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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:

Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review
Stefania Della Vecchia, Alessandra Tessa, Claudia Dosi, et al.
Journal of Neurology (2021) Vol. 269, Iss. 1, pp. 437-450
Closed Access | Times Cited: 18

Showing 18 citing articles:

Insights into Clinical, Genetic, and Pathological Aspects of Hereditary Spastic Paraplegias: A Comprehensive Overview
Liena E. O. Elsayed, Isra Eltazi, Ammar Ahmed, et al.
Frontiers in Molecular Biosciences (2021) Vol. 8
Open Access | Times Cited: 59
“Trafficking Disorders: Phenotypical Similarities and Differences With Other IMDs”
Àngels García‐Cazorla, Éva Morava, Jean‐Marie Saudubray
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
A Case Series and Review of Febrile-Infection Related Epilepsy Syndrome (FIRES)
Tahnee Spoden, Alice Hoftman, Nanci Rascoff, et al.
Children (2025) Vol. 12, Iss. 4, pp. 485-485
Open Access
Association of variants in the KIF1A gene with amyotrophic lateral sclerosis
Panlin Liao, Yanchun Yuan, Zhen Liu, et al.
Translational Neurodegeneration (2022) Vol. 11, Iss. 1
Open Access | Times Cited: 16
Heterogeneity of comprehensive clinical phenotype and longitudinal adaptive function and correlation with computational predictions of severity of missense genotypes in KIF1A-associated neurological disorder
Khemika K. Sudnawa, Wenxing Li, Sean Calamia, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 8, pp. 101169-101169
Open Access | Times Cited: 3
A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A
Annalaura Torella, Ivana Ricca, Giulio Piluso, et al.
Journal of Neurology (2023) Vol. 270, Iss. 10, pp. 5057-5063
Open Access | Times Cited: 7
A Novel De Novo Missense Mutation in KIF1A Associated with Young-Onset Upper-Limb Amyotrophic Lateral Sclerosis
E Bernard, Florent Cluse, Adrien Bohic, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 15, pp. 8170-8170
Open Access | Times Cited: 2
Positive charge in the K-loop of the kinesin-3 motor KIF1A regulates superprocessivity by enhancing microtubule affinity in the one-head–bound state
Taylor M. Zaniewski, William O. Hancock
Journal of Biological Chemistry (2022) Vol. 299, Iss. 2, pp. 102818-102818
Open Access | Times Cited: 11
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
Dravet syndrome and hemorrhagic shock and encephalopathy syndrome associated with an intronic deletion of SCN1A
Hiroaki Hanafusa, Hiroshi Yamaguchi, H. Kondo, et al.
Brain and Development (2023) Vol. 45, Iss. 6, pp. 317-323
Open Access | Times Cited: 4
Heterogeneity of comprehensive clinical phenotype and longitudinal adaptive function and correlation with computational predictions of severity of missense genotypes in KIF1A-associated neurological disorder
Khemika K. Sudnawa, Wenxing Li, Sean Calamia, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
A Novel de Novo Missense Mutation in KIF1A Associated with Young-Onset Upper-Limb Amyotrophic Lateral Sclerosis
E Bernard, Florent Cluse, Adrien Bohic, et al.
(2024)
Open Access | Times Cited: 1
Illustration of a rare case of hereditary spastic paraplegia type 30 associated with a missense variant in the non-motor domain of KIF1A
Halil Önder, Atay Vural, Neslihan Düzkale, et al.
Journal of Neurology (2022) Vol. 269, Iss. 6, pp. 3343-3346
Closed Access | Times Cited: 1
The net charge of the K-loop regulates KIF1A superprocessivity by enhancing microtubule affinity in the one-head-bound state
Taylor M. Zaniewski, William O. Hancock
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
Long-term Observation of a Japanese Patient with a Multiple-system Neurodegenerative Disorder with a Uniallelic <i>de novo</i> Missense Variant in <i>KIF1A</i>
Katsuya Nakamura, Tsuneaki Yoshinaga, Minori Kodaira, et al.
Internal Medicine (2023) Vol. 62, Iss. 20, pp. 3047-3051
Open Access
Enfermedad neurológica asociada al gen KIF1A: correlación genotipo/fenotipo
Ana Ortiz‐Ortigosa, Rocío Calvo Medina, C. Ruiz-García, et al.
Revista de Neurología (2023) Vol. 77, Iss. 06, pp. 141-141
Open Access
Autosomal dominant neurodevelopmental disorders associated with &lt;italic&gt;KIF1A&lt;/italic&gt; gene variants in 6 pediatric patients
Jingqi Lin, Niu Li, Ruen Yao, et al.
Journal of Zhejiang University (Medical Sciences) (2023) Vol. 52, Iss. 6, pp. 693-700
Open Access
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