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 2021-06-01 to 2025-06-01.)
ArticleCitations
Estimating sequence diversity of prion protein gene ( PRNP ) in Portuguese populations of two cervid species: red deer and fallow deer28
Transcriptomic analysis identifies novel potential biomarkers and highlights cilium-related biological processes in the early stages of prion disease in mice21
Expression of the cellular prion protein by mast cells in the human carotid body14
Differentiated cultures of an immortalized human neural progenitor cell line do not replicate prions despite PrP C overexpression8
Variability in prion protein genotypes by spatial unit to inform susceptibility to chronic wasting disease7
Post COVID-19 AA amyloidosis of the kidneys with rapidly progressive renal failure6
Exploring CJD incidence trends: insights from Slovakia6
Polymorphism of prion protein gene (PRNP) in Nigerian sheep6
Prion 2024 Conference Abstracts5
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
Chronic wasting disease as a model for human prion therapy5
Insight into the conserved structural dynamics of the C-terminus of mammal PrPC identifies structural core and possible structural role of pharmacological chaperones3
Functional amyloid protein FXR1 is recruited into neuronal stress granules3
A family with mental disorder as the first symptom finally confirmed with Gerstmann–Sträussler–Scheinker disease with P102L mutation in PRNP gene – case report2
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
Differential involvement of amyloidogenic evolvability in oligodendropathies; Multiple Sclerosis and Multiple System Atrophy2
Specific early electroencephalogram for the diagnosis of sporadic Creutzfeldt-Jakob disease2
A systemic analysis of Creutzfeldt Jakob disease cases in Asia2
Prion 2022 Conference abstracts: pushing the boundaries2
Developing neuropalliative care for sporadic Creutzfeldt-Jakob Disease1
Chronic Wasting Disease Research in North America: A systematic review highlighting species-wise and interdisciplinary research trends1
Canine detection of chronic wasting disease (CWD) in laboratory and field settings1
18F-FP-CIT PET/CT in a case of probable sporadic Creutzfeldt-Jakob disease with parkinsonism as initial symptom1
Preventive pharmacological treatment in subjects at risk for fatal familial insomnia: science and public engagement1
Anti-recoverin antibody positive Heidenhain variant CJD: a case report1
Cellular prion protein distribution in the vomeronasal organ, parotid, and scent glands of white-tailed deer and mule deer1
The first non-prion pathogen identified: neurotropic influenza virus1
Correction1
A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom1
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