Sandra Pritzkow

3.1k total citations · 3 hit papers
24 papers, 2.0k citations indexed

About

Sandra Pritzkow is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, Sandra Pritzkow has authored 24 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 5 papers in Neurology and 4 papers in Physiology. Recurrent topics in Sandra Pritzkow's work include Prion Diseases and Protein Misfolding (19 papers), Alzheimer's disease research and treatments (4 papers) and Trace Elements in Health (4 papers). Sandra Pritzkow is often cited by papers focused on Prion Diseases and Protein Misfolding (19 papers), Alzheimer's disease research and treatments (4 papers) and Trace Elements in Health (4 papers). Sandra Pritzkow collaborates with scholars based in United States, Chile and Italy. Sandra Pritzkow's co-authors include Claudio Soto, Mohammad Shahnawaz, Luis Concha‐Marambio, Nicolás Méndez, Ah-Lim Tsai, Abhisek Mukherjee, Wolfgang Singer, Phillip A. Low, Xiangan Liu and K. Peter R. Nilsson and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Nature Neuroscience.

In The Last Decade

Sandra Pritzkow

23 papers receiving 2.0k citations

Hit Papers

Protein misfolding, aggregation, and conformational strai... 2018 2026 2020 2023 2018 2020 2023 250 500 750

Peers

Sandra Pritzkow
Allison Kraus United States
Samantha L. Eaton United Kingdom
Wei Xiang Germany
M Novák Slovakia
Jennifer N. Rauch United States
Sandra Pritzkow
Citations per year, relative to Sandra Pritzkow Sandra Pritzkow (= 1×) peers Fabio Moda

Countries citing papers authored by Sandra Pritzkow

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Pritzkow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Pritzkow

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra Pritzkow. A scholar is included among the top collaborators of Sandra Pritzkow 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 Sandra Pritzkow. Sandra Pritzkow 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.
Donadio, Vincenzo, Martin Ingelsson, Giovanni Rizzo, et al.. (2025). Diagnostic biomarkers for α-synucleinopathies- state of the art and future developments: a systematic review. Molecular Neurodegeneration. 21(1). 1–1.
2.
Pritzkow, Sandra, et al.. (2024). Screening of Anti-Prion Compounds Using the Protein Misfolding Cyclic Amplification Technology. Biomolecules. 14(9). 1113–1113. 1 indexed citations
3.
Pritzkow, Sandra, Paul E. Schulz, Brian S. Appleby, et al.. (2023). Detection of prions in the urine of patients affected by sporadic Creutzfeldt–Jakob disease. Annals of Clinical and Translational Neurology. 10(12). 2316–2323. 4 indexed citations
4.
Concha‐Marambio, Luis, Sandra Pritzkow, Mohammad Shahnawaz, Carly M. Farris, & Claudio Soto. (2023). Seed amplification assay for the detection of pathologic alpha-synuclein aggregates in cerebrospinal fluid. Nature Protocols. 18(4). 1179–1196. 113 indexed citations breakdown →
5.
Concha‐Marambio, Luis, et al.. (2023). Development of a methodology for large-scale production of prions for biological and structural studies. Frontiers in Molecular Biosciences. 10. 1184029–1184029. 1 indexed citations
6.
Chahine, Lana M., Thomas G. Beach, Charles H. Adler, et al.. (2023). Central and peripheral α‐synuclein in Parkinson disease detected by seed amplification assay. Annals of Clinical and Translational Neurology. 10(5). 696–705. 23 indexed citations
7.
Urayama, Akihiko, et al.. (2022). Preventive and therapeutic reduction of amyloid deposition and behavioral impairments in a model of Alzheimer’s disease by whole blood exchange. Molecular Psychiatry. 27(10). 4285–4296. 21 indexed citations
8.
Wang, Fei, Sandra Pritzkow, & Claudio Soto. (2022). PMCA for ultrasensitive detection of prions and to study disease biology. Cell and Tissue Research. 392(1). 307–321. 9 indexed citations
9.
Pritzkow, Sandra, Rodrigo Morales, Manuel V. Camacho, & Claudio Soto. (2021). Uptake, Retention, and Excretion of Infectious Prions by Experimentally Exposed Earthworms. Emerging infectious diseases. 27(12). 3151–3154. 6 indexed citations
10.
Shahnawaz, Mohammad, Abhisek Mukherjee, Sandra Pritzkow, et al.. (2020). Discriminating α-synuclein strains in Parkinson’s disease and multiple system atrophy. Nature. 578(7794). 273–277. 535 indexed citations breakdown →
11.
Tetz, George, et al.. (2020). Bacterial DNA promotes Tau aggregation. Scientific Reports. 10(1). 2369–2369. 55 indexed citations
12.
Escobar, Luis E., Sandra Pritzkow, Daniel A. Grear, et al.. (2019). The ecology of chronic wasting disease in wildlife. Biological reviews/Biological reviews of the Cambridge Philosophical Society. 95(2). 393–408. 49 indexed citations
13.
Medina, Sarah J., Christine Mesa, Catherine C. Robertson, et al.. (2019). Identification of circulating microRNA signatures as potential biomarkers in the serum of elk infected with chronic wasting disease. Scientific Reports. 9(1). 19705–19705. 11 indexed citations
14.
Mays, Charles E., et al.. (2019). Application of PMCA to screen for prion infection in a human cell line used to produce biological therapeutics. Scientific Reports. 9(1). 4847–4847. 7 indexed citations
15.
Soto, Claudio & Sandra Pritzkow. (2018). Protein misfolding, aggregation, and conformational strains in neurodegenerative diseases. Nature Neuroscience. 21(10). 1332–1340. 798 indexed citations breakdown →
16.
Pritzkow, Sandra, et al.. (2018). Efficient prion disease transmission through common environmental materials. Journal of Biological Chemistry. 293(9). 3363–3373. 41 indexed citations
17.
Pritzkow, Sandra, et al.. (2017). Detection of Prions in Blood of Cervids at the Asymptomatic Stage of Chronic Wasting Disease. Scientific Reports. 7(1). 17241–17241. 39 indexed citations
18.
Concha‐Marambio, Luis, Sandra Pritzkow, Fabio Moda, et al.. (2016). Detection of prions in blood from patients with variant Creutzfeldt-Jakob disease. Science Translational Medicine. 8(370). 370ra183–370ra183. 113 indexed citations
19.
Morales, Rodrigo, Sandra Pritzkow, Ping Hu, Claudia Duran‐Aniotz, & Claudio Soto. (2013). Lack of prion transmission by sexual or parental routes in experimentally infected hamsters. Prion. 7(5). 412–419. 6 indexed citations
20.
Pritzkow, Sandra, Martin L. Daus, Karin Lemmer, et al.. (2011). Quantitative Detection and Biological Propagation of Scrapie Seeding Activity In Vitro Facilitate Use of Prions as Model Pathogens for Disinfection. PLoS ONE. 6(5). e20384–e20384. 39 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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