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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:

Insights into Clinical, Genetic, and Pathological Aspects of Hereditary Spastic Paraplegias: A Comprehensive Overview
Liena E. O. Elsayed, Isra Z. M. Eltazi, Ammar Ahmed, et al.
Frontiers in Molecular Biosciences (2021) Vol. 8
Open Access | Times Cited: 57

Showing 1-25 of 57 citing articles:

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
The Role of Spastin in Axon Biology
Ana Catarina Costa, Mónica Mendes Sousa
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 26
The Puzzle of Hereditary Spastic Paraplegia: From Epidemiology to Treatment
Arun Meyyazhagan, Haripriya Kuchi Bhotla, Manikantan Pappuswamy, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 14, pp. 7665-7665
Open Access | Times Cited: 23
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model
Ruizhi Deng, Eva Medico Salsench, Anita Nikoncuk, et al.
Acta Neuropathologica (2023) Vol. 146, Iss. 2, pp. 353-368
Open Access | Times Cited: 13
The role of the PLA2G6 gene in neurodegenerative diseases
Xinyue Deng, Lamei Yuan, Joseph Jankovic, et al.
Ageing Research Reviews (2023) Vol. 89, pp. 101957-101957
Closed Access | Times Cited: 13
Development and validation of TreatHSP-QoL: a patient-reported outcome measure for health-related quality of life in hereditary spastic paraplegia
Jekaterina Malina, Eva‐Maria Huessler, Karl‐Heinz Jöckel, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 5
A Retrospective Review of 18 Patients With Childhood-Onset Hereditary Spastic Paraplegia, Nine With Novel Variants
Mehmet Akif Kılıç, Edibe Pembegül Yıldız, Adnan Deniz, et al.
Pediatric Neurology (2024) Vol. 152, pp. 189-195
Closed Access | Times Cited: 4
Pluripotent Stem Cells as a Preclinical Cellular Model for Studying Hereditary Spastic Paraplegias
Devid Damiani, Matteo Baggiani, Stefania Della Vecchia, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 5, pp. 2615-2615
Open Access | Times Cited: 4
Neurodevelopmental Implications Underpinning Hereditary Spastic Paraplegia
Yiqiang Zhi, Yan Shi, Danping Lu, et al.
CNS Neuroscience & Therapeutics (2025) Vol. 31, Iss. 2
Open Access
“Ears of the Lynx” Sign on Brain MRI in Siblings With Spastic Paraplegia: A Case Report
Qingqing Wang, Manikum Moodley
Annals of the Child Neurology Society (2025)
Open Access
Mechanisms underlying phenotypic variation in neurogenetic disorders
Jean‐Marc Burgunder
Nature Reviews Neurology (2023) Vol. 19, Iss. 6, pp. 363-370
Closed Access | Times Cited: 10
TFG regulates secretory and endosomal sorting pathways in neurons to promote their activity and maintenance
Jennifer L. Peotter, Iryna Pustova, Molly M. Lettman, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 40
Open Access | Times Cited: 14
The hereditary spastic paraplegias
John K. Fink
Handbook of clinical neurology (2023), pp. 59-88
Closed Access | Times Cited: 8
De novo variants cause complex symptoms in HSP-ATL1 (SPG3A) and uncover genotype–phenotype correlations
Julian E. Alecu, Afshin Saffari, Catherine Jordan, et al.
Human Molecular Genetics (2022) Vol. 32, Iss. 1, pp. 93-103
Open Access | Times Cited: 12
GRID1/GluD1 homozygous variants linked to intellectual disability and spastic paraplegia impair mGlu1/5 receptor signaling and excitatory synapses
Dévina C. Ung, Nicolas Pietrancosta, Elena Baz Badillo, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 4, pp. 1205-1215
Open Access | Times Cited: 2
Diving deep: zebrafish models in motor neuron degeneration research
Vranda Garg, Bart R. H. Geurten
Frontiers in Neuroscience (2024) Vol. 18
Open Access | Times Cited: 2
SARM1 deletion delays cerebellar but not spinal cord degeneration in an enhanced mouse model of SPG7 deficiency
Carolina Montoro-Gámez, Hendrik Nolte, Thibaut Molinié, et al.
Brain (2023) Vol. 146, Iss. 10, pp. 4117-4131
Closed Access | Times Cited: 6
Neuroimaging in hereditary spastic paraplegias: from qualitative cues to precision biomarkers
Grainne Mulkerrin, Marcondes C. França, Jasmin Lope, et al.
Expert Review of Molecular Diagnostics (2022) Vol. 22, Iss. 7, pp. 745-760
Closed Access | Times Cited: 10
Expanding the Knowledge of KIF1A-Dependent Disorders to a Group of Polish Patients
Justyna Paprocka, Aleksandra Jezela‐Stanek, Robert Śmigiel, et al.
Genes (2023) Vol. 14, Iss. 5, pp. 972-972
Open Access | Times Cited: 5
Power of NGS-based tests in HSP diagnosis: analysis of massively parallel sequencing in clinical practice
Daniele Galatolo, Rosanna Trovato, Arianna Scarlatti, et al.
Neurogenetics (2023)
Closed Access | Times Cited: 5
A review of the genetic spectrum of hereditary spastic paraplegias, inherited neuropathies and spinal muscular atrophies in Africans
Amokelani C. Mahungu, Nomakhosazana Monnakgotla, Melissa Nel, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 8
A missense mutation in the Hspa8 gene encoding heat shock cognate protein 70 causes neuroaxonal dystrophy in rats
Miyuu Tanaka, Ryoko Fujikawa, Takahiro Sekiguchi, et al.
Frontiers in Neuroscience (2024) Vol. 18
Open Access | Times Cited: 1
Axon demyelination and degeneration in a zebrafishspastizinmodel of hereditary spastic paraplegia
Vranda Garg, Luisa Heyer, Torben Ruhwedel, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Atlastin-1 regulates endosomal tubulation and lysosomal proteolysis in human cortical neurons
Eliska Zlamalova, Catherine Rodger, Francesca Greco, et al.
Neurobiology of Disease (2024) Vol. 199, pp. 106556-106556
Open Access | Times Cited: 1
Generation of a human induced pluripotent stem cell line (FSMi001-A) from fibroblasts of a patient carrying heterozygous mutation in the REEP1 gene
Matteo Baggiani, Filippo M. Santorelli, Serena Mero, et al.
Stem Cell Research (2024) Vol. 79, pp. 103472-103472
Open Access | Times Cited: 1
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