Caroline Powell

902 total citations
11 papers, 475 citations indexed

About

Caroline Powell is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, Caroline Powell has authored 11 papers receiving a total of 475 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Neurology and 3 papers in Physiology. Recurrent topics in Caroline Powell's work include Prion Diseases and Protein Misfolding (9 papers), Neurological diseases and metabolism (7 papers) and Trace Elements in Health (3 papers). Caroline Powell is often cited by papers focused on Prion Diseases and Protein Misfolding (9 papers), Neurological diseases and metabolism (7 papers) and Trace Elements in Health (3 papers). Caroline Powell collaborates with scholars based in United Kingdom, Belgium and Denmark. Caroline Powell's co-authors include Sebastian Brandner, Jacqueline M. Linehan, John Collinge, Emmanuel A. Asante, Jonathan D. F. Wadsworth, Adrian M. Isaacs, Catherine O’Malley, Elizabeth Fisher, John Collinge and Kristina E. Froud and has published in prestigious journals such as Brain, Human Molecular Genetics and PLoS Pathogens.

In The Last Decade

Caroline Powell

11 papers receiving 466 citations

Peers

Caroline Powell

MB

NEURO

PHYSI

CB

Andreas Heiseke Germany

Angela Richard‐Londt United Kingdom

Kori Kosberg United States

Bernard Bonaïti France

Anna Meshcheriakova Israel

N. Tomokane Japan

Lauren R. Kett United States

Lisa Schwarz Germany

Simon Nicot France

Prachi Mehta Australia

Andreas Heiseke Germany

Caroline Powell

306 ×1.0

MB

128 ×0.8

NEURO

86 ×0.6

NEURO

157 ×1.2

PHYSI

73 ×0.8

CB

Citations per year, relative to Caroline Powell Caroline Powell (= 1×) peers Andreas Heiseke

Countries citing papers authored by Caroline Powell

Since Specialization

Citations

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

Fields of papers citing papers by Caroline Powell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Powell

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

All Works

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11 of 11 papers shown

1.

Wadsworth, Jonathan D. F., Gary Adamson, Susan Joiner, et al.. (2017). Methods for Molecular Diagnosis of Human Prion Disease. Methods in molecular biology. 1658. 311–346. 11 indexed citations

2.

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

3.

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

4.

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

5.

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

6.

Urwin, Hazel, Jørgen E. Nielsen, Daniel Metcalf, et al.. (2010). Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations. Human Molecular Genetics. 19(11). 2228–2238. 142 indexed citations

7.

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

8.

Hyare, Harpreet, S. Wroe, Tom Webb, et al.. (2010). Magnetization transfer ratio may be a surrogate of spongiform change in human prion diseases. Brain. 133(10). 3058–3068. 6 indexed citations

9.

Isaacs, Adrian M., Caroline Powell, Tom Webb, et al.. (2008). Lack of TAR‐DNA binding protein‐43 (TDP‐43) pathology in human prion diseases. Neuropathology and Applied Neurobiology. 34(4). 446–456. 22 indexed citations

10.

Wadsworth, Jonathan D. F., Caroline Powell, Jonathan Beck, et al.. (2008). Molecular Diagnosis of Human Prion Disease. Methods in molecular biology. 459. 197–227. 38 indexed citations

11.

Kim, Tae Min, et al.. (1992). Delayed acute measles inclusion body encephalitis in a 9-year-old girl: ultrastructural, immunohistochemical, and in situ hybridization studies.. PubMed. 5(3). 348–52. 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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