6× 90 2.1k
Oscar Murillo United States 14 782 0.8× 14 0.0× 20 0.1× 99 0.7× 94 1.4× 19 1.3k
Luciane V. Mello United Kingdom 24 888 0.9× 5 0.0× 42 0.1× 91 0.7× 169 2.4× 54 1.5k
N. G. Holmes United Kingdom 15 367 0.4× 31 0.1× 59 0.2× 4 0.0× 115 1.7× 27 773
Dessislava Georgieva Germany 18 671 0.7× 42 0.1× 57 0.2× 39 0.3× 24 0.3× 47 1.1k
Neil Harris United Kingdom 17 534 0.6× 12 0.0× 16 0.0× 23 0.2× 22 0.3× 32 877
Richard H. Smith United States 21 328 0.3× 7 0.0× 20 0.1× 24 0.2× 39 0.6× 37 1.1k
Sandra S. Ristow United States 20 476 0.5× 6 0.0× 22 0.1× 106 0.8× 77 1.1× 43 1.5k
Rudolf Hoffmann Germany 10 148 0.2× 59 0.1× 62 0.2× 11 0.1× 442 6.4× 21 1.0k
Henry L. Levin United States 30 2.7k 2.9× 7 0.0× 22 0.1× 23 0.2× 121 1.8× 69 3.5k

Countries citing papers authored by Eric M. Nicholson

Since Specialization
Citations

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

Fields of papers citing papers by Eric M. Nicholson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric M. Nicholson. 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 Eric M. Nicholson. The network helps show where Eric M. Nicholson may publish in the future.

Co-authorship network of co-authors of Eric M. Nicholson

This figure shows the co-authorship network connecting the top 25 collaborators of Eric M. Nicholson. A scholar is included among the top collaborators of Eric M. Nicholson 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 Eric M. Nicholson. Eric M. Nicholson 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.
Popichak, Katriana A., Jifeng Bian, Eric M. Nicholson, et al.. (2025). Microglia-specific NF-κB signaling is a critical regulator of prion-induced glial inflammation and neuronal loss. PLoS Pathogens. 21(6). e1012582–e1012582. 1 indexed citations
2.
Nicholson, Eric M., et al.. (2024). Aqueous extraction of formalin-fixed paraffin-embedded tissue and detection of prion disease using real-time quaking-induced conversion. BMC Research Notes. 17(1). 266–266. 2 indexed citations
3.
4.
Dassanayake, Rohana P., Adam S. Mullis, Shollie M. Falkenberg, et al.. (2021). Bovine NK-lysin peptides exert potent antimicrobial activity against multidrug-resistant Salmonella outbreak isolates. Scientific Reports. 11(1). 19276–19276. 8 indexed citations
5.
Greenlee, Justin J., et al.. (2021). Real-Time Quaking-Induced Conversion Detection of PrPSc in Fecal Samples From Chronic Wasting Disease Infected White-Tailed Deer Using Bank Vole Substrate. Frontiers in Veterinary Science. 8. 643754–643754. 15 indexed citations
6.
Moore, S. Jo, Catherine E. Vrentas, M. Heather West Greenlee, et al.. (2020). Novel Strain of the Chronic Wasting Disease Agent Isolated From Experimentally Inoculated Elk With LL132 Prion Protein. Scientific Reports. 10(1). 3148–3148. 23 indexed citations
7.
Greenlee, Justin J., et al.. (2020). Role of donor genotype in RT-QuIC seeding activity of chronic wasting disease prions using human and bank vole substrates. PLoS ONE. 15(1). e0227487–e0227487. 5 indexed citations
8.
Mammadova, Najiba, et al.. (2020). Evaluation of Antemortem Diagnostic Techniques in Goats Naturally Infected With Scrapie. Frontiers in Veterinary Science. 7. 517862–517862. 3 indexed citations
9.
Dassanayake, Rohana P., et al.. (2019). PAD-Beads enrichment enhances detection of PrPSc using real-time quaking-induced conversion. BMC Research Notes. 12(1). 806–806. 1 indexed citations
10.
Dassanayake, Rohana P., et al.. (2018). Antimicrobial activity of bovine NK-lysin-derived peptides on Mycoplasma bovis. PLoS ONE. 13(5). e0197677–e0197677. 21 indexed citations
12.
Moore, S. Jo, M. Heather West Greenlee, Jodi D. Smith, et al.. (2016). A Comparison of Classical and H-Type Bovine Spongiform Encephalopathy Associated with E211K Prion Protein Polymorphism in Wild-Type and EK211 Cattle Following Intracranial Inoculation. Frontiers in Veterinary Science. 3. 78–78. 14 indexed citations
13.
Brunelle, Brian W., et al.. (2016). Disparate Modes of Evolution Shaped Modern Prion (PRNP) and Prion-Related Doppel (PRND) Variation in Domestic Cattle. PLoS ONE. 11(5). e0155924–e0155924. 1 indexed citations
14.
Greenlee, Justin J., Robert A. Kunkle, Jürgen A. Richt, Eric M. Nicholson, & Amir N. Hamir. (2014). Lack of Prion Accumulation in Lymphoid Tissues of PRNP ARQ/ARR Sheep Intracranially Inoculated with the Agent of Scrapie. PLoS ONE. 9(9). e108029–e108029. 10 indexed citations
15.
Vrentas, Catherine E., Justin J. Greenlee, Thierry Baron, et al.. (2013). Stability properties of PrPScfrom cattle with experimental transmissible spongiform encephalopathies: use of a rapid whole homogenate, protease-free assay. BMC Veterinary Research. 9(1). 167–167. 13 indexed citations
16.
Vrentas, Catherine E., et al.. (2012). Relationships between PrPSc Stability and Incubation Time for United States Scrapie Isolates in a Natural Host System. PLoS ONE. 7(8). e43060–e43060. 15 indexed citations
17.
Nicholson, Eric M., Brian W. Brunelle, Jüergen A. Richt, Marcus E. Kehrli, & Justin J. Greenlee. (2008). Identification of a Heritable Polymorphism in Bovine PRNP Associated with Genetic Transmissible Spongiform Encephalopathy: Evidence of Heritable BSE. PLoS ONE. 3(8). e2912–e2912. 58 indexed citations
18.
Brunelle, Brian W., Marcus E. Kehrli, Judith R. Stabel, et al.. (2007). Short Communication: Allele, Genotype, and Haplotype Data for Bovine Spongiform Encephalopathy-Resistance Polymorphisms from Healthy US Holstein Cattle. Journal of Dairy Science. 91(1). 338–342. 19 indexed citations
19.
Brunelle, Brian W., Amir N. Hamir, Thierry Baron, et al.. (2007). Polymorphisms of the prion gene promoter region that influence classical bovine spongiform encephalopathy susceptibility are not applicable to other transmissible spongiform encephalopathies in cattle1,2. Journal of Animal Science. 85(12). 3142–3147. 35 indexed citations
20.
Nicholson, Eric M., Jüergen A. Richt, Mark A. Rasmussen, et al.. (2007). Exposure of sheep scrapie brain homogenate to rumen-simulating conditions does not result in a reduction of PrPSclevels. Letters in Applied Microbiology. 44(6). 631–636. 10 indexed citations

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