Katie Williams

760 total citations
26 papers, 355 citations indexed

About

Katie Williams is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, Katie Williams has authored 26 papers receiving a total of 355 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 12 papers in Neurology and 5 papers in Physiology. Recurrent topics in Katie Williams's work include Prion Diseases and Protein Misfolding (24 papers), Neurological diseases and metabolism (7 papers) and Neuroinflammation and Neurodegeneration Mechanisms (6 papers). Katie Williams is often cited by papers focused on Prion Diseases and Protein Misfolding (24 papers), Neurological diseases and metabolism (7 papers) and Neuroinflammation and Neurodegeneration Mechanisms (6 papers). Katie Williams collaborates with scholars based in United States, Italy and Netherlands. Katie Williams's co-authors include Brent Race, Bruce Chesebro, James A. Carroll, James F. Striebel, Andrew G. Hughson, Christina D. Orrú, Bradley R. Groveman, Cathryn L. Haigh, Lori Lubke and Simote T. Foliaki and has published in prestigious journals such as Nature Communications, PLoS ONE and Journal of Virology.

In The Last Decade

Katie Williams

26 papers receiving 344 citations

Peers

Countries citing papers authored by Katie Williams

Since Specialization

Citations

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

Fields of papers citing papers by Katie Williams

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katie Williams

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Prion-induced ferroptosis is facilitated by RAC3 2025 ·Nature Communications ·Hao Peng, Susanne Pfeiffer, (unknown), Mei Qiu, (unknown), Xiang Jin, Xin Zhang, Katie Williams, Bradley R. Groveman, Simote T. Foliaki, Brent Race, T. TURNER THOMAS, Chengxuan Chen, Constanze Müller, Krisztina Kovács, Thomas Arzberger, Stefan Momma, Cathryn L. Haigh, Joel Schick	1
2	Limbic system synaptic dysfunctions associated with prion disease onset 2024 ·Acta Neuropathologica Communications ·Simote T. Foliaki, Bradley R. Groveman, (unknown), Katie Williams, (unknown), Benjamin Schwarz, Jacqueline M. Leung, Christine A. Schneider, Cindi L. Schwartz, Eric Bohrnsen, (unknown), Brent Race, Cathryn L. Haigh	1
3	Sporadic Creutzfeldt–Jakob disease infected human cerebral organoids retain the original human brain subtype features following transmission to humanized transgenic mice 2023 ·Acta Neuropathologica Communications ·Bradley R. Groveman, Brent Race, Simote T. Foliaki, Katie Williams, Andrew G. Hughson, (unknown), Gianluigi Zanusso, Cathryn L. Haigh	10
4	Neural cell engraftment therapy for sporadic Creutzfeldt-Jakob disease restores neuroelectrophysiological parameters in a cerebral organoid model 2023 ·Stem Cell Research & Therapy ·Katie Williams, Simote T. Foliaki, Brent Race, Anna Smith, T. TURNER THOMAS, Bradley R. Groveman, Cathryn L. Haigh	3
5	Altered energy metabolism in Fatal Familial Insomnia cerebral organoids is associated with astrogliosis and neuronal dysfunction 2023 ·PLoS Genetics ·Simote T. Foliaki, Anna L. Smith, Benjamin Schwarz, Eric Bohrnsen, Catharine M. Bosio, Katie Williams, Christina D. Orrú, (unknown), Bradley R. Groveman, Cathryn L. Haigh	9
6	Hereditary E200K mutation within the prion protein gene alters human iPSC derived cardiomyocyte function 2022 ·Scientific Reports ·(unknown), Simote T. Foliaki, Bradley R. Groveman, Ryan O. Walters, Katie Williams, Jue Yuan, Wen‐Quan Zou, Cathryn L. Haigh	4
7	Second passage experiments of chronic wasting disease in transgenic mice overexpressing human prion protein 2022 ·Veterinary Research ·Brent Race, (unknown), Katie Williams, James F. Striebel, Andrew G. Hughson, Bruce Chesebro	7
8	Microglia have limited influence on early prion pathogenesis, clearance, or replication 2022 ·PLoS ONE ·Brent Race, Katie Williams, (unknown), James F. Striebel, Dan Long, T. TURNER THOMAS, Lori Lubke, Bruce Chesebro, James A. Carroll	6
9	Innate immune responses after stimulation with Toll-like receptor agonists in ex vivo microglial cultures and an in vivo model using mice with reduced microglia 2021 ·Journal of Neuroinflammation ·James A. Carroll, Brent Race, Katie Williams, James F. Striebel, Bruce Chesebro	11
10	Cerebral organoids as a new model for prion disease 2021 ·PLoS Pathogens ·Bradley R. Groveman, Anna Smith, Katie Williams, Cathryn L. Haigh	7
11	Reduced SOD2 expression does not influence prion disease course or pathology in mice 2021 ·PLoS ONE ·Simote T. Foliaki, Brent Race, Katie Williams, (unknown), Bradley R. Groveman, Cathryn L. Haigh	1
12	RNA-seq and network analysis reveal unique glial gene expression signatures during prion infection 2020 ·Molecular Brain ·James A. Carroll, Brent Race, Katie Williams, James F. Striebel, Bruce Chesebro	44
13	Prion-associated cerebral amyloid angiopathy is not exacerbated by human phosphorylated tau aggregates in scrapie-infected mice expressing anchorless prion protein 2020 ·Neurobiology of Disease ·Brent Race, Katie Williams, James F. Striebel, Bruce Chesebro	1
14	Prion protein N1 cleavage peptides stimulate microglial interaction with surrounding cells 2020 ·Scientific Reports ·James A. Carroll, Bradley R. Groveman, Katie Williams, Roger A. Moore, Brent Race, Cathryn L. Haigh	14
15	Microglia are not required for prion-induced retinal photoreceptor degeneration 2019 ·Acta Neuropathologica Communications ·James F. Striebel, Brent Race, Katie Williams, James A. Carroll, Mikael Klingeborn, Bruce Chesebro	9
16	Altered distribution, aggregation, and protease resistance of cellular prion protein following intracranial inoculation 2019 ·PLoS ONE ·Anne Ward, Jason R. Hollister, (unknown), Brent Race, Katie Williams, (unknown), Roger A. Moore, Suzette A. Priola	1
17	Transmission studies of chronic wasting disease to transgenic mice overexpressing human prion protein using the RT-QuIC assay 2019 ·Veterinary Research ·Brent Race, Katie Williams, Bruce Chesebro	28
18	Inactivation of chronic wasting disease prions using sodium hypochlorite 2019 ·PLoS ONE ·Katie Williams, Andrew G. Hughson, Bruce Chesebro, Brent Race	17
19	Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein 2018 ·Acta Neuropathologica Communications ·Brent Race, Katie Williams, Andrew G. Hughson, Casper Jansen, Piero Parchi, Annemieke J.M. Rozemüller, Bruce Chesebro	16
20	Toll-like receptor 2 confers partial neuroprotection during prion disease 2018 ·PLoS ONE ·James A. Carroll, Brent Race, Katie Williams, Bruce Chesebro	18

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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