Prion

Papers
(The median citation count of Prion is 1. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-05-01 to 2025-05-01.)
ArticleCitations
Estimating sequence diversity of prion protein gene ( PRNP ) in Portuguese populations of two cervid species: red deer and fallow deer27
Expression of the cellular prion protein by mast cells in the human carotid body19
Transcriptomic analysis identifies novel potential biomarkers and highlights cilium-related biological processes in the early stages of prion disease in mice14
Differentiated cultures of an immortalized human neural progenitor cell line do not replicate prions despite PrP C overexpression8
Polymorphism of prion protein gene (PRNP) in Nigerian sheep6
Variability in prion protein genotypes by spatial unit to inform susceptibility to chronic wasting disease6
Prion therapeutics: Lessons from the past5
A review of chronic wasting disease (CWD) spread, surveillance, and control in the United States captive cervid industry5
Two Chinese patients of sporadic Creutzfeldt–Jacob disease with a S97N mutation in PRNP gene5
Post COVID-19 AA amyloidosis of the kidneys with rapidly progressive renal failure5
Prion 2024 Conference Abstracts5
Exploring CJD incidence trends: insights from Slovakia5
Insight into the conserved structural dynamics of the C-terminus of mammal PrPC identifies structural core and possible structural role of pharmacological chaperones4
A family with mental disorder as the first symptom finally confirmed with Gerstmann–Sträussler–Scheinker disease with P102L mutation in PRNP gene – case report3
Differential involvement of amyloidogenic evolvability in oligodendropathies; Multiple Sclerosis and Multiple System Atrophy3
Creutzfeldt-Jakob disease after COVID-19: infection-induced prion protein misfolding? A case report2
Serial changes in regional cerebral blood flow in Gerstmann–Sträussler–Scheinker disease caused by a Pro-to-Leu mutation at codon 105 in the prion protein gene2
Specific early electroencephalogram for the diagnosis of sporadic Creutzfeldt-Jakob disease2
A systemic analysis of Creutzfeldt Jakob disease cases in Asia2
18F-FP-CIT PET/CT in a case of probable sporadic Creutzfeldt-Jakob disease with parkinsonism as initial symptom2
Prion 2022 Conference abstracts: pushing the boundaries2
Cellular prion protein distribution in the vomeronasal organ, parotid, and scent glands of white-tailed deer and mule deer1
Chronic Wasting Disease Research in North America: A systematic review highlighting species-wise and interdisciplinary research trends1
Anti-recoverin antibody positive Heidenhain variant CJD: a case report1
Developing neuropalliative care for sporadic Creutzfeldt-Jakob Disease1
The first non-prion pathogen identified: neurotropic influenza virus1
Canine detection of chronic wasting disease (CWD) in laboratory and field settings1
Preventive pharmacological treatment in subjects at risk for fatal familial insomnia: science and public engagement1
Correction1
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