OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Genetic aspects of human prion diseases
Brian S. Appleby, Shashirekha Shetty, Mohamed Elkasaby
Frontiers in Neurology (2022) Vol. 13
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

Smart Nanoscale Extracellular Vesicles in the Brain: Unveiling their Biology, Diagnostic Potential, and Therapeutic Applications
Akanksha Onkar, Fatima Khan, Anshika Goenka, et al.
ACS Applied Materials & Interfaces (2024) Vol. 16, Iss. 6, pp. 6709-6742
Closed Access | Times Cited: 10

Viruses and amyloids - a vicious liaison
Per Hammarström, Sofie Nyström
Prion (2023) Vol. 17, Iss. 1, pp. 82-104
Open Access | Times Cited: 20

UPF1—From mRNA Degradation to Human Disorders
Jacek Staszewski, Natalia Lazarewicz, Julia Kończak, et al.
Cells (2023) Vol. 12, Iss. 3, pp. 419-419
Open Access | Times Cited: 13

The Knowns and Unknowns of Prion Protein in Immune Modulation and the Pathogenesis of Neuroautoimmune Diseases
Naghmeh Abbasi Kasbi, Olaf Stüve
Current Treatment Options in Neurology (2025) Vol. 27, Iss. 1
Closed Access

Identification of the Highly Polymorphic Prion Protein Gene (PRNP) in Frogs (Rana dybowskii)
Hans‐Jürgen Möller, Sae‐Young Won, Sanghun Park, et al.
Animals (2025) Vol. 15, Iss. 2, pp. 220-220
Open Access

Gerstmann‐Sträussler‐Scheinker Disease Presenting as Late‐Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology
Christopher D. Stephen, Claudio Melo de Gusmão, Sharan R. Srinivasan, et al.
Movement Disorders Clinical Practice (2024) Vol. 11, Iss. 4, pp. 411-423
Closed Access | Times Cited: 2

Cerebrospinal fluid p‐tau181, 217, and 231 in definite Creutzfeldt–Jakob disease with and without concomitant pathologies
Andreja Emeršič, Nicholas J. Ashton, Agathe Vrillon, et al.
Alzheimer s & Dementia (2024) Vol. 20, Iss. 8, pp. 5324-5337
Open Access | Times Cited: 2

Accumulation Area of a Japanese PRNP P102L Variant Associated With Gerstmann-Sträussler-Scheinker Disease: The Ariake PRNP P102L Variant
Kohei Suzuyama, Makoto Eriguchi, Hiromu Minagawa, et al.
Journal of Clinical Neurology (2024) Vol. 20, Iss. 3, pp. 321-321
Open Access | Times Cited: 1

Human prion diseases - state of the art 2023
Egon Kurča, Štefan Sivák, Pavol Skáčik
Neurologie pro praxi (2024) Vol. 25, Iss. 1, pp. 19-25
Closed Access | Times Cited: 1

Understanding Creutzfeldt-Jakob disease in Iran: a systematic review of case reports
Alireza Mohebbi, Parastoo Motamedaria, Malihe Naderi, et al.
Journal of International Medical Research (2024) Vol. 52, Iss. 5
Open Access | Times Cited: 1

The advances in the early and accurate diagnosis of Creutzfeldt–Jakob disease and other prion diseases: where are we today?
Hitaru Kishida, Naohisa Ueda, Fumiaki Tanaka
Expert Review of Neurotherapeutics (2023) Vol. 23, Iss. 9, pp. 803-817
Closed Access | Times Cited: 3

Prion Disease After COVID-19: A Case Report
Karim Makhoul, Tova Beeber, Ryan Cordero, et al.
American Journal of Case Reports (2023) Vol. 24
Open Access | Times Cited: 2

Predicting Symptom Onset of Genetic Prion Diseases Using Fluid Biomarkers
Brian S. Appleby
Neurology (2024) Vol. 103, Iss. 2
Closed Access

Genetic prion disease – fatal familial insomnia (clinical case)
T. V. Sorokovikova, А. М. Morozov, A. N. Kryukova, et al.
Acta Biomedica Scientifica (East Siberian Biomedical Journal) (2024) Vol. 9, Iss. 3, pp. 90-94
Open Access

Unfolding Mechanism and Fibril Formation Propensity of Human Prion Protein in the Presence of Molecular Crowding Agents
Manoj Madheswaran, Nataliia Ventserova, Gianluca D’Abrosca, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 18, pp. 9916-9916
Open Access

Démences neurodégénératives
J Cambier, M Masson, Catherine Masson-Boivin, et al.
Elsevier eBooks (2024), pp. 483-496
Closed Access

Theoretical Aspects of Protein Aggregation and Neurodegenerative Diseases
Vishal Singh, Priya Dey
IntechOpen eBooks (2024)
Closed Access

An introduction to neurodegenerative disorders: Pathophysiology, hallmarks, and mechanisms at a glance
Rahul Dilawari, Meghna Barik, Ekta Singh
Elsevier eBooks (2024), pp. 3-16
Closed Access

Overview of human transmissible spongiform encephalopathies
Rebeca Benavente, Celso S. G. Catumbela, Rodrigo Morales
Elsevier eBooks (2024), pp. 529-545
Closed Access

Difficulties in lifetime diagnosis of Creutzfeldt—Jakob disease
О. А. Кичерова, Л. И. Рейхерт, E S Ostapchuk, et al.
S S Korsakov Journal of Neurology and Psychiatry (2024) Vol. 124, Iss. 11, pp. 19-19
Closed Access

Role of Enzymes in Prion Disease: A Molecular Mechanism
Sayed Mohammed Firdous, Sourav Pal, Subhajit Mandal
(2024), pp. 127-151
Closed Access

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