S. J. DeArmond

8.3k total citations · 2 hit papers
78 papers, 6.4k citations indexed

About

S. J. DeArmond is a scholar working on Molecular Biology, Neurology and Nutrition and Dietetics. According to data from OpenAlex, S. J. DeArmond has authored 78 papers receiving a total of 6.4k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 35 papers in Neurology and 26 papers in Nutrition and Dietetics. Recurrent topics in S. J. DeArmond's work include Prion Diseases and Protein Misfolding (50 papers), Neurological diseases and metabolism (32 papers) and Trace Elements in Health (25 papers). S. J. DeArmond is often cited by papers focused on Prion Diseases and Protein Misfolding (50 papers), Neurological diseases and metabolism (32 papers) and Trace Elements in Health (25 papers). S. J. DeArmond collaborates with scholars based in United States, United Kingdom and Germany. S. J. DeArmond's co-authors include Stanley B. Prusiner, Marilyn Torchia, H. A. Kretzschmar, S. B. Prusiner, Shuyan Yang, Darlene Groth, Linda Stowring, Albert Taraboulos, K. Jendroska and Patrick Tremblay and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genes & Development and The Journal of Immunology.

In The Last Decade

S. J. DeArmond

77 papers receiving 6.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies.

1993 373 citations Stanley B. Prusiner, Darlene Groth et al. profile →
Scrapie prion proteins are synthesized in neurons.

1986 357 citations H. A. Kretzschmar, Stanley B. Prusiner et al. PubMed profile →

Peers

S. J. DeArmond

NEURO

PHYSI

NEURO

Jun Tateishi Japan

H. A. Kretzschmar Germany

Sabina Capellari Italy

Andreas W. Sailer Switzerland

Hansruedi Büeler Switzerland

Stefan Isenmann Germany

Gerald V. Raymond United States

Kjeld Møllgård Denmark

Yoshigoro Kuroiwa Japan

O. Robain France

Jun Tateishi Japan

S. J. DeArmond

5.2k ×1.0

2.6k ×0.9

NEURO

1.5k ×0.7

1.7k ×1.5

PHYSI

1.3k ×1.7

NEURO

Citations per year, relative to S. J. DeArmond S. J. DeArmond (= 1×) peers Jun Tateishi

Countries citing papers authored by S. J. DeArmond

Since Specialization

Citations

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

Fields of papers citing papers by S. J. DeArmond

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. J. DeArmond. 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 S. J. DeArmond. The network helps show where S. J. DeArmond may publish in the future.

Co-authorship network of co-authors of S. J. DeArmond

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Caverzasi, Eduardo, Roland G. Henry, Paolo Vitali, et al.. (2014). Application of quantitative DTI metrics in sporadic CJD. NeuroImage Clinical. 4. 426–435. 30 indexed citations

Kim, Eunice, Gil D. Rabinovici, William W. Seeley, et al.. (2007). Patterns of MRI atrophy in tau positive and ubiquitin positive frontotemporal lobar degeneration. Journal of Neurology Neurosurgery & Psychiatry. 78(12). 1375–1378. 45 indexed citations

Diez, Margarita, S. J. DeArmond, Darlene Groth, Stanley B. Prusiner, & Tomas Hökfelt. (2001). Decreased MK-801 Binding in Discrete Hippocampal Regions of Prion-Infected Mice. Neurobiology of Disease. 8(4). 692–699. 10 indexed citations

Scott, Michael R., et al.. (2000). Transgenic models of prion disease. PubMed. 113–124. 18 indexed citations

Hökfelt, Tomas, Christian Broberger, X. Zhang, et al.. (1998). Neuropeptide Y: some viewpoints on a multifaceted peptide in the normal and diseased nervous system1Published on the World Wide Web on 4 December 1997.1. Brain Research Reviews. 26(2-3). 154–166. 101 indexed citations

Evatt, Bruce L., Harland Austin, Elizabeth R. Barnhart, et al.. (1998). Surveillance for Creutzfeldt‐Jakob disease among persons with hemophilia. Transfusion. 38(9). 817–820. 56 indexed citations

Wong, Ka Lam, Yushan Qiu, William C. Hyun, et al.. (1996). Decreased receptor-mediated calcium response in prion-infected cells correlates with decreased membrane fluidity and IP sub 3 release. Neurology. 47(3). 741–750. 55 indexed citations

Mastrianni, James A., et al.. (1996). Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease. Neurology. 47(5). 1305–1312. 38 indexed citations

Kretzschmar, H. A., James W. Ironside, S. J. DeArmond, & J Tateishi. (1996). Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease. Archives of Neurology. 53(9). 913–920. 210 indexed citations

10.

Tatzelt, Jörg, Milos Pekny, Christer Betsholtz, et al.. (1996). Scrapie in mice deficient in apolipoprotein E or glial fibrillary acidic protein. Neurology. 47(2). 449–453. 42 indexed citations

11.

DeArmond, S. J. & Stanley B. Prusiner. (1996). Transgenetics and Neuropathology of Prion Diseases. Current topics in microbiology and immunology. 207. 125–146. 7 indexed citations

12.

Jendroska, K., W. Poewe, Jane S. Paulsen, et al.. (1995). Ischemic stress induces deposition of amyloid ? immunoreactivity in human brain. Acta Neuropathologica. 90(5). 461–466. 136 indexed citations

13.

Carlson, George A., S. J. DeArmond, Marilyn Torchia, David Westaway, & S. B. Prusiner. (1994). Genetics of prion diseases and prion diversity in mice. Philosophical Transactions of the Royal Society B Biological Sciences. 343(1306). 363–369. 6 indexed citations

14.

Prusiner, Stanley B. & S. J. DeArmond. (1994). Prion Diseases and Neurodegeneration. Annual Review of Neuroscience. 17(1). 311–339. 132 indexed citations

15.

Kretzschmar, H. A., Peter Kufer, G. Riethmüller, et al.. (1992). Prion protein mutation at codon 102 in an Italian family with Gerstmann‐Straussler‐Scheinker syndrome. Neurology. 42(4). 809–809. 52 indexed citations

16.

Snow, Alan D., Thomas N. Wight, David Nochlin, et al.. (1990). Immunolocalization of heparan sulfate proteoglycans to the prion protein amyloid plaques of Gerstmann-Straussler syndrome, Creutzfeldt-Jakob disease and scrapie.. PubMed. 63(5). 601–11. 141 indexed citations

17.

Snow, Alan D., Robert Kisilevsky, J Willmer, Stanley B. Prusiner, & S. J. DeArmond. (1989). Sulfated glycosaminoglycans in amyloid plaques of prion diseases. Acta Neuropathologica. 77(4). 337–342. 100 indexed citations

18.

Rosenblum, Mark L., et al.. (1989). Isolation and partial purification of growth factors with TGF-like activity from human malignant gliomas. Journal of neurosurgery. 71(6). 875–883. 13 indexed citations

19.

Rutka, James T., et al.. (1985). XX Canadian Congress of Neurological Sciences Abstracts of the Scientific Program. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 12(2). 169–220. 3 indexed citations

20.

Barry, Ronald A., Michael P. McKinley, Paul E. Bendheim, et al.. (1985). Antibodies to the scrapie protein decorate prion rods.. The Journal of Immunology. 135(1). 603–613. 60 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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