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 2021-02-01 to 2025-02-01.)
ArticleCitations
Preventive pharmacological treatment in subjects at risk for fatal familial insomnia: science and public engagement19
Differential involvement of amyloidogenic evolvability in oligodendropathies; Multiple Sclerosis and Multiple System Atrophy11
Estimating sequence diversity of prion protein gene ( PRNP ) in Portuguese populations of two cervid species: red deer and fallow deer9
A systemic analysis of Creutzfeldt Jakob disease cases in Asia5
Viruses and amyloids - a vicious liaison5
Cellular prion protein distribution in the vomeronasal organ, parotid, and scent glands of white-tailed deer and mule deer5
Penetrance of the V203I variant of the PRNP gene: report of a patient with stroke-like onset of Creutzfeld-Jacob Disease and review of published cases5
A case of V180I genetic mutation Creutzfeldt Jakob disease (CJD) with delusional misidentification as an initial symptom5
The first non-prion pathogen identified: neurotropic influenza virus5
Differentiated cultures of an immortalized human neural progenitor cell line do not replicate prions despite PrP C overexpression5
Expression of the cellular prion protein by mast cells in the human carotid body3
A family with mental disorder as the first symptom finally confirmed with Gerstmann–Sträussler–Scheinker disease with P102L mutation in PRNP gene – case report3
Transcriptomic analysis identifies novel potential biomarkers and highlights cilium-related biological processes in the early stages of prion disease in mice3
Genetic assessment of apolipoprotein E polymorphism and PRNP genotypes in rapidly progressive dementias in Pakistan2
Cerebral cortex swelling in V180I genetic Creutzfeldt–Jakob disease: comparative imaging study between sporadic and V180I genetic Creutzfeldt–Jakob disease in the early stage2
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
A review of chronic wasting disease (CWD) spread, surveillance, and control in the United States captive cervid industry2
Prion meeting 2023: implications of a growing field2
Unmet needs of biochemical biomarkers for human prion diseases2
Prion2022-pushing the boundaries1
Prion 2022 Conference abstracts: pushing the boundaries1
Prion 2024 Conference Abstracts1
Difference of geographic distributions of the Chinese patients with prion diseases in the permanent resident places and referring places1
A case report of fatal familial insomnia with cerebrospinal fluid leukocytosis during the COVID-19 epidemic and review of the literature1
Two Chinese patients of sporadic Creutzfeldt–Jacob disease with a S97N mutation in PRNP gene1
Sheep scrapie and deer rabies in England prior to 18001
Variability in prion protein genotypes by spatial unit to inform susceptibility to chronic wasting disease1
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