Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Hereditary spastic paraplegia: Genetic heterogeneity and common pathways
Emanuele Panza, Arun Meyyazhagan, Antonio Orlacchio
Experimental Neurology (2022) Vol. 357, pp. 114203-114203
Closed Access | Times Cited: 29

Showing 1-25 of 29 citing articles:

Disruption of axonal transport in neurodegeneration
Sarah H. Berth, Thomas E. Lloyd
Journal of Clinical Investigation (2023) Vol. 133, Iss. 11
Open Access | Times Cited: 54
Sphingolipids in neurodegenerative diseases
Xueyang Pan, Debdeep Dutta, Shenzhao Lu, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 24
Betz cells of the primary motor cortex
Matthew Nolan, Connor Scott, Patrick R. Hof, et al.
The Journal of Comparative Neurology (2024) Vol. 532, Iss. 1
Open Access | Times Cited: 8
DDHD2, whose mutations cause spastic paraplegia type 54, enhances lipophagy via engaging ATG8 family proteins
Fei Jia, Xiaoman Wang, Yuhua Fu, et al.
Cell Death and Differentiation (2024) Vol. 31, Iss. 3, pp. 348-359
Closed Access | Times Cited: 7
Clinical and Genetic Spectrum in a Large Cohort of Hereditary Spastic Paraplegia
Yuwen Cao, Haoran Zheng, Zeyu Zhu, et al.
Movement Disorders (2024) Vol. 39, Iss. 4, pp. 651-662
Closed Access | Times Cited: 6
Targeting MDM2 affects spastin protein levels and functions: implications for HSP treatment
Francesca Sardina, Federica Polverino, Sonia Valentini, et al.
Cell Death Discovery (2025) Vol. 11, Iss. 1
Open Access
Biomarkers in Hereditary Spastic Paraplegias
Emanuele Panza, Antonio Orlacchio
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 5, pp. 1950-1950
Open Access
A Case of Hereditary Spastic Paraplegia Type 54 Characterized by Ataxia and Tremor
颖洁 刘
Bioprocess (2025) Vol. 15, Iss. 01, pp. 1-5
Closed Access
Glycerophospholipids: Roles in Cell Trafficking and Associated Inborn Errors
Foudil Lamari, Francis Rossignol, Grant A. Mitchell
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
The metabolism and function of phospholipids in Mitochondria
Jun Dong, Fei Ye, Jiacheng Lin, et al.
Mitochondrial Communications (2022) Vol. 1, pp. 2-12
Open Access | Times Cited: 20
Loss of Fic causes progressive neurodegeneration in a Drosophila model of hereditary spastic paraplegia
Amanda G. Lobato, Natalie Ortiz-Vega, Tijana Canic, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2024) Vol. 1870, Iss. 7, pp. 167348-167348
Open Access | Times Cited: 3
The various forms of hereditary motor neuron disorders and their historical descriptions
Stéphane Mathis, Diane Beauvais, Fanny Duval, et al.
Journal of Neurology (2024) Vol. 271, Iss. 7, pp. 3978-3990
Closed Access | Times Cited: 2
Experimental Cell Models for Investigating Neurodegenerative Diseases
Cecilia Evangelisti, Sherin Ramadan, Antonio Orlacchio, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 17, pp. 9747-9747
Open Access | Times Cited: 2
The Role of Small Heat Shock Proteins in Protein Misfolding Associated Motoneuron Diseases
B. Tedesco, Veronica Ferrari, Marta Cozzi, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 19, pp. 11759-11759
Open Access | Times Cited: 11
Hereditary spastic paraplegias proteome: common pathways and pathogenetic mechanisms
Chiara Martinello, Emanuele Panza, Antonio Orlacchio
Expert Review of Proteomics (2023) Vol. 20, Iss. 7-9, pp. 171-188
Closed Access | Times Cited: 6
A Novel MAG Variant Causes Hereditary Spastic Paraplegia in a Consanguineous Pakistani Family
Rabia Akram, Haseeb Anwar, Humaira Muzaffar, et al.
Genes (2024) Vol. 15, Iss. 9, pp. 1203-1203
Open Access | Times Cited: 1
Biallelic DDHD2 mutations in patients with adult‐onset complex hereditary spastic paraplegia
Ying‐Tsen Chou, Shao‐Lun Hsu, Yu‐Shuen Tsai, et al.
Annals of Clinical and Translational Neurology (2023) Vol. 10, Iss. 9, pp. 1603-1612
Open Access | Times Cited: 4
Movement disorders in hereditary spastic paraplegias
José Luiz Pedroso, Thiago Cardoso Vale, Júlian Letícia de Freitas, et al.
Arquivos de Neuro-Psiquiatria (2023) Vol. 81, Iss. 11, pp. 1000-1007
Open Access | Times Cited: 4
Multiple roles for TFG ring complexes in neuronal cargo trafficking
Ziheng Zhang, Molly M. Lettman, Amber L. Schuh, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Clinical Manifestations Associated with the Domain-Containing Protein 2 Gene Mutation in an Iranian Family with Spastic Paraplegia 54
Abolfazl Yari, Shokoofeh Etesam, Shannaz Zarifi, et al.
Neurodegenerative Diseases (2022) Vol. 22, Iss. 3-4, pp. 139-150
Closed Access | Times Cited: 6
Chiropractic Care in a Patient With Hereditary Spastic Paraplegia and Chronic Pain
Eric Chun‐Pu Chu, Kevin Hsu Kai Huang, Kenny Cheng, et al.
Cureus (2023)
Open Access | Times Cited: 2
Case report: Novel mutations in the SPG11 gene in a case of autosomal recessive hereditary spastic paraplegia with a thin corpus callosum
Ji-Qing Duan, Hui Liu, Jia-Qiao Wu
Frontiers in Integrative Neuroscience (2023) Vol. 17
Open Access | Times Cited: 2
Upregulation of Heat-Shock Protein (hsp)-27 in a Patient with Heterozygous SPG11 c.1951C>T and SYNJ1 c.2614G>T Mutations Causing Clinical Spastic Paraplegia
Juan Antonio García-Carmona, J. Amores, José Soler-Usero, et al.
Genes (2023) Vol. 14, Iss. 7, pp. 1320-1320
Open Access | Times Cited: 2
Hereditary spastic paraplegias
R. F. Kutlubaeva, М А Кутлубаев, Р. В. Магжанов, et al.
Neuromuscular Diseases (2024) Vol. 13, Iss. 4, pp. 74-82
Open Access
AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia
Salimata Diarra, Saikat Ghosh, Lassana Cissé, et al.
Neurobiology of Disease (2024) Vol. 198, pp. 106537-106537
Open Access
Page 1 - Next Page

Scroll to top