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 2022-05-01 to 2026-05-01.)
ArticleCitations
Plaque-type dura mater graft-associated Creutzfeldt-Jakob disease: an autopsied case report30
Detection of chronic wasting disease prions in soil at an illegal white-tailed deer carcass disposal site27
Estimating sequence diversity of prion protein gene ( PRNP ) in Portuguese populations of two cervid species: red deer and fallow deer24
Differentiated cultures of an immortalized human neural progenitor cell line do not replicate prions despite PrP C overexpression12
Expression of the cellular prion protein by mast cells in the human carotid body11
Variability in prion protein genotypes by spatial unit to inform susceptibility to chronic wasting disease9
Transcriptomic analysis identifies novel potential biomarkers and highlights cilium-related biological processes in the early stages of prion disease in mice9
Polymorphism of prion protein gene (PRNP) in Nigerian sheep8
Maternal chronic wasting disease infection restricts fetal head size in white-tailed deer ( Odocoileus virginianus )8
Exploring CJD incidence trends: insights from Slovakia7
Prion 2024 conference: from two decades of growth to a new journey forward7
Post COVID-19 AA amyloidosis of the kidneys with rapidly progressive renal failure7
Chronic wasting disease as a model for human prion therapy6
Addressing chronic wasting disease in Korean farms: topsoil removal and 2N NaOH treatment before cervid restocking6
A review of chronic wasting disease (CWD) spread, surveillance, and control in the United States captive cervid industry6
Prion 2024 Conference Abstracts4
Two Chinese patients of sporadic Creutzfeldt–Jacob disease with a S97N mutation in PRNP gene4
Prion therapeutics: Lessons from the past3
Prion 2025: advancing the understanding and treatment of prion diseases in dialogue with patients and families3
Functional amyloid protein FXR1 is recruited into neuronal stress granules3
Efficient induction of motor neuron disease in transgenic G93A SOD1 mice by prion-like seeding2
Differential involvement of amyloidogenic evolvability in oligodendropathies; Multiple Sclerosis and Multiple System Atrophy2
Prion 2022 Conference abstracts: pushing the boundaries2
A systemic analysis of Creutzfeldt Jakob disease cases in Asia2
Insight into the conserved structural dynamics of the C-terminus of mammal PrPC identifies structural core and possible structural role of pharmacological chaperones2
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 family with mental disorder as the first symptom finally confirmed with Gerstmann–Sträussler–Scheinker disease with P102L mutation in PRNP gene – case report2
Development of a user guide to support administration of the MRC Prion Disease Rating Scale in research and clinical settings for prion diseases2
Canine detection of chronic wasting disease (CWD) in laboratory and field settings1
Specific early electroencephalogram for the diagnosis of sporadic Creutzfeldt-Jakob disease1
Preventive pharmacological treatment in subjects at risk for fatal familial insomnia: science and public engagement1
Correction1
Prion meeting 2023: implications of a growing field1
18F-FP-CIT PET/CT in a case of probable sporadic Creutzfeldt-Jakob disease with parkinsonism as initial symptom1
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
Genetic assessment of apolipoprotein E polymorphism and PRNP genotypes in rapidly progressive dementias in Pakistan1
Cellular prion protein distribution in the vomeronasal organ, parotid, and scent glands of white-tailed deer and mule deer1
Differential pathology of P102L-associated Gerstmann–Stäussler–Scheinker disease: exclusive presence of 8-kDa protease-resistant prion protein vs. co-existence of 8-kDa and type-1 protease-resistant p1
Creutzfeldt-Jakob disease after COVID-19: infection-induced prion protein misfolding? A case report1
In memoriam of Pawel P. Liberski (1954–2025)1
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